EDITOR Charles J. Epstein, M.D. University of California San Francisco, CA ASSISTANT EDITOR Shelley F. Diamond University of California San Francisco, CA EDITOR, HUMAN GENETICS EDUCATION SECTION Kenneth L Garver, M.D., Ph.D. Western Pennsylvania Hospital Pittsburgh, PA ASSOCIATE EDITORS Michael L. Boehnke, Ph.D. University of Michigan Ann Arbor, Ml John C. Carey, M.D. University of Utah Medical Center Salt Lake City, UT Aravinda Chakravarti, Ph.D. University of Pittsburgh Pittsburgh, PA William A. Gahl, M.D., Ph.D. National Institute of Child Health and Human Development Bethesda, MD Jane Gitschier, Ph.D. University of California San Francisco, CA Lynn Jorde, Ph.D. University of Utah School of Medicine Salt Lake City, UT David H. Ledbetter, Ph.D. Baylor College of Medicine Houston, TX Neil J. Risch, Ph.D. Yale University School of Medicine New Haven, CT Stephanie Sherman, Ph.D. Emory University School of Medicine Atlanta, GA Lap-Chee Tsui, Ph.D. The Hospital for Sick Children Toronto, Ontario David Valle, M.D. Johns Hopkins University School of Medicine Baltimore, MD Dorothy Warburton, Ph.D. Columbia University College of Physicians and Surgeons New York, NY Huntington F. Willard, Ph.D. Stanford University Stanford, CA Business communications in connection with nonmember subscriptions and advertising should be addressed to the publisher: The Univer- sity of Chicago Press, Journals Division, 5720 South Woodlawn, Chicago, IL 60637. Remittance for nonmember subscription is payable to the publisher on a calendar-year basis. For domestic nonmember individuals and institutions, the single-copy rate is $21.00 and the calendar- year rate is $250.00; for foreign nonmember individuals and institutions, the single-copy rate is $21.00 (U.S. currency) and the calen- dar-year rate is $250.00 (U.S. currency). Subscription agent for Japan: Kinokuniya Company, Ltd. Nonmembers in other countries add the following rates for each year's subscription to cover postage: Surface mail-$24.00; Airmail: Canada and Mexico-$63.00; Central America-$72.00; Europe, North Africa, and South America-$99.00; all other countries (including Africa, Asia, Australia, Near and Middle East, Oceania, and the USSR)- $131.00. Postmaster: send address changes to The American Journal of Human Genetics, Journals Division, P.O. Box 37005, Chicago, IL 60637. Advertising space in The American Journal of Human Genetics is available, as is rental of its subscriber list. For information and rates, please contact the advertising sales staff, The University of Chicago Press, Journals Division, 5720 South Woodlawn Avenue, Chicago, IL 60637; phone (312) 702-8187 or (312) 702-7361. Advertising and list rental is limited to material of professional interest to our subscribers and does not imply endorsement by The University of Chicago Press or by The American Society of Human Genetics. Memberships.-Student subscriptions are accepted only via membership. For student and all other membership information, contact the Administrative Office, American Society of Human Genetics, 9650 Rockville Pike, Bethesda, MD 20814; phone (301)571-1825. A member- ship application and dues schedule appear at the back of each issue of the Journal. Notice of change of address, which should indude the member's old and new addresses, should be sent to the administrative office at least 30 days before the date of the issue for which the change is to be effective. Correspondence concerning editorial matters should be directed to the Editor. Copying Beyond Fair Use. -The code on the first page of an artide in this journal indicates the copyright owner's consent that copies of the article may be made beyond those permitted by Sections 107 and 108 of the U.S. Copyright Law, provided that copies are made only for personal or internal use or for the personal or internal use of specific clients and provided that the copier pay the stated per-copy fee through the Copyright Clearance Center, Inc., 27 Congress Street, Salem, MA 01970. To request permission for other kinds of copying, such as copying for general distribution, for advertising or promotional purposes, for creating new collective works, or for resale, kindly write to Permissions Department, The University of Chicago Press, 5801 South Ellis Avenue, Chicago, IL 60637. If no code appears on the first page of an article, permission to reprint may be obtained only from the author. Back issues are available from 1980 (vol. 32). Complete volumes are available in microfiche from Kraus Reprint and Periodicals, Route 100, Millwood, NY 10546. Complete volumes and individual issues are available in microform from University Microfilms International, 300 North Zeeb Road, Ann Arbor, MI 41806; phone (313)761-4700. © by The American Society of Human Genetics. All rights reserved.
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EDITORCharles J. Epstein, M.D.University of CaliforniaSan Francisco, CA
ASSISTANT EDITOR
Shelley F. DiamondUniversity of CaliforniaSan Francisco, CA
EDITOR, HUMAN GENETICSEDUCATION SECTIONKenneth L Garver, M.D., Ph.D.Western Pennsylvania HospitalPittsburgh, PA
ASSOCIATE EDITORS
Michael L. Boehnke, Ph.D.University of MichiganAnn Arbor, Ml
John C. Carey, M.D.University of Utah Medical CenterSalt Lake City, UT
Aravinda Chakravarti, Ph.D.University of PittsburghPittsburgh, PA
William A. Gahl, M.D., Ph.D.National Institute of Child Health andHuman Development
Bethesda, MD
Jane Gitschier, Ph.D.University of CaliforniaSan Francisco, CA
Lynn Jorde, Ph.D.University of UtahSchool of Medicine
Salt Lake City, UT
David H. Ledbetter, Ph.D.Baylor College of MedicineHouston, TX
Neil J. Risch, Ph.D.Yale University School of MedicineNew Haven, CT
Stephanie Sherman, Ph.D.Emory UniversitySchool of Medicine
Atlanta, GA
Lap-Chee Tsui, Ph.D.The Hospital for Sick ChildrenToronto, Ontario
David Valle, M.D.Johns Hopkins University School
of MedicineBaltimore, MD
Dorothy Warburton, Ph.D.Columbia University
College of Physicians andSurgeons
New York, NY
Huntington F. Willard, Ph.D.Stanford UniversityStanford, CA
Business communications in connection with nonmember subscriptions and advertising should be addressed to the publisher: The Univer-sity of Chicago Press, Journals Division, 5720 South Woodlawn, Chicago, IL 60637. Remittance for nonmember subscription is payableto the publisher on a calendar-year basis. For domestic nonmember individuals and institutions, the single-copy rate is $21.00 and the calendar-year rate is $250.00; for foreign nonmember individuals and institutions, the single-copy rate is $21.00 (U.S. currency) and the calen-dar-year rate is $250.00 (U.S. currency). Subscription agent for Japan: Kinokuniya Company, Ltd. Nonmembers in other countries addthe following rates for each year's subscription to cover postage: Surface mail-$24.00; Airmail: Canada and Mexico-$63.00; CentralAmerica-$72.00; Europe, North Africa, and South America-$99.00; all other countries (including Africa, Asia, Australia, Near andMiddle East, Oceania, and the USSR)- $131.00. Postmaster: send address changes to The American Journal ofHuman Genetics, JournalsDivision, P.O. Box 37005, Chicago, IL 60637. Advertising space in The American Journal of Human Genetics is available, as is rental ofits subscriber list. For information and rates, please contact the advertising sales staff, The University of Chicago Press, Journals Division,5720 South Woodlawn Avenue, Chicago, IL 60637; phone (312) 702-8187 or (312) 702-7361. Advertising and list rental is limited to materialof professional interest to our subscribers and does not imply endorsement by The University of Chicago Press or by The American Societyof Human Genetics.Memberships.-Student subscriptions are accepted only via membership. For student and all other membership information, contact the
Administrative Office, American Society ofHuman Genetics, 9650 Rockville Pike, Bethesda,MD 20814; phone (301)571-1825. A member-ship application and dues schedule appear at the back of each issue of the Journal. Notice of change of address, which should indudethe member's old and new addresses, should be sent to the administrative office at least 30 days before the date of the issue for which thechange is to be effective.
Correspondence concerning editorial matters should be directed to the Editor.Copying Beyond Fair Use. -The code on the first page of an artide in this journal indicates the copyright owner's consent that copies
of the article may be made beyond those permitted by Sections 107 and 108 of the U.S. Copyright Law, provided that copies are madeonly for personal or internal use or for the personal or internal use of specific clients and provided that the copier pay the stated per-copyfee through the Copyright Clearance Center, Inc., 27 Congress Street, Salem,MA 01970. To request permission for other kinds of copying,such as copying for general distribution, for advertising or promotional purposes, for creating new collective works, or for resale, kindlywrite to Permissions Department, The University of Chicago Press, 5801 South Ellis Avenue, Chicago, IL 60637. If no code appears onthe first page of an article, permission to reprint may be obtained only from the author.Back issues are available from 1980 (vol. 32). Complete volumes are available in microfiche from Kraus Reprint and Periodicals, Route
100, Millwood, NY 10546. Complete volumes and individual issues are available in microform from University Microfilms International,300 North Zeeb Road, Ann Arbor, MI 41806; phone (313)761-4700. © by The American Society ofHuman Genetics. All rights reserved.
HOW TO USE THIS ABSTRACTS VOLUME
The Abstracts volume for the 8th International Congress of Human Genetics serves as the Proceedings andis published as a supplement to The American Journal of Human Genetics. It includes more than 2,800abstracts, an author index and a permuted title index. It will be distributed on site to all scientific registrantsand will be sent to all institutional subscribers to The American Journal of Human Genetics, as well as toall members of the American Society of Human Genetics who do not attend the Congress.
AbstractsThis book contains Congress abstracts whose numbers correspond with those in the separate Program.Asterisks indicate presenters. Each abstract has ONE number located above the title. The same numberidentifies the abstract in the indices described below, and in all listings in the Program. For poster presenta-tions, this is also the number of the board on which the abstract is displayed.
* Oral Presentations: Abstracts on pages 1-89 represent oral presentations inchronological order by day of presentation. Abstracts for Poster Symposia arereferenced in this section on pages 57 and 77 may be found on pages 93-504.
* Poster Presentations: Abstracts on pages 93-504 represent poster presentations.They appear in the author's first-choice topic category, alphabetically by pre-senting author. The term Poster Symposium followed by a session numberindicates that the abstract, in addition to being displayed as a poster presentation,has been chosen by the Program Committee for special presentation in one ofeight Poster Symposia.
Author and Presenter IndexThis index begins on page 505 and includes two types of entries merged into one alphabetical listing.Asterisks indicate presenters.
* Names of all authors on abstracts provided by invited speakers and names of allauthors of contributed abstracts, followed by their numbers.
* Names of all invited speakers from whom abstracts were not available at presstime. Because there is no abstract (and consequently no number), the invitedspeaker's name is followed by the session number.
Permuted Title IndexA permuted title index has been computer generated from key words in abstract titles. This index appearsat the end of the book. Each entry refers the reader to the appropriate abstract by its number (1-2883). Keywords in the title of a paper for which no abstract was supplied are referenced by session (S) number.
i
ii
SPONSORS AND CONTRIBUTORSGeneral Sponsors:American Society of Human GeneticsGenetics Society of AmericaNational Institutes of HealthIntegrated GeneticsMarch of Dimes Birth Defects Foundation
Robert J. Kleberg, Jr. andHelen C. Kleberg Foundation
Applied BiosystemsWellcome Trust
Sponsors of Specific Events:Plenary Lectures .................................................. Imagenetics
Symposia:Gene Therapy and Treatment of Genetic Disease .................................................. Cystic Fibrosis FoundationReproductive Genetics .................................................... Genetics & IVF InstituteGenetic Determinants of Common Metabolic Disorders .................................................... Cetus Corporation
Workshops:Genetics and the Eye .................................... RP Foundation Fighting Blindness, Baltimore, Maryland, and
RP Eye Research Foundation, CanadaNeurofibromatosis .........................................................................*National Neurofibromatosis Foundation
Contributors to Specific Events:Workshops:Heritable Connective Tissue Disorders:Molecular and Phenotypic Correlations ........................ Coalition for Heritable Disorders of Connective Tissue
Molecular Cytogenetics .................................... Oncor, Inc.Skeletal Dysplasias .................................... Shriners Hospitals for Crippled ChildrenPrenatal Biochemical Screening for Chromosomal Abnormalities ................ .................. Amersham CorporationMolecular and Cellular Biology of Duchenne Muscular Dystrophy and
Becker Muscular Dystrophy ...................... Muscular Dystrophy AssociationMitochondrial DNA Mutations in Neuromuscular Disease .............................. Muscular Dystrophy AssociationMyotonic Dystrophy .......................................... Muscular Dystrophy AssociationMolecular Genetic Methods .......................................... MediGene, Inc.Cystic Fibrosis .......................................... MediGene, Inc.Human Neurogenetics .......................................... Muscular Dystrophy AssociationEthical Aspects of Human Genetics ............................ .............. National Society of Genetic CounselorsMolecular Aspects of Fragile X .......................................... Oncor, Inc.Heritable Connective Tissue Disorders:Molecular and Phenotypic Correlations ........................................ Osteogenesis Imperfecta Foundation, Inc.
Union Station Reception ........ ....... Beckman Instruments, Inc. and Perceptive Scientific Instruments, Inc.
General Contributors:RGK FoundationUnited Nations Educational, Scientific and
Cultural OrganizationE. I. du Pont de Nemours & CompanyMerck Sharp & Dohme Research LaboratoriesMerck Sharp & Dohme International DivisionNational Science FoundationBecton Dickinson and CompanyMonsanto CompanyGenetrix, Inc.
Roche Diagnostics ResearchSpringer-Verlag New York, Inc.AmgenGenentech, Inc.Life Technologies, Inc.PromegaGenetics InstituteFisher ScientificLilly Research LaboratoriesRobert Maciel Associates, Inc.
iv
8TH INTERNATIONAL CONGRESS OF HUMAN GENETICS
Officers and Committees
Executive Committee
Victor A. McKusick, President, Baltimore, MarylandWalter F. Bodmer, Vice-President, London, EnglandAndrew Czeizel, Vice-President, Budapest, HungaryLuo Huiyuan, Vice-President, Beijing, P. R.C.John J. Mulvihill, Secretary General,
Pittsburgh, PennsylvaniaMaimon M. Cohen, Treasurer, Baltimore, MarylandLarry 1. Shapiro, Chairperson, Program Committee,
Torrance, CaliforniaMalcolm A. Ferguson-Smith, ex officio,
Glasgow, Scotland
Program Committee
Larry 1. Shapiro, Chairperson, Torrance, CaliforniaArthur L. Beaudet, Houston, TexasAravinda Chakravarti, Pittsburgh, PennsylvaniaDavid M. Danks, Victoria, AustraliaAlbert de la Chapelle, Helsinki, FinlandBeverly S. Emanuel, Philadelphia, PennsylvaniaCharles J. Epstein, San Francisco, CaliforniaUta Francke, Stanford, CaliforniaMitchell S. Golbus, San Francisco, CaliforniaJudith G. Hall, Vancouver, CanadaPeter S. Harper, Cardiff, WalesArmin Dale Kaiser, Stanford, CaliforniaThaddeus E. Kelly, Charlottesville, VirginiaRuben Lisker, Mexico City, MexicoWalter E. Nance, Richmond, VirginiaDavid L. Valle, Baltimore, MarylandAnn P. Walker, Orange, CaliforniaHuntington F. Willard, Stanford, California
Finance Committee
Maimon M. Cohen, Chairperson,Baltimore, Maryland
Alexander G. Bearn, New York, New YorkKaire Berg, Oslo, NorwayNikolai P. Bochkov, Moscow, U.S.S.R.Walter F. Bodmer, London, EnglandHenry Nadler, Chicago, IllinoisEberhard Passarge, Essen, GermanyLeonard Pinsky, Montreal, CanadaDavid L. Rimoin, Los Angeles, CaliforniaJoe Leigh Simpson, Memphis, Tennessee
Editorial Advisory CommitteeCharles J. Epstein, San Francisco, CaliforniaPeter S. Harper, Cardiff, WalesHarold P. Klinger, Bronx, New YorkShiro Miwa, Tokyo, JapanJan Mohr, Copenhagen, DenmarkJohn M. Opitz, Helena, MontanaElizabeth B. Robson, London, EnglandFriedrich Vogel, Heidelberg, Germany
v
8TH INTERNATIONAL CONGRESS OF HUMAN GENETICS
International Advisory CouncilKhalid Al-Ali, Doha, QatarSadika A. Al-Awadi, Safat, KuwaitSergio Arias, Caracas, VenezuelaSalvador Armendares, Mexico City, MexicoRamiro M. Barrantes, San Jose, Costa RicaChristos S. Bartsocas, Athens, GreeceNestor 0. Bianchi, La Plata, ArgentinaMartin Bobrow, London, EnglandHelge Boman, Bergen, NorwayBatsheva Bonne-Tamir, Tel Aviv, IsraelCyril Chapman, Wellington South, New ZealandWan Kyoo Cho, Seoul, KoreaJames F. Crow, Madison, WisconsinRicardo Cruz-Coke, Santiago, ChileMaria de Sousa, Porto, PortugalMaximo Drets, Montevideo, UruguayAdedayo Ejiwunmi, Ogun State, NigeriaTalaat 1. Farag, Sulibikaht, KuwaitF. Clarke Fraser, Montreal, CanadaNewton Freire-Maia, Curitiba, BrazilJean Frezal, Paris, FranceH. Galjaard, Rotterdam, The NetherlandsJose M. Garcia-Castro, San Juan, Puerto RicoEloise Giblett, Seattle, WashingtonE. K. Ginter, Moscow, U.S.S.R.John L. Hamerton, Winnipeg, CanadaNemat Hashem, Cairo, EgyptLuis Heredero, Havana, CubaJerry L. Hsueh, Shanghai, P.R.C.Maricela Jaquez de Gutierrez, Santo
Domingo, Dominican RepublicTrefor Jenkins, Johannesburg, South AfricaOlafur Jensson, Reykjavik, IcelandEi Matsunaga, Mishima, JapanConstantin Maximilian, Bucharest, RomaniaMargareta Mikkelsen, Glostrup, DenmarkFelix Mitelman, Lund, SwedenArno G. Motulsky, Seattle, WashingtonJames V. Neel, Ann Arbor, MichiganIvan G. Nikolov, Sofia, BulgariaReijo Norio, Helsinki, FinlandAndrzej Pawlak, Poznan, PolandC~sar Paz y Mifio, Quito, EcuadorTeresa Perez de Gianella, Irigoyen, PeruNguyen Thi Phuong, Hanoi, VietnamJanchivyn Radnaabazar, Ulan Bator, MongoliaGiovanni Romeo, Genoa, ItalyLeon E. Rosenberg, New Haven, ConnecticutWalter Rosenkranz, Graz, AustriaNadia Sakati, Riyadh, Saudi ArabiaAndres Sanchez-Cascos, Madrid, SpainBekir Sitki Sayli, Ankara, TurkeyAlbert Schinzel, Zurich, SwitzerlandCharles R. Scriver, Montreal, CanadaEva Seemanova, Prague, CzechoslovakiaMargery W. Shaw, Houston, TexasGrant R. Sutherland, North Adelaide, AustraliaGeorge Szemere, Szeged, HungaryIrene Uchida, Hamilton, CanadaHerman van den Berghe, Leuven, BelgiumP. M. Vengesa, Harare, Zimbabwe
Ishwar C. Verma, New Delhi, IndiaFriedrich Vogel, Heidelberg, GermanyTso-Ren Wang, Taipei, ChinaRegine Witkowski, Berlin, GermanyEmilio T. Yunis, Bogota, ColombiaLjiljana Zergollern, Zagreb, Yugoslavia
ICHG Permanent CommitteeMalcolm A. Ferguson-Smith, Chairman,
Glasgow, ScotlandJohn L. Hamerton, Vice-Chairman, Winnipeg, CanadaNikolai P. Bochkov, Vice-Chairman, Moscow, U.S.S.R.Luigi Gedda, Secretary General, Rome, ItalyMarco Milani-Comparetti, Assistant Secretary General,
Ancona, Italy
ICHG Permanent Committee: Area RepresentativesPertti P. Aula, Turku, Finland1. 1. S. Bansal, Patiala, IndiaChristos S. Bartsocas, Athens, GreeceKare Berg, Oslo, NorwayNikolai P. Bochkov, Moscow, U.S.S.R.Angelo Carbonara, Torino, ItalyTirza Cohen, Jerusalem, IsraelAndrew Czeizel, Budapest, HungaryJean De Grouchy, Paris, FranceMalcolm A. Ferguson-Smith, Glasgow, ScotlandEnrique C. Gadow, Buenos Aires, ArgentinaJoe P. M. Geraedts, Maastricht, The NetherlandsWerner Gohler, Leipzig, GermanyJohn L. Hamerton, Winnipeg, CanadaAntoni Horst, Poznan, PolandLuo Huiyuan, Beijing, P.R.C.Trefor Jenkins, Johannesburg, South AfricaJan Lindsten, Stockholm, SwedenRuben Lisker, Mexico City, MexicoEi Matsunaga, Mishima, JapanOrlando J. Miller, Detroit, MichiganJan Mohr, Copenhagen, DenmarkManuel Molina, Bilbao, SpainFrancisco Rothhammer, Santiago, ChileP. H. Saldanha, Sao Paulo, BrazilWerner Schmid, Zurich, SwitzerlandH. G. Schwarzacher, Vienna, AustriaGrant R. Sutherland, North Adelaide, AustraliaG. van den Berghe, Leuven, BelgiumFriedrich Vogel, Heidelberg, GermanySalvador Armendares, ex officio, Mexico City, MexicoBatsheva Bonne-Tamir, ex officio, Tel Aviv, IsraelArno G. Motulsky, ex officio, Seattle, WashingtonJames V. Neel, ex officio, Ann Arbor, MichiganArthur G. Steinberg, ex officio, Cleveland, OhioBernard S. Strauss, ex officio, Chicago, IllinoisS. 1. Geerts, I.G.F. Representative,
Nijmegan, The NetherlandsVictor Buiyzhenkov, W.H.O. Representative,
Geneva, Switzerland
vi
8TH INTERNATIONAL CONGRESS OF HUMAN GENETICS
Congress Management Staff
ASHG/GSA Administrative Office
Gerry Gurvitch, Executive DirectorKaren Gould, ComptrollerMargot Kiley, Membership ManagerKrista Koziol, Publications ManagerMarsha Ryan, Meetings ManagerElaine Strass, Deputy Director
FASEB Office of Scientific MeetingsGeri Goodenough, DirectorDiane Doub, RegistrarNoel Marnane, Administrative AssistantNancy Nootenboom, Meetings ManagerEd Quinones, Meetings AssistantJohn Rice, ComptrollerRobin Roth, Meetings AssistantNancy Sledge, Exhibit ManagerIris Stratton, Accounts ManagerGeorge Wingate, Assistant Comptroller
With special thanks for the invaluable assistance of support staff in bothoffices: Barbara Abbott, Sharon Adler, Judy Ashton, Joan Friedman, GloriaGarber, Candis Galkin, Anne Marie Langevin, Damita McVeigh, Jane Pavlick,Sharon Robinson, Jane Salomon and Gerry Smith.
vii
ABSTRACTS OF ORAL PRESENTATIONS
Abstracts of oral presentations are published in chronological order by day of presentation.Each abstract has ONE number located above the title. The same number identifies theabstract in all listings in the separate Program, and in the author and presenter index and thepermuted title index included in this book. Asterisks indicate presenters.
Abstracts for Poster Symposia are referenced in this section on pages 57 and 77 and may befound on pages 93-504.
Session Number and Type Abstract Numbers Page Numbers
Monday 2: Plenary Lecture3: Plenary Lecture4-15: Concurrent Workshops16-20: Concurrent Slide Sessions
Tuesday 21: Plenary Lecture22-25: Concurrent Symposia26-37: Concurrent Workshops38-42: Concurrent Slide Sessions
Wednesday 43: Plenary Lecture44-47: Concurrent Symposia48-53: Concurrent Workshops54-57: Concurrent PosterSymposia
58-64: Concurrent Workshops
Thursday 65: Plenary Lecture66-69: Concurrent Symposia70-77: Concurrent Workshops78-81: Concurrent PosterSymposia
82-89: Concurrent Workshops
Friday 90: Plenary Lecture91-94: Concurrent Symposia95: Plenary Lecture96: Plenary Lecture97: Plenary Lecture
1No Abstract2-6263-112
113114-127128-185186-235
236237-251252-276
Random Numbers277-310
311312-326327-379
Random Numbers380-420
421422-433No Abstract434435
1
1-1214-23
2424-2627-3738-47
4848-5051-56
5758-63
6464-6667-76
7778-85
8686-88
8889
57CONCURRENT POSTER SYMPOSIA-WEDNESDAY, 9 OCTOBER
Abstracts printed in the Poster Presentation section of this book will also be pre-sented in these poster symposia in the following order by the authors listed.
Session 54: Alzheimer Disease
M. A. Pericak-VanceG. D. SchellenbergR. ParshadL. Fidani
2381:1071:1504:2667:1584:
R. E. TanziS. NaruseH. PotterL. A. FarrerM. l. Melaragno
2057:739:845:
2244:
J. P. CharlieuT. KatsuyaK. SanfordM. Yasunami
Session 55: Chromosome Structure and Function
J. W. ljdoV. M. ParkK. GandelmanT. Haaf
1580:1858:1647:2120:
S. LeskoA. BaldiniK. H. ChooM. Cummings
1645:1657:1643:2575:
D. BroccoliK. GardinerW. BickmoreJ. A. Ciccarelli
Session 56: Sex Determination
RY FechnerX. HeJ. C. C. de AlmeidaL. E. McMorrowH. Ostrer
1685:2395:2238:2341:
G. MarachettiS-W. WangE. K. PivnickD. McElreavey
1190:2393:2227:2343:1859:
R. J. JagerM. A. WalterJ. GriffinM. J. MitchellC. E. Bishop
Session 57: Lipoproteins and Atherosclerosis
H. G. KraftH. HamaguchiA. DunningM. J. Kotze
2682:515:996:
2689:
M. HavilandC. F SingR. R. FrantsM. Kamboh
471:2463:470:
2656:
R. A. HegeleR. WilliamsonM. R. HaydenS. Cole
1992:2811:807:
2290:
2147:1701:1655:1663:
2225:1665:982:
1692:2237:
2434:567:986:
1036:
CONCURRENT POSTER SYMPOSIA-THURSDAY, 10 OCTOBER
Abstracts printed in the Poster Presentation section of this book will also be pre-sented in these poster symposia in the following order by the authors listed.
Session 78: Fluorescent In Situ HybridizationA. Geurts van KesselK. YoshiuraJ. M. HolmesA. J. WyrobekT. Arinami
1626:1673:1607:1355:
S. SchwartzA. KuwanoC. A. GriffinM. B. Qumsiyeh
1306:2156:1697:2066:1696:
E. BryantW. L. KuoL. MorrisonR. FetniJ. Meyne
Session 79: Parent of OriginC. TurleauL. A. CupplesH. TraupeJ. M. FisherD. J. Driscoll
1459:1116:1056:1035:1723:
M. A. GreensteinC. A. WilliamsM. J. MascariH-L. KokkonenR. Weksberg
767:1712:1588:1582:2077:
M. MannensL. D. SpotilaM. B. PetersenR. H. LindenbaumR. A. Lewis
Session 80: Neural Tube Defects and Alpha-fetoprotein Screening
D. A. KingJ. M. ConnorK-J. HsiaoC. J. LimbB. K. Burton
923:1238:1274:1172:1214:1157:
G. KohnG. E. PalomakiR. M. WagnerD. GrayL. LustigG. Cunningham
1205:1173:1135:1235:1183:
K. E. KronquistP. GretherM. Ben-YishayL. A. Oman-GanesW. Hogge
Session 81: Abnormalities of Lysosomal MetabolismN. W. BartonY. A. loannouE. I. GinnsC. B. Whitley
2473:495:
2359:2345:
M. HaskinsM. PotierM. A. RafiC. P. Morris
1075:1067:2356:1018:
A. OshimaE. H. MulesL. PeltonenM. Horowitz
77
1605:1728:1184:1281:1131:
621:2660:2765:1567:2224:
1201:1155:1186:1211:1144:
553:2475:2503:564:
91
ABSTRACTS OF POSTER PRESENTATIONS
All posters are on display throughout the Congress in Exhibit Halls B (board numbers436-1771) and D (board numbers 1772-2883) of the Convention Center. Remember whenentering the poster display area in Exhibit Hall B that the first board number is 436.
The abstracts on the following pages appear in the author's first-choice topic category, andwithin category, alphabetically by presenting author. Each abstract has ONE number locatedabove the title. The same number identifies the abstract in all listings in the separate Program,in the author and presenter index and the permuted title index included in this book, and onthe poster board. Asterisks indicate presenters.
The term Poster Symposium followed by a session number indicates that the abstract, inaddition to being displayed as a poster, has been chosen by the Program Committee forspecial presentation in one of eight Poster Symposia. Thus, the numbers of contributedabstracts selected for Poster Symposia appear twice in the Program: once in the PosterSymposia sessions (random number order) and once in thefollowing poster listings (sequentialnumber order).
Presenting authors will be at their poster boards according to the following schedule. Twoone-hour presentation times are scheduled on different days for each presenting author.
Exhibit Hall B: Poster board numbers 436-1771.Exhibit Hall D: Poster board numbers 1772-2883.
Authors Will Be PresentAt Their Boards On: For Abstracts Ending In:Monday 12:00 PM-1 :00 PM 0 or 2Monday 1:00 PM-2:00 PM 1 or 3
Tuesday 12:00 PM-1 :00 PM 4 or 6Tuesday 1:00 PM-2:00 PM 5 or 8
Wednesday 12:00 PM-1 :00 PM 7 or 9Wednesday 1:00 PM-2:00 PM 0 or 2
Thursday 12:00 PM-i:00 PM 1 or 3Thursday 1:00 PM-2:00 PM 4 or 6
Friday 12:00 PM-1 :00 PM 5 or 8Friday 1:00 PM-2:00 PM 7 or 9
92
Abstracts of Poster Presentations
Topic Category
Biochemical GeneticsCharacterization of Disorders ........................Ecogenetics/Pharmacogenetics .......................Management .............................................Methodology .............................................
Clinical GeneticsCancer .....................................................Characterization of Disorders ........................Embryo-fetal Development/Pathology ..............Management .............................................Molecular Diagnosis ...................Reproductive Genetics (Prenatal/Perinatal).Teratogenesis .............................................
CytogeneticsCancer .....................................................Chromosomal Syndromes .............................Mechanisms ..............................................Methodology .............................................Molecular .................................................
Educational, Psychosocial andSocietal Aspects of GeneticsGenetic Counseling and Psychosocial Issues .....Genetics Education (Patient, Public, Professional)Genetics Service Delivery and Public Policy .....Legal and Ethical Issues ...............................Screening .................................................
Gene MappingComparative ..............................................Linkage ....................................................Methodology .............................................Physical ....................................
Molecular GeneticsDevelopmental Mechanisms .........................Gene Identification and Characterization .........Gene Regulation and Function ......................Gene Therapy ............................................Methodology .............................................Mutagenesis ..............................................Oncogenesis .........
Population GeneticsEvolution ..................................................Genetic Epidemiology .................................Methodology .............................................Mutation ...................................................Population Structure ....................................
Abstract Numbers Page Numbers
436-536537-551552-564565-581
582-623624-907908-946947-957958-11261127-12871288-1296
1297-13971398-15501551-16021603-16381639-1729
1730-17711772-17821783-18121813-18231824-1856
1857-18711872-20522053-21002101-2221
2222-22442245-24052406-24672468-24942495-25322533-25652566-2609
2610-26422643-27802781-27932794-28212822-2883
93-109110-112112-114115-117
118-124125-172172-178179-180181-209209-236236-237
238-254255-280280-289289-295295-310
310-317317-319319-324324-326326-332
332-334335-365365-373373-393
393-397397-424424-434435-439439-445446-451451-458
459-464464-487487-489490-494494-504
505AUTHOR AND PRESENTER INDEX
This index includes two types of entries merged into one alphabetical listing. Asterisks indicatepresenters.* Names of all authors of abstracts provided by invited speakers and names of all authors of
contributed abstracts, followed by their numbers.* Names of all invited speakers from whom abstracts were not available at press time. Because
there is no abstract (and consequently no number), the invited speaker's name is followed by thesession number.
A-
Aase, J.M., 661Abaci, E., 2830Abassi, R., 1693Abbad, A., 839Abbas, N., 2341Abdelhak, S., 1223, 2101*Abdel-Hamid, J., 624Abdel Meguid, N., 624Abdel-Salam, M., 624, 879Abe, K., 1348Abe, M., 545Abe, S., 1052Abe, T., 2148, 2171, 2172Abel, K., 2102*Abel, L., 2643*Abeliovich, D., 1916, 2245*,
2255, 2883Abidi, F., 373Aboul-Ezz, E.H.A., 624*, 715,879
Abrahamson, D.R., 383Abrahamson, M., 1026, 2183Abramson, R.K., 625*Abreu, M.K.C., 580Abuelo, D.N., 626*Abulaban, M., 1346Acaron, S., 1357Accadia, L., 667Acevedo, S., 1334Ackenheil, M., 1094, 2043Acquila, M., 2652, 2794*Acton, R., 2771, 2844Adachi, H., 2172Adam, S., 211*Adams, K.J., 1909, 2340Adams, M., 2026Adams, M.B., 321*Adams, M.D., 2179Adams, P., 1944Adams, R.M., 2469Adams, V., 2406*Adams, W.B., 1127*, 1216Adelsberger, P.A., 1707, 2094Adewale, O., 1398*Adhikary, D., 2833Adler, D., 2421Adler, W., 2694Adler-Brecher, B., 696, 1962Adra, C.N., 736, 958*Aerts, H., 436*, 837Affara, N.A., 598, 2097, 2207Afzal, M., 1164, 1403, 2822*Agarwal, N., 2459Agarwal, S., 565Agarwal, S.S., 565*, 856Aggarwal, A., 944Aguilar, L.C., 950Aguirre, G., 2473Ahmann, P., 2045Ahn, C., 1668Ahnine, L., 2181
Ahrens, E.M., 686Ahuja, Y.R., 1297*, 1363, 1571,2843
Ai, S-X., 2533*Aiken-Hunting, D., 1128*, 1251Ainbender, E., 1261Ainscough, R., 238Airall, E., 1619Aissani, B., 1657, 2256Aitken, D.A., 1155Ajioka, J., 239Ajmar, F., 980Akaboshi, S., 627*Akalin, N., 2246*Akarsu, A. N., 628*Akbas, E., 2537Akierman, A., 927Akifyev, A.P., 1473, 1574Akkerman, C., 1152Akli, S., 1029Akots, G., 74Aksenrod, E., 1730*Aksentijevich, I., 1872*Akstein, E., 461Aktan, G., 628Alagappan, R., 433Ala-Kokko, L., 46, 2461Alali, K., 1346, 1400*Alameida, A., 2118Al Arrayed, S.S., 1399*Alavaikko, M., 2595Al-Awadi, S.A., 1477Albert, D., 2603Albertson, D.G., 2214Alcaide-Loridan, C., 2103*Aldini, A., 1151Aldred, M.A., 1016Aleck, K.A., 1140, 1242Alegria, M., 52Alembik, Y., 537*, 1290, 1442Alexander, D., 860Alexandre, J-A., 1881Alexandrov, I., 1639*, 1694Alexandrov, l.A., 1721Al Hussain, M., 839Ali, M., 981, 2495*Ali, V.R.A., 1617Alitalo, K., 2570Al-Jandal, N., 1313Allan, L., 603Allanson, J., 215Allanson, J.E., 629*AlIderdice, P.W., 1687, 2104*Alleman, J., 52Allen, B., 2105*Allen, C., 1940Allen, L.J., 243Allen, N.A., 200Allen, R.C., 959*Allen, R.G., 1874, 1962Allen, S.L., 1327Allen, W., 630*Alley-Hay, R., 912
Alliende, M.A., 664, 1299*,1309
Allikmets, R.L., 2098, 2579Allison, P., 882Alloisio, N., 1063Allsopp, C.E.M., 2618Almeida, M.R., 960*, 2747Almeida, V.M., 1995Alonzo, A., 1667Alp, N., 2537Alperovitch, A., 2742Al Saadi, A., 1298*Alsaleh, Q.A., 878Altherr, M.R., 961*, 1516, 1651,
2088, 2204, 2210, 2217,2336, 2384
Altland, K., 309, 960, 2747Alvarado, C., 267Alvarez, A., 725Alvarez-Arratia, M., 950Alves, l.L., 2747Alvino, A., 1401Alvira, G., 2761Al Zaman, A., 1346Amacker-North, E., 1783*Amador, A.G., 2566*Amar, A.M., 2877Amaral, O., 837Amato, M., 1401*, 1418Ambinder, R., 623Amemiya, C., 52, 176Amendoeira, M.R.R., 2651Amendt, B.A., 459Amfoh, K.K., 159Amiel, A., 923, 1196, 1551*,
1826Ammala, P., 1847Ammann, W., 227Ammini, A.C., 1229Amorim, A., 1995Amorosi, A., 595Amos, C.l., 582*Amos, J.A., 79, 106, 1913Amselem, S., 437*, 1927, 2455Amster, R., 1208Amyot, K., 1178An, J., 2876Anagnou, N.P., 337*Anand, R., 18, 376Anandaraj, M.P.J.S., 445, 486,
731Anand Rao, G.A., 691Andermann, E., 1913, 2289,2662
Andersen, L., 2339Andersen, L.B., 98*, 223, 2133,
2328, 2818Andersen, R.N., 1844Andersen, T.I., 218, 2567*Anderson, B., 2813Anderson, C.E., 1467Anderson, G.J., 2363Anderson, I.J., 1723
Anderson, K., 129*Anderson, K.P., 1589, 2247*Anderson, L., 1888, 2811Anderson, L.H., 1592Anderson, M.A., 2163Anderson, M.D., 15Anderson, R., 2248*Anderson, R.A., 1059Anderson, S.J., 2249*Anderson, V.E., 833Anderson, W.F., 2479Andersson, B.S., 1709Andersson, Y., 25*Ando, A., 1862Andrade, J.A.D., 2823*Andreadis, A., 2334Andres, R., 2694Andresen, B., 195Andresen, P.A., 1107Andrews, E., 532Andrews, J., 1139Andria, G., 805, 872Andriuskeviciute, I., 1595Angastiniotis, M., Session 30Angelicheva, D., 962*Angrist, M., 2020Anguiano, A., 106*Anhalt, G.J., 1597Annab, L.A., 2134Annas, G.J., 209*Anner6n, G., 2106*Anokhin, A., 2028Antich, J., 1153Antignac, C., 2252Antonarakis, S.E., 74, 410, 416*,
1588, 1682, 1690, 1707,1968, 2094, 2196, 2283, 2453
Antonelli, A., 677, 1873*, 1937Antozzi, C., 35Anusri, Y., 1621Anvret, M., 1044, 2293Anyane-Yeboa, K., 1453, 1824*Aoki, K., 1071Aoki, T., 438*, 512Apak, M.Y., 797, 838Apak, S., 1987Appelman, Z., 1130*Applebaum, M., 1278Applegarth, D., 563, 804Aprelikova, O., 2544Ara, F., 1019Arana, R., 1328Aranda, M., 1299Aranha, I.P., 1552*Arcas, J., 761Archibald, A.L., 429Ardinger, H., 2369Arechaederra, M., 754Arena, J.F., 716, 963*, 1104,2015
Arenas, S., 1328Arenstorf, H.P., 2511Argente, J., 2084
Author and Presenter Index
Arias, S., 1553*Arias-Mendoza, F., 908*Arinami, T., 567, 1131*, 2672Aristi, G., 908Armanet, L., 2655Armatis, P.E., 1438Armendares, S., 840Armfield, K., 457Armour, J., 1965Armstrong, D., 924Armstrong, M., 541Armstrong, M.J., 1232Armstrong, R.M., 2222*Arn, P.H., 827, 1132*Arnaud, D., 146Arnaudo, E., 34Arnheim, N., Session 34Arnold, G.L., 439*Arnold, J., 2121Arnold, N., 1857*Arnoldus, E.P.J., 180Arnopp, J., 2701Arnos, K.S., 22, 28*, 79Aronson, Jr., N.N., 458, 2355Arosa, F., 1624Arps, S., 1300*Arregoces, C., 725Arrieta, M.I., 631*Arroyo, P., 1604Artan, S., 1301, 1302Arteaga, M., 908Arwert, F., 1990, 2250*, 2408Asaka, A., 1531, 2644*, 2693,
2721, 2772Asakawa, J., 440*, 506, 2793Asaoka, H., 2286Aseev, M., 965Asher, D.M., 1003Asher, J., 79Asherson, P., 1986Ashhar, E., 1164Ashizawa, T., 2222, 2287,
2407*, 2501Aslanidis, C., 52, 176, 405Asmundsson, P., 1902Astete, C., 847, 2659Astolfi, P., 2645*Aston, C., 2656, 2669, 2689,2708
Astruc, J., 510Atalianis, P., 2047Atasoy, S., 2830Athwal, R.S., 1627, 2314, 2547,
2568*, 2587, 2601Attanasie, M., 1797Attardi, G., 36Attree, O., 2352Aubin, G., 2840Aubry, M., 2166, 2191, 2251*Auerbach, A.D., 696, 1874*,
1962, 2535Aughton, D.J., 632*Augustus, M., 583*Aula, P., 1022, 1482, 2013Aulehla-Scholz, C., 2280, 2302Aupetit, J., 447Austin, M.J.F., 2534*Austruy, E., 2252*Autenrieth, M., 1633Autio, S., 1630Aventuro, J., 1602Avigad, S., 584*, 2883Avila, C., 794Aviram, A., 640, 1245, 1554*Aviv, H., 1546
Avivi, L., 1312, 1554, 1577,1640, 1653
Avner, P., 146*, 2259Avraham, K.B., 418Awata, H., 987Axelrod, F.B., 1880Axelrod, J., 2488Axelsen, P.H., 2632Aylsworth, A.S., 1651Aylward, E., 828Ayme, S., 135*, 234, 1529,
1799, 1825*Azen, C., 836Azen, E., 2253*Azevedo, E.S., 2651Azfer, M.A., 1164, 1403*Azimi, F., 1472Azouz, E.M., 633*Azuma, T., 2090, 2148, 2254*
Babron, M-C., 1881Babu, A., 748, 1521Bacchetti, S., 1559Bach, G., 2255*Bach, I., 11, 24Bach, J., 781Bachinski, L., 2107*, 2287,
2310, 2321, 2368, 2501Bachner, L., 2371Bachy, A., 891Bachynski, B., 682Badiali, M., 602Baenziger, J., 2303Baer, R., 634*Bagent, S., 1327Bagga, P.S., 2314Bagley, R., 2212Bahuau, M., 635*Bai, J., 1449Baiget, M., 1875, 1984, 2674Bailey, J., 1940Bailey, L.C., 2352Bailey-Wilson, J.E., 71Bailly, J., 404Bainton, J., 2554Baird, P.A., 355*, 2745Baird, W., 1638Baker, E., 379Baker, J., 225, 423Baker, J.C., 1555*, 1659Bakker, E., 964*, 984, 989, 1100Baktha, A., 237Balarin, M.A.S., 2673Balazs, I., 2824*Balbul, A., 452Balcells, S., 1875*Balci, S., 636*Baldini, A., 91, 1722, 1858*,2147
Baldrich, K., 2346Baldrich, M., 2346Baldwin, C.T., 2497Bale, A.E., 595, 1353, 2583Baley, P., 2478Ball, M.J., 2811Ballabio, A., 55*, 96*, 204, 805,
2092, 2174, 2259, 2294, 2307Ballard, L., 2150Ballerini, G., 444Ballesta, F., 1404*, 1515Ballester, F., 383Ballester, R., 98Ballester, S., 2591Ballhausen, W., 2206
Ballinger, S.W., 2610*Balogh, E., 1350Balow, Jr., J.E., 1872Baltimore, D., 119*Bamba, M., 491Bamberger, E., 1686Bamforth, J., 1488Bandini, S., 595Bankier, A., 133*, Session 27,2125, 2646*
Bankovi, G., 2874Banks, S., 2056Bansal, I.J.S., 2825*, 2832Bao, Y., 2277Bapat, B., 1876*Bar, S., 16Bar-Am, I., 1640*, 1653Baran, B., 2663Baranov, V., 965*, 1004, 1615Barba, H., 2558Barbieri Neto, J., 1308, 1360Barbosa, C.A.A., 2673Barbujani, G., 2882Barby, T., 1089Bardoni, B., 2092Barichard, F., 1572Barinova, E.l., 2333Barisheva, E., 1947Barkai, G., 640, 1245Barker, D.F., 1126, 1998, 2220Barker, P.E., 2249Barletta, C., 1405*, 1451Barlow, D., 1272Barlow, G.K., 164Barlow, K., 1772*Barnea, E., 16Barnes, D.E., 295*Barnes, G., 82Barnes, I., 1551, 1826*Barnes, L., 1362Barnstein, B., 468Baron, M., 2029Barr, C.L., 1877*, 1941, 1988Barr, F., 370Barranger, J.A., 436, 552*, 557,
2486, 2492Barrett, i.C., 2134Barrick, J., 2123Barrios, B., 1791, 1827*Barron, L., 966*, 1884Bartels, C.F., 546Barth, M.L., 2675Bartholomei, M.L., 1339Bartlett, R.i., 967*, 2272Bartley, J., 474Bartnoff, N., 1261Bartolomei, L., 437Barton, D., 1281Barton, N.W., 553*Barton, S.A., 803Bartsch, O., 1588Bartsocas, C.S., 637*Barwell,J.A., 2116Baparan, A., 1301*, 1302Baparan, N., 1301, 1302*, 1374Baparan, S., 1402, 1406*, 1707Bascom, R.A., 10Bashan, N., 2551Baska, R.E., 712Baskaran, N., 2511Baskaya, G., 2831Bassan, M., 1554Bassett, A.S., 638*Basso, G., 602Basu, S.K., 2678Basys, V., 1595
Batanian, J.R., 1641*Bateman, J.B., 1945Bates, F., 1347, 1450Bates, G.P., 102*, 298, 2204,
2336, 2348, 2383Batista, D.A.S., 1407*Bat7Miriam Katznelson, M., 585*,
640, 1245Batsone, P.J., 1441Battin, J., 639*, 751Baty, B., 214*Baumiller, R., 1813*Baxendale, S., 102Baxter, B.T., 460, 496, 534Beall, M.H., 1133*Beall, S., 100*Bear, C.E., 2364Bear, J.C., 226*Beards, F., 970Beasley, S.W., 2646Beaty, T., 864, 2724Beauchamp, R.L., 2553, 2605Beaudet, A.L., 251*, 1897, 2157Beauregard, L.J., 1203, 1134*Bebelman, J.P., 2408*Bebout, J., 80, 1992Beccaro, F., 654Bech-Hansen, N.T., 1878*Beck, J.S., 1097, 2059Beck, L., 1086Becker, D., 2435Beck-Lippert, W., 1519Bedford, H.M., 1378, 1662Beer, A.E., 932Beer-Romero, P., 433Beggs, A., 1062Behbehani, A., 1313Behm, G., 850Behnke, C., 488Behrend, C., 1664Behrendt, H., 1331Beighton, P., 23*, 24, 79, 344*Beiguelman, B., 2647*Beitel, L., 267Bejerano, M., 585Beker, R., 2883Belani, K.G., 564Beldjord, C., 90Belen, G., 932Belfroid, R., 1100Bell, D.A., 2500Bell, M.V., 376Bell, N., 1821Bell, W., 880Bellec, V., 1408*Bellis, M., 2057Bello, M.J., 1310, 1332Belmaaza, A., 2513, 2611Belmar, P., 443Belmont, J.W., 959, 2468*Belon, C., 751Belsham, D.D., 441*Belt, M., 1715Belyaev, I.Y., 1574Benacerraf, B., 276*Bender, B., 213Bender, J.C., 712, 810Benedetti, L., 2223*Bengtsson, U., 1651, 2168Benham, F., 2108*, 2136Benke, P.J., 443*, 716, 1465Benkendorf, J., 1814*Benkhalifa, M., 1684Benlian, P., 2804Benn, P.A., 586*Bennett, H.S., 1409*
506
Author and Presenter Index
Bennett, J. D., 1481Bennett, W., 592Bennett, W.P., 587*, 610Benninger, M.S., 1385, 1393Ben-Nun, I., 1196Benoy Kurian, G., 746Benson, G., 2196Bentley, D.R., 18, 1005, 1089,
2109*, 2125Bent-Williams, A., 1457, 1549Ben-Yishay, M., 1135*, 1165,
1243Ben-Yoseph, Y., 442*Berdoukas, V., 968*Berg, C.M., 2505Berg, D.E., 2505Berg, K., 39*, 161*, 2658, 2755Berg, M.A., 969*Berg, R.L., 2795*Berg-de Ruiter, E.v.d., 1311Berger, C.S., 1377, 1642*Berger, W., 11Bergere, M., 1258Bergin, A., 864Berk, T., 1876Berkenstadt, M., 640*Berkman, N., 2329Berkovitz, G.D., 2225Berlin, Y.A., 1095Bernal, ).E., 2761Bernard, L.E., 2110*Bernardi, F., 444*, 1685Bernardi, G., 1657, 2256Bernini, L.F., 1865, 2517Bernstein, J., 740Beroud, C., 2247Berquin, P., 769Berrettini, W.H., 1879*Berry, K., 1565Berry, M., 1509Berry, R., 1410*, 1505Berry, S.A., 641*Berson, E.L., 8, 9*, 799, 2173Bertheas, M.F., 1323, 1572Berthelon, M., 449Berthelot, J., 559, 2712Bertin, T.K., 2801Bertolini, S., 980Beschorner, W., 623Beskrovnaya-lbraghimov, O., 20Besmond, C., 437, 463, 588Bessis, J.L., 502Besson, J., 860Bessudnova, S.S., 1136*Best, R.G., 1821, 1828*Bester, R., 1494Betard, C., 515, 2682Betournay, N., 815Bettecken, T., 2256*Beutler, E., 279*Bever, R.A., 2854Beverstock, G.C., 1303*, 1556Bhagyavathi, M., 746Bhatnagar, D.P., 2752Bhatt, M., 2163Bhattacharya, S.S., 1661, 1974Bhattacharyya, N., 2569*, 2638Biaggioni, I., 1037Bialer, M.G., 642*Bianchi, D.W., 60*Bianchi, F., 2762Bianchi, M.S., 2228, 2570Bianchi, N.O., 2228, 2570*Bichlmaier, R., 2262Bick, D.P., 1841Bickmore, W., 1643*
Biddison, W., 100Bidichandani, S., 1244Bieber, F.R., 26, 2338Biegel, J.A., 219*, 370Bies, R., 2174, 2385Bigbee, W.L., 2535*, 2541, 2546Bigelow, L.B., 909Bijisma, EK., 2585Biller, D., 809Billingsley, G.D., 1979Billotto, R., 2138, 2198Billstrand, C., 932, 1829*Binkert, F., 647, 1707, 1711Birch, P.H., 1909Bird, T., 1083, 1952, 2811Bishop, C.E., 1859*, 2238, 2343Bishop, D.F., 2475Bishop, D.T., Session 58, 2026Bishop, T.R., 2409*Bissell, M., 2797Bistritzer, T., 1446Bitoun, P., 643*Bittner, M., 1697Bixenman, H.A., 1137*, 1316Blachmann, T., 659Black, S.H., 1841Black, T., 82Blackburn, B., 214Blackburn, E., 236*Blackman, V., 1532Blackston, R.D., 88, 1411*, 1517Blaese, M., Session 91Blagowidow, N., 1138*Blaichman, S., 773, 1502Blake, D., 17, 835Blakemore, A., 195Blakemore, K., 1139, 1714Blancato, J., 1412*, 1693Blanchet-Bardon, C., 1927Blanco, G., 2595Blangero, J., 2648*, 2764Blank, C., 1413*Blanquet, V., 588*, 621Blanton, S.H., 1013, 1871, 1981Blasi, F., 1948Blau, H.M., 21*Blazar, B.R., 564Blecher, S.R., 2227Bliek, J., 767, 2144Blitzer, M.G., 561, 975, 1139*,
1832, 2709Bloch, M., 211Block, A.W., 1304*Blonde, L., 2361Blonden, L.A.J., 2357Bloom, K.E., 641Blouin, J.L., 1528, 2119Blount, P., 2571*Blum, L., 1194Blume, J.E., 2445Blumenfeld, A., 1880*Blumenthal, D., 1414*, 1444Bnait, K.S., 1296Boavida, M., 767Bobrow, M., 380*, 970*, 1011,
1089, 1965, 2109Bocharova, T., 992Bochkov, N.P., 335*, 2796*Boddy, A.V., 538*Bodmer, J., 589*, 590Bodmer, W.F., 1*, 590*, 2206Bodrug, S.E., 1966, 2042Bodurtha, J., 28, 663, 1160,
1280, 1415*, 2790Boegman, R.J., 233Boehm, C., Session 83, 1182
Boehnke, M., 158*, 2040Boeke, J., 188Boerwinkle, E., 67*, 2631, 2800Boespflug-Tanguy, O., 971*Boezeman, J., 2765Bogaert, R., 349, 522Bogan, J., 433Boggs, S., 2486, 2492Bohlander, S.K., 2053*Bohlman, M.C., 995Boileau, C., 1881*, 1883, 2804,2848
Bojsen-Moller, M., 821Bokesoy, I., 644*Bokkala, S., 445*Boldog, F., 2098, 2579Bolhuis, P., 1990Bollag, G., 12Bolle, R., 1107Bolognia, J.L., 1353Bolos, A.M., 1882*, 1907Bolton, B., 2054*Bolton, K.D., 669Boltshauser, E., 645*Bolund, L., 92*, 195, 1948, 2476Boman, H., 228Bonatti-Pelli6, C., 90, 1881,2848
Bonanno, C.T., 2838Bonaventure, J., 446*Bond, S.L., 2410*Bonifas, J.M., 2257*Bonizzato, A., 1078Bonkovsky, J., 433Bonneau, D., 1061Bonnefont, J-P., 259, 447*Bonnet, F., 2725Bonne-Tamir, B., 2883Bonney, G.E., 159, 601, 1963,
Session 58Bono, M.R., 2103Bonthron, D.T., 2111*, 2415Boone, L.Y., 1601Boorn, N.v.d., 2042Boosalis, M., 2258*Booth, C., 1829Bootsma, D., 293*B66varsson, M., 1902Bordet, S., 267Borecki, I.B., 2649*, 2714, 2739Borell, T., 216Borenstein, P.E., 1790Borenstein, T., 1202Borgaonkar, D.S., 358*Borghgraef, M., 2672Borglum Jensen, A., 1948Borgo, G., 1078Borochowitz, Z., 646*, 1833Borot, N., 2827*Borowitz, S., 533B~rresen, A-L., 218*, 2567,2593, 2803, 2813
Borsani, G., 96, 2259*Bosch, D.A., 2585Bose, D., 1911Bosman, F., 1386Bosque, P.J., 2390Bots, G.T.A.M., 616Bottani, A., 647*Bottema, C.D.K., 70, 2632, 2821Bottema, M.J., 2821Bouchard, C., 2649, 2878Bouchard, J-P., 1900, 2004Boudailliez, B., 769Boue, A., 108*, 1747, 1849,2058
BouWJ., 1042, 1747Boughman, J.A., 780, 2650*,2668
Boulay, B., 2289Bourdarias, J-P., 1881Bourgeron, T., 503Bournikos, K., 1793Boutte, M.I., 233, 544Bowcock, A.M., 2254, 2373Bowden, D.W., 74*, 2008Bowen, J.H., 2829Bowyer, S., 749Boxer, M., 1441, 1883*Boyajian, M., 834, 956Boyce, A., 1733Boyce, F.M., 15, 1943, 2112*,2332
Boyd, E., 1455, 1644*Boyd, P.A., 112, 1567Boyd, S.B., 1934Boyd, Y., 2260*Boye, E., 1011Boyer, S.H., 2409Boyer Smith, S.B., 554*Bozon, D., 2261*Bozorgi, N., 1278Bracha, H.S., 909*Brachman, D., 2577Bracken, R.B., 2606Bradley, A., 2493Bradley, D., 1012Bradley, J., 2646Bradley, L.A., 1140*, 1242, 1828Bradt, D.W., 1898Brady, R.O., 553, 2471Brady, S., 1257Brahe, C., 2113*Brainerd, E., 2548, 2554Brambati, B., 935Brancati, C., 1964, 2727Brandi, M.L., 595Brandriff, B., 176, 182Brandriss, M.C., 2279Brandt, C.A., 1416*, 1596Brandt, J., 1751, 1822Brandt, M., 2469*Brandt, N.J., 1848Brandt, T., 1256Branscomb, E., 176, 182, 2203Brantly, M., 2326, 2797*Bras, M., 1240Bratthauer, G.L., 2580Braun, A., 2262*Braun, G., 672Braun, J., 2812Brauner, R., 2341Bray, J., 2030Bray, P., 2263*Brdicka, R., 2826Breakefield, X.O., 1880, 2196,
2303, 2353Breed, A.S.P.M., 1527Breg, W.R., 728Brenholz, P., 1453Brennecke, S.P., 1156Brenner, J., 1413Brereton, A., 2818Bressler, S., 2421Bressman, S., 2353Breukel, C., 2132, 2216Breuning, M.H., 185, 1303,
1556*, 1994, 2371Brewer, G.J., 947*, 1871Brewster, S., 1956Briard, M.L., 755, 1223, 1939,1959
507
Author and Presenter Index
Bricarelli, D., 1685Bridge, J., 1305*Bridge, P.J., 972*, 1888Brin, M., 2353Brink, L., 1920Brink, P.A., 1920Briscioli, V., 752Brisebois, J.J., 2536*Brito, J., 1492Britt, B.A., 429Britt, D.E., 2149Brivet, M., 259Brizard, A., 1323Broadhead, W., 14, 2037Broccoli, D., 1645*Brock, D.J.H., 77, 306*, 966,
1016, 1842, 1884*, 1919,2311
Brockdorff, N., 1106Brocker-Vriends, A.H.J.T., 984Brockington, M., 1010, 2032Brodeur, G.M., 2133, 2193,2215
Brody, B., 2479Brody, L.C., 202, 2519Broekman, A., 1470Bragger, A., 2803, 2813Bronson, S., 2114*Bronstein, I., 2518Bronstein, S., 461Brook, J.D., 1916, 2115*Brooks, C.C., 2264*Brooks, L.D., 2055*Brooks-Wilson, A.R., 1956Broome, D., 1129, 1417*Bross, P., 195Brostram, K., 187Brouwer, R., 2585Brower, A., 789Brown, C.A., 283Brown, CQ., 97*, 2307Brown, D., 207Brown, D.R., 2051Brown, G.K., 2416Brown, J., 1661Brown, J.A., 1713Brown, K., 1165, 2740Brown, L., 433Brown, L.J., 1646*Brown, M.D., 973*Brown, N.C., 2499Brown, P., 1003Brown, R., 768, 2394Brown, R.H., 1910Brown, R.M., 2416Brown, W.T., 1141*, 1501,
1550, 1908Browne, D., 53, 1126Brownstein, B., 2204, 2339Brubacher, M.G., 2411*Brun, J.L., 1142*Brunner, H.G., 24*, 194Brunner, P.O., 645Bruns, G., 196*, 1572, 2173,2241
Brunschwig, A., 709Brunzell, J., 470, 2434Brusco, D.M., 2091Brusnicky, J., 2176Bryant, E., 1306*Bryke, C.R., 1628Brynes, R.K., 619Brzustowicz, L.M., 1239, 1885*,
1943, 2112, 2332Bu, X., 2781*Bucan, M., 298
Buchan, H.L., 2589Bucher, M., 1417Buchwald, M., 2376, 2496*Buckle, V., 376Buckler, A.J., 223, 2201, 2383Buckley, D., 1603*Buckley, M.F., 1307*Budak, T., 2537*Budarf, M.L., 57, 86, 199*Budden, S., 2293Buehler, B., 496, 534Buentello, L., 791Buetow, K.H., 772, 1754, 1901,
1966, 1971, 2017, 2265*,2350, 2369, 2774
Buijs, A., 2582Buikstra, J., 2617Buist, N., 2264Bukler, A., 2115Bull, L.N., 299Bull, P.C., 2116*Bulman, D., 2319Bulman, D.E., 810Bulut, A., 838Bunchman, T.E., 705Bundey, S., 1942Buraczynska, M., 203, 1654Burch, M., 1763Burd, L., 1256, 1641Burger, H., 2295Burger, J., 2703Burghes, A.H.M., 205, 1886*,
2319, 2443, 2489Burk, C.D., 219Burke, B.M., 1784*Burke, J., 2030, 2663Burke, R., 2353Burkhart-Schultz, K., 2550Burkholder, S.W., 1467Burlet, P., 1223, 2101Burn, J., 591*, 816, 901, 1518,
1661, 1664Burns, A.L., 2266*Buroker, N., 2828*, 2836, 2852,2867
Burough, F., 160Burschyk, M., 110Burt, B.A., 1143*Burton, B.K., 1144*, 1197, 1233,
1256, 1787Buser, M., 2788Bussaglia, E., 547Bustos, T., 648*, 812Butler, B.B., 2603Butler, J.D., 448*Butler, J.H., 684Butler, M.G., 655, 709, 948*,
1056, 1365, 1459Butler, W., 1178Buxton, J., 2310Buyakova, O.1., 2333Buys, C.H.C.M., 224*, 1093,
1926, 2607Buzhievskaya, T., 2782*Byers, P.H., 347*, 626, 2464Byrd, L.K., 649*Byrum, R., 2248Byskov, A., 1948Byth, B.C., 17, 2379
-C-
Cabello, P.H., 2651*Cacheiro, N.L., 1487Cadiou, H., 2073Cadle, R.G., 137
Caffarelli, M., 1278Cahill, T.C., 1681Cai, H., 239Cai, S.P., 391Cai, Y., 2288Caillaud, C., 449*I;akmak, A., 1301, 1302Calabro, A., 2762Calabr6, V., 1964Calandra, S., 980Calarco, P.G., 2239Call, K., 2258Callahan, D., 1580Callan, H.G., 317Callanan, N.P., 1651, 1814Callegari-Jacques, S.M., 256Callen, D.F., 2124Calvano, S., 1703Calzolari, E., 949*, 1685, 2762Calzone, R., 1401, 1418*Camargo-Guerrero, M., 1557*Camerino, G., 2092Cameron, C., 974*, 2599Cameron, J., 1289Campbell, E.W., 2167, 2499Campbell, K.P., 20*, 2385Campbell, M.L., 2167, 2499Campbell, T., 1692Campell, B., 1619Campo Sampedro, F.M., 692Camurri, L., 910*, 911Canapa, A., 2555Can Baaer, K.H., 1301Canick, J.A., 1238Canki-Klain, N., 650*Cann, R.L., 168*Cans, C., 1562Cantarelli, M., 910, 911*Cantor, R.M., 1945, 2783*Cantu, E.S., 1558*Cantu, J.M., 685, 844, 950*Cantu-Reyna, C., 450Cao, A., 150*, 250*, 392*Cao, N., 1853Cao, Q., 1389Capecchi, M., 2418Capel, B., 2393Capelli, E., 2561Caporossi, D., 1559*Capossela, A., 2137Cappellacci, S., 1993Capra, J.D., 425*Capra, V., 96, 204Caprino, D., 2652*, 2794Capua, A., 389Cara, A., 2420Carapetian, J., 651*Carbonen, C., 437Cardesa Garcia, J.J., 692Cardieri, J.M., 2863Cardinet, G.H., 464Carey, A., 901, 1518Carey, J.C., 174*, 214Carey, T.E., 1385, 1393Carlin, M.E., 716, 1146, 1755,
1773*Carlock, L., 1651, 2267*, 2335,
2391, 2399Carlson, A., 1394Carlson, D.E., 652*, 704Carlson, E.J., 2229Carlson, G.A., 2056*Carmi, R., 653*, 1139, 1413Carmichael, P., 592*Carmody, G.R., 2829*Carnevale, A., 450*
Carpenter, A., 963Carpenter, N.J., 848, 1887*Carpenter, S., 1955Carrano, A.V., 52, 176*, 182,2203
Carrazana, M., 2845Carreau, M., 2412*Carrera, P., 654*Carrillo, J., 1173Carritt, B., 224Carroll, A.J., 225, 1804Carrozzo, R., 805, 2092, 2294Carskadon, M., 2763Carson, N.L., 1888*Carson, W.J., 1889*, 1900Carstens, B., 1410Carter, D., 2057Carter, N.P., 1680, 2214Carter, P., 889Cartier, L., 1145*, 1273Cartron, J.P., 2625Carvajal, M.V., 1419*Carver, V.H., 1146*Casalaro, A., 2420Casals, T., 988, 1074, 1084Casamassimi, A., 373, 2122Casartelli, C., 1308*, 1360Casetti, A.V., 203Casey, G., 1687Casey, J., 1200Caskey, C.T., 19*, 51*, 65, 375*,
959, 978, 1033, 1038, 2005,2174, 2357, 2361, 2472,2477, 2480, 2484, 2493,2506, 2526
Casper, R.F., 1284Caspi, B., 1130Cassidy, S.B., 169*, 655*Cassiman, J.J., 1387, 1392,
1870, 1925Castagnoli, A., 1685Castellano, J., 656Castellano, T.M., 730Castellanos, T., 2845Castiglione, C.M., 1941, 1988Castillo, J., 1604*Castillo, S., 2659Castillo-Taucher, S., 1420*Castro, J., 1827Castro, O., 725Castroviejo, I.P., 1486Catalano, E., 1828Catanzarite, V., 1277Cattanach, B.M., 241, 242*Cavagna, A., 971Cavalli-Sforza, L.L., 254, 1877,
2373, 2623, 2882Cedeho Rinc6n, R., 656*Cederbaum, S.D., 1007, 2431Cedrone, E., 1389Cedrone, M., 1485Cenani, A., 1782, 2665, 2677,
2830*Cerbone, A.M., 872Cervantes, A., 1328, 1560*Cesarman, G., 1357Cetta, G., 1065Ceylaner, S., 2831*Chader, G.J., 2523Chaganti, R.S.K., 611Chahal, S.M.S., 2825, 2832*,2870
Chaillet, J.R., 1860*Chaki, R., 1245
508
Author and Presenter Index
Chakraborty, R., 65, 252*, 803,978, 983, 2506, 2615, 2758,2837
Chakraborty, S., 451*Chakraborty, T., 326Chakravarti, A., 64, 410*, 1830*,
1958, 2020, 2060, 2076, 2209Chakravarti, S., 1890*Chakravarty, A., 1147*, 1244Chamberlain, J., 19, 978, 2220,2385
Chamberlain, P.F., 112Chambers, C., 2268*Chambon, P., 120*Chan, T.K., 388Chan, V., 388*Chance, P., 1952Chandley, A.C., 406*, 2205Chandra, H.S., 2236Chandra, R.S., 817Chandra, T., 657*Chang, D-Y., 1614Chang, F-M., 1614Chang, M-H., 1778Chang, P.L., 2470*, 2481Chang, S.l., 2572*Chang, S.P., 1798Chang, W-C., 2304Chang, Y.C., 75*Channabasavanna, S.M., 766Chao, M., 1666, 1854Chaplin, D., 2114Chapline, C., 543Chapman, P., 591Chapman, V., 2421Charak, B., 619Charlieu, J.P., 2057*Charpentier, C., 259Charrin, C., 1323Chartier, M.C., 2290Chartrand, P., 2202, 2513, 2556,2611*
Chatkupt, S., 1953, 2653*Chau, A.S., 1785*, 1795Chaudhuri, G., 2563Chautard-Freire-Maia, E.A., 539*,580
Chauvet, M.L., 755Chaventre, A., 2827Chawla-Gupta, M., 2120Chayko, C.A., 1583Chebotarjova, N., 2806Chehab, F.F., 1113, 2612*Chehensse, V., 90, 1572Chelly, J., 1029, 2269*Chelsky, D., 199Chemke, J., 1217, 1561*Chen, A., 2188Chen, A.K.Y., 2324Chen, A.T.L., 1852, 2737Chen, C., 52Chen, C.H., 1120Chen, C-P., 1148*, 1149Chen, C.Y., 1120Chen, D., 2573*, 2592Chen, D.J., 1891*Chen, D.S., 2270*Chen, E., 2312Chen, F., 1021, 2413Chen, G., 454Chen, H-T., 1186Chen, H-Y., 1614Chen, I-K., 1186Chen, J., 1091, 2401, 2538*Chen, L-C., 217Chen, M-F., 718, 1421*
Chen, M-H.W., 1149*Chen, M.J., 1087Chen, P-L., 71Chen, R., 2403Chen, S-H., 658*Chen, T.H., 1261Chen, T.P., 1523Chen, X., 2573, 2592Chen, X-Q., 1601Chen, Y., 2573, 2592, 2685Chen, Y.T., 475, 574, 1119,
1533, 2277Chenevix-Trench, G., 400, 2574*Cheng, E.Y., 1150*Cheng, J.Q., 1380Cheng, L.Y.L., 2324Cheng, S., 1657Cheng, T.C., 326Cheng, Z., 1447, 1537, 1544,
1616Chen-Majransayeva, T.P., 1288*Chernos, J.E., 1422*, 1513, 1723Cherryson, A., 14Chessa, L., 294, 677, 2654*Chettouh, Z., 1430, 1528Cheung, S., 1423*Chi, S.M., 2453Chiang, S-H., 1186Chiara, T., 2826Chidambaram, A., 1892*, 2624Chieffo, C., 2473Chien, C.H., 593, 2413*Chieri, P., 1151*Chifu, Y., 1070Child, A., 77Childs, B., 396*Chillon, M., 1074Chimoy E, P.J., 566*Chin, E., 748Chinault, A.C., 2065, 2092,
2135, 2157, 2174, 2220, 2287Ching, N.S.P., 1831*Chini, B., 2182Chinn, R., 1978Chinoy, N.J., 1506Chinsky, J., 975*, 1413Chitayat, D., 452*, 454, 470,
524, 633, 698, 718, 779, 804,815, 899, 1145, 1217, 1421,1462, 2442
Chitrikova, L.E., 1523Chiurazzi, P., 2349Chivilev, I.V., 2333Cho, K.R., 1991Cho, S., 912*Cho, Y., 1289Cholerton, S., 540*Cholin, S., 453*Chomyn, A., 36*Choo, K.H., 1647*Choopanya, K., 387Chorney, M.J., 785, 1066, 2117*Choudhary, R.P., 2833*Chow, N.H., 1383Chow, S.N., 593*Chowdhury, J.R., 423Chowdhury, N.R., 423Choyke, P., 1122Chretien, D., 447, 503Christensen, B., 2231Christensen, K., 69*Christensen, M., 182Christiaens, G.C.M.L., 1152*Christian, C.L., 1424*, 1516Christian, J., 921Christine, B., 1410
Christodolou, Z., 376Christopher, K.L., 1379, 1592Christopoulos, G., 1023Chu, B.M., 976*, 1185, 1831,
1839, 2679Chu, E.H.Y., 2807Chu, M-L., 73, 2387Chu, W.M., 1123Chudley, A.E., 1425*Chueh, J., 659*Chui, D.H.K., 387, 1839Chung, B-C., 2414*Chung, L.C., 73, 2387Chung, M-Y., 2001Chung, W.L., 1143Ciafaloni, E., 977*Ciaffoni, F., 526Cibis, G.W., 712, 810Ciccarelli, J.A., 2575*Cicchi, P., 595Ciccodicola, A., 373, 2122Cieply, K., 1566Ciesla, W., 1670Cieslak, J., 107, 2525Cifuentes, L., 2655*Cifuentes, S., 843Ciminelli, B.M., 2628Cinti, C., 2122Cirillo, F., 872Cisternino, M., 665Civelli, O., 1903Civitello, A.B., 2357Clark, A., 2438Clark, C., 227Clark, R., 234Clark, S., 2486, 2492Clarke, A., 951*, 1106, 1126Clarke, C., 1888Clarke, L., 804Claus, E.B., 277*Claussen, U., Session 13, 376,
2181Claxton, D., 1709Clayton, C.M., 2237Clayton, J., 2742Clayton-Smith, J., 170*Cleaver, J.E., 2539*Clemens, M., 660*Clemens, P., 19, 978*, 983,2295
Clementi, F., 2182Clementi, M., 2762Clerget-Darpoux, F., 270*Clericuzio, C., 661*, 730, 2676Cleve, H., 2262Cliche, D., 2002Clift, S.M., 192*Cloney, D., 533Cloninger, C.R., 1076Clow, C.L., 389*, 452, 462, 524Clusellas, N., 1153*Coates, P.M., 262*, 2724Cobben, J.M., 1093Cobo, A.M., 1875, 1984Cocchi, G., 949Coccia, M., 2586Cocco, E., 2423Cochaux, P., 662*Cochran, C., 305Cochrane, S., 1914Cockcroft, D., 2685Coelho, T., 2747, 2757Coerdt, W., 1519Coetzee, G.A., 2329Coghlan, G., 1055Cohen, Jr., M.M., 339*
Cohen, O., 1562*Cohen, Z., 1876Cohen-Overbeek, T.E., 926Cohen-Salmon, M., 2252Cohen-Solal, L., 446Cohn, D.H., 45, 287*, 349*, 522Colby, C., 2642Cole, C.G., 2109Cole, D., 2293Cole, H., 663*Cole, J., 2814Cole, S., 2656*Cole, T., 172*, 951Cole, W., 717Coleman, M., 1357Coleman, M.P., 1974Colige, A., 2497*Colilla, S., 2471Coll, M.J., 1153Collazo, T., 2504Collet, M., 1079Colley, A., 99Colley, P., 99Collier, D., 1986Collier, S., 2375Collins, A., 2017, 2657*Collins, C., 2271*, 2396Collins, D.L., 206*Collins, F., 77, 102, 1028Collins, F.S., 14, Session 6, 82,
98, 223, 421*, 2133, 2204,2210, 2339, 2814, 2818
Collins, J., 2125Collins, T., 720, 2111, 2415*Collis, E., 729Collu, R., 1476Colman, M., 2000Colman, S., 2118*Colwell, K., 1154*Combes, C., 2613*Comeau, F., 1060Cometto, M., 1029Comings, D., 979*Concannon, P., 294Cong, N.V., 2252Conneally, P.M., 1896, 2660Connelly, P.W., 471Conner, J.M., 1894Connolly, M., 833Connor, A., 2834*Connor, J.M., 1155*, 1644, 1932Connor, L., 2667Constantiniu, L., 1344Constantinou, C.D., 967, 2272*,2497
Conte, R.A., 1563*, 1717Contreras, A., 2864Contreras, M., 516Conway, T., 1977Cook, E.J., 310Cook, J.D., 958Cooke, H., 2498*Cooney, P., 1774*Coons, G., 1426*Cooper, D.W., 1156*Cooper, J.A., 2861Cooper, K.F., 198*Coopland, G.R., 2104Copeland, A., 52C6rdova, A., 1352C6rdova, S., 1625Corell, B., 722Corey, L.A., 2232, 2658*Corey, M., 2261Cork, L., 1861*Cormier, V., 502
509
Author and Presntsr Index
Coronel, L., 634Corpus, G., 225Correll, P.H., 2471*Corridori, L., 1467Corson, G.M., 94Corson, V., 1731*Cortelazzo, A., 2561Cortes, F., 664*Cortez, M.D., 2287Cortner, J., 2724Coss, C.A., 1682, 1714, 1933Costa, M.l.A., 1308Costa, P.P., 2747Coto, E., 2371Cotter, F., 1605Cotton, R.G.H., 193*Cotton, R.W., 2861Cottrell, S., 2206Coucke, P., 2371Couillin, P., 1042, 2058*, 2103Coulon, M., 1881Coulson, A., 238, 2126Courter, A.M., 1714Courtier, B., 146Cousineau, A.J., 2059*Coutinho, P., 1889, 1995Coutinho, W.G., 1467Couvreur, J.M., 2243Covello, M., 2727Coviello, D.A., 980*Cowan, T., 561, 975, 1832*Cowell, J.K., 613Cowles, T., 689, 1648*, 1650Cowley, G.S., 8Cox, D., Session 13, Session 89,
1465, 1781Cox, D.M., 1422, 1513Cox, D.R., 299, 2184, 2185Cox, D.W., 1726, 1979, 2116,
2411Cox, R., 2083Cox, T.K., 1830, 2060*Cox, T.M., 981*, 2214Cox, V., 701Coyle, H., 1364Coyle, M.C., 1455Crabb, J.W., 543Craig, J., 1649*Craig, R.J., 2276Craig, R.W., 2589Cramer, B.C., 226Cramer-Giraud, U., 1522Crandall, B.F., 1205, Session 64Crane, A.M., 532Crane, J., 1172, 1423Craufurd, D., 208, 1732*, 1768Craxton, M., 238Creacy, S., 2854Cr~au-Goldberg, N., 621, 2119*,2625
Cremer, T., 91, 184*, 2160,2641
Cremers, C.W.R.J., 24Cremers, F., 11 *, 24Cremonesi, L., 985Crespo, A., 1427*Crete, N., 2119Criado, B., 631Crisp, M., 2508Crist, W., 225Croci, G., 910Croft, P., 1828Crombleholme, W.R., 1740,
1758Cromwell, S.C., 1262Croquette, M.F., 1430
Cross, I., 591, 816, 901Cross, N.C.P., 981Cross, S., 670Crossley, J.A., 1155Crow, S., 1916, 2115Crowe, C., 215Crowley, M., 419Croxson, M., 853Crozet, N., 1590Cruickshank, D., 603Cruz, G., 1586Cruz-Coke, R., 2659*Crystal, R., Session 91Cserjesi, P., 326Cuccaro, M.L., 625Cuccia, M., 665*, 2838Cuckle, H., 307*Cui, M.Y., 1719Cullen, M., 933Cullen, R.F., 1481Culpi, L., 2835*Cummings, E., 1841Cummings, K.R., 1235Cummings, M., 2120*Cummins, J.H., 1601Cunniff, C.M., 1179Cunningham, G., 1157*, 1214,
2701Cunningham, M., 28Cupp, C., 2188Cupples, L.A., 2660*, 2667Curfs, L.M., 2672Curotto, B., 1309*Currie, .L., 1335Curristin, S., 2798*Curry, C.J.R., 366*, 884, 1547,
1631Curtis, A., 966, 1661, 1884Curtis, D., 195, 323Curtis, L., 1455Curtis, M.T., 913*Cury, P.R., 2673Cuticchia, A.J., 2121*Cutillo, S., 602*, 1063Cutting, G.R., 2245, 2273*,
2703, 2798Czeizel, A.E., 151*, 360*,
Session 74, 1166, 1267, 1271Czernuszewica, G.Z., 1920
-D-
Dabholkar, D., 207Dackowski, W., 111, 1708Dadey, B., 1304Daga, A., 36Dagna Bricarelli, F., 1428*Dahl, H-H.M., 2416*Dahl, N., 2200Dahlen, P., 1022Dahoun-Hadorn, S., 1161Dai, H.W., 1543, 2288Dai, Y., 2488Daiger, S.P., 1013, 2023, 2631Daigneault, J., 2840Dakou, C., 1489Dale, S., 1647D'Alessandro, E., 759Dallaire, L., 666*Dallapiccola, B., 667*, 910,
1703, 1984Dalton, J.D., 1454Daly, A.K., 541*Daly, M., 1733*, 1754Dam, A., 614, 1311, 1384Dan, K., 1369
Danan, C., 437Dancis, A., 2363Dandolo, L., 146, 2259D'Andrea, F., 759Dangel, A., 2403Daniel, S., 953Daniel, W., 1289*, 1666Danks, D.M., 249, 328Danner, D.B., 2400Danpure, C.J., 132*Dar, H., 646, 1833*Darlington, G., 2469, 2482Darnuade, M.T., 1159Das, K., 1239, 2576*Das, T., 2563Dasovich, M., 455Dastugue, B., 971, 2804Datson, N.A., 2088Daugherty, E.A., 1200Dauhajre, J., 1759Dautigny, A., 971Dauwerse, H., 1303, 2132, 2216Dauwerse, J.G., 185, 1556, 1994Davenport, C.M., 2378Davi, G., 872David, A., 234David, K., 1158*David, M., 1833Davidson, M., 191Davidson, R., 328Davies, J., 2310Davies, K.E., 17*, 376*, 1974,
2109, 2146, 2379Davies, K.P., 1106Davignon, J., 515, 2682Davila, L., 1827Davis, G., 920, 1276Davis, J., 1082Davis, J.G., 696Davis, M.B., 224, 2032Davison, D., 2616Davisson, M.T., 1863Dawid, I., 2263Dawson, D.V., 2661*Dawson, S.J., 2417*Day, C.E., 2784*Day, J., 2828, 2836*, 2852,2867
Day Ill, R., 2568Day-Salvadore, D-L., 1257, 1669Dayton, S.H., 221, 2577*d'Azzo, A., 280*D'Costa, A., 1893*De, M., 2760Deadman, M.E., 2447de Almeida, J.C.C., 982*, 1683Dean, J., 234Dean, J.C.S., 670*, 889Dean, M., 106, 1872, 1882,
1907, 1973, 2418*Dean, P., 2571de Andrade, M., 978, 983*Dear, S., 238, 970Deaven, L.L., 2151, 2167, 2499*de Barsy, T., 529de Beer, F.C., 616Debevec, M., 650Debiec-Rychter, M., 1467De Braekeleer, M., 470, 2002,
2289, 2662*, 2840Debrinski, M., 671*De bruyn, A., 2038de Buendia, P.G., 2578*de Campos, J.M., 1310*, 1332de Canache, M.F., 2680De Carli, L., 2182
DeCarlo, R., 862Decary, F., 2202D1cary, F., 2513Decruyenaere, M., 1738de Die-Smulders, C.E.M., 1429*Deeb, S., 2398, 2419*de Elejalde, M., 61Defesche, J.C., 1990Defize, J., 2408DeGala, G., 286, 2359Degennes, J-L., 2804Degioanni, A., 2645de Graaff, W.E., 614de Grouchy, J., 621, 1590Degtiarev, G., 2067Deguchi, T., 545DeGuzman, M., 1366DeHaven, M., 1160*Deidda, G., 2799Deisseroth, A.B., 1709, 2466,2785*
deJong, B., 614, 1311*, 1384,1386
de Jong, D., 618de Jong, G., 668*de Jong, P., 52*, 176, 182, 405,2203
De Jonghe, P., 1998Deka, R., 410, 2615, 2837*de Klerk, J.B.C., 263de Knijff, P., 996Delabar, J.M., 1430*, 1528,2119
de la Chapelle, A., 76, 1046,1918, 1991, 2196, 2570
de la Cruz, F., 212, 836Delaroche, I., 1703de la Torre, A., 2845Delattre, O., 2130, 2191, 2251Delaunay, J., 1063del Castillo, V., 672*De Leo, R., 1001, 2799de Leon, D., 2353Delgado-Escueta, A.V., 2041Delhanty, J., 591Delicado, A., 1159, 1431*, 1486Delisio, J., 605, 2161Del Mastro, R.G., 1894*Delneste, D., 1421, 1529, 1585DeLorenzo, R.J., 2658DeLozier-Blanchet, C.D., 1064,
1161*Delp, K.J., 1776*del Rio, E., 2674DeLuca, H., 1870Deluchat, C., 2058Delvenne, V., 2038Demacker, P.N.M., 996DeMaio, M.S., 1257Demant, P., 594*De Marchi, M., 2362DeMarini, D.M., 2500*Demaugre, F., 259DeMayo, J.L., 2462Dembure, P., 457Demczuk, S., 1432*De Mello, M., 1859Demenais, F.M., 1963, 2786*Demers, D., 2790de Miranda, E., 831Demongeot, J., 1562, 2221Demple, B., 2270Demyttenaere, K., 1738Den Dunnen, J.T., 18, 185Deng, G., 80
510
Author and Presenter Index
Deng, H-X., 1348, 1543, 1728,2061*, 2510, 2515
Deng, P., 2386De Nigris, E., 2555Denison, M.S., 1291Denning, C., 1769, 1836Denny, C.T., 2162De Paepe, A., 354*de Parscau, L., 2712de Pater, J.M., 1152de Paula, I.D., 1407DePaulo, J.R., 2091de Perdigo, A., 1408de Ravel, T.J.L., 669*de Recondo, J., 1922Derfler, B., 2258, 2401Dergunova, L.V., 2333Deriagin, G.V., 2197Der Kaloustian, V.M., 454*, 773,
1502, 1512, 1529, 1585Dermody, J.)., 1953Derom, R.M., Session 85de Rooij, F.W.M., 1008de Saint-Basile, G., 2221Deshmukh, D., 862Desnick, R.)., Session 31, 530,2475, 2491
de Sousa, M., 2731Desposito, F., 781, 1261, 1546,1766
Destrempes, M., 1691Detera-Wadleigh, S.D., 1879,2123*
de Toledo, S.R.C., 2823De Tollis, G., 1418de Torres, M.L., 1159*, 1431,
1486Deugau, K.V., 974Deutsch, C.K., 673*, 723Deutz-Terlouw, P.P., 984*deVere White, R., 1642Devilee, P., 2234Devine, G., 2089de Visser, M., 1093Devor, E.J., 1076, 1895*, 1924Devoto, M., 985*DeVries, G.H., 2232Devys, D., 377Dewald, G., 216, 1228, 1603de Wet, W.J., 534De Wolf-Peeters, C., 1387, 1392Dey, S., 2749, 2868Dhar, U., 1356Dhaunsi, G., 516Dho, S., 2364Diamond, N., 1261Diamond, T.M., 210, 674*Diatloff-Zito, C., 296, 2274*Diaz, L.A., 2387Diaz, M.O., 124, 2053Diaz de Leon, L., 450Dickinson, L., 323Dickson, J.G., 17Di Cola, M., 759DiDonato, S., 35, 1873, 1937,2178, 2382
Diehl, S.R., 79, 2030, 2062*,2600, 2681
Dieli, F., 2838Dierks, P., 2409Dietrich, A., 374Dietz, G., 979Dietz, H.C., 77Dietz-Band, J., 2124Digweed, M., 2275*Dijkhuizen, T., 1311, 1384
DiLella, A.G., 2276*Dillon, N., 118ADi Maio, S., 805Di Martino, D., 2420*DiMauro, S., 34, 977Di Minno, G., 872Dimitroff, T.J., 1819Dimmick, J., 698, 804, 1145Di Natale, P., 204, 500Ding, J.H., 475, 1119, 2277*Ding, Y., 2063*DiNovo, C., 1433*Dionne, F.T., 2878DiPersio, C.M., 2430Di Rienzo, A., 2614*Dirks, R.W., 180, 1728DiRocco, M., 507diSibio, G., 2185Disteche, C.M., 1678, 2421*Ditta, S.D., 2019Divelbiss, J., 1325, 1622Dixon, J., 941, 2163Dixon, M., 2163Djurdjinovic, L., 1219Dlouhy, S.R., 1896*, 2358D'mello, N., 820Doane, W., 2676Dobin, S.M., 1162*, 1241Dobkin, C.S., 376, 2175Dobler, K.D., 2568Dobrenis, K., 955Dobyns, W.B., 230*, 1981Docherty, Z., 1176Dochin, M., 2857Dockter, M., 109Dodd, S.N., 1844Dodge, A., 1732Dodinval, P., 675*Dodson, A.E., 1007Dodson, L.A., 1090Doehmer, J., 2547Doering, J., 2120Doggett, N.A., 2124*Dognini, M., 1078Dokras, A., 1272Doll, J., 2120Doll, R., 1101Dombroski, B.A., 2278*Donahue, R.P., 1146, 1465,
1804Dondi, E., 665, 2838*Dongier, M., 2725Donis-Keller, H., 1950, 2145,2165, 2718
Donlon, T., 2301Donnai, D., 99, 208, 229, 289*Donnenfeld, A., 1163*Doppelt, S.I., 553Dorfmann, A., 1201Dorman, J.S., 2663*, 2708Dorman, T., 2212Dornan, J.C., 1232Dorval, J., 1737Dosman, J., 2685Dotan, A., 1312*, 1577Dott, B., 537, 1290*, 1442Doty, L., 1170Dou, S., 1950, 2145Dougherty, K.M., 2279*Dougherty, N., 814Douste-Blazy, P., 2804Dover, G.J., 75, 2634Dovrat, A., 1196Dowler, L.L., 2810Dowling, C.E., 1067Dowling, P., 1434*
Doyle, A., 2054Doza, B., 1164*Draaijers, T.G., 224Drabkin, H., 2087, 2195, 2198Drabkova, H., 1734*Dracopoli, N.C., 223Dressler, G., 2282Drevon, C., 2058Drews, B., 2043Driesen, M.S., 185Driscoll, D., 1062Driscoll, D.A., 57, 86*, 913,
1485Driscoll, D.J., 1116, 1457, 2224*Dronamraju, K.R., 2664*Drouant, G., 1843Drouin, R., 2066, 2085, 2540*Drumheller, T., 1385, 1393Drumm, M., 2814Drwinga, H.L., 505, 1435*, 2081Dryja, T.P., 8*, 9, 221, 799,2575
Drysdale, J.W., 2117D'Silva, G., 656D'Souza, C.R., 972Du, Y-Z., 2404Du, Z., 238Duara, R., 963, 1957, 1997Duba, C., 1436*Dube, I., 225*Dubel, JR., 2222, 2287, 2407,2501 *
Dubertret, L., 1927DuBois, J., 2212DuBow, M.S., 2536Dubrova, Y., 2787*Duchaud, E., 296Duckworth-Rysiecki, G., 1876Duclos, F., 81Ducluzeau, M.T., 1063Dudzinski, M., 1335Duerr, R., 2773Duffty, P., 889Dufier, J.L., 1939Duggan, M., 958, 1699Dumez, Y., 929Dumie, M., 1466Dumoulin, J.C.M., 1240Dunbar, J., 2335Duncan, A.M.V., 1437*, 2366Duncan, B., 2812Duncan, C., 1612, 1667, 2199Duncan, I.W., 239Duncan, L., 369Dunham, I., 2125*Dunne, C.J., 2407Dunne, P.W., 2287Dunning, A., 66, 986*Dunwoodie, D., 1619DuPont, B.R., 2541*Duquesnoy, P., 1927, 2455Duran, M., 263*Durand, D., 689, 1564*Durbin, R., 238Durfee, K., 912Durie, P., 2261Duros, C., 2848D'Urso, M., 204, 373, 2122*Dutchik, J., 237Duthie-Nurse, G., 1478du Toit, J.L., 1792Dutra, J., 2675Dutra-Filho, C., 2675Dutta, S.K., 2422*, 2569, 2576,2630, 2638
Duvic, M., 2372
Duvick, L.A., 2001Duyk, G., 299, 1325Dworniczak, B., 1027, 2280*,2302
Dwyer, D., 1781Dyer, K., 920Dykstra, M., 967Dynlacht, B., 118Dzeranova, N.Y., 1095
- E-
Eallonardo IlIl, S.J., 1623Earle, E., 1647Earle-MacDonald, J., 1105Earley, E.M., 1438*Earnshaw, W.E., 1597Easton, D., 13, 1965Eaves, L., Session 24Ebers, G.C., 1917Ebihara, M., 2281*Eccles, M., 2282*Economou-Petersen, E., 2283*,2426
Eddy, Jr., R.L., 2400Edelman, C., 1692Edenberg, H.J., 2284*Edgley, M.L., 2126*Edman, B., 2106Edmonds, L.D., 232, 2686,
2697, 2702Edmondson, D., 326Edwards, A.O., 959, 2506Edwards, E., 2064*Edwards, J., 1752, 1821Edwards, J.H., Session 86Edwards, M., 2295Edwards, M.J., 995Edwards, Y.H., 2379Eeg-Olofsson, O., 1535Egbuta, J.O., 2127*Egeland, J.A., 1940Eggers, S., 1735*Egorova, M., 121*Egozcue, J., 1629Eich, G., 1526Eichenlaub-Ritter, U., 409*Eicher, E.M., 432*Eidlitz-Markus, T., 688Eigel, A., 2302, 2344Eiken, H.G., 228Eik-Nes, S., 821Eipers, P., 2128*Eisenman, R., 196Eisensmith, R.C., 455*Ekblom, L., 1565*Ekins, M., 1055Elam, R., 2485Elbadramany, M.H., 1736*Elbl, F., 1463Elder, F.F.B., 1564, 1648, 1650*Eldridge, R., 676*, 806Elejalde, B.R., 61*El-Fouly, M.H., 868, 1291*Elias, S., 109, 209, 1262, 1844El Kalla, S., 2799Ellard, J., 47Elli, R., 677*Ellingham, T.J., 1439*, 2089Elliott, J., 52, 200Ellis, P.M., 1455Ellison, J.W., 2285*, 2402Ellison, K.A., 2065*Ellston, J., 101Elorza, M.A., 1747Elsas, L.)., 457, 485
511
Author and Presenter Index
Elsassaer, D., 1774Elston, R.C., 71, 1997Ely, J., 2615*El-Zawahri, M., 1313*Emanuel, B.S., 57*, 86, 199,
219, 370*, 1419, 1507, 1716,1901, 2169
Embury, S., Session 83Emery, D.W., 2490Emi, M., 2286*Encio, I.J., 2123Endicott, B., 897Endo, F., 987*, 1058Endo, K., 1321Eng, C.M., 1897*Engel, E., 1064, 1161Engelhart, C.M., 1240Engstrom, P., 1733, 1754Enomaa, N., 466Enomoto, I., 2856Ephrussi, A., 323Epner, E., 338Eppig, J.T., 1898*Epstein, C.Q., 2229, 2239, 2244Epstein, Jr., E.H., 2257Epstein, H.F., 2222, 2287*,2310, 2501
Ercal, M.D., 636Ercolani, P., 2555Eren, Z., 1302Erginel, A., 2665*Erikson, M.S., 60Eriksson, A.W., 2666*Eriksson, S., 680Erlandsson, R., 2098, 2579*Erlich, H., 426*Ermakov, A.V., 2564Ermert, K., 1857Ernstoff, M.S., 223Ertl, M., 2043Ervasti, J.M., 20Ervin, F.R., 678*, 2725Espinel, A., 2839*, 2842Espinosa, R., 1705, 2053Espinoza, C., 743Esposito, P., 602Essig, Y.P., 1748Estabrooks, L.L., 1651*Estivill, X., 988*, 1074, 1084,
1111Estop, A., 774, 1566*, 2153Estupinain, D., 1789Eswara, M.S., 1440*Eto, Y., 523, 2315Etzioni, A., 688Eunpu, D.L., 1737*Eussen, B.E., 378, 1720, 2389Evans, D.G.R., 229*Evans, J.A., 679*Evans, M., 29*Evans, M.E., 1113Evans, M.l., 1174, 1189, 1192,
1195Evans, S., 2473Evans, S.S., 1304Evers, J.L.H., 1240, 1386Evers-Kiebooms, G., 1738*Evsikov, S., 107Ewens, W., Session 58Ewens, W.J., 2711Exeler, J.R., 1575Extermann, P., 1161Eyal, N., 1018Eyre, D., 45, 349, 522
F-
Faa, G., 1534Fabacher, P., 2709Faber, J-P., 680*, 2397Facchiano, A., 448Faed, M.J.W., 1441*Fagan, R.J., 2450Fahn, S., 2353Fairbrother, U., 2379Fairfull, R.W., 2080Fairweather, N., 1914Fajans, S.S., 74Fakharzadeh, S.S., 1361Fakoury, M., 2877Falcao-Conceicao, D.N., 989*Falchetti, A., 595*Falik-Borenstein, T., 914*Falk, C., 1899*Falk, R.E., 1719Fallet, S., 555*Fallon, L., 1201, 1841Falls, K., 74, 1940, 2212Fan, Y-S., 1666, 2129*Fanen, P., 463, 985Fang, B., 990*, 1021, 1114Fann, W.E., 2011Fanning, T.G., 2580*Fantes, J., 1643, 2498Farag, T.l., 681*, 1477, 1736Farah, S., 991*Farber, R.A., 1651, 2581*Fardeau, M., 1904Farkas, L.G., 629, 673Farlow, M., 1896Farndon, P.A., 1905Farnham, J., 2037Faround, T., 2861Farquharson, D.F., 946Farr, C., 2498Farrantz, G., 2567Farrar, G.J., 7Farrell, P., 1006Farrer, L.A., 79, 2660, 2667*Faucher, M.C., 1900*, 2009,2191
Fawcett, M.., 2167, 2499Fechner, P.Y., 2225*Fedde, K.N., 456*, 472Fedorov, A., 992*Fedortseva, R., 1314*Feduchi, E., 2591Fei, Y., 1928Feigelson, H.S., 2739Feil, R., 2190, 2320Feinberg, A., 767Feingold, J., 2242Feitell, D., 2005Feitosa, M.F., 2696Fejgin, M., 923, 1196, 1551,
1826Felber, S., 1376Feldman, D., 559Feldman, G.L., 682*Felicetti, L., 1001, 2799*Fellman, J.O., 2666Fellous, M., 2103, 2341, 2826Fellowes, A., 853Feng, L., 2288*Fenger, K., 1765Fenton, W.A., 508Fenwick, R., 51, 978, 983Ferencz, C., 2650, 2668*Ferguson-Smith, A.C., 241Ferguson-Smith, M.A., 183*,
598, 1680, 2097, 2207
Fernandes, M., 2289*Fernandez Moya, J.M., 843Fernhoff, P., 457*Ferrari, M., 654, 985Ferraro, M., 1652*Ferreira, P., 683*Ferreira, R., 2504Ferreira-Rajabi, L., 2840Ferrell, R.E., 64, 410, 703, 867,
1892, 1960, 1999, 2615,2624, 2656, 2669*, 2689,2775, 2837
Ferrie, R.M., 993*, 1047Fertitta, A., 182Feschenko, S.P., 2233Festenstein, H., 590Fetni, R., 1476, 2066*, 2085Feuchtbaum, L., 1214Feunteun, J., 1977Feussner, G., 2434Fex, J., 79Fiamengo, S., 931Fibison, W.J., 1901*Fidani, L., 2290*Fidler, A., 2282Field, B., 1749Field, L.L., 2670*Fielder, A.R., 1905, 1942Fields, C.R., 684*Figlewicz, D.A., 1910, 2130*,2251
Figueiredo, M.S., 994*Figuera-Villanueva, L.E., 685*Filatov, L., 2131*Filkins, K., 1793Filling-Katz, M.R., 686*Filosa, S., 1964Finck, S., 1442*Finegan, J., 172Finegold, M.J., 2462, 2469Fink, J.K., 2291*Fink, S., 2303Fink, T., 54Finkelstein, J., 48Finley, W., 2070, 2671*Finn, J., 1135, 1165*Finn, P., 111Finnerty, V., 2312Finniear, R., 101Finocchiaro, G., 2382Finucane, B., 1443*Fiorani, O., 2882Fiorucci, S., 2382Firth, H.V., 112Fisch, G.S., 2672*Fischbeck, K.H., 95, 1886, 1914,2007
Fischel-Ghodsian, N., 995*Fischer, H., 92Fish, B., 1235Fisher, J.M., 1567*Fisher, K.J., 458*, 2355Fishman, G.A., 1097Fitz, C.R., 699FitzGerald, K., 1814Fitzgerald, M.G., 2179Fitzgerald, P.H., 2597Flandermeyer, B., 1283Fleming, J., 2392Fletcher, F., 2468Fletcher, J.A., 1364, 1391, 2232,2600
Fletcher, J.C., Session 11Fleury, P., 2585Flint, A., 59, 60Flinter, F., 381*, 970, 1011
Flodman, P., 753, 2022Flomen, R., 2109Florentin, L., 2292*Fluharty, A., 285Fluharty, A.L., 2492Fodde, R., 1865, 2132*, 2216,2517
Fogarty, P., 1232Fogh-Andersen, P., 69Foitzik, M., 404Folstein, S.E., 301*Fonda, J., 1731Fong, C-T., 2133*, 2339Font, U., 2674Fontaine, G., 488, 2519Fontoura, S.E., 539Foote, S., 433Forabosco, A., 1685Ford, A., 2451Ford, C.E., 2795Ford, D., 1965Forman, L., 314*, 2861, 2871Forman, N., 1653*Formstone, Ci., 1967Fornage, M., 2800*Fornerod, M., 125, 2582*Foroud, T., 294, 1896Forrai, G., 2874Forrester, W.C., 338Forse, R.A., 1889Forsthoefel, K.F., 1081Foskett, J.K., 2364Fossdal, R., 1902*Fountain, J.W., 223*Fourney, R.M., 2829Fowlow, S.B., 1723Fox, J.E., 1414, 1444*Fox, M.F., 2136Foy, C., 27, 79Fraga, J., 2731Francis, M., 376Francke, U., 969, 1658, 1867,
1987, 2293*, 2388Franco, B., 1702, 2092, 2294*,2307
Franco, M.F., 2673Francomano, C.A., 48*, 77, 1996Frangione, B., 964Franssila, K., 1333Frants, R.R., 143, 996*, 1093,
2012, 2042Frantzen, M., 415Fraser, C.M., 1907Fraser, D., 2274Fraser, F.C., 915*, 1835Fraser, J.R.E., 467Fraser, P., 118AFrebourg, T., 449Freeman, S.B., 916*, 1411Freese, D., 157*Freidman, E., 836Freije, D., 373Freimer, N.F., 1944Freire-Maia, D.V., 2673*Frelin, L.P., 2409Freneaux, E., 459*, 513Frerman, F.E., 2322Fresia, A., 1335Frets, P.G., 1767Freudin, M.l., 1445*Freund, L., 828Frezal, J., 1939, 1223, 2101Frias, J.L., 692, 2761Fried, K., 1446*Friedberg, E.C., 2301Friedes, J., 1658
512
Author and Presenter Index
Friedman, A.J., 1364Friedman, C., 1306Friedman, J.M., 1815*, 1909Friedman, K.J., 997*, 1014, 1099Friedman, T., 79Friedmann, T., 478, 1681, 2074,2485, 2488
Friedrichs, K., 1373Friend, S., 218Frieri, M., 1366Fries, J., 2415Fries, M.H., 687*, 1207, 1237Frisch, A., 584, 998*Frischauf, A-M., 298*, 1869,
2206, 2218, 2371Frisoli, G., 851Fritz-Wolz, G., 1166*Frontali, M., 1937, 1993Froster-Iskenius, U.G., 139*Fryburg, J., 1257, 1503Frydman, M., 640, 688*, 998Frydman, R., 1258Fryer, A., 14Fry-Mehltretter, L., 1786*Fryns, J.P., 343*, 1925, 2672Fu, H., 1537Fu, S., 1447*, 1537, 1544Fu, S-B., 1315*Fu, X-W., 2395Fu, Y-H., 2174Fucharoen, G., 2354Fucharoen, S., 387*, Session 83,2354
Fuhrmann, W., 309*, 2003Fujii, J., 429Fujiki, K., 999*, 1019Fujiki, N., 1739*, 2857Fujimoto, A., 215*, 1143, 1581Fujimoto, H., 1862*Fujio, K., 1862Fujishima, M., 2644, 2693Fujita, R., 81Fujiwara, T.M., 493, 2725,2840*
Fukuhara, Y., 1075Fukumaki, Y., 2354Fukushima, Y., 1028, 1324,
1348, 1448*Fuller, N., 1686Fullwood, P., 1905, 1942Fundia, A., 1449*Funk, R., 2740Furlong, C.E., 543Furman, P., 689*Furman, Y., 1938Furth, E.E., 913Furtun, Y., 538Furukawa, M., 2437Furuyama, J., 690*, 2584Fusaris, K.W., 2449Fusaro, L., 1316Fusaro, R., 1316*Futreal, P.A., 2134*Fyer, A., 1944
G-
Gabizon, R., 1000*Gabriel, A., 188Gabriele, A.L., 2727Gade, R., 691*Gadhia, M., 2542*Gadhia, P., 2542Gadner, H., 1320Gadow, E.C., 1167*Gagne, R., 1816*
Gahl, W.A., 281*, 571Gahmberg, N., 1847Gailani, M., 2583*Gajdusek, D.C., 1003Gala, N., 1607Galanello, R., 250Galan Gomez, E., 692*Galeva, I., 962Galjaard, H., 435*Gall, J.G., 317*Galla, A., 1568*Gallagher, J.E., 2500Gallagher, P., 2724Gallano, P., 2674*Gallego, M.l., 2591Gallisai, D., 2423Galluzzi, G., 1001*Galt, J., 1654*Galton, D.J., 2759Gamble, K., 1256, 1787*Gamel, J., 686Gammack, A., 101Gammaro, L., 1110Gan, G.C., 1040Gan, T., 760Gandelman, K., 1655*, 1727Gandhi, P., 1524Gandini, E., 949Ganshirt-Ahlert, D., 110Gao, C., 1447, 1537, 1544,
1616Gao, S-W., 2540Gao, X., 257, 990Gaon, E., 1826Gaona, A., 1074Garabedian, B., 915Garani, G.P., 949Garber, A., 704, 1834*Garber, M.F., 917Garbern, J., 2226*Garcea, N., 2349Garcia, C.A., 1958Garcia, D., 1978Garcia, E., 52, 176, 200Garcia-Cavazos, R., 693*, 908Garcia-Cruz, D., 685, 694*, 844Garcia-Cruz, M.O., 694Garcia-Esquivel, L., 844Garcia-Heras, J., 1656*Garcia-Pelaez, I., 908Garcia-Sagredo, J.M., 695*Gardiner, G.B., 1777, 1788*Gardiner, K., 1657*Gardiner, R.M., 1972Gardner, E., 2347Garneau, Y., 2002Garner, C.E., 1811Garner, D.D., 2861, 2871, 2877Garnica, A., 1450*Garofalo, G., 1405Garritsen, H.S.P., 110Garson, O.M., 369*, 1307Gartler, S.M., 147*, 2452Gartner, J., 190*Garver, K., 1566Gasbarra, R., 1451*Gaskell, P.C., 78Gasparini, P., 1078Gasparini, R., 954, 1569*Gass, A., 809Gasser, K., 1385, 1393Gaston, S.M., 2348Gatti, R., 204Gatti, R.A., 294*Gaupman, K., 1452*Gaustad, A., 2567
Gavis, L., 323Gavrilov, I., 596*Gawinowicz, M.A., 960Gayle, A., 2576Gazit, E., 2551Gearhart, J.D., 419, 2453Gebhardt, M., 2788*Gedda, L., Session 85Gedeon, A., 968Geethanjali, D., 2543*Gehrels, C., 599Geifman, O.H., 1168*Geiser, A., 2435Gelb, B.D., 2135*, 2385, 2406,2616
Gelernter, J., 1877, 1903*, 2100Gelinas, Y., 2878Geller, L.N., 1504Gellera, C., 35Gelman-Kohan, Z., 1561Gemmati, D., 444Genco, P., 625Genest, D.R., 917*, 934Gennarelli, M., 910, 1984Genovese, M.J., 1570*, 1612Gentil-Filho, V., 2050Genuardi, M., 1317*, 2349George, C.F.P., 2019George, D.L., 1361George, J., 1412, 1607, 1693George, Jr., J.F., 2240George, M., 2500George, P., 853Geraedts, J.P.M., 1240, 2502*Geraghty, D., 2114Geraghty, M.T., 202*, 2153Gerder, M., 1553Gerdes, M., 2840Gerdes, T., 1618Gericke, G.S., 1494German, J., 292*, 597*Germino, G.G., 1869, 2371Gerrard, B., 2418Gersen, S.L., 1453*Gershon, E.S., 1879Gershoni-Baruch, R., 688Gerwin, B.I., 610Gessler, M., 196, 2241Gettig, E., 1793Geurts van Kessel, A., 1386,
1605*Gevers Leuven, J.A., 996Gewitz, M.H., 1235Geypes, M., 711Ghalib, M.A., 734, 952*Ghanem, N., 463, 2674Ghetti, B., 1896Ghezzi, M., 805Ghisellini, M., 980Ghorbani, K., 651Ghosh, A., 2563Ghosh, B.B., 2563, 2576Ghosh, S., 2563Giacalone, J., 1658*Giambernardi, T.A., 2588Giampietro, P.F., 696*, 1175Giannelli, F.B., 1002*, 1005,
2109, 2125Giardine, R., 1138, 1169*Gibas, Z., 938Gibbs, R., 51, 978, 2174, 2295*Gibson, K.M., 488, 1217Gibson, L., 1484Gibson, L.F., 1555, 1659*Giebel, L.B., 189, 525, 2296*Giere, I., 1334
Gieselmann, V., 285, 2492Gieser, L., 2531Giger, U., 518Gilbert, A.D., 1835*Gilbert, F., 1175, 1836*Gilbert, J.G., 1904*, 2272Gilbert, J.R., 2368Gilboa, E., 2491Gilchrist, D., 697*Gilchrist, J.M., 78Giles, A.R., 1068Giles, H.R., 1200Giles, M.G., 1905Giles, R., 2740, 2824Gilfillan, A., 1842Gilfillan, T., 1541Gilgenkrantz, H., 1029Gilgenkrantz, S., 1430Gill, M., 1986Gillard, E.F., 429, 1911Gillberg, C., 1535Gillberg, I.C., 1535Gillerot, Y., 891, 1475Gillespie, G.A.J., 2371Gillett, A., 1342Gillett, G.T., 2108, 2136*Gilliam, T.C., 1239, 1885, 1943,
1944, 2029, 2044, 2112, 2332Gillis, A., 1318*Gilman, J.G., 2423*Gimenez, F.J., 1074Gingrich, J., 2156Ginns, E.I., 514, 1940, 2483,2503*
Ginsberg, N., 107, 1278Ginsburg, O., 698*Ginter, E.K., 1947, 2841*Ginzburg, E., 2067*Ginzinger, D., 2198, 2297*Giordano, P.C., 2517Giovagnoni, A., 2555Giraldo, A., 725, 1789*Girbau, E., 988Girijamani, K., 2560Girimaji, S.R., 766Girmen, A.S., 2196, 2303Girodon, E., 2674Gispert, S., 2504Gitelson, A., 1759Gitschier, J., 2154Giudice, G., 2387Giugliani, R., 2675*, 2863Giunti, P., 1993Glamotanin, S., 1326Glaser, J., 1263Glass, I.A., 1894, 1905*, 1942Glass, R.B.J., 699*Glatt, K., 59, 87Glaves, M., 1723Glenn, G., 1122Glick, A., 383Glicksman, A., 1908Glodek, A., 2179Glomstein, A., 1345Glorieux, F.H., 2698Glover, T.W., 222*, 1925, 2328,
2339, 2818Gluck, E., 1098Go, R., 2771, 2844Goate, A., 2290Goatley, C., 1463Gobran, F., 700*Godeau, G., 1061Godfrey, M., 93, 345*, 460*,
496, 534Goding, J.W., 1307
513
Author and Presanter Index
Goedde, H.W., 1373, 1671,2596
Goede, W., 1575Goedert, M., 2156Goei, V., 2137*Goetz, P., 854, 2106Gogate, S., 1244Goh, J.C., 1327Gojobori, T., 2621Golabi, M., 659, 687, 701*Golbus, M.S., 115*, 155*, 687,
991, 1204, 1207, 1283,1740*, 1758, 2196
Gold, W.R., 1241Goldberg, B., 2676Goldberg, J.D., 365*Goldberg, M.D., 1446Goldberg, R., 768, 1518Goldberg, R.B., 1741*Golden, J., 1569Golden, W.L., 1170*Goldenfum, S., 2675Goldfarb, L.G., 1003*Goldgaber, D., 1003, 2298*Goldgar, D., 2068*Goldin, L.R., 1879, 1906*Goldman, A.S.H., 1171*Goldman, B., 461*, 494, 640,
1245, 1554Goldman, D., 1882, 1907*, 1973Goldman, H., 560Goldman, M., 1660*, 2118Goldsmith, T.H., 394*Goldwitch, Z., 2883Golembieski, W., 2138*, 2195,2198
Golkova, I., 1615Golla, A., 2808Gollin, S.M., 1319*, 1362, 1368,
1378, 1662, 2708Golmard, ).L., 2643Golubovskaya, V., 2544*G6mez, J.C., 1449Gomez Lira, M., 1065Gonsebatt, M., 1608Gonzales, G., 1604Gonzalez, A., 1159GonzAlez, A., 1625Gonzalez, C.H., 702*, 1329Gonzalez, F.J., 540, 551Gonzalez, I.L., 165*, 1716Gonzalez, O.L., 2845GonzAlez-Duarte, R., 1875Gonzalez-Portal, M.E., 2591Good, P., 1905Goodchild, N., 2337, 2424*Goodfellow, P., 2393, 2498Goodfellow, P.J., 1909, 1956,1982,2170,2340
Goodfellow, P.N., 430*, 2109,2282
Goodman, C.S., 325*Goodman, S.l., 264*, 439, 535,2322
Goodship, J.A., 901, 1518,1661*
Goodwin, D., 1893Goodyer, P., 462*Goonewardena, P., 1141, 1908*Goorha, S., 2458Goossens, M., 437, 463*, 588,
985, 1927, 2455, 2674Gopinath, P.M., 2560Gorbunova, V., 1004*Gordon, J.W., 799Gordon, L., 182
Gordon, P.L., 1454*Gorin, A.l., 2564Gorin, M.B., 703*, 1077Gorius, A., 296Gorlin, R.J., 340*, 738Gorospe, J.R.M., 464*Gorski, M., 2179Gorski, S.M., 1909*Goswami, H.K., 1508, 1524,
1606*Goto, J., 1910*Goto, Y., 1017Gottesman, I.1., 123*, 909Gottlieb, B., 267Gottlieb, W., 1056, 1558, 1593,2224
Goud, J.D., 2862, 2866Goudie, D.R., 598*, 2097Gough, N.M., 2360Gould, S.J., 131*Goulding, M., 311Gourgiotis, D., 1568Govea, N., 1515Goverde, A., 2216Goyle, S., 1292*Grabbe, J., 1539Grabowski, G.A., 4*, 555, 2365,2545
Grasa, C.H.N., 1617Grace, E., 1455*Grace, M.E., 2365, 2545*Gradle, K., 1811Graeber, M.B., 1949Graham, G.W., 1155Graham, J.G., 652, 704*, 914,
1516Graham, Jr., J.M., 87, 995, 1202,
1424, 1426, 2392Granados, J., 693Granda, H., 1791, 1827, 2504*Grandchamp, B., 1008Grandone, E., 872Grange, D.K., 705*Grant, A., 1521Grant, D., 2425*Grant, P., 1898Grant, S.G., 2535, 2541, 2546*Grant, S.S., 1238Grantham, M., 916Gras, N., 829Grasela, J.F., 554Grass, F., 1456*Grasso, M., 1428Gras-Vincendon, A., 1442Grattagliano, B., 529Graves, K., 2531Gravius, T., 1940Gravius, T.C., 74Graw, S.L., 223, 2201Gray, B.A., 1457*, 1549Gray, D., 1172*Gray, J.W., 217, 1283, 1635,
1724, 2087, 2151, 2156Gray, M.R., 2069*, 2449Gray, P., 2505*Graziadio, C., 777Graziano, S.L., 1380Greally, M., 1458*Grebe, T., 2676*Grechanin, B.E., 1837Grechanina, E.Y., 1837*Greco, S., 1451Green, E.D., 49*, 2160Green, E.P., 2109Green, F., 2417Green, J., 599*
Green, J.R., 1758Green, P.M., 160*, 238, 1002,
1005*Green, R.C., 600*, 833Greenberg, C.R., 441, 1055,
191 1*Greenberg, F., 87, 140*, 655,
1255, 1702, 2139, 2392Greenberg, J., 79, 732Greene, A.E., 2081Greene, C.L., 439Greene, M.F., 917Greenhaw, G., 706*Greenstein, M.A., 1459*Greenstein, R.M., 1790*Greenswag, L., 655Greenwood, B.M., 2618Greer, J., 247*Greer, W.L., 1912*Gregersen, N., 195*, 498Gregg, R.G., 1006*, 2180Greggio, N., 654Gregory, C.A., 2299*Gregory, P., 2818Gregory, W., 542*Grenningloh, G., 325Gress, T., 2330Grether, P., 1173*, 1221Grevengood, C., 1174*Gribble, T.J., 556*Grierson, H., 968, 1082Griffin, C.A., 50, 615, 623,
1335, 1367, 1607*Griffin, D., 591Griffin, J., 2227*Griffin, L.D., 485, 2135, 2406,2616*
Griffin, W., 1797Griffioen, G., 609Griffiths, A.J.F., 395*Grifo, J., 1175*Griggs, R., 2212Grimm, T., 2776, 2808Grinberg, D., 1875Grinell, S., 397*Grinzaid, K.A., 88Gripenberg, U., 2228*Grisard, M.C., 2058, 2103Grishchenko, O.V., 1837Grisolia, S.V., 2722Grison, O., 1060, 1142, 1253Grix, A., 2014Grobstein, R., 1814Grody, W.W., 1007*, 1133,
2431Groenewald, I., 2093Groffen, J., 2597Gromov, P.S., 465*Grompe, M., 1033, 2259, 2472*,2477
Groner, Y., 418*Groot, P.C., 594Groot de Restrepo, H., 2839,
2842*Grootscholten, P.M., 18Gross, B., 178, 374Gross, M., 489Grosschedl, R., 1867Gross-Glenn, K., 1957, 1997Gross-Kieselstein, E., 234Grossman, A., 586Grossman, M., 423Grossman, S.A., 615Grosveld, F., 118A*, 336*Grosveld, G., 125*, 2582Groudine, M., 338*
Growdon, J., 2303Growdon, J.H., 2667Grubb, A., 1026Gruber, H.E., 45, 349, 522Gruberg, L., 1872Grubs, R.E., 1662*Grudda, K., 2280Gruen, J.R., 2137Gruenert, D., 991Grundfast, K., 79*Gruss, P., 311*Gu, H., 1612Gu, J.R., 610Gu, X-F., 1008*Gu, Z., 2300*Gubbay, J., 2393Guckenberger, S., 2686Guellaen, G., 2130Guenet, J.L., 240*Guerin, D., 2024Guerra, D., 754, 1791Guerra, S., 444Guerra Valdez, R., 1460*Guest, A., 2469Guggino, W.B., 2273Guillouf, C., 296, 2559Guinsburg, S., 2629Guioli, S., 2092Guion-Almeida, M.L., 707*Gulati, K., 224Guler, A., 1406GuIle, M., 409Gunn, A., 591Gunwar, S., 383Guo, G.M., 2509Guo, S., 1050Guo, Y-F., 558Gupta, S., 423Gursel, T., 644Gurusinghe, A., 17Gusella, J.F., 82, 102, 298,
Session 62, 961, 1727, 1880,1913, 1992, 2009, 2035,2162, 2169, 2189, 2204,2210, 2336, 2348, 2353,2381, 2383, 2802
Gusew, N., 2611Gustafson, G., 2003Gustafson, S.R., 708*Gustashaw, K.M., 1701Gustavson, K-H., 2200, 2671Gutfriend, A., 586Guthrie, E., 1741Gutierrez, E., 1827Guti&rez, G., 1173Gutierrez, M.J., 1460Guti&rez, S., 1352Gutmann, D., 2339, 2818Guttler, F., 2426*Guttmacher, A.E., 1777*Guzzetta, V., 1702, 2139*
H-
Ha, T.H., 793Haaf, T., 1663*Haagerup, A., 1948Haan, J., 964Haapala, K., 937Haas, O.A., 1320*Haataja, L., 2013Haber, G.D., 718Habibian, R., 1177, 1351,
1461*, 1491, 1675, 1700Habibullah, C.M., 504Hacihanefioglu, S., 2677*
514
Haddad, F.S., 1642Haddow, J.E., 308*, 1134, 1169,
1203, 1224, 1238, 1250Hadjizadeh, E., 2678*Hadro, T., 1666Hagemeijer, A., 368*, 1323Hager, H.D., 1269Hagerman, R.J., 709*, 1410Haggitt, R., 2571Hagiwara, H., 2281Hahn, L.B., 8Hahn, T., 2462Haile, V.F., 1037Haines, J., 2169Haines, J.A., 2009Haines, J.L., 1880, 1913*, 1992,
2035, 2381Hainline, B., 2316Haites, N.E., 603, 1914*Hajianpour, A., 1176*, 1231,
1965Hajianpour, M.J., 1177*, 1491,1700
Hakoda, M., 2538Halal, F., 1462*Hale, D.E., 498, 2316, 2377Halford, S., 1518Halila, R., 466*, 2356Halimi, M., 1000Hall, B.D., 137*, 710*Hall, B.K., 2328Hall, J.G., 89, 245*, Session 45,
291*, 352*, 762, 2679*Hall, K., 742Hall, L.V., 2208Hall, M.H., 603Hall, R.E., 482Hall, T., 2671Haller, R.G., 482Haller, V.L., 83Halley, D.J.J., 1915*Halliday, J., 2646Halliday, J.W., 2137Hallmayer, J., 1877, 2043Halloran, N., 238Halper, M., 608Haltia, M., 866Hamada, H., 1131Hamaguchi, H., 567*, 1118,
1131Hamalainen, E. R., 1011Hamard, G., 1029Hamazaki, M., 1321Hameister, H., 918*Hamel, B.C.J., 2235Hamels, J., 891Hamers, A.J.H., 1429Hamers, G., 1386Hamerton, J.L., 2299Hamilton, J.D., 2011Hammad, I., 1477Hamman, R., 2656, 2669, 2689Hammans, S.R., 1010, 2427*Hammond, F.G., 2680*Hammond, H.A., 65, 2506*Hampe, C.L., 63Hampsch, K., 605Hampton, G., 2206Hamsten, A., 986, 2417Han, H., 606Han, J., 2070*Han, T., 1304Han, Y-H., 2534Hanchett, J., 655Handa, K., 2022
Handelin, B., 1009*, 1239,1691, 1786, 2524
Handyside, A., 1210Handyside, A.H., 116*Hani, V., 452Hanis, C.L., 2801*Hankenson, L.G., 711 *, 1761Hanley, W., 212, 836Hanmanth Rao, P., 2843*Hann, E., 1619Hanscombe, O., 118AHansen, J., 359, 1458, 2441Hansen, L., 2416Hansen, R.S., 147Hansen, S., 2452Hansen, T., 453Hansma, D.l., 1841Hansmann, I., 1664*, 2183,2374
Hanson, J., 1458Hanson, M., 1969Hanzlik, A.J., 2507*Hao, Y-C., 1048Happ, A., 1178*Happle, R., 290*, 2765Hara, M., 438, 512Harada, N., 1728Haralson, M.A., 383Harding, A.E., 32*, 1010*, 2032,2427
Hardy, J., 2290Hargreave, T.B., 2205Harikrishna, J.A., 1045Hariti, G., 1881Harley, H.G., 1916*, 2115Harman, L., 2844*Harpending, H., 2639, 2869Harper, G., 467*Harper, P.S., 14, 143, Session
28, 300*, 951, 1126, 1817*,1916, 1961, 2012, 2037, 2088
Harris, A., 970, 1011 *Harris, C.C., 587, 610Harris, D.J., 712*, 810Harris, E., 1 774Harris, H., 472Harris, J., 884Harris, M., 1470, 1670Harris, P., 1549, 1742*Harris, R., 37*, 99, 208, 229,
329*, 1732, 2375Harris, R.M., 1680Harrison, D., 2497Harrison, M.R., 154, 1192Harrison, W.R., 1648, 1650Hart, M., 557*Hart, P.S., 468*Hart, T.C., 684, 2681*Harteveid, C. L., 2517Hartge, P., 582Hartd, D.L., 239*Hartsfield, Jr., J.K., 1293*Hartz, J., 2532Hartzer, M.R., 857Harvey, J.F., 85, 1567Harvey, R., 111, 2608Hasan, Q., 1571*Hasegawa, T., 1321*Hashem, N., 713*Hashimoto, L.L., 1917*Hashimoto, T., 2584*Hasholt, L., 1743*Haskin-Leahy, L., 742Haskins, M., 2473*Hassed, S.J., 1179*Hassell, J.R., 1890
Hassemer, D., 1006Hassett, C., 543Hassock, S., 2109, 2125Hassold, T.J., 85, 408*, 916,
1411, 1567Hasstedt, S., 1969Hastbacka, J., 1918*Hastie, N., 304*, 413*Hatanaka, M., 2171Hatase, O., 477Hauser, E.R., 2040Hauser, M.A., 2507Havekes, L.M., 996Havenga, C., 1965Haviland, M., 2682*Hawkins, A., 1607Hawkins, H., 1520Hawkins, T., 238Haworth, R., 931Hayakawa, K., 68*Hayakawa, M., 999Hayashi, A., 469*Hayashi, S., 2622Hayashi, Y., 1028Hayden, M.R., 211, 227, 248*,
470*, 1488, 1585, 1771,1807, 2271, 2396, 2442
Haydon, R., 2617*Hayflick, S., 1067Haynes, C., 1992Hayward, C., 1883, 1919*Hazel, M., 2418Hazlett, L.D., 1174He, A., 587He, G-S., 2545He, H., 2486, 2492He, X., 1543, 1665*, 2061, 2515He, Z.J., 1853Headings, V., 499Headrick, E.G., 1841Healey, S., 400Healy, J.M.S., 1012*Heard, E., 146Hebert, M., 916Hecht, J.T., 48, 1013*, 1650,2774
Hechtman, P., 2246, 2289,2327, 2662
Hedge, P.J., 101*Hedrick, A., 227, 1488, 1807,2442
Heffron, J.J.A., 1012Hegde, S., 1270Hegele, R.A., 471*Hegi, M., 305Heidenreich, R., 1058Heier, L., 931Heikkinen, M., 2595Heim, R., 1955Heiskanen, T., 466Heisler, K.L., 1200Heisterkamp, N., 2597Heitz, D., 377Hejtmancik, J.F., 1920*, 2023,2165, 2407, 2501
Heju, Z., 2139Hekele, A., 1320Held, K.R., 1613, 1671Helderman, J.H., 383Helen, B.K., 1627, 2547*Helio, T., 714*Heller, S., 1886Helminen, H., 2461Helmy, S.M.H., 715*, 879HelzIsouer, K., 615Henderson, A., 2598
515
Henderson, D.J., 919*Henderson, H., 470Hendricks, S.K., 1180*Hendrickson, J., 1116Hendrickx, J., 1921*Heng, H.Q., 2071*Henke, A., 2360Hennessy, M.D., 1533Henney, A., 2417Henning, K.A., 2301*Henriksen, K.F., 2426Henriksson, K.G., 482Henry, I., 90, 767, 1572*, 2181,2252
Henske, E.P., 2140*Henson, V., 2056Hentati, A., 1922*Henthorn, P.S., 456, 472*Hentzen, D., 559Hepburn, M., 1997Heppel-Portan, A., 2161Herbergs, J., 1605Herbstreith, M., 2272Heredero, L., 1791 *Herit, S., 1664, 2374Herman, T., 2270Hermans, M.M.P., 568*Hemandez, D., 1967Hernandez, E., 2719Hernried, L., 2676Herrera, C.H., 2023Herrera, G.E., 221, 2605Herrera, L.A., 1608*Herrero, F., 1159Herrmann, M.E., 1322*Herro, G.J., 577Herron, B.J., 2802*Hersey, J., 916Hersh, J.H., 686, 1463*Herta, N., 1886Hertz, J.M., 1416, 1923*Herva, R., 896Herzing, L.B.K., 2548*, 2554Heslop-Harrison, J.S., 2141*Hesse, A., 960Hesseling-janssen, A.L.W., 1915Heston, L., 2753Heumann, L.E., 716*Heutink, P., 1924*, 1954, 2045,2766
Hevey, K., 1619Hewett-Emmett, D., 2528Heymann, W.R., 904Hiasa, Y., 1118Hibiya, Y., 2398, 2419Hickok, D.E., 1150Hidalgo, P.C., 2845*Hiemstra, J.L., 2133Hieter, P., 50*Higgins, J.V., 737, 868, 1218,
1468, 1925*Higgins, M., 2142*Highsmith, Jr., W.E., 997, 1014*,1099
Higurashi, M., 1531Hiilesmaa, V., 1847Hildebrand, C.E., 2124, 2499Hildesheim, J., 2326, 2797Hill, A.V.S., 2618*Hill, K.A., 2619*Hill, R., 1920Hillier, I., 238Hilliker, C., 1387, 1392Hillman, R.E., 554Hilt, D., 419Himmelbauer, H., 1869
Author and Presenter Index
Author and Presenter Index
Hindkjer, J., 92Hinshaw, M.T., 1099Hinton, L.M., 201, 2208Hiraga, K., 473*Hirata, G.l., 1181*Hirayama, M., 1739, 2857Hirning, U., 918Hirota, T., 2510Hirsch, N., 537Hirst, M.C., 376, 2109Hirvasniemi, A.; 756Hittner, H., 1960Hitzeroth, H.W., 1792*Hixson, J.E., 2631, 2690Hiyama, K., 506, 2793Ho, J., 1668Ho, M., 179Ho, S.C., 1212Hoa, D.P., 793Hoa, T.T., 793Hoar, D., 1488Hobbins, J.C., Session 53, 758,
794, 835Hobbs, F., 199Hobbs, F.W., 2078Hobbs, H., 67Hockey, A., 717*Hodes, M.E., 1896, 2358, 2508*Hodge, S.E., 2683*Hodgkinson, K.A., 718*, 1421Hoefsloot, E.H., 581Hoehe, M., 1879Hoehn, H., 1609*Hoeijmakers, J.H.J., 293Hoekx, J., 763Hoey, T., 118Hoffman, E., 1435Hoffman, E.P., 464, 1096, 1207,2394
Hoffman, L., 931Hofstra, R.M.W., 224Hogan, K., 2180Hogg, A., 613Hogge, J., 1182*, 1183Hogge, W., 1182, 1183*Holder, S.E., 1015*Holland, J., 2125Hollen, C., 1347Hollenbach, K.A., 1150Hollister, D.W., 93, 345, 460,
496, 534Holloway, S., 1016*, 1884Holloway, T.L., 2088Hollstein, M.C., 587Holm, C., 891Holm, N.V., 69Holm, V., 655Holman, K., 379Holmberg, E., 719*Holme, E., 228Holmes, E.W., 489Holmes, J.M., 1184*Holmes, L.B., 673, 720*, 723,
871, 917, 1168, 1211Holmgren, G., 719Holmgren, J., 829Holmquist, G.P., 411 *, 2540Holzgreve, W., 110*, 114*,
274*, 309, 1195, 1225, 1254Hommes, F.A., 569*, 848Hong, H.K., 703Hong, S.S., 2846*Honig, P.H., 904Honnaiah, S., 2143*Honore, L., 366Hoo, J.J., 1580, 1666*
Hood, L., 100Hood, O.J., 721*Hooper, H.R., 683Hoovers, J.M.M., 1596Hoovers, J.M.N., 767, 1209,
1572, 2144*Hopcus, D., 1450Hopkins, P.N., 164Hopkinson, D.A., 2073Hoppel, C.L., 535, 536Hopwood, J.J., 204, 282*, 467,
1042, 2200, 2255, 2345Horai, S., 1017*, 2622Hordinsky, M.K., 641, 2684*Horikoshi, Y., 1321Horn, E., 1719Horn, G.T., 2522Horne, S., 2685*Horng, C-J., 570*Hornstra, l.K., 2428*Horovitz, J., 1142, 1253Horowitz, M., 1018*, 2439Hors, M.C., 1959Horst, A., 722*Horst, J., 110, 114, 235, 1027,
1225, 1254, 1539, 2280,2302*, 2344
Horsthemke, B., 56*, 87, 197,376, 1079, 1860, 1868, 2181
Horst-Sikorska, W., 722Horton, W., 47*, 48, 474*, 706Horwitz, A.L., 492Horwitz, J.A., 1242Hosenfeld, D., 234Hoshino, H., 1531Hoshino, Y., 790Hosoe, S., 1122Hosokawa, K., 477Hotamisligil, G.S., 2196, 2303*Hoth, C., 79Hotta, Y., 999, 1019*Hou, G.Y., 2474Hou, Y-L., 2429*Houck, G., 1667*Houck, Jr., G., 550, 1470, 1670Housman, D.E., Session 14,
126*, 223, 2115, 2201, 2383Houwen, R.H.J., 1926*Hovig, E., 218, 2803*, 2813Hovnanian, A., 1927*Howard, J., 664Howard-Peebles, P.N., 1200,
1610*, 1688, 2672Howe, C., 2206Howe, JR., 1950, 2145*Howells, D.W., 193Hoyle, S., 974Hoyme, H.E., 661, 1295, 1723Hozier, J., 1400Hreczko, T., 723*Hruban, R., 615Hruz, P., 488Hsia, Y.E., 385*, 976, 1185*,
1831, 1839, 1855, 2679Hsiao, K-J., 570, 1120, 1186*,
1854Hsieh, F-J., 1034, 1108, 1614Hsieh, W-T., 1879, 2123Hsu, L.C., 2304*Hsu, L.Y.F., 1187*Hsu, W-T., 1668*Hsueh, ).L., 2474*, 2487Hu, D.N., 2706Hu, N., 601 *
Hu, P., 80, 1020*Hu, X., 1124, 2549*, 2769, 2778
Hu, Y., 1125, 1928*, 2487Hu, Y.F., 2820Huang, A., 2530Huang, B., 1611*Huang, C-H., 1186Huang, J-H., 2609Huang, L.H., 1744*Huang, M-C., 1778*Huang, M-F., 1186Huang, P.Y., 2820Huang, S., 990, 1021*, 1114,
1117Huang, S.Z., 1087, 1856, 2305*Huang, T., 1641Huang, T.T., 2229*Huang, W., 1978Huang, Y., 1856Hubbard-Smith, K., 2598Hudgins, L., 724*, 832Hudson, B.G., 383*Hudson, J., 383Hudson, J.D., 1238Hudson, K., 2306*Hudson, T.C., 1293Huether, C., 2686*, 2697Huff, D.S., 920*Huff, V., 220*Huggins, M.J., 1745*, 2745Huggins, R., 2700Hughes, A.E., 1929*, 2016Hughes, C., 678Hughes, H., 172, 1086Hughes, M., 1210, 1520Hughes, R., 1105Hugnot, J.P., 1029, 2269Huie, M.A., 2237Hulsebos, T.J.M., 1990, 2585*Hulten, M.A., 1051, 1171, 1951Humbert, R., 543*Humphreys, W.F., 708Humphries, M.M., 7Humphries, P., 7*Humphries, S., 66, 986, 2417Hung, W-Y., 80, 2021Hungerford, J., 613Hunt, D.M., 2108, 2136Hunt, J.A., 976, 1185, 1831,2679
Hunt, M., 1412Hunt, S.C., 164Hunter, D.W., 641Hunting, D.J., 2412Huoponen, K., 1022*Hupkes, P.E., 1946Hur, M.W., 2284Huret, J.L., 1061, 1323*Hurk, J.v.d., I 1Hurst, D., 2671Hurtado, S., 829Huschenbett, J., 2146*Huson, S.M., 13, 14, 112*, 229,
356*Hussein, F., 624Hussein, H.A., 715, 879Hux, C., 1257Huymans, J.G.M., 263Hvozdikova, E., 1188*Hyden-Granskog, C., 1930*Hyland, K.M., 1669*Hyser, C., 143, 1886, 2012,2212
lafolla, A.K., 475*, 1119lannello, R., 2416
lannuzzi, M., 2814Ibraimov, A., 1579, 1730, 2620*Idle, J.R., Session 93, 538, 540,
541, 542Idle, M.E., 540, 541Idriss, J-M., 476*, 479leiri, T., 662Igarashi, S., 1071Igarashi, T., 2644, 2693Iglesias, E., 1159Iglesias-Gamarra, A., 725*Ignatius, J., 896, 2687*Ihalainen, j., 617li, S., 2632lihara, K., 1071lijima, S., 1531, 2644, 2772ljdo, J.W., 1655, 2147*Ikeda, S., 578Ikeno, K., 412Ikeuchi, T., 1395Ikonen, E., 235611gin, H., 1236Ilyina, H., 726*llyinskikh, N.N., 741, 813, 1136,
1354, 1838*Imachi, J., 1019Imaizumi, K., 727*Imaizumi, Y., 2688*Imamura, T., 1070Imanishi, T., 2621*Immken, L., 1631Inana, G., 1057, 1931*Inati, M.N., 728*, 835Inazawa, J., 2148*, 2171, 2172Incerti, B., 2294, 2307*Indo, Y., 1058Inmon, J., 2500Inoko, H., 1862Inomata, T., 2030Inoue, K., 2148, 2172Insel, R., 783, 1389Inserra, J.A., 1484, 1503Inuzuka, T., 1071loan, D., 770loannou, P., 1023*, 2047loannou, Y.A., 2475*lolascon, A., 602*, 1063Ireland, J.H., 1839*Irion, O., 1161Isa, M.N., 1644Isaac, G.S., 1573*Isada, N.B., 1174, 1189*, 1192,
1195Isakova, G., 2067Isenberg, K.E., 1895Ishikiriyama, S., 1324*Isichei, U.P., 2127Islas, A., 950Isobe, M., 903Israel, J., 28Israel, N., 1833Issac, G.S., 734Itakura, H., 2286Itano, T., 477Ito, K., 876Ito, Y., 1862Itratunnisan 1164Ivanchshenko, V.E., 2317Ivanov, V.I., 1464*Ivaschenko, T., 1004Ives, E., 729*Iwasaki, H., 1131Iwata, T., 1931Iyengar, S., 2669Izquierdo, L., 1932*Izquierdo, L.A., 730*
516
Author and Presenter Index
-I-
Jabali, M., 2221Jaber, L., 1746*, 2781Jabs, E.W., 827, 1597, 1682,
1714, 1933*Jackon, L.G., 1467Jackson, A., 2308*, 2459Jackson, C., 1793Jackson, C.E., 1934*, 1982, 2090Jackson, C.L., 2149*Jackson, D., 2430*Jackson, L., 938, 1276Jackson, M., 2500Jackson-Cook, C.K., 83*, 1200,
1415, 1611, 1713Jackson-Grusby, L., 266Jacobs, P.A., 85, 1567Jacobsen, S.J., 2212Jacobson, H.R., 383Jacobson, S., 143Jacobson, S.G., 1931Jaeger, E., 1443Jagadeesh, G., 731*Jager, R.J., 1190*Jahan, B., 2843Jain, P.K., 1024*Jain, S., 877, 2565Jakubowski, L., 1670Jalal, S., 1603Jalbert, P., 1562Jallad, B.J., 1957Jam, K., 1834Jamehdor, M., 732*, 1417James, G., 326James, O., 542Jamot, B., 2024Jamry, I., 2114Janco, R.L., 2821Janecka, I., 1362Janjua, N.A., 477*Janka, M., 2808Jankowski, S.A., 2586*Janny, L., 1684Jansen, G., 405Jansen, R., 532Jansen, S., 1025*, 1965Janson, M., 612Janssen, L.A.J., 1915Jansson, S-E., 617Jantke, I., 1373Jaquez, F., 733, 2756Jaquez, M., 733*, 2756Jarai, Z.K., 205*, 1886Jaramillo-Pasquale, M., 2175Jartseva, N., 1314Jarvela, I., 1935*Jarvinen, H., 1991Jauch, A., 2641Jaume-Roig, B., 1747*Javed, A., 2309*Jaworski, M.A., 2064, 2072*Jayakar, P., 1465*Jayamony 746Jayasimha, N., 766Jeanpierre, C., 2181, 2252Jeanpierre, M., 1191*Jedlicka, A.E., 1936*Jeenah, M.S., 2329Jeffers, A.J., 80Jeffery, S., 982Jeffreys, A.J., 313*, 2789Jeison, M., 584Jelsema, R.D., 1192*Jen, J., 2539
Jenkins, E.C., 550, 745, 1141,1470, 1570, 1612*, 1667
Jenkins, H., 2340Jenkins, R., 216*Jenkins, T., 258*, 1478, 2000,
2633, 2635, 2872Jennings, K., 670Jensen, K., 366Jensen, P.K.A., 2476*Jensen, R.H., 2535, 2541, 2546Jensen, T.G., 2476Jensen, U.B., 2476Jensson, 0., 1026, 1902Jervis, G.A., 1748*Jeziorowska, A., 1470, 1670*Jha, K., 2598, 2601Jia-Hsu, Y., 2295Jiang, S., 940Jiang, Z., 2509*Jin, F., 2211Jin, K-L., 2230*, 2395Jin, L., 65*, 2506Jinnah, H.A., 478*Jinno, Y., 1728, 2510*Jirikowic, J., 1540Jockusch, H., 1864Jodice, C., 1937*, 1993, 2628Joe, C.0., 2691Johannesson, T., 1535Johannisson, R., 1193*John, R., 2144Johnson, A., 887, 1194*, 1195,
1276Johnson, C., 1172, 1500Johnson, D., 207Johnson, D.H., 1731Johnson, J., 941, 1319Johnson, K., 1012, 2310*, 2848Johnson, K.R., 1863*Johnson, M.P., 1174, 1189,
1192, 1195*Johnson, P., 1896Johnson, P.A., 1681Johnson, P.H., 2073*Johnson, S.K., 204, 373Johnson, T.L., 2150*Johnson, V., 961Johnson, W.G., 1938*, 1953,
2653Johnston, A.W., 603*, 860, 1914Johnston, P., 350Jolay de Portugal, L., 648Jonas, A., 476, 479*Jonat, W., 1373, 2596Jondeau, G., 1881Jones, C., 2136, 2181, 2310,
2311*, 2771Jones, I.M., 2550*Jones, J., 1942Jones, K.L., 1045Jones, M., 1 126Jones, M.C., 1277Jones, OW., 1072Jones, P.G., 2480Jones, R., 239Jones, S.L., 1201, 1841Jones, S.N., 2406, 2472, 2477*Jones, T., 2083J6nsd6ttir, S., 1026*Jordan, B., Session 77, 2221Jordan, D., 1325*Jordan, S., 7Jargensen, A.L., 2231*Joseph, A.M., 1270Joseph, G., 953*Joseph, N., 1196*
Joshi, A., 1508Josifovska, O., 2423Josso, N., 891Jouannet, P., 1258Journel, H., 2712Jovanovic, V., 309Joyce, A., 1197*Juda, S., 1530Judd, S.A., 2807Juji, T., 876, 2211, 2876Julaine, F., 1886Julian, C., 1799, 1825Julien, J-P., 2166, 2251Julien, P., 470Junien, C., 90*, 1572, 1881,
2181, 2252, 2804, 2848Junker, S., 92Jurecki, E., 1237Just, C., 2473Just, W., 1633Jyothi, A., 952Jyothy, A., 734*
-K-
Kaariainen, H., 735*, 1046Kaback, M.M., 207*Kaddoura, R., 736*, 846, 958Kadysheva, E.K., 2879Kaepernick, L.A., 737*, 1776,
1925Kaffe, S., 1187Kaganer-Breit, M., 1749*Kahkonen, M., 1035, 1198*Kahler, S.G., 475, 1533Kahn, A., 1029, 2269Kaic, Z., 1466*Kainulainen, K., 77*Kaiser, R., 2344Kaiser-Kupfer, M.l., 676, 806,2519
Kaitila, I., 77, 765, 1918Kajii, T., 888, 1199*, 1348Kajii, Y., 2281Kalaitsidaki, M., 2094Kalaydjieva, L., 962, 1027*,2280, 2302
Kaler, S.G., 571*Kalitsis, P., 1647Kallioniemi, A., 217, 1283,2151*
Kallioniemi, O-P., 217*, 1283,2151
Kalluri, R., 383Kalnins, V.I., 10Kalousek, D.K., 288*, 364*,
Session 75, Session 75, 1154Kalscheuer, V., 1710Kaluzewski, B., 1467*, 1670Kamat, A., 2138Kamatani, N., 2538Kamboh, M., 2669, 2689*Kamdar, K., 2312*Kamei, T., 1028*Kamel-Reid, S., 225Kamen, B., 882Kamholz, J., 1672Kaminsky, E., 1613, 1671*Kammerer, C., 2690*Kamp, J.J.P.v.d., 1767Kampsch, K., 2161Kan, Y.W., 391, 1113Kanai, A., 999, 1019Kanamori, M., 604*Kanazawa, I., 551, 1946Kandpal, R.P., 2511*
Kaneko, K., 1071, 2152*, 2527Kang, H., 1654Kang, K.W., 2691*Kansara, M.S., 2587*Kant, J.A., 1090Kantaputra, P., 738*Kao, F., 2532Kaplan, D., 2199Kaplan, E.B., 2661Kaplan, F., 389, 1716, 2246,2289, 2662
Kaplan, G., 1840*, 2676Kaplan, J., 1939*Kaplan, J.C., 1029*, 2269Kappler, J., 285Kaprio, J., 402*Kapur, S., 737, 1468*Kaput, J., 1289Kar, B., 480*, 1493, 1591Karam, S., 2686Karaman, B., 1402, 1406Karatzas, C., 2080Karayalcin, G., 1469*Karayiorgou, M., 223Kardon, N., 1470*Karimi-Nejad, M.H., 1471*,
1472Karimi-Nejad, R., 1471, 1472*Karlsson, S., 2435, 2471Karna, P., 1468Karras, D., 921*Karson, E.M., 2490Kartner, N., 2364Kasai, K., 2313*Kascheeva, T., 1615Kashatus, W.C., 953Kashima, K., 491, 2171, 2172Kashuba, V.I., 2098, 2579Kastelein, J., 470Kastner, D.L., 1872Kasturi, R.V., 310Kato, N., 438Kato, S., 2512*Kato, Y., 604Katosova, L.D., 2796Katsuya, T., 739*Katz, J., 1412Katz, K., 1030*Kaufman, B., 2215Kaufman, M., 267Kaul, R., 573Kaupmann, K., 1864*Kauppinen-Makelin, R., 714Kaur, G.P., 2314*, 2568, 2587,2601
Kavalakkatt, T., 1524Kawai, K., 2148, 2254Kawame, H., 2315*Kawasaki, K., 177Kay, H., 574Kay, M.A., 2478*, 2482Kayes, L., 2372Kazazian, Jr., H.H., Session 4,
1690, 2278, 2283Kazemi-Esfarjani, P., 267Kazi, R., 1510Kazimiroff, P., 481Kazzi, N., 1192Kearney, L., 1605Kearney, M., 821Kearns, W.G., 202, 1690, 1706,2153*
Keath, A.M., 1725Keats, B., 81, 159*, 820, 1893,2052
Keel, B., 912
517
Author and Presenter Index
Keenan, K., 922*, 1178Keener, S.L., 1205Keighley, M., 1051Keil, R., 2205Keiles, S., 481*Keilman, K., 701Keinanen, M., 1031*Keith, T., 1940*Keller, S.M., 1380Kelly, D., 1518, 2316*, 2377Kelly, K.F., 603, 1914Kelly, T.E., 1032*Kelsell, D., 2026Kendler, K., 2030Kenna, P., 7Kennaway, N.G., 482*, 1057Kennedy, B.H., 1796Kennedy, J.L., 1877, 1903, 2100Kennedy, L., 590Kent, C., 1538Kenwrick, S., 2154*Kenyon, J.B., 1077, 2750Kerber, S., 1613*, 1671Kerbrat, P., 2024Kere, J., 201, 2122Kerem, B., 2261, 2551*Kern, R., 2431Kerr, J., 1490Kerr, M., 1793*Kersey, J.H., 564Kerzin-Storrar, L., 208*, 1732Kessel, M., 311Kessling, A., 2682Keston, M., 77Ketterer, D.M., 1200*Ketterling, R.P., 70*, 2632, 2821Kevles, D.J., 319*Keyes, C.D., 1819Khan, A.A., 208, 1732Khan, M.A., 1750*Khan, T.A., 1558Khandogina, E.K., 1473*Khane, I.E., 942Khannanova, F.K., 2692*Khidiyatova, I.M., 2317Khillan, J.S., 2461Khoo, SK., 2574Khouri, S., 1749Khoury, M.J., 232*, 2702Khudoliy, G.A., 1574*Khusnutdinova, E.K., 1599,2317*
Kibbelaar, R., 1303Kida, K., 507Kidd, J.R., 1941, 1988Kidd, K.K., 167, 312*, 1877,
1903, 1918, 1941*, 1956,1988, 2045, 2079, 2100,2170, 2792
Kidd, V., 2128Kielman, M.F., 1865*Kiely, D.K., 2660Kiely, F., 2083Kikuchi, S., 567Kilis, G., 1402Kilimann, M.W., 19, 1033*Killary, A.M., 2588*Kilpatrick, M.W., 77, 1883,
1894, 1905, 1942*Kim, C., 579, 2081Kim, C.A., 702, 1329Kim, C.G., 338Kim, D.K., 2572Kim, H-S., 2253Kim, J., 2192Kim, M.A., 1575*
Kim, N., 2512Kim, S., 299Kimak, M., 2486, 2492Kimberling, B., 850Kimberling, W.J., Session 8,
1077, 2023, 2155, 2750Kimble, J., 324*Kimchi-Sarfati, C., 1576*Kimura, K., 1071Kincaid-Smith, P., 249King, B., 467King, D.A., 1201*King, M-C., 127*King, M.P., 191*King, R., 2318*King, T., 945King, T.M., 1751*Kingston, H., 208Kinoshita, T., 2693*Kinsley, G., 2797Kinugawa, N., 1324Kinzler, K., 101Kioschis, P., 178Kiras, S., 1302Kirby, L.T., 2829Kirillova, l.A., 2699Kirimer, N., 1301Kirkilionis, A.J., 2299Kirkman, H.N., 1456Kirkness, E.F., 1907, 2392Kirkwood, J.M., 223Kirson, L., 1170Kiss, A., 1350Kiss, J.G., 484Kissel, J.T., 1887Kisselev, L.L., 1639, 2098Kitagawa, K., 412Kitahama, M., 572Kitajima, S., 2511Kitchener, H., 603Kitoh, Y., 2351Kitsiou, S., 1568Kittur, S., 2694*Kiuchi, A., 1071Kiviniemi, H., 2595Klapp, J., 1269Klausner, R.D., 2363Kleeman, C., 1752*Kleijer, W.J., 2200Kleiman, S., 740*, 2883Klein, C.., 2319*Klein, D., 1007, 2431*Klein, D.F., 1944Klein, G., 2098, 2579, 2594Klein, J., 652, 704, 1202*, 1426Klein, K.A., 2232*Kleinman, C.S., 275*Kleyn, P.W., 1885, 1943*, 2112,2332
Klift, H.M.v.d., 2132Kline, A.D., 1672*, 1695, .2188Kline, S., 938Kling, S., 1005Klinger, K.W., 60, 111*, 1239,
1279, 1634, 1708, 2163Klinnert, M., 789Kluin-Nelemans, J.C., 618Knapik, M., 1366Kneppers, A., 989Knight, A.B., 1162, 1241Knight, G.J., 1203*, 1238Knight, R., 2695*Knight, S.J.L., 376Knobler, H., 418Knoll, J.H.M., 59, 87*, 1502,
1860, 2392
Knoppers, B.M., 40*Knowles, J., 1944*Knowlton, R.G., 73*, 2010,2025, 2387
Knutson, C., 1456Knuutila, S., 1333, 1676Ko, T-M., 1034*, 1108, 1614Kobayashi, H., 1071, 1112,
2521, 2527Kobayashi, K., 567, 1118Kobayashi, N., 2211Kobrynski, L., 815Kobyliansky, E., 585Koch, J., 92, 1698Koch, R., 212, 836Kochhar, D.M., 268*Kochl, S., 427Kochorova, L.V., 2741Kock, K., 69Kotova, M., 1326*Kodaira, M., 440, 2793Kodama, K., 295Kodama, T., 2286Kodunov, L.A., 942Koduru, P.R.K., 1327*Koehl, C., 537, 1290Koenig, M., 81*Koenigsberger, M.R., 1953, 2653Koetters, P., 479Kofman-Alfaro, S., 693, 908,
1328*, 1560Koga, J., 2351Koga, Y., 191Kogure, T., 572*Koh, G.A.S., 1040Kohli, Y., 2857Kohn, G., 923*Kohsaka, T., 2211Koiffmann, C.P., 1329*Koike, R., 2320*Kojima, T., 1071Kojis, T.L., 1945*Kok, K., 224Kokkonen, H-L., 1035*Kolker, A., 1753*Koller, B., Session 9Kolomiytsev, A., 741*Kalvraa, S., 92, 195, 498Komoltri, C., 1764Komori, T., 2320Kondo, I., 551, 1946*Kondo, K., 332*, 1794*Kondo, R., 2622*Konecki, D.S., 2160, 2432*,2462
Konig, U., 1474*Konradi, C., 2303Kontusaari, S., 2461Koppitch, F.C., 1189Koprivnikar, K., 2367Koren, Z., 1243Korenberg, J.R., 203, 417*Korenstein, A., 1577*Korf, B.R., 742*, 958, 1699Kormann-Bortolotto, M.H., 1584Korn, B., 374Korneev, S.A., 2333Kornegay, J., 967Korneluk, B., 405Korneluk, R.G., 404*, 778, 1043,
2036, 2370Korokhov, N., 2815Korotkov, A.V., 942Korotkov, E.V., 2433*Korovaitseva, G., 1947*Korsmeyer, S., 2156
Korson, M.S., 2300Kosciolek, B.A., 2602Kosik, K., 2334Koskenvuo, M., 402Koskimies, O., 735Koskiniemi, M., 76Kosowsky, M.R., 1898Kostense, P.J., 2666Kottke, B., 2775Kotze, M.J., 1036*Koulischer, L., 334*, 529, 1475*Kouri, R.E., 2514Koury, S.T., 2453Kousseff, B.G., 674, 743*, 1498,1748
Kouts, S., 2386Kovacs, I., 1350Kovalev, L.l., 576, 2233*Kovalev, Y.R., 1095Kovaleva, N.V., 1578*Kowbel, D., 2271, 2396Koyata, H., 473Kozak, C., 1973Koza-Taylor, P., 2368Kozich, V., 2300, 2323Kozinetz, C., 2479*Kozono, H., 2114Kozono, Y., 238Kozopas, K.M., 2589*Kozyra, A., 1846Krabchi, K., 1476*Kraft, H.G., 427, 2434*Krahe, R., 2287, 2321*Kraker, W., 216Kramer, M.H.H., 618Kramer, P., 1126, 2353Krantz, D.A., 310Krasikov, N., 744*, 796, 1425Kratz, L.E., 2322*Kratzer, P.G., 1204*Kraus, J.P., 2300, 2323*Krauss, M., 1470Krauss, R.M., 192Kraut, J., 1829Kravtsov, V.I., 1354Krawczun, M.S., 745*, 1141,
1570, 1612Kremensky, I., 1027Kremer, E., 379Kren, V., 1866Kreysing, J., 285Krieger, H., 2651, 2696*Krishnamani, M.R.S., 1037*Krishnamoorthy, K.S., 562Krishna Murthy, D.S., 1477*Krishnan Nair, M., 1358Kristensen, T., 1948Kristidis, P., 2261Kristoffersson, U., 1330*Krivchenia, E., 2686, 2697*Krivit, W., 156*, 564Krizus, A., 1910Kroes, W., 1331*Krol, R.B., 781Kromberg, J.G.R., 1478*Kronick, M., 2062Kronquist, K.E., 1205*Kroos, M.A., 568, 581Kruse, B., 457Kruse, T.A., 1923, 1948*Kruyer, H., 1111Ktsoeva, T.V., 1095Kubota, J., 438, 512Kucera, L., 1160KuterovS, G., 1188
518
Author and Presenter Index
Kucheria, K., 877, 1206*, 1229,2565
Kuchinski, A.P., 1095Kudoh, J., 177Kuffardjieva, A., 962Kugoh, T., 477Kuhl, D., 375, 1038*, 2005,2174
Kuhnlein, U., 2080, 2590*Kuik, D.J., 2666Kukharenko, V.I., 1479*Kuklik, M., 2003Kukull, W.A., 2811Kulakova, T., 1480*Kuliev, A.M., 149*, 1278Kulkarni, A.B., 2435*Kulkarni, M.L., 746*Kuller, J.A., 701, 1207*, 1237Kullmann, F., 2808Kumar, S., 2155*Kumashiro, H., 790Kumbnani, H.K., 747*, 786Kunaviktikul, C., 1621Kuncl, R.W., 1887Kunert, E., 2302Kunkel, L.M., 15*, 1062, 1943,
2112, 2332Kunst, D.B., 2526Kuo, A.C-F., 1778Kuo, B.A., 2436*Kuo, P-L., 1614*Kuo, W.L., 1547, 2156*Kupchik, G.S., 748*Kupfer, A., 542Kupke, K.G., 1949*Kupsky, W., 1391Kurachi, K., 2437, 2494Kurachi, S., 2437*Kurbatova, O., 2847*Kurczynski, T.W., 1481*Kurdi-Haidar, B., 2074*Kurer, C.C., 1414Kurimasa, A., 875Kurki, L., 1847Kurlan, R., 1941Kurmanova, G., 1579*, 1730,2620
Kurnit, D.M., 203, 1654, 2507Kuroda, N., 903Kuroki, Y., 727Kurth, J.H., 2623*Kurtz, A., 2177, 2188Kurtz, M., 1443Kurtz, T., 1866*Kurzion, S., 862Kusak, M.E., 1310, 1332*Kusanno, K., 523Kuseyri, F., 797, 1987Kushch, A., 1957Kushnick, T., 749*Kuster, W., 2003Kusuma Kumari, C., 734Kusuma Kumari, P., 1358Kuthy, I., 2719Kuwaki, Y., 572Kuwano, A., 1673*Kuwata, S., 876Kuykendall, D., 2630Kuznetzova, T., 1615*Kwak, J., 932Kwiatkowski, D.J., 1913, 1981,
1996, 2140, 2353, 2618Kwiatkowski, M., 1041Kwiatkowski, Jr., T.J., 2157*Kwong, L.C., 753
L'AbbW, D., 2513*Labeille, B., 769, 1079Labella, T., 2158*Labelle, Y., 483*Labuda, D., 1039*, 2018, 2099,2454
Labuda, M., 2698*Lacassie, Y., 750*, 859, 1419Lacerda, L., 837Lachman, R., 1260Lacombe, D., 639, 751*Ladanyi, M., 1674*Ladanyi, T., 2201Ladda, R.L., 785, 1056, 1066,
1593, 2117La Du, B.N., 546Laemmli, U.K., Session 67Lafer, C., 827Lafferty, E., 1692Lafferty, M.A., 472Laframboise, R., 1760Lafreniere, R.G., 97, 2366Lagerquist, A., 1041Lagerstrom, M., 2075*Lagrew, D., 1761Lahdetie, J., 1482*Lai, P.S., 1040*Laing, S., 1850Lairmore, T.C., 1950*, 2145Lakatua, D., 1375Lake, S.P., 600Lakkala, T., 1333*, 1482Lalande, M., 59*, 87, 1502,
1860, 2116, 2392Lalatta, F., 752*, 935Lalley, P.A., 1322Lalouel, J-M., Session 92, 2286Lalov, V., 962Lam, R.W., 2745Lam, S.T.S., 1785, 1795*Lam, V.M.S., 2324*LaMarca, M.E., 2503Lamb, A.N., 1651Lambert, B., 2813Lambert, C., 2301Lambert, M., 666, 1029Lammer, E.J., 924*, 2350Lamoureux, L., 2840Lamy, C., 1922Lamy, M., 1475Lan, G., 1675*Lanctot, A., 21Landegren, U., 1041*, 2075Landenburger, G., 1796*Lander, E.S., Session 36, Session95
Landers, C.J., 2773Landers, J.E., 2342Landes, G., 111, 1708, 2163Landrieu, P., 90Landsberger, D., 2329Lane, D., Session 63Lane, D.P., 587Lane, M.A., 1340Lange, E., 294Lange, K., 158, 294, 2040Langenhoven, E., 1036Langevitz, P., 1554Langford, L., 706Langley, S.D., 485Langlois, R.G., 2535, 2541, 2546Langlois, S., 104, 753*, 1154Langnas, A., 557Lania, A., 602
Lanman, J.T., 1533Lantiqua, A., 754*, 1791Lanyon, W.G., 1894Laosombat, V., 2354LaPorte, P., 2074Laptev, A.V., 576Larin, Z., 179, 1859, 1869Larman, J., 574Larramendy, M.L., 1676*Larregue, M., 1061Larripa, I., 1334*, 1449Larsen, L., 1948Larson, E. B., 2811Larson, R.A., 2581Larsson, C., 612Larsson, N.G., 228*Lasher, L., 2076*Laskarzewski, P.M., 2739La Spada, A., 95*, 2007Lasselin, C., 446LaszI6, A., 484*Lathrop, G.M., Session 32, 1927,2095
Latif, F., 605*, 785, 1066, 1122,2161
Latimer, F., 1298Latimer, J.)., 2325*Latimer, K., 556Latino, J., 1158LaTorre, G., 579LaTrenta, G., 905, 931Lau, A., 804Lauandos, J.E., 1617Laubach, V., 2326*Laubscher, L., 2093Laval, S.H., 2260Lavallie, S., 1502Lavedan, C., 2848*Law, J.C., 2624*Lawler, M., 7Lawn, R.M., 162*Lawrence, C., 96Lawrie, M.N., 1951*Laxman, R., 1335*Laxminarayana, K., 2849*Laxova, A., 1006Laxova, R., 1538Lazar, R., 1208Lazaris-Karatzas, A., 2450Lazaro, C., 1084Lazarou, L.P., 2088Lazarow, P.B., 505Lazjuk, G.l., 2699*Lazo, O., 516Lazo, P.A., 2591*Lazzarini, R., 2226Lea, D.H., 1777Leach, R.)., 1978, 2150Leadon, S.A., 2229Leana-Cox, J., 1189, 1542, 1626,
1677*, 1715Learish, R.D., 2020Le Beau, M.M., 124, Session 76,
1705, 2053, 2581Lebedev, V., 1615Leblond, S.C., 1043*Lebo, R., 687, 1952*, 2196Lecca, U., 1534Leclerc, B., 1816Le Corvaisier, B., 1684LeCouter, J.E., 1979Ledbetter, D., 968, 1641Ledbetter, D.H., 58*, 230, 1673,2077, 2139, 2165, 2400
Ledbetter, S.A., 1673, 2165Leder, P., 266
Lederfein, D., 16Ledley, F.D., 453, 532, 1818*,
2469, 2479Ledoux, P., 2327*Lee, B., 93*, 345, 460, 474Lee, C., 238Lee, C-C., 19, 2480*, 2846Lee, C.P., 388Lee, J.E., 2272, 2368Lee, J-S., 1044*Lee, J.T., 2159*Lee, M., 920Lee, M.I., 897Lee, M-L., 1257, 1669Lee, R., 1965Lee, R.E., 557Lee, S-Y., 1186Lee, T., 433Lee, T-Y., 1034, 1108, 1614Lee, W.L., 1040Lee Carter, C., 601Leeuwen, E.v., 1331Lefevre, M., 1475Leffell, D.J., 2583Leffert, C., 67Le Gales, C., 1799LeGall, J-Y., 2117Legator, M., 1697Leger, J.J., 2480Leger, W.J., 928Legius, E., 222, 737, 1925,
2328*, 2339LeGuern, C., 2490Le Guern, E., 1042*, 2058Legum, C., 1098, 1208*Legum, S., 1653Lehane, M., 1012Lehesjoki, A-E., 76*Lehman, T.A., 610Lehmann, R., 323*Lehner, T., 1885, 1938, 1943,
1953*, 2029, 2034Lehrach, H., 102, 175*, 178,
179, 298, 374, 1859, 1869,2204, 2330, 2336, 2348, 2383
Lehto, V-P., 466Leiba, H., 906Leicht, B., 2438*Leigh, I., 590Leinonen, A., 2405Leisti, J., 756*, 818, 896, 1035,
1198Leitch, A.R., 2141Leitersdorf, E., 2329*Lekanne Deprez, R.H., 1954*Leland, F., 2478, 2482Lele, K., 745, 1612Lelikhova, G.P., 2333Lelli, N., 980Le Marec, B., 1959, 2712Le Merrer, M., 635, 755*, 1959Lemieux, N., 2085Lemieux, R., 2202Lemyre, L., 1760Lench, N., 1955*Lengauer, C., 184, 2160*Lenkey, S.L., 1601Lennon, F., 2039Lennon, G., 2330*Lenoir, G., 502, 1977Lenz, W., 235, 1539Leone, P., 1352Leong, S.P.L., 1377Le Paslier, D., 2119, 2215Lepore, F., 2155Leppert, M., 833, 1316, 1969
519
520
Leppig, K.A., 1678*Leren, T., 821Lerer, I., 2245, 2883Lerman, C., 1733, 1754*Lerman, M.l., 605, 785, 1066,
1122, 2161*Lerner, T., 2162*, 2163, 2169Leroy, J.G., 1679*Leschot, N.J., 767, 1209*, 2144Lesh, D.H., 2020Leshner, R.T., 510Lesko, J., 1210*Lesko, S., 1580*Lesny, I., 854Lester, L., 1829Lestienne, P., 1115Letcher, R., 2339Letouz6, B., 2103Lettau, K., 936Leu, S., 1390Leuteriz, G., 2206Levan, G., 1870Levene, C., 688Leverone, B., 111Leversha, M.A., 1680*Levin, B., 1957, 1997Levin, S.W., 448, 1483*, 1677Levin, T., 1755*Levine, F., 1681 *, 2074Levine, M., Session 69Levinson, B., 2154Levinson, F., 1566Levitan, R., 638Levitt, D., 2293Levitt, R.C., 1936, 1983Levy, H., 212*, 563, 836, 2439*Levy, N., 207Lewis, J.G., 2094Lewis, K.E., 757*Lewis, M.B., 1054Lewis, M.E., 2514*Lewis, R.A., 1981, 2077*, 2342Leysens, N.J., 1966Li, C.C., 64*Li, F.P., 271*, 2607Li, H., 1125Li, J., 990, 1114Li, K-H., 2387Li, L., 326, 1543, 1665, 2061,2515*
Li, P., 1315, 1336*, 2404Li, Q., 544, 1285Li, S., 1286, 1854Li, S-B., 606*Li, S-C., 803Li, S.S-L., 2331*Li, S-Y., 1612Li, W-B., 2609Li, X., 925*, 1682*, 1933, 2509Li, X-M., 2440*Li, Z., 1836Liang, J.C., 1337*, 1396Liang, Y., 2595Liberati, M., 758*Liberman, B., 940Lichtenstein, Z., 1826Lichter, J.B., 1956*, 2079, 2170Lichter, P., 54*, 2263Lichter-Konecki, U.L., 2432,2462
Lidral, A., 2369Lieb, M., 2552*Lieber, C., 1797*Lieberman, E., 893Lieberman-Tangi, I., 584Liedgren, S., 1535
Lien, L.L., 1943, 2112, 2332*Lifchez, A., 107Ligas, C., 759*Lijoi, S., 872Lillicrap, D., 974, 1068, 2599Lim, L., 2380Lima, A.M.D., 2651Limb, CQ., 1211*Limber, E., 1178Limborska, S.A., 992, 2333*Limpens, J., 618Lim-Steele, J., 207Lin, A., 660Lin, C., 102, 1488, 1666, 2129,
2336, 2383Lin, C.K., 1120Lin, D., 1045*Lin, H.H., 1120Lin, J., 1366Lin, M.S., 1581*Lin, P-Z., 601Lin, S.J., 1778Lin, S-M., 2533Lin, S.N., 1383Lin, S-P., 1484*, 1655Lina, R.A., 2185Lincoln, S., 1270Lindahl, T., 295Lindal, S., 821Lindblom, A., 607*Lindeman, R., 2219, 2386Linden, M., 213Lindenbaum, M., 118ALindenbaum, R.H., 112, 1567,
1582*Linder, C., 2334*Lindhout, D., 1915Lindl6f, M., 1046*Lindmark, B., 680Lindsay, E., 1518Lindsay, S., 1974Lindsey, D., 2419Linehan, M., 605, 1122Lingenfelter, P., 1306Linke, R.P., 960Linnainmaa, K., 610Linss, G., 2003Linyear, A., 2730Lipnick, N., 1551Lippold, S., 1167Lipson, A.H., 943Lipson, M., 215Lisa, A., 2645, 2882Lisanti, J., 1102Lish, J., 1944Lisker, R., 253*, 1698Liston, W.A., 1842, 1919Litt, M., 53*, 1126, 1931Little, P., 2144Little, R.D., 373Little, S., 993, 1047*Littlefield, J.W., 1706Littler, A.J., 376Liu, A., 2041Liu, C., 1048, 1616*Liu, C.C., 1212*Liu, C-X., 1315, 1336Liu, F.X., 2395Liu, G-Y., 1048*Liu, I.H., 2481*Liu, J.Z., 1049*, 1117, 1123Liu, L-W., 760*Liu, P., 1649, 1709, 2321, 2501,2516*
Liu, Q., 1962, 2573, 2592*Liu, Q-Z., 1315
Liu, T.J., 2478, 2482*Liu, T-T., 570Liu, W., 2254Liu, XX., 1050*Liu, Y.E., 2706Liu, Z.D., 2474, 2487Livak, K.J., 2078*Livingstone, J., 1919Livini, E., 752Livneh, A., 858LizArraga, B., 634Ljung, R., 1005Llerena, Jr., J.C., 1683*Lloyd, J., 2812Lloyd, R.S., 2314Lo, D., 1124Lo, F.J., 1212Lo, L., 1125Lo, W., 2246Lo, W.H.Y., 558*, 990, 1021,
1114Loader, S., 1846Lobacarro, J-M., 751Lobato, L., 2757Lobato, N., 631LoBue, J., 1341, 1371Lockhart, L., 836, 1688Loesch, D.Z., 2700*Loffredo, C., 2650, 2668Loghin-Grosso, N.S., 1617*Lohr, G.W., 1269Lohrs, U., 1193London, J., 2625*London, W.T., 772Long, R.T., 1940Long, W., 1485*Longmire, J.L., 2499Longo, N., 485*Looijenga, L.H.J., 1318, 2234*Lopes, H., 2629L6pez, A., 1586Lopez, L.R., 111, 2163*Lopez-Arlandis, J., 1989L6pez-Flores, J.C., 893Lopez-Larrea, C., 2371L6pez Martin, V., 761*, 1486Lopez-Ortiz, J., 1557L6pez Pajares, I., 1159, 1431,
1486*Loprest, L., 2039Lo Re, M.L., 759Lorenzetti, D., 2178Lorey, F., 2701*Lorincz, M., 2267, 2335*Lorsung, E.M., 1235Los, F.J., 926*Losanowa, T., 1382Losekoot, M., 2517*Lostao, C., 631Lothe, R.A., 2593*Lotosh, E.A., 2850*Lott, M.T., 671, 973Louard, D., 678Loukopoulos, D., 390*Loulseged, H., 2472Loureiro, J.L., 1995Loux, N., 2804*Love, D.R., 17, 2379Lovell-Badge, R., Session 94,2393
Lovett, M., 201*, 2208Lovrien, E.W., 658Low, E-F., 1186Low, P.S., 1040Lowry, R.B., 762*Lozano, C., 695
Lozano, G., 2441*Lozovskaya, E.R., 239Lozzio, C.B., 1487*, 1686Lu, D-P., 2230, 2395Lu, G.H., 1338*Lu, J.M., 2163Lu, J.X., 2851*Lubetsky, M.J., 757Lubin, M.B., 608*Lubs, H.A., 963, 1104, 1465,
1804, 1957*, 1997, 2015Lubs, M.L., 1997Lucas, A., 2039Lucas-Derse, S., 1907Lucca, E.J., 1339*Lucek, P.R., 2653Lucente, D.E., 1880Ludecke, H-)., 197*Ludeke, B.I., 221, 2553*Lue-Shing, H., 501Lukash, F., 1499Luke, S., 1409, 1598, 2626*Lulli, P., 1993Lum, J.K., 168Lumbroso, R., 267Lumsden, A., 311Lun, Y.L., 1287Lund, C., 415Lundin, G., 1044Lundsteen, C., 1618*Lunga, I.N., 1213*Lunt, P., 143, 2012, 2037Luo, H-Y., 1048, 1117Luo, J.S., 758, 835Luo, Y., 2029Luoh, S-W., 433Lupski, J.R., 1702, 1958*, 2077,2139
Luria, D., 584Lurie, l.W., 2805*Luscombe, S., 1585Lustbader, E.D., 72*, 772Lustig, L., 1157, 1214*Lutchman, M., 1910Lutfalla, G., 1968Luthy, D.A., 1150Lutte, J.)., 887Lutterbach, B., 238Luty, J.A., 53Lutz, R., 912Lutze, L.H., 2539Luz, R., 2859Luzina, F.A., 2850Luzzatto, L., 1964Lyberg, T., 800Lyckegaard, E., 2438Lynberg, M.C., 2702*Lynch, E., 1952Lynch, H.T., 273*, 1316, 1977Lynch, J., 1316, 1977Lynch, M., 379Lyon, M.F., 144*Lyonnet, S., 449, 635, 1959*,2712
Lyons, L., 1960*Lystad, S., 218Lytle, C.H., 2600
Ma, K., 2205Ma, P., 2470, 2481Ma, S., 1537Ma, Y., 470Maahr, J., 1618Maas, R., 1495
Author and Presenter Index
Author and Presenter Index
Maass, H., 1373, 2596Maaswinkel-Mooij, P., 763, 890Maat-Kievit, A., 763*, 890Maayan, C., 1880MacCollin, M., 2169MacDonald, D., 904MacDonald, F., 1051*MacDonald, M., 298, 1828MacDonald, M.E., 82, 102, 961,
1727, 2204, 2210, 2336*,2348, 2383
MacDonald, M.L., 1137, 1215*,1274
Macedo, G., 2731Macek, M., 2703Macek, Jr., M., 2703*Macera, M.J., 1346, 1370, 1717,2164*
MacGillivray, M.H., 2237Macgregor, D., 2442*MacGregor, G.R., 2406Machado, M., 47, 474Maciel, R.j., 1127, 1216*Maciel-Guerra, A.T., 764*MacKenzie, A.E., 404, 2036MacKenzie, I.Z., 112Mackenzie, M.J., 85*MacLaren, D., 2836, 2852*MacLaren, L., 697, 1488*MacLean, C., 2030, 2062MacLennan, D.H., 429*, 1911MacLeod, P.L., 1889MacLeod, P.M., 233, 544*, 1437MacMillan, J.C., 1961*MacMurray, J., 979Macoska, J.A., 1340*Macquart-Moulin, G., 1799,
1825Macri, J.N., 310*Madan, K., 1495Madan, S., 560, 814, 1263Maddalena, A., 1841*, 2790Madiyan, M., 2754Madlom, H., 1441Mador, M.L., 2079*Madrazo, I., 908Madrazo, M., 908Maeda, N., 2425, 2463Maerzke, S., 1710Maestrelli, S.R.P., 2791Magalhaes Faria, R., 1427, 1514Magalong, D., 2770Magarino, C., 2504Magee, C., 653Magenis, R.E., 243*, 1600, 1718Mager, D., 2337*, 2424Mager, W.H., 2408Magistrelli, R., 2555Magnani, C., 949, 985Magnusson, K.P., 2594*Magovcevic, I., 2338*Magzanov, R.V., 2728Mah, D., 1807Mahadevan, M., 404, 2036Maher, E., 785Maher, T., 106Maheshwari, M.C., 877, 2565Mahoney, M.J., 758, 835, 1257Mahony, B.S., 1150Mahuran, D.J., 283*, 528, 2246Maichele, A., 2385Maier, W., 2043Maisch, B., 960Majoor-Krakauer, D., 2704*,2744
Majumder, P.P., 867, 1999,2705*
Mak, T.W., 1917Maki, M., 2171Makitie, O., 765*Makover, A., 16Malaspina, P., 1937, 1993Malcolm, S., 1015Malet, P., 1684*Malik, S.A., 848Malinen, T., 617Malkin, D., 218Mallet, A., 2643Malmgren, H., 2075Malone, P.S., 1362Malone, V., 1162Malysheva, O., 965Mamaeva, S., 2131Mamer, O.A., 452, 524, 1217*Mammi, I., 2762Mamunes, P., 1737Manca, L., 2423Manchester, D.K., 1343Mancini, A., 759Mancuso, S., 1475Mandahl, N., 371*Mandava, R., 1218*Mandel, J-L., 81, 377*Mandell, R., 562Mandrikina, E.V., 465Manenti, E., 910Mangat, H., 486*Manjunatha, K.R., 766*Mankin, H.J., 553Mankinen, C., 827, 1132Mann, R., 623Mann, S.S., 1181Mann, W.R., 1874, 1962*Mannaerts, G.P., 260*, 527Mannens, M., 767*, 1572, 2144Mannermaa, A., 2595*Manning, D., 1699Mano, K., 1739, 2857Mansour, S.L., 30*Mantei, N., 1948Manuelidis, L., 414*Mao, J., 2031Mao, X., 1052*Mao, Y., 2028Maraldi, N.M., 2122Marazita, M.L., 22*, 2030, 2681,
2706*, 2730Marsais, B., 2057Marchau, F., 1921Marchese, S., 552, 1530Marchetti, G., 444, 1685*Marchuk, D.A., 98, 2133, 2328,2339*
Marcotte, P., 2002Marcouillier, M., 2725Marcoz, i-P., 1064Marcsec, Z., 2098Marcucci, L., 677Marcus, S., 1053*, 1829Mares, Jr., A., 2165*Margaglione, M., 872Mariman, E.C.M., 2235*Marin, E., 783Marineau, C., 2166*, 2191, 2251Marinello, M.J., 1219*Marini, C., 759Marini, J.C., 1054*Marini, T., 954*, 1569Marion, R.W., 768*, 1741Mark, H.F.L., 1619*, 2149Mark, Y., 1619
Markalous, H., 1341 *, 1371Markham, A.F., 101, 2306Markiewicz, D., 2261Marks, J.H., 1779*Marles, S.L., 1055*Marom, M., 1245Maroteaux, P., 446, 650Marques, C., 1514Marquet, J., 133, Session 27Marquez, C., 1629Marquez-Solis, E., 893Marras, S., 1534Marshall, K.J., 1878Marshall, T., 497Marsteller, F., 1828Marstrander, M., 1345Martens, P., 1262Martha, A., 1960Martin, B.M., 2483, 2503Martin, C., 2518*Martin, C.A., 203Martin, C.J., 226Martin, G., 1975Martin, G.M., 2811Martin, J., 463, 2674Martin, J.J., 1998Martin, M.L., 232Martin, N., 1342Martin, N.G., 400*Martin, R.H., 362*, 407*, 1184Martin, W., 227Martin-DeLeon, P.A., 1552,
1583*, 1594Martinetti, M., 665Martinez, A., 2499Martinez, B., 631Martinez, G., 2504Martinez, I., 791, 908Martinez Frias, M.L., 692Martinez, M.M., 1963*, 1879Martinez-Martinez, R., 844Martin-Gallardo, A., 2392Martini, G., 1964*Martini, M.E., 2349Martinsson, T., 1535Martinuzzi, A., 36Martorell, M.R., 1629Marx, S.J., 595Marynen, P., 1392, 1870Marzullo, L., 768Masaki, M., 2707*Masala, B., 2423Mascari, M.J., 1056*, 1593Maschio, G., 1110Mascio, L., 2087, 2151Mashima, Y., 1057*, 1931Mashimo, M., 545*Mashkova, T., 1639, 1694Maslen, C.L., 94*Massa, H.F., 182Mastella, G., 1078Masters, S., 2185Mastrangelo, P., 2227Mastroiacovo, P.P., 2762Masturzo, P., 980Masukata, H., 412Masumoto, H., 412Masumura, S., 1028Masumura, T., 2351Matalon, R., 212, 468, 573*, 836Matayoshi, T., 1167Mathes, A.C.S., 1308Mathew, C., 970, 1965*Mathews, A., 2799Mathews, K., 143, 1966*, 2012Mathews, T., 1220*
Mathias, S.L., 188*, 2278Mathieu, J., 1900Mathieu, M., 769*, 1079Matiaszuk, N., 501, 511Matsubara, Y., 265*Matsuda, I., 987, 1058*Matsumoto, A., 2286Matsumoto, M., 1862Matsumura, K., 20Matsunaga, T., 1118Matsuo, M., 2351Matsushita, M., 2231Matsuta, K., 876Matsuta, M., 1635, 1635Matt, B., 1519Mattei, J.F., 1528Mattei, M-G., 93, 2387Matteson, K.J., 1487, 1686*Matthews, B.W., 246*Matthews, P.M., 403*Matthopoulos, D., 1605Matton, M., 354Mattson, K., 610Matuoka, M., 2688Maugey, B., 1142, 1253Mauldin, C., 443Maumenee, I.H., 885, 2051Maunoury, C., 1430Mavrou, A., 1489*, 2292, 2672Maximilian, C., 770*May, D., 2686, 2697May, H., 1884May, K.M., 88*, 1517May, M., 1104, 2242May6n, D.G., 1221*MayerovA, A., 2047Mayfield, J., 909Mayo, J., 2084Mayr, U., 1376Mayr, W.R., 2853*Maziade, M., 2002Mazor, G., 646Mazoyer, S., 2024Mazurczak, T., 1756*McAfee, M.W., 26McAlpine, P.J., 1055, 1687*,2104
McAndrew, P.E., 2443*McArthur, R.G., 2670McBride, L., 2062McBride, OW., 1901, 2266McCabe, E.R.B., 810, 2135,
2220, 2385, 2406, 2616McCall, A.E., 2157McCall, S., 771*McCanna, K., 2681McCarthy, B., 2663, 2708*McCarthy, C., 1342*McCarthy, J., 826McCarthy, T.V., 1012McCauley, B., 237McCaw, G., 1155McClatchey, A., 2381McClure, M., 1840, 2676McCollin, M., 2162McCombie, W.R., 1003McCombs, J., 1688*McConkie-Rosell, A., 574, 1533McConnell, J., 850McConville, C.M., 1967*McCorkle, R.D., 1201McCormick, D., 789McCormick, F., 12*McCormick, M.K., 1682, 2167*,2499
McDaniel, L.D., 1689*, 2301
521
Author and Presenter Index
McDevitt, H.O., 2859McDonald, D., 2482McDonald, H., 2340*McDonald-Jones, G., 2590McDowell, G.A., 2709*McDuffie, H.H., 2710*McElreavey, D., 2341*McElree, C., 2770, 2773McEwen, A.J., 683McFadden, D.E., 104*, 1154McFarland, H., 100McFarlin, D., 100McGavran, L., 1343*, 1410,
1541McGee, T.L., 8McGill, ).J., 1217McGillivray, B.C., 1154, 1781McGinnis, R.E., 2711 *McGinniss, M.J., 1690*McGlynn, K.A., 772*McGuffin, P., 122*, 1986McGuinness, M.C., 454, 487*McGuire, N., 1691*McInerney, J.D., 1780*McInnes, B., 2530McInnes, R.R., 10*, 2530McInnis, M.G., 1968*, 2094McIntosh, I., 2311McIntosh, N., 773*McIvor, R.S., 1059*McKay, T.R., 1972McKechnie, D., 101McKeithan, T.W., 1705McKenna, W., 1763McKeown, C., 1051McKinney, C.E., 2483*McKusick, V.A., Session 73McLaren, A., 431*McLeod, D.R., 927*McMahan, M.R., 1490*McMahon, B.i., 2265McMahon, J., 2168McManus, J., 1643McMichael, A.i., 2618McMichael, J., 1540, 1620*McMorrow, L.E., 920, 1692*McPherson, E., 660, 774*McPherson, J.D., 1943, 2168*McQuarrie, P.S.R., 464McQuillan, G.M., 1852, 2737McWilliam, P., 7Meagher-Villemure, K., 1512Meaney, F.J., 948, 1798*Meck, J., 1412, 1693*Mecklin, J-P., 1991Mecucci, C., 1387, 1392Medvedev, L., 1639, 1694*Meehan, B.W., 2854*Meeker, T.C., 2184, 2608Meera Khan, P., 185, 609*,
1303, 2132, 2216Meglioli, G., 1222*Meguid, N., 1491*, 1675Mehm, W.I., 1592Mehra, S., 775*Mehta, L., 776*Meier-Ewert, S., 179Meijer, H., 2502Meijerink, P.H.S., 2408Meincke, L.1., 2167, 2499Meinecke, P., 234Meiner, V., 2329Meiner, Z., 1000Meisler, M.H., 2444*Melancon, D., 899Melancon, M., 1816
Melanson, S., 666, 2004, 2018,2289
Melaragno, M.I., 1584*Melendez, R., 1560Melenhorst, J., 194Melki, J., 971, 1223*, 1922,
2101, 2223Melle, D., 449, 2712*Mellon, C., 1969*Mellott, J., 2118Melmer, G., 2496Melnick, M., 2706Melo, M.S., 2050Meltzer, E., 494Meltzer, P., 2586Menard, E., 1585Mencher, J., 585Mendelbaum, K., 2038Mendell, J.R., 1886, 2212, 2319,2489
Mende-Muller, L., 488Mendes, R.P., 2673Mendez, H.M.M., 777*, 811Mendlewicz, J., 2038Mendoza, A.E., 1277Menendez, F., 1791Meng, X-W., 2404Menko, F., 1990Menkveld, R., 2176Mennie, M., 1842*Menninger, J., 2332, 2392Mennuti, M.T., 913, 1138, 1169,
1224*, 1250, 1485Menon, A.G., 2162, 2169*Menozzi, P., 254, 2882Mensink, H.J.A., 1384Mentink, M., 2318Menzel, H.J., 2434Meo, T., 2211Meola, G., 36Mercier, J., 2004Merel, P., 1060*Mrette, C., 1970*Merin, S., 906Merkens, E.C., 1915Merksamer, R., 1833Merkx, G., 1632Merlob, P., 1746Mermet, M.A., 1562Merril, C.R., 2049, 2179Merry, D.E., 2342*Messerli, J., 1064Messier, P-E., 1476, 2066, 2085Metaxotou, C., 1489, 2292Metcalf, R.A., 587, 610*Metcalfe, M., 670Metintas, M., 1374Metsaranta, M., 46Mettey, R., 1061*Mettler, G., 778*Metzenberg, A., 2154Metzstein, M., 238Meunier, C., 779*Mevatee, U., 1621*Mewar, R., 1695*, 2188Meybohm, I., 1373, 2596*Meyer, J., 1611, 1713, 2062Meyers, C.M., 109, 780*, 1262,
1844Meyers, D.A., 75, 1751, 1861,
1933, 2091Meyers, M., 592Meyn, M.S., 1727, 2548, 2554*Meyne, J., 1696*Mhatre, A., 267Micale, M.A., 1340
Michaeli, )., 1674Michaels, J., 781*Michals, K., 573Michaud, J., 1039, 2519*Michaud, L., 495Michelle, M.P., 456Michels, V., 1013, 1062*, 2774Mickle, J., 1913Middleton, L., 1023Midgley, C., 587Midro, A.T., 1757*Miezejeski, C., 1141Migeon, B.R., 148*, 2152Migeon, C.., 2225Mihalache, D., 1344*Mikamo, K., 1199Mikhail, I., 2771Mikhalevich, H., 2806Mikhalevich, L., 2806*Miki, T., 739, 1916, 1975Mikkelsen, M., 359*, 415*,
1416, 1474, 1588Mikuni, M., 790MilA, M., 1404, 1515Milan, M., 949Milani-Comparetti, M., 2555*Milatovich, A., 1658, 1867*Miles, J.H., 782*Miles, R., 2483Miller, D.A., 1645Miller, D.G., 608Miller, D.L., 2170*Miller, F., 1062Miller, J., 1843*Miller, J.M., 1943Miller, J.N., 2208Miller, K., 2398Miller, L., 709Miller, M., 783*Miller, M.W., 2409Miller, O.J., 1645, 2138, 2195,2297
Miller, P.L., 2079Miller, R., 1163Miller, R.D., 2627*Miller, S.A., 2810Miller, W.L., 1045Millington, D.M., 475Millman, R., 2763Mills, K.A., 1966, 1971*Milner, B.J., 603Milner, E.C.B., 2212Milner, R.D.G., 736, 1965Milot, E., 2556*Milot, J., 815Milunsky, A., 79, 106, 1263,
1394Mimaya, J., 1321Minc, D., 418Minoletti, F., 2178Minoshima, K., 903Minoshima, S., 177Miny, P., 110, 114, 309, 1195,
1225*, 1254Miraglia del Giudice, E., 602,
1063*Misawa, S., 2148, 2171*, 2172Misericordia, M., 2555Mishkin, M., 1194Mitani, K., 2484*Mitchell, A., 2339Mitchell, D.A., 442Mitchell, D.L., 2539Mitchell, G.A., Session 4, 488*,
666, 1039, 2519Mitchell, J., 1585*
Mitchell, L.E., 2713*, 2739Mitchell, M.J., 1859, 2343*Mitchell, T.N., 2051Mitchison, H.M., 1972*Mitelman, F., 367*, 1330Mitkevich, S., 1639Mitra, J., 1341, 1371Mitsubuchi, H., 1058Mitsumoto, H., 1886Mitter, N.S., 1226*Mittman, I., 1740, 1758*Miura, I., 1380Miura, K., 1862Miura, Y., 1052Miyakawa, F., 1185Miyanohara, A., 2485*Miyatake, T., 1071, 1112, 2152,
2320, 2521, 2527Miyawaki, S., 523, 627, 798,875
Mize, S.G., 784*, 2479Miziorko, H., 488Mizunoe, T., 1227*, 1282Moatti, J-P., 1799*Mobraaten, L.E., 1898Modell, B., 149, 152*, 1024Modelo, R., 579Moderau, I., 2344*Modi, W.S., 605, 785*, 2161Modiano, G., 2628*, 2727, 2826Moe, J.P., 1345Moen, C.J.A., 594Moerer, P., 2042Moertel, C.A., 1228*Mogensen, J., 92Mohamed, A., 1322, 1340Mohammad, F.M., 1477Mohandas, T.K., 2285Mohanlal, K.N., 1851Mohapatra, I., 1206, 1229*Mohrenweiser, H.W., 176, 182,
2203, 2807*Moises, H., 1877Molday, R.S., 10Moldin, S.O., 2714*Mole, S.E., 2347Moll, P., 163, 1062, 2729Moller, C., 2750Maller, P., 1345*Mollevanger, P., 1303, 1556Molloy, K., 11Molnar, L., 1488Mommadov, I.M., 2715*Monaco, A.P., 18, 102, 179*,
202, 374, 1974, 2112, 2153,2206, 2346
Monaco, T., 2083Monard, S., 1605Monckton, D.G., 2789*Mondal, P.R., 786*Monk, M., 62*Monkman, S.C., 541Monnens, L., 194Montanaro, V., 373, 2158Montandon, A.J., 1002, 1005Montero, R., 1608, 2558Montes de Oca-Luna, R., 1702,
1958Moore, B.J., 1878Moore, C., 921Moore, C.C.D., 1045Moore, G.E., 919Moore, J.A., 398*, 1622*Moore, K., 2468Moorthy, A., 1341, 1371Moorti, M., 2114
522
Author and Presenter Index
Mor, O., 1640Mora, F., 754Morabito, E., 500Moraes, C.T., 34Morales, E., 754Moralli, D., 2182Moran, E., 1759*Moran, T., 419Morawietz, S., 2262Mordaunt, V., 2701Moreira, C., 989Morell, R., 79Morellini, M., 1937Moreno, F., 2558Moreno, R.F., 2179Moreno, R.S., 2659Moretti, T., 1973*Moretti-Ferreira, D., 787*, 1329Morgan, C., 1342Morgan, C.D., 1844Morgan, G., 1800*Morgan, J.M., 226Morgan, K., 6*, 493, 2004,
2018, 2725, 2840Morgan, M., 1763Morgan, P., 1276Morgan, S., 802Morgan-Hughes, J.A., Session 10,
1010, 2427Mori, M., 604Mori, P.G., 2652, 2794Morimoto, K., 1531, 2716*Morisaki, H., 489Morisaki, T., 489*Morishita, H., 690Morizon, G., 1492*Mornet, E., 1747, 1849Morocutti, C., 1937Morpurgo, G., 2628Morral, N., 988Morrell, J., 1861, 2190Morris, C.M., 2597*Morris, C.P., 282, 2345*Morris, G.E., 2379Morris, G.J., 17Morris, M.A., 1064*Morris, P., 204Morrison, L., 1697*Morth, C.M., 2819Morton, C.C., 26, 944, 1364,
1391, 2186, 2232, 2338, 2400Morton, D., 1051Morton, N., 2812Morton, N.E., 85, 2017, 2657Moscetti, A., 2113Moseley, A., 2484Moser, A., 454, 487, 505, 533,864
Moser, H., 130*, 190, 505, 804,864, 2190
Mosgoller, W., 2141Mosher, R., 433Mosimann, S., 2788Moskovitz, J., 2686, 2697Mostafavipour, S.H., 1346*Mota, N.J., 2673Motoiu, I., 1344Mott, C., 1829Motta-Vieira, L., 2058Mottes, M., 1065*Motulsky, A., 322*, 2231, 2398,2419
Mou, L., 2080*Mountain, i.L., 2623Mourino, A., 1151
Moustacchi, E., 296*, 2274,2559
Mowery, P.A., 928*Mowrey, P.N., 785, 1066*Moyer, S.L., 788*, 883Moyzis, R.K., Session 36, 1696,
2124, 2167, 2499Mrazek, D., 789*Muckle, G., 1760*Mueller, O.T., 210*, 1498Muenke, M., 1509, 1672Muglia, M., 2727Muhleman, D., 979Mukai, T., 2286Mukherjee, A.B., 448Mukoyama, H., 2313Mules, E.H., 1067*Mulhauser, L., 1731Mulivor, R.A., 472, 2081*Muller, B., 2808*Muller, C.R., 2256, 2346*, 2808Muller, D., 2694Muller, F., 108, 929*Muller, H., 269*Muller, H., 2788Muller, U., 105*, 1949, 2238Muller-Navia, J., 1519Mulley, J.C., 379, 968Mulligan, L.M., 2347*Mulligan, R.C., 2503Multani, A.S., 1230*, 1506, 1525Mulvihill, J.J., 1530Mundlos, S., 930*, 1121Muneer, R., 1347*, 1450Munne, S., 2153Munnich, A., 447, 449, 502,
503, 559*, 635, 1223, 1922,1939, 1959, 2101, 2223, 2712
Munsat, T.L., 1885, 1943Muntefering, M., 1519Murakami, K., 2148Murali, G., 2199Muratovska, O., 1326Murayama, K., 2622Murday, V.A., 2026Murdock, C., 2169Murer-Orlando, M., 1176,
1231*, 1965Murgia, A., 2159Murigande, C., 601Murken, J., 2808Muro, Y., 412Murphey, W.W., 1931, 2014Murphy, B., 2030Murphy, C., 317Murphy, S., 2676Murphy, W., 1109Murray, E.W., 1068*Murray, J., 143Murray, J.C., 410, 1716, 1966,
1971, 1974*, 2012, 2042,2265, 2350, 2369, 2774
Murray, L., 45Murray, R., 1986Murthy, S.K., 480, 1230, 1493*,
1525, 1591Murty, J.S., 575, 824, 2664,
2849, 2855*, 2862Murty, V.V.V.S., 611*Musgrave, M.A., 233Mutangadura-Mhlanga, T., 2557*Mutchinick, O., 1698*Mutoh, T., 1739Mutovin, G.R., 1473Mutter, G.L., 1069*Mutton, D.E., 357*
Myburgh, E., 1494*Myers, J., 1011Myers, N.A., 2646Myers, R.H., 2348*, 2660Myers, R.M., 299*, 2184, 2185Myers, S., 1888Myerson, D., 1306
-N-
Nabavinia, N., 1472Nabel, E., 2494Nabel, G., 2494Nacheva, M., 596Nadeau, J.H., 1898, 2056Nadon, N., 622Nagai, H., 2249Nagai, T., 2856*Nagano, K., 739, 1975Nagao, M., 490*Nagaraja, R., 373Nagashima, T., 2320Nahum, M., 2628Naidu, S., 864Naim, R., 1699*Nair, S., 1503Najafi, A.H., 1472Nakabayashi, H., 2584Nakagawa, A., 567Nakagawa, H., 2148, 2171,2172*
Nakagawa, S., 1135, 1165Nakagawara, A., 2215Nakahori, Y., 376Nakai, H., 2281Nakai, S., 438Nakajima, A., 999, 1019Nakajima, T., 2351Nakamura, H., 2351Nakamura, M., 1019Nakamura, N., 440Nakamura, Y., 101, 302*, 604,2087, 2347
Nakanaga, M., 2857*Nakano, I., 1071Nakano, K., 876Nakashima, H., 1070*Nakazaki, S., 1739Nakazato, H., 2172Nakura, J., 739, 1975*Nanba, E., 2446Nancarrow, J., 379Nance, M.A., 1976*Nance, W., 22, 28, 79, 399*,2658, 2790*
Nanjundiah, V., 2236*Nanko, S., 790*Nanthakumar, E.J., 2278Nara, T., 1448Narang, M., 404Narayanan, H.S., 766Narcisi, P., 350Narinsky, R., 998Narod, S.A., 1977*, 2006, 2009,2024
Naruse, S., 1071*Nasyrova, F., 992Nathans, J., 2378Natowicz, M., 1101Natt, E., 507Naumov, l.M., 1819*Navarrete, C., 791*, 840Naveed, M., 565Navia, B., 2173*Naviaux, R., 2488Navon, R., 3*
Naylor, E.W., 1102Naylor, J.A., 1002Naylor, S.L., 1978*, 2588Nayudu, N.V.S., 2717*Naz, R., 2309NazarA, Z., 844Nazer, H., 846Nazer, J., 2655Neary, W., 229Nebert, D.W., 428*Nebesn~kovA, E., 1188Neckrasova, E.P., 2879Nederlof, P.M., 181*Neethling, E., 1494Neff, J., 1305Neidhardt, A., 1801*, 1812Neidich, J., 905, 931*Neilly, M.E., 1705Neilsen, K., 1512Neish, A.S., 792*, 944Neitzel, H., 1710Nejfelt, M.K., 2453Nel, J.J., 1792Nelen, M., 194, 1985Nelis, E., 1998Nelson, D.L., 375, 378, 1038,2005, 2159, 2174*, 2352,2361, 2389, 2526
Nelson, I., 1115Nelson, L., 2150Nemiroff, R., 1163Neri, G., 1317, 2113, 2349*Nesland, J.M., 218, 2567Neto, J.C., 702Neuber, M., 936Neufeld, N., 1424Neuman, R., 2718*Neuman, W.L., 2581Neumann, H.P.H., 231*Neumann, P.E., 1868Neve, R., 196, 2241Nevedrova, N.V., 1837Neville, C.E., 404, 2036, 2370Nevin, J., 1232Nevin, N.C., 1232*Nevo, S., 2883Nevo, Y., 1653Newkirk, P., 210Newton, V., 27, 79, 229Nezarati, M.M., 233*, 544, 1889Ng, H.T., 1120Ng, J.T., 388Ng, W., 1832Ngo, J.T., 217, 1945Ngo, K.N., 1072*N'guyen, C., 2221Nguyen, C.K., 793*Nguyen, P., 2295Nguyen, T., 2539Nguyen, T-H., 1461Nguyen, T-T., 1461Nguyen, V.T.T., 1979*Nicholas, T.W., 1205Nicholls, A.C., 350Nicholls, M., 943Nicholls, R.D., 1056, 1116,
1549, 1558, 1593, 1868*,2224
Nichols, B.E., 2520*Nickerson, J.M., 2523Nicoletti, B., 1388, 1559Nicolini, H., 2719*Nie, L., 2030, 2062Nieb, B., 1144, 1197, 1233*Nieburh, E., 2221Niederecker, M., 1094
523
Author and Presenter Index
Niederwieser, D., 1436Nielsen, B.R., 1107Nielsen, D.A., 2445*Nielsen, l-M., 1115Nielsen, J., 359Niermeijer, M.F., Session 30,
378, 1767, 2389Nieuwint, A.W.M., 1495*Nihoul-Fekete, C., 23'41Niikawa, N., 1028, 1348*, 1448,
1728, 1946, 2510Nikolaev, D.L., 2699Nikoskelainen, E.K., 1022Nilsson, I.M., 1005Nilwarangkur, S., 1764Nimmannit, S., 1764Nimmermann, C., 1234*, 1264Ni Nuallain, M., 2030Nippert, I., 1802*Nirmala, A., 2713, 2720*Nishida, T., 1448Nishigaki, I., 491*Nishikawa, M., 2688Nishimoto, J., 2446*Nishimura, D.Y., 2350*Nishio, H., 2351*Nisson, P., 2082*Nitowsky, H.M., 560*, 814,
1135, 1165, 1243, 1263Niveloni, S., 1449Nizetic, D., 178Niznik, H.B., 1903Nobukuni, Y., 1058Noel, B., 1528Noel, P., 216Noelken, M.E., 383Nolin, S.L., 2175*Noll, W.W., 2008Nomura, T., 1369Nonaka, I., 1017Nootens, S., 1816Nopparatana, C., 2354Norbury, C.G., 1582Norby, S., 1073*, 1115, 2221'Nordenskjold, M., 612*Nordlund, J.J., 2705Nordmann, Y., 1008Nordshus, T., 800Nordstrom, A-M., 1980*Norn,; O., 1948Nores, J.A., 728, 794*Norio, R., 5*, 76, 896Norman, D., 592Noro, M., 999Northrup, H., 1981*Norum, R.A., 1934, 1982*Nouri, N., 1983*Novak, G., 1433Novak, M., 443Novelletto, A., 1937, 1993, 2799Novelli, G., 910, 1984*Novikova, I.V., 2699Novitsky, V.V., 1354Nowak, J.S., 2858*Nowicki, G.A., 1496*Nuccio, J., 916Nudel, U., 16Nuell, M.J., 2400Nuez, A.N., 1003Nukina, N., 1071Nunes, V., 988, 1074*Nurbekov, M.K., 2098Nurnberg, P., 1382Nussbaum, R.L., 904, 2014,
2159, 2174, 2342, 2352Nutile-McNenemy, N., 2008
Nwokoro, N.A., 795*Nyberg, R., 937Nygaard, M., 92Nygaard, T.G., 2044
-0-
Oates, R., 106Ober, C., 932*, 1829Oberle, I., 377O'Brien, P.J., 429O'Brien, S.i., 1907, 1973O'Brien, T., 1828Ocampo, L., 1352O'Connell, M.P., 1109O'Connell, P., 14, 1952, 2150,2253
O'dahl, S., 2811Odenwald, W., 2226Odievre, M., 507Odone, V., 1329O'Donnell, J.J., 2802Odrezin, G., 744, 796*Oetting, W., 2318Offermans, J.P.M., 1429Ogasawara, N., 491Ogawa, K., 1448Ogden, M., 2316, 2377Ogier, H., 447Ogihara, T., 739, 1975Ogilvie, D., 2306O'Gorman, A.M., 524Ogren, J., 1289Ogur, G., 797*, 838, 1406Ogura, K., 1858Oh, M.Y., 2846Oh, S., 2512Oh, S.J., 744Ohama, K., 1199O'Hara, B.F., 2273Ohashi, H., 1448Ohashi, T., 436, 552, 2486*,2492
Ohba, Y., 68Ohlendieck, K., 20, 2385Ohno, K., 627, 798*, 875Oiuonbilig, A., 1497*Okabe, I., 2352*Okano, K., 551, 1946Okano, Y., 455Okazaki, T., 412*Okimoto, Y., 1324Okten, G., 1349*Okumura, K., 2124Olafsson, I., 1026Olah, E., 1350*Old, J.M., 1024, 1272Oldenburg, M., 2132Oldfors, A., 228O'Leary, L., 2663Olek, K., 680, 2344, 2397Olert, J., 1519Oliva, J.A., 1791Oliveira, N.R.B., 702Oliveira, S.E., 2751Oliveri, D.R., 492*Olivero, O.A., 1343Olsen, D.A., 52, 176, 182,
1962, 2203, 2535Olson, E., 326*Olson, M.V., 49, 237*, 2160Olson, S., 243, 1718Olsson, J.E., 799*Olsson, K., 1940O'Malley, K.L., 1076Oman-Ganes, L.A., 1235*
Omiecinski, C., 543Ommen, G.J.B.v., 1767Onadim, Z., 613*O'Neil, A., 2030Oniki, R., 2068Onodera, K., 2281Onodera, O., 2521*Ooki, S., 2721*Oomen, L.C.J.M., 594Oosterhuis, J.W., 614*, 1311,
1318, 1384, 1386, 2234, 2607Oosterwijk, J.C., 1152, 1985*Oosthuizen, C.i.J., 2176*Oostra, B.A., 378*, 568, 1720,
1954, 2005, 2045, 2174,2361, 2389, 2766
Opp, J.S., 1859, 2238Oppenheim, A., 2883Oran, O., 636Oranje, A.P., 1985Orazova, G.A., 2879Orcutt, M.L., 605, 2161O'Reilly, A., 1772Orioli, I.M., 2722*Orkin, S., Session 9, Session 71Orlander, P., 706Ormsby, J.E., 1898Orozco, M., 1698Orr, H.T., 2001Orrison, B.M., 10540rstavik, K.H., 800*, 2755Ortega, R., 2845Orti, R., 2057Ortiz, C., 1586*Ortiz Romo, E., 1604Osella, P., 1394Osemlak, M., 2507Oshima, A., 1075*Oshimura, M., 875, 1395, 1891Oshiro, O., 68Osinga, J., 224Osman, M., 615*Osorio, R.V., 449Ossowski, O.K., 1700*Oster-Granite, M.L., 419Ostrer, H., 2105, 2237*Ostrosky-Wegman, P., 1608,
2558*Ota, S., 1324Otanlo, L., 1167Othman, A.H., 1313Otsu, K., 429Ott, J., 714, 1885, 1943, 1944,
1970, 2029, 2034, 2063,2095
Ott, R.N., 2019Ottestad, L., 2567Ottman, R., 2704, 2723*, 2744Otto, P.A., 787, 2791*Overby, H., 1356Overhauser, J., 1672, 1695,2177*,2188
Overkamp, W.J.L., 2250Owen, M., 1986*Oza, A., 589Ozawa, T., 33*Ozbek, U., 797Ozselik, T., 1987*, 2293Ozdemir, M., 1374Ozdemir, N., 1374Ozelius, L., 2140, 2353*Ozer, H.L., 2598, 2601Oztas, S., 644Oztaa, S., 1236*
Paabo, S., 315*Packman, S., 535, 1237*Padberg, G.W., 143*, 616*,
2012, 2042Paddy, M.R., 199Padma, T., 575, 657, 691, 801*,
895, 2664Paetkau, D., 1687Page, D.C., 433*, 2421Page, T., 478Pagon, R.A., 869Pai, G.S., 771, 802*, 1558Pairitz, G., 2724*Pakkala, S., 617Pakstis, A.J., 1877, 1924, 1941,
1988*, 2045Pal, K., 1231Palao, A., 2558Palatnik, M., 2629*Palau, F., 1989*Palazazolo, M., 239Palha, J.A., 2747Palit, S., 2563Palmer, B., 853Palmer, L., 2056Palmgren, M., 1843Palmieri, G., 204*, 373Palmour, R.M., 493, 517, 678,2725*
Palomaki, G.E., 1169, 1203,1224, 1238*, 1250
Palomaki, G.F., 1134Palomino, H., 803*Palomino, H.M., 803Palotie, A., 617*, 714, 2013Pals, G., 1990*, 2408Pan, X.F., 2769, 2778Pan, X.L., 1021Panarello, C., 2652, 2794Panayidou, K., 1023Pandolfo, M., 1873, 1937, 2178*Pangalos, C., 1528Panich, V., 2354*Panizza, D.S., 1238Panny, S., 1832Panter, S., 2684Pantova, I.G., 1523Pantzar, T., 804*Papadopoulo, D., 296, 2559*Papas, C.B., 637Papayannopoulou, T., 338Papenhausen, P.P., 1498*, 1748Papi, L., 2347Papp, A.C., 1081Paraswanath, S., 1372Parboosingh, J.S., 493*Pardinas, J., 2598Pardue, M.L., 316*Parent, P., 2712Parente, M.G., 73, 2387Parenti, G., 805*Parfitt, E., 1986Parfrey, P.S., 226Parik, J., 1041, 2075Parikh, H., 1462Parimoo, B., 490Parimoo, P., 747Parimoo, S., 2511Park, H., 574*, 2355*Park, K.S., 2876Park, M.H., 2876Park, M.S., 1891Park, V.M., 1701*Parke, J.C., 1783
524
Author and Presenter Index
Parke, Jr., J.C., 1456Parker, E., 1660Parker, N.B., 1343Parker, R.A., 2863Parkin, D., 603Parmenter, M., 1619Parmiter, A.H., 219Parnes, B., 1499*Parodo, L., 1534Parry, D.M., 676, 806*Parshad, R., 807*, 845, 2695Parsian, A., 1076*Parsons, P.G., 2574Parsons, Y.M., 1156Partalci, A., 1987Partridge, T.A., 424*Parvizpour, D., 1351*Parvizpour, S., 1177Pascual Castroviejo, I., 761Paskulin, G.A., 777, 811Passage, M.B., 2285Passarge, E., 1721Passarino, G., 2826Passos-Bueno, M.R., 2050Pasti, G., 1350Pastores, G., 1062Pastushenko, A.S., 942Patanjali, S.R., 2511Patel, K., 2083*Patel, L., 1911Patel, P.l., 1702*, 1958, 2011,
2077, 2139Patil, S., 1325, 1458, 1622Patois, E., 2742Patracchini, P., 444, 1685Patsalis, P., 2598*Patterson, D., 2119, 2189Patterson, D.F., 518Patton, M.A., 1763Patzak, A., 1373Paul, S.M., 1940Paul, T.O., 703Paula, F.A., 1407Pauls, D.L., 789, 1924, 1940,
1941, 2766Paulus-Thomas, J., 774, 1102Pautler, S.E., 2116Pavan, W., 50Pavanello, R., 1735Pavelka, K., 111Pavlath, G.K., 21Pawar, H., 2308, 2459Pawlak, A.L., 2726*Pawlowitzki, I-H., 1254Pawlyk, B.S., 799Payami, H., 592Payao, S.L.M., 1584Paz-y-Mino, C., 1352*Peacock, M.L., 2291Peacock, R., 66, 986Peacocke, M., 1912Pearce, W.G., 1878Pearson, M.A., 1295Pearson, P.L., 202, 1690, 1706,2153
Pecorara, M., 2652, 2794Pedersen, M.B., 187Pedersen, R.A., 2325Pedersen, S., 92Pedreira, S., 1449Pedrotti, A., 777Pegram, D., 552Pei, J., 2114Peissel, B., 1110Peleg, L., 461, 494*Pelet, A., 559, 1939, 1959
Pelias, M.Z., 1820*, 2023Pellestor, F., 1587*Peltomaki, P., 1991 *Peltonen, L., 46*, 77, 466, 1935,2013, 2356*
Penia, R., 840Peflaherrera, M.S., 1352Pehialoza, R., 840Pencarinha, D., 1821*Penchaszadeh, G.K., 1239*Penchaszadeh, V.B., 748, 1521,
1803*Pennington, R.D., 1642Penswick, J., 2599Pentao, L., 1702, 2077Pepe, G., 2727*Pepkowitz, S.H., 652, 1426Peraza, I., 1827Pereira, E., 982Pereira, L.V., 2491Perepetskaja, G., 2806Peretz, H., 1208Perez-Andrade, M.E., 893Perez Jurado, L.A., 2084*Perheentupa, J., 765Pericak-Vance, M.A., 78, 80,
143, 1904, 1992*, 2021, 2039Perilla, Y., 716Perizonius, R., 2502Perl, A., 1304Perlin, M., 2060Perret, J., 662Perrone, R., 1501Perroni, L., 1685Perrotta, S., 602, 1063Perry, B.A., 2807Perry, T.R., 997Perryman, M.B., 1920, 2165,2222, 2287, 2310, 2407, 2501
Persichetti, F., 1937, 1993*Persico, G., 2294, 2307Pertcev, G.S., 2728*Perusse, L., 2729*Pession, A., 602Pestafna, A., 1332Peters, A.C.B., 890Peters, D., 2087, 2151Peters, D.J.M., 1994*Peters, J., 1761*Petersen, D.D., 428Petersen, G.B., 359Petersen, M.B., 415, 1588*,1968
Peterson, G., 118Petrella, R., 1602, 1623*Petrinelli, P., 677Petrou, M., 1024Pettay, D., 85, 916Pettenati, M.J., 1490, 1500*,
1509Pettersson, T., 1031Pettersson, U., 1041, 2075,2106, 2200
Pettigrew, A., 808*Petty, E.M., 728, 1353*, 1484Petty, T., 2814Petzl-Erler, M.L., 2859*Pfeifer, G.P., 2540Pfeiffer, R.A., 1190, 1959Pfendner, E.G., 89*Pflueger, S., 809*, 954, 1569Phadke, S., 856Pham-Dinh, D., 971Phaneuf, D., 483Phelan, M.C., 1589*, 1804Philbert, P.M.P., 1308
Philip, J., 359, 2231Philip, N., 234*Philipps, S., 1055Phillips, C., 916Phillips IlIl, J.A., 70, 1037, 1840,2031, 2084, 2390, 2632,2821, 2863
Phillips, N., 2138Phillips, O.P., 109, 1262, 1844*Phipps, P., 1940Piantadosi, S., 615Piazza, A., 254*Piccinelli, A., 1873, 1937, 2178Piche, C., 1760Picheth, G., 580Picketts, D.J., 974, 2599*Pieke Dahl, S., 1077*, 2155,2750
Piel, J.L., 635Pierce, J., 2797Pieretti, M., 375, 2092, 2174,
2357, 2361Pierluigi, M., 1428Pierpont, M.E., 498Pieters, M.H.E.C., 1240*Pignatti, P.F., 1065, 1078*, 1110Piguzzi, M.T., 752Pihlajaniemi, T., 1011Pilia, G., 373Pillers, D.M., 810*Pilz, A., 224Pimenov, M.G., 1103Pimentel, M., 989Pinheiro, S., 1178Pinkel, D., 217, 1132, 1281,2087, 2151, 2156
Pino, W., 725Pinsky, L., 267*Pinto, L.l.B., 777, 811*Pinto-Cisternas, J., 648, 812*Piserchio, J., 1415Pitter, J.H., 1409Piussan, C., 769, 1079*Pivetta, O., 2344Pivnick, E.K., 2238*Pizzuti, A., 96, 2295, 2357*,2361
Plachot, M., 1590*Plaisted, L., 1628Platt, L., 652, 704, 914, 1202,1834
Plavsic, N., 2366Pletcher, B.A., 508, 1501*Plonk, S.G., 1459Plotnikova, N.N., 813*Ploughman, L.M., 22, 2030,2730*
Plummer, S., 961, 2210, 2384Plutalov, O.V., 1095Pobedonostseva, E., 2847Poge, A., 196Poggi, V., 509PohIschmidt, M., 1869*Pohlson, E., 1181Pohodich, A.J., 1162, 1241*Poirier, J., 2004Poirier, M.C., 1343Poje, Z., 1466Pokala, P., 814*Pokorney, W., 2478Pol, D.v.d., 1 1Polakis, P., 12Pollack, M., 2052Pollard, H.B., 2266Poller, W., 680Poll-The, B.T., 263
525
Polomeno, R.C., 454, 815*Polten, A., 285Poluha, D., 2465Polukarova, L.G., 2333Polychronakos, C., 1502*Polymeropolous, M.H., 2100Polymeropoulos, M.H., 2049,2179*
Pomponio, R.J., 1069Poncin, J., 675Ponder, B.A.J., 13*, Session 63,2347
Ponder, M., 13Pons, F., 2480Ponting, N.R., 1140, 1242*Poort, S.R., 984Pope, F.M., 350*Popish, A., 1180Popovich, B.W., 1080*Popp, S., 184Porfirio, B., 1703*Porta, G., 373Porteous, D., 2144Porteous, M.E., 816*, 1932Porteus, M., 234Porto, B., 1624*Porto, G., 1624, 2731*Pospekhova, N.l., 2564Post, E., 1335Potier, M., 495*, 1462Potier, M-C., 2156Potluri, V.R., 1503*Potter, H., 1504*Potter, T.G., 1904, 2368Potts, A., 2149Poulsen, H., 415Poulton, J., 2447*Poustka, A.M., 125, 178*, 179,374*
Povey, S., 1582, 2136Povirk, L.F., 2534Powell, B.R., 810Powell, C.M., 817*, 1439Powell, l.A., 1340Powell, J., 1986Powell, L.W., 2137Powell, M.F., 1642Powers, P.A., 2180*Powers, V.E., 1666, 1704*Poyhonen, M., 818*Prabhakara, K., 480, 1591*Prader, A., 645Pragliola, A., 2294, 2307Prantera, G., 1652Pras, M., 858, 1554, 1872Prasad, V.S., 1297Prata, M.J., 1995*Pratibha, N., 575*Pratt, V.M., 2358*Pravenec, M., 1866Preicak-Vance, M., 2012Prencipe, M., 759Prescott, K.E., 1505*Prevost, C., 1900Price, F., 807, 845, 2695Price, J., 109Price, R.A., 401Priest, J., 1565, 2686Prieto, F., 1989Prieur, F., 1572Prieur, M., 635, 1430, 1528Primo-Parm6, S.L., 546*Pringle, J., 433Prior, T.W., 1081*Pritchard, C.A., 299Pritchard, D.J., 2732*
Author and Presenter Index
Pritchard, M., 379Privitera, O., 935Prochazka-Graf, G., 819*, 874Prockop, D.J., 44*, 1712, 2025,
2461, 2497Profumo, L.E., 1463Proietti, M., 677Prokhorov, A.Y., 2564Prokofjev, G.V., 1523Promchainant, C., 1249Propert, D., 2733*Proshin, S.N., 1354*Provost, S., 2202Prozorova, M.V., 1770Pruchno, C., 2464Prusiner, S.B., 1000Pruzina, S., 118APrytkov, A.N., 2025Przybyla, B.D., 909Pshytycki, A., 1446Puech, A., 90, 1572, 2181*Puffenberger, E.G., 1996*Pugh, F., 118Pulijaal, V., 1243*, 1263Pulst, S.M., 203Pulyaeva, E.V., 576Punales-Morejon, D., 1762*Punnett, H.H., 1398Purandare, H., 1147, 1244*Purandare, S., 1244Purdue, P.E., 132Purohit, K., 820*Purtilo, D.T., 968, 1082*, 1263Putnam, E., 47Puymirat, J., 483Pyankov, S., 2815Pyeritz, R.E., 48, 77, 351*, 1996Pylkkanen, L., 1991
Qian, C., 2090Qian, J.F., 2242Qin, J., 760Qin, S., 2102Qionghua, A., 2860*Qiu, Q., 238Qiu, W-Q., 2734*Qiu, X.F., 2474, 2487*Qiu, X.K., 1087Quaid, K.A., 1822*Quandt, K.R., 2861*Quintana, A., 695Quintana, V., 2845Qumsiyeh, M.B., 1355*, 1381,
1454, 2458Qyan, P.H., 2851
-R-
Raap, A.K., 180, 181Rabago, R., 843Rabbitts, P.H., 224, 785, 2161Rabbitts, T.H., 2604Rabier, D., 259, 447, 559Rabin, M., 1957, 1997*Rabinovitch, P., 2571Rack, K., 376Radhakrishna, U., 1230, 1506*,
1525Radnaabazar, J., 1497, 2735*Rado, T., 2070Raducha, M.R., 472Radvany, J., 1889Raeburn, ).A., 1894Raees-Dana, J., 1472
Raeke, T., 1861Raeymaekers, P., 1921, 1998*,
2038, 2046Raez, E., 634Raffel, L., 561*, 1832Rafi, M.A., 286, 451, 2359*Rafi, S.K., 1379, 1592*Rafikov, K.S., 2317Raghavan, L., 2560*Raghoebier, S., 618*Ragusa, R.M., 1451Raguthu, S., 1570Rahimi, M., 1471, 1472Rahman, R., 1356*Rahmani, Z., 1528Rahuel, C., 2625Raimondi, E., 2113, 2182*Rajpurohit, Y., 518Ramel, S., 2571Ramer, J.C., 1066Ramesar, R., 79Ramesh, A., 1999*Ramesh, V., 2300, 2802Ramesh Babu, B., 2855, 2862*Rami Reddy, V., 1845*Ramirez, C., 1789Ramirez, F., 93, 345, 353*, 460,474
Ramirez, J., 733Ramirez, Z.H., 1460Ramirez-Duehas, M.L., 685, 694Ramos, C., 991Ramos, F.J., 1507*Ramqvist, T., 2594Ramsammy, R., 2630*Ramsay, M., 2000*Ramsay, N.K.C., 564Ramsha, U., 1615Ramsing, M., 821*Ramzy, M.I., 771, 822*Randolph, L.M., 823*, 1675Rangan, S.R., 1438Rangnekar, G.V., 1508*Ranney, H., 1072Ranum, L.P.W., 2001*Rao, B.S.S., 766Rao, D.C., 2649, 2713, 2720,2739
Rao, D.N., 519, 521Rao, K.W., 1651, 1804*Rao, N., 1490, 1500, 1509*Rao, P.H., 1357*Rao, P.S., 824*, 2849Rao, V.H., 460, 496*, 534Rao, V.V., 2849Rao, V.V.N.G., 2183*, 2374Rao, Y.S., 521Rapaport, D., 2050Rapaport-Blachman, D., 16Rapola, J., 1935Rapoport, S., 845Rapp, R., 1762Rappaport, R., 2341Rappold, G.A., 2360*Raschke, H., 2218Raskin, S., 1840, 2863*Raskind, W., 1083*, 2231, 2571Rassool, F.V., 1705*, 2053Rastan, S., 1106Rasulov, E., 992Rattazzi, M.C., 955*Rauch, J.B., 2575Rauskolb, R., 309Ravella, A., 1084*Ravia, Y., 1245*Ravindran, A., 1358*
Ravine, D., 249*Ravise, N., 2058Rawlings, B., 22Rawlings, L., 1749Ray, J.H., 1141, 1501Ray, M., 1085*Ray, P.N., Session 7, 810, 1876,2042, 2549
Raycroft, L., 2441Raymond, J.P., 2341Raymond, V., 2002*Read, A.P., 27*, 79Reade, T.M., 462, 524Reardon, W., 1086*Rebbeck, T., 2736*RMcan, D., 1029Recchia, F., 2138, 2198Rechitsky, S., 107, 2525Reddy, G.M., 825*Reddy, P.C., 2713, 2720Reddy, P.P., 520, 521, 734,2543
Redeker, B., 767Redford, A., 2770Redline, R.W., 720Redline, S., 2763Redwine, F., 1160, 1280Reed, A., 932Reed, T., 921Reed, V., 2260Reeders, S.T., 384*, 1869, 2147,2371
Reefer, J., 2076Rees, A.H., 1463Reeve, A., 2282Reeves, R., 50, 419*Reguigne, I., 2058Rehder, H., 900Rehm, J., 325Reich, E., 826*Reich, T., 1076Reichardt, J.K.V., 186*Reichel, E., 2173Reichl, D., 2759Reid, B., 2571Reid, C.S., 1246*, 1692Reid, J.A., 889Reid, T., 2603Reid, T.J., 1379Reidy, J.A., 1852, 2737*Reilly, S.L., 163, 2738*Reilly-Gendzier, G., 827*Reimer, D.L., 2448*Rein, M.S., 1364Reindollar, R.H., 2449*Reiner, A.H., 1898Reiner, O., 375, 2174, 2361*Reis, A., 2003*, 2703Reiser, N., 358Reiss, A., 828*Reitsma, P.H., 984Rekate, H., 832Remick, R.A., 2745Ren, L., 1359*Ren, S., 2232Ren, Z.R., 1087*, 1856, 2305Renges, H., 66*, 986Renieri, A., 2362*Renlund, M., 2013Renolen, O., 800Renterfa, R., 844Resau, J.H., 587Reshef, A., 2329Resnick, J.M., 564Resnick-Silverman, L., 2475Resta, R.G., 1150
Restrepo, M., 725Retief, A.E., 1036, 2093, 2176Reus, B.E., 2150Reuser, A.J.J., 568, 581Rey, F., 449, 2712Rey, J.A., 449, 1310, 1332Reyes, J., 829*, 1420Reynolds, J., 1565Reynolds, J.E., 2600*Rezai, K., 1225Reznik, H., 640Rezvani, I., 788Rhead, W.)., 459, 497*, 498,
513, 535Ricachnevski, N., 811Riccardi, S.L., 830, 1805*Riccardi, V.M., 333*, 830*,
1177, 1491, 1805, 2372Ricci, E., 977Rice, J.P., 2714, 2718Rice, T., 2649, 2713, 2720,2739*
Rich, S.S., 2001Richard Ill, C.W., 2184*Richards, A.J., 350Richards, B., 2522*Richards, C.S., 2824Richards, J., 82Richards, M.A., 841Richards, R.l., 379Richards, S., 1030, 2740*Richardson, W.R., 383Richaud, F., 2341Richer, C-L., 1039, 1476, 2066,
2085*, 2454Richieri-Costa, A., 707, 831*Richkind, K.E., 1247*, 1248Richman, L., 1458Richter, A., 1512, 2004*Richter, B., 543Richter, S., 724, 832*Riconda, D., 933*Riddell, D.C., 1088*Riddle, D.L., 2126Rider, S.H., 2185*Ried, T., 91*, 1858, 2263Riess, O., 2271, 2396Riethman, H., 2160Riggins, G.J., 1038, 2005*Riggs, A.D., 2540Rigo, J., 529Riles, L., 237Rimoin, D.L., 45*, 173*, 349,
522, 957, 1260Rimsza, M.E., 1295Rinaldo, P., 498*, 2377Rinaldy, A., 2314Rince, P., 1258Rinchik, G., 1868Rindl, M., 1051Ringer, D., 622, 2495Rininsland, F., 2261Rinsky, J., 1510*Riordan, J.R., Session 51, 2364Rios, R., 2581Rippin, J., 1437Risch, N.J., Session 32, 1248*,2353
Riscile, G.R., 1511*, 1748Rita, P., 2543Ritchie, S., 941, 1526Ritvanen, A., 735Rivas, M.L., 780, 1725Riviere, M., 1870Riviin, Y., 2551Rizza, C.R., 1002
526
Author and Presenter Index
Roach, E.S., 1981Robb, A.S., 1879Robb, L.J., 779, 1512*Robbins, C.A., 299Robbins, J., 807Robbins, P., 2486, 2492Robert, M-F., 488, 2519Roberts, A., 1342Roberts, D.)., 792, 934*, 944Roberts, M., 499*Roberts, R., 1089*, 1920, 2165,
2407, 2431Roberts, S.H., 1086Robertson, D.M., 400Robertson, N.G., 26*, 2186*Robertson, N.H., 993, 1047Robertson, R.M., 1037Robinson, A., 213*Robinson, B.H., 447Robinson, E., 1628, 2451Robinson, H., 1850Robinson, M.A., 2784Rocchi, M., 500*Roche, A., 376Roche, M.C., 761Rochette, C., 2018Rockwood, S., 1898Rodeck, C.H., Session 15, 919Rodeheffer, R., 1062Rodewald, A., 1300, 1474Rodgers, G.P., 2305Rodnan, L., 870Rodriguez, A.L., 2403Rodriguez, Jr., E., 1981Rodriguez, L., 1791Rodriguez, M.A., 829, 2845Rodriguez, V., 2761Rodriguez Gamero, L., 648Rodriguez-Larralde, A., 2864*Rodriquez, H., 754Roe, C.R., 475, 1119, 2277Roederer, G., 470Roels, F., 129*Roemer, K., 2074Roettger, V., 497Rogaev, E., 1103, 1947, 2187*,2194
Rogan, P.K., 1056, 1066, 1593*Rogatko, A., 2006*Rogatto, S.R., 1308, 1360*Rogers, J., 167*Roizes, G., 2057Rojas, C.V., 2394Rojas, E., 1608Rojas, I., 754Rojas, K., 2177, 2188*Roland, B., 1513*Roldan, A., 1948Roling, D., 2007*Rolleri, M., 980Rolo, M., 1553Roman, D.G., 2363*Roman, M., 2488*Romanenko, O.P., 2741*Romano, A., 1499Romano, D., 2162, 2189*, 2381Romano, G., 204, 373Romanov, K., 402Romem, I., 1139Romeo, G., 985Romero, N., 502Romero, R., 794Romi, M.M., 2470Romitti, L., 935*Rommens, J.M., 2261, 2364*Romyanan, O., 1249*
Ronchetto, P., 985Ronen, G.M., 833Rood-Breithaupt, J.A., 1090*Rooijmans, H.G.M., 1767Rooke, K., 2290Roos, R.A.C., 964, 1767Roos, R.P., 80Ropers, H. H., 11, Session 5, 24,
194, 405, 1990, 2196Rorman, E.G., 2365*Rosales, T.O., 833*Rosamond Pinto, M.C., 1427,
1514*Rosario, N.A., 2863Rosatelli, C., 250Rose, E., 1255Rose, N.C., 913, 1169, 1224,
1250*Rose, R., 402, 921Rosell, J., 1404, 1515*Rosenbaum, K.N., 28, 699,
834*, 842, 1439Rosenberg, C., 1690, 1706*Rosenberg, M.P., 2444Rosenberg, P., 931Rosenberg, R.N., 1889Rosenberg, T., 1073Rosenblatt, B., 1462Rosenblatt, D.S., 501*, 511, 531Rosenblatt, M., 1446Rosenblum-Vos, L.S., 1361*Rosenfeld, S., 1886Rosensaft, J., 1561Rosenstein, B.J., 2798Rosenthal, G., 608Roses, A.D., 78, 967, 1904,
1914, 1992, 2021, 2039,2272, 2368
Rosette, C.D., 1635Roshd, S., 700Rosner, B., 9Ross, B., 2684Ross, E., 1754Ross, J.L., 89Ross, M., 179, 2698Ross, S., 2670Rosselli, F., 296, 2274Rossi, A.B., 2185Roth, A., 2603Roth, D.E., 1020Roth, M.P., 537, 1290, 2742*Rothberg, P.G., 712, 810Rothenberg, S., 2478Rothhammer, F., 2865*Rothman, A.L., 2257Rothschild, C.B., 74, 2008*Rothschild, H., 71Rothstein, W., 1752Rotig, A., 502*, 503Rotmensch, S., 758, 794, 835*Rotshenker, S., 418Rotter, J.l., 1834, 2770, 2773,2781
Roubicek, M., 547*Rouleau, G.A., Session 28, 1889,
1900, 1910, 2009*, 2035,2130, 2162, 2166, 2169,2191, 2251
Roulston, D., 1516*Round, A.P., 2086*Rouse, B., 212, 836*, 1688Rousseau, F., 377Rousseau, J.J., 675Roux, D., 2221Rowell, J., 1342Rowland, L.P., 2704
Rowley, J.D., 124*, 2053, 2581Rowley, P.T., 1846*, 2602Rowley, S., 1367Roy, M., 515Roy, R., 638Royal, S., 796Roychowdhury, A., 2760Rozear, M., 1914Rozen, R., 2450*, 2840Rozmahel, R., 1924, 2366*Rozov, T., 2863Ruano, G., 167, 2514, 2792*Rubboli, F., 2182Rubenstein, C., 1158Ruberto, G., 2561*Rubin, C.H., 1128, 1251*, 1275Rubin, C.M., 2581Rubin, E.M., 192Rubin, J.D., 2668Rubinfeld, B., 12Rucknagel, D.L., 1774, 2743*Rudd, N.L., 1422Rudduck, C., 369Rufz, M.X., 694Ruiz-Barnbs, P., 1310Rundle, S.A., 1916Rupert, J.L., 97Rush, P.W., 1701Russell, J., 970Russell, M., 953Russell, P., 2268Russo, J., 1793Russo, S., 1132Rustin, P., 447, 502, 503*Rutgers, J., 1761Ruther, K., 11Ruther, K., 2218Rutter, S., 172Ruutu, T., 617Ruvalcaba, R.H.A., 24Ruz, L., 1698Ryan, W.J., 2326Rysiecki, G., 1582Ryynanen, M., 73, 2010*, 2387
_ W
Sa, C.M., 436Saal, H.M., 28, 699, 817, 842,
956*, 1678Sabbaghian, N., 267Sabnekar, P., 2866*Sacco, R., 2744*Saccucci, F., 2555Sachendranath, A., 504*SAnchez-Corona, J., 694Sachs, D.H., 2490Sachs, G.S., 1135Sack, G., 864, 1861, 2190*Sadek, S., 715Sadhana Chowdary, P., 2809*Sadovnick, A.D., 2745*, 2811Safneck, J., 1055Safran, A., 1064Sagai, Y., 1208Sagi, M., 572, 906, 2245Saha, B.K., 2196Saha, N., 2746*, 2873, 2875Sahenk, Z., 2489Sahhar, M., 328Sahn, E.E., 802, 841Sahota, A., 1091*, 2538Sainio, M., 838*Saint-Jore, B., 2804Saito, Y., 438, 512Sakai, I., 2313
Sakai, J., 1019Sakai, L.Y., 94Sakamoto, M., 1283, 1724,2087*
Sakati, N., 736, 839*, 846, 958Sakuma, T., 999Sakuraba, H., 1075Salamanca, F., 791, 840*Salamanca Maesso, C., 692Salbenblatt, A., 1410Salber, S., 1163Salbert, B.A., 663Salcedo, J.R., 851Salerno, A., 2838Salido, E.C., 2367*, 2402, 2440Salinas, C.F., 802, 822, 841*Saller, D.N., 1238Salomao, O., 702Salonen, R., 1847*, 1930Salvador, A.M., 1440Salvat, C., 1881Salvioli, R., 526Salzano, F.M., 256*Samango-Sprouse, C.A., 834,
842*, 870Samelson, R., 1178Samet, J., 610Samiotakis, M., 1041SA Miranda, M., 837*Samollow, P., 2451*Sampson, J.R., 1915Samson, F., 1904, 2368*Samson, K., 1088Samson, L., 2258, 2401Samuelson, J., 1338Samuelson, L.C., 2444Samulski, R.J., 2477, 2492San Agustin, T., 79Sanal, O., 294SAnchez, A., 1404Sanchez, C., 2571SAnchez, J., 950SAnchez, M.E., 1352SAnchez, O., 950SAnchez-Cascos, A., 843*SAnchez-Corona, J., 844*SAnchez-Pernaute, R., 843Sand, A., 415Sandberg, A.A., 1316, 1377,
1642, 2586Sandberg, M.A., 9Sanders, A.R., 2011*Sandholzer, C., 427, 2434Sandhu, A.K., 2568, 2587, 2601*Sandhu, S.S., 2547Sandkuijl, L.A., 1916, 1961,
2038, 2088Sandkuyl, L.A., Session 32, 1915,
2042, 2766Sandier, A., 2471Sandlin, C., 711, 1761Sando, G., 2248Sands, C., 1733, 1754Sane, K.S., 1976Sanford, K., 807, 845*, 2695Sangalli, A., 1065Sangiuolo, F., 1984Sanjad, S., 736, 839, 846*Sankary, S., 1362*Sanocki, E., 2419San RomAn, C., 695Sanson, M., 2191*Santachiara Benerecetti, A.S.,
2628, 2826*Santa-Maria, M., 535Santavouri, P., 1935
527
528
SantillAn, S., 1625*Santolamazza, C., 2628Santoro, K., 1619Santos, G., 1367Santos, H., 234Santos, M.J., 505*Santos, M.T., 1995Santos, R., 837Sanyal, M., 1294Sanz, J., 847Sanz, P., 2659Sanz-Mujica, P., 847*Saperstein, D.A., 2523*Sapienza, C., 244*Sapp, M.C., 1594*Saraiva, M.J.M., 960, 2747*Sarasa, J.L., 1310, 1332Sardas, O., 538Sardas, S., 538Sarfarazi, M., 143, 1109, 1883,
2012*, 2037Sargeant, M., 1986Sargent, C.A., 1680Sargent, I., 1272Sarikayalar, F., 636Saris, ).J., 1994Saritha, B.T., 1363*Sarkany, R.P., 2214Sarras, M., 383Sarto, G.E., 730Sartorato, E., 991Sasabe, T., 1931Sasaki, T., 727, 2452*Sasi, R., 2129Satish, J., 1294*, 1540, 1620Sato, M., 1252*Satoh, C., 440, 506*, 2793Saucedo-Cardenas, O., 1958Saudubray, J-M., 259*, 447, 502,
503, 2712Sauer, R., Session 46Saul, R., 1452Saulino, A., 98, 2339, 2818Saunders, A.M., Session 86Saunders, G.F., 220, 1960Saura, R., 1060, 1142, 1253*Saus, J., 383Sauvage, P., 2242Savoia, A., 1078Savontaus, M-L., 1022Savoy, D., 2848Sawada, T., 532Sawai, S., 1748Sawamura, D., 2387Saxe, D.F., 1517*Saxon, P., 2239*Say, B., 636, 848*Sayli, B.S., 628, 849, 1236,
1806*, 2831Sayli, U., 849*Scaduto, L., 1699Scambler, P.J., 901, 1518*Scarano, G., 2349Scarpelli, H., 1585Schaap, T., 1576Schaefer, B., 850*Schaefer, D., 768Schaefer, F., 622, 1092*, 2084,2495
Schaefer, G.B., 460Schaid, D., 216, 1062Schalt, F., 2028Schanfield, M.S., 2810*Schantz, L., 1978Schapiro, M., 845Schechter, A.N., 2305
Scheffer, H., 1093*, 1527, 1926Scheglova, M.V., 465Scheinker, V., 2365, 2545Schellenberg, G. D., 1975, 2811*Schendel, L., 768Schenkein, H.A., 2681Scherer, A., 851*, 1766Scherer, G., 507*, 1190Scherer, J., 1094Scherer, S., 2192*Scherthan, H., 184Schertzer, M., 2048Schickler, M., 418Schiff, E.B-S., 2255Schiffer, T., 1243Schimke, R.N., 206, 681Schinaia, G., 1937, 1993Schindler, D., 1609Schinzel, A., 647, 1690, 1707*,
1711Schisler, N.J., 2448, 2619Schlack, L., 1492Schlang, A.M., 2480Schleiermacher, E., 1519*Schlessinger, D., 204, 373*, 379,
2092, 2122Schleutker, J., 2013*Schlichtemeier, T., 882Schloo, R., 1254*Schlote, D., 2374Schlotter, M., 2432Schmerler, S., 1814Schmidt, A., 1721Schmidt, B.J., 1617Schmidt, D., 1255*Schmidt, F., 2043Schmidt, R., 1434Schmidt, S., 2043Schmidtke, J., 2703Schmidt-Sommerfeld, E., 498Schnatterly, P., 1183Schneider, H.P.G., 274Schneider, M., 1520*Schneider, S., 2193*Schnittger, S., 1664, 2183Schnur, R.E., 904, 2014*Schoenberg, M.L., 1364*Schoenfeld-Dimaio, M., 835Schoenmakers, E., 1392Schofield, B., 748, 1521*Schon, E.A., 34*, 191, 977Schonberg, S., 687, 701Schoof, J., 658Schoonmaker, M., 2694Schoos, R., 529Schoot, C.E.v.d., 1331Schor, P.L., 2499Schorderet, D.F., 136*Schorry, EK., 852*, 1536Schot, J.D.L., 616Schouten-V. Meeteren, A.Y.N.,
1331Schraffordt Koops, H., 614Schramm, A.M., 1878Schreck, R., 914, 1202, 1424,
1426, 1516Schreiber, R., 454Schreder, C., 194Schroeder, Jr., H.W., 2240*Schroeder, W.T., 2372Schroeder-Kurth, T.M., 1522*,
1609Schuback, D., 2353Schuchman, E.H., 2491Schulman, J.D., 1201, 1841,2790
Schulman, P., 1327Schultz, C., 1641Schultz, D., 2603Schultz, E., 2440Schultz, R.A., 1689, 2301Schulz, C., 1256*Schumacher, M.C., 164Schumann-Rogge, B., 1710Schuper, A., 906Schuring-Blom, G.H., 1209Schurr, T.D., 2637Schurr, T.G., 2610Schuster, M.K., 2008Schut, L.J., 2001Schutgens, R.B.H., 128*Schwab, S., 1094*, 2043Schwartz, B., 259Schwartz, C.E., 642, 963, 1104,
2015*, 2672Schwartz, D.R., 1385Schwartz, E.l., 1095*Schwartz, F., 196, 2241*Schwartz, G., 740Schwartz, H.S., 1365*Schwartz, l.D., 712Schwartz, J.L., 326, 2581Schwartz, L., 1096*Schwartz, M., 1107, 1848*Schwartz, P.E., 606, 1338Schwartz, S., 1139, 1189, 1413,
1542, 1626*, 1636, 1656,1677, 1715
Schwartz-Richstein, C., 1612Schwarz, M.J., 993, 1047Schwarzacher, T., 2141Schwienbacher, C., 444Schwinger, E., 936*, 1193, 1588Sciamanna, D.S., 868Sciorra, L.J., 1257*, 1669Scott, A.F., 188, 2278Scott, C.R., 658, 1443, 2828,
2836, 2852, 2867*Scott, H.S., 282, 2345Scott-Emuakpor, A.B., 327*Scozzari, R., 2628Scrimshaw, B., 853*Scriver, C.R., 153*, 389, 393*,
422*, 452, 524, 2246, 2289,2327, 2662, 2712
Seagal, S., 1058Searle, S., 2206Seashore, M.R., 508*, 1484Seaver, L.H., 1295*Sebastio, G., 509*Secor McVoy, J.R., 468, 510*Sedat, J.W., 199Sedun, K., 1781*Seebach, C., 847Seedorf, T., 1064Seeley, G., 1342Seely-Sloan, L., 1262Seemanova, E., 854*, 2106Seftel, H.C., 2329Segal, P., 2329Segraves, M., 1281Segraves, R., 1283, 1724Seharaseyon, J., 2489*Seia, M., 985Seibert, T., 2227Seizinger, B.R., 303*Sekhon, G., 1538Sekine, S., 2512Selby, P., 2562*Self, S., 625Selicorni, A., 752, 935Selig, A., 917
Seller, M.J., 1231, 1296*Sellers, T.A., 71*Sellinger, B., 370Sellitto, D., 2628Seltzer, W.K., 810Selva, J., 1258*Semenza, G.L., 1948, 2453*Semino, O., 2826Sengupta, L.K., 1508Senior, M., 1224Sequeiros, J., 1889, 1995, 2748*,2757
Sereda, L., 1712, 2497Serfas, K., 1911Seri, M., 2362Serjeant, G., 75Serjeantson, S.W., 257*Seror, V., 1799Serra, A., 2113Serrano, H., 1173Serratosa, J.M., 2041Serre, J-L., 1747, 1849*, 2703Servidei, S., 1001Serville, F., 1959Sessa, A., 2362Seth, P.K., 2749, 2868*Seth, S., 2749*, 2868Seva-Pereira, A., 2647Seven, H., 2665, 2677Severson, S.L., 577Seyschab, H., 1609Shacham, H., 1312Shafer, G.E., 2490*Shaffer, L.G., 1647, 1713Shaffer, R., 358Shah, H., 1366*Shah, H.O., 1501Shah, N.K., 1367*, 1607Shah, V.C., 1230, 1506, 1525Shalash, B.A., 879Shanahan, F., 2770, 2773Shandlorenko, S.K., 1523*Shanske, A., 855*, 1433, 1469,
1499, 1510Shanske, S., 977Shapira, E., 531, 1532, 1843,2709
Shapiro, B.J., 2431Shapiro, D.J., 2445Shapiro, L.J., 2285, 2367, 2402,2440
Shapiro, L.R., 1235, 1259*,1602, 1623, 2672
Shapiro, L.S., Session 29Shapiro, R.S., 641Shapiro, S.M., 510Sharief, F.S., 2331Sharkey, A., 2205Sharland, M., 1763*Sharma, A.K., 856*, 2563*, 2760Sharma, O.P., 1524*Sharony, R., 1260*Sharp, E.M., 7Sharp, N., 967Shastry, B.S., 857*Shaw, B., 557Shaw, D.J., 1916, 2088, 2115Shaw, G.L., 582Shea, T.J., 2871Shearman, A.M., 1929, 2016*Shedlousky, A., 2482Sheer, D., 2083Sheetz, K., 2684Sheffield, L.J., 249, 328*, 2812*Sheffield, V.C., 1097*, 1325,
1458, 2059, 2265, 2520
Author and Presenter Index
Author and Presenter Index
Sheidler, V.R., 615Sheils, D., 7Shekhter-Levin, S., 1368*Shelbourne, P., 2310Shelton, M., 2312Shen, G.P., 1287Shen, L.M., 2403Sherer, C., 660Sherer, M.E., 1319, 1368Sherman, R., 1162Sherman, S.L., 159, 1411,
1850*, 1962, 1978, 2005,2812
Sherrington, P.D., 2604Sherry, S., 2869*Sherwood, M., 1467Sheshadri, S., 766Sheth, F.J., 1525*Shevell, M.I., 511*Shevtsov, S.P., 1095Shew, J-Y., 2429Shi, H-P., 558, 2246Shiang, R., 2369*Shibata, A., 1028Shidoji, Y., 438, 512*Shields, D.C., 2017*, 2657Shifrin, H., 836Shih, L.Y., 1261*Shih, V.E., 562*, 2300, 2802Shiloh, Y., 294, 740, 1098Shimatake, H., 438, 512Shimizu, M., 1395Shimizu, N., 177*Shimizu, T., 68, 1071Shimizu, Y., 1378Shimmoto, M., 1075Shimoda, S-l., 662Shindoh, H., 2584Shinkwin, R., 2030Shinohara, T., 1369*Shiono, T., 999, 1057Shiota, K., 103*Shipley, J., 2083Shipley, W.U., 2577Shirahama, K., 2856Shirai, M., 1862Shirai, Y., 1739Shires, A., 513*Shirneshan, K., 1471Shirvan, A., 2266Shishkin, S.S., 576*, 2233Shizawa, Y., 2281Shlensky, A., 2187, 2194*Shoba, S., 766Shoeb, M.A., 715Shoffner, J.M., 31, 671Shohat, M., 858*, 1746, 2781Shomrat, R., 1098*, 1208, 1653Shook, D., 111, 1634, 1708*Short, M.P., 1913Shoshani, T., 2551Shownkeen, R., 238Shows, T., 2102, 2142, 2400Shprintzen, R.J., 1518, 1741Shreffler, D.C., 2627Shridhar, V., 1858, 2138, 2195*,2297
Shrimpton, A., 966, 1016, 1884Shriver, M.D., 2631*Shtybel, W., 227*Shuber, A., 1009, 2524*Shuber, T., 1786Shugart, Y.Y., 1077, 2750*Shukla, H., 2511Shulman, L.P., 109, 1262*, 1844Shultz, L.D., 21
Shuman, C., 941, 1526Shung, R., 1397Shung, W., 1397Shushval, O.N., 1523Shuster, R.S., 485Shutler, G., 404, 405, 2036,2370*
Shwed, N., 1615Si, J-S., 2523Sicard, D., 2839, 2842Siciliano, J., 1709, 2516Siciliano, M.J., 1649, 1709*,
1891, 2107, 2287, 2310,2321, 2368, 2501, 2516
Siddique, T., 80*Siddiqui, M.A.Q., 2164Sidhu, M.S., 1627*Sidransky, E., 514*, 2503Siegel-Bartelt, J., 941, 1526*Siest, G., 2800Siewertsen, M.A., 1979Siitari, H., 1022Sijmons, R.H., 1527*Silahtaroglu, A.N., 1782*Silengo, M., 234Silicorni, A., 234Sill, A.M., 2650Silva, B., 693Silva, B.M., 2731Silva, C., 2865Silva, M.A., 1407Silven, B., 1691Silver, A., 970Silver, K., 454, 773Silver, R.T., 586, 1370*Silverman, G., 2156Silverman, J., 2524Silverman, L.M., 997, 1014,
1099*Silvestre, E., 1153Silvestri, G., 977Sim, C-B., 570Simaraks, S., 1621Simard, F., 2840Simard, L.R., 2018*Simensen, R., 2672Siminovitch, K.A., 1912Simmler, M.C., 146, 2259Sim6es, A.L., 2751*Simoes, M., 2629Simola, K.O.J., 937*Sim6n, A., 631Simon, M., 1373, 2848Simonaro, C.M., 1341, 1371*Simon-Bouy, B., 1747, 1849Simoneau, I., 859*Simonet, L., 1866Simoni, G., 935Simons, J.W., 1991Simons, J.W.I.M., 2250Simosa, V., 648, 812Simpson, E., 433, 1678Simpson, J.L., 109, 361*, 780,
1262, 1844, 2238Simpson, N.E., 1888, 2340Simpson, S.A., 860*Simpson, S.G., 2091Simpson, W.J., 1888Sims, K., 2196*Sinaniotis, C., 1568Sinet, P.M., 1430, 1528*, 2119Sinev, E.M., 2197*Sing, C.F., 163*, 515*, 2682,
2729, 2736, 2738, 2775Singer, F., 957Singer, M.F., 2460
Singh, A., 747Singh, A.P., 1710Singh, C., 747Singh, D.N., 1372*Singh, I., 516*, 2547Singh, P., 2870*Singh, R., 7Singh, R.P., 2752*Singh, S., 1373*, 1671, 2466,2596
Singh, S.M., 2019*, 2410, 2448,2619
Sinha, A.K., 861*Sinkovec, J., 650Sinkus, A., 1595*Sinnett, D., 1039, 2099, 2454*Sinnott, P.)., 2375Sinosich, M.J., 1749Siri, E., 2882Sirinavin, C., 1764*Sirokvasheva, E.Y., 1103Sirugo, G., 81Sistonen, P., 76, 1918, 1991Sites, C., 2438Sjogren, B., 1877Sjostrom, H., 1948Sjoukes, P.F.J., 890Skare, J., 79, 1263*Sklower Brooks, S.L., 862*,
1570, 1667Skoletsky, J., 1009, 1691, 1786Skorski, M., 1467Skoulakis, E., 2438Skovby, F., 187*Skraastad, M.l., 185, 1100*,
1767Skrinjarit, I., 1466Skuse, G.R., 2602*Skyberg, D., 1107Slater, C.P., 2379Slater, R.M., 1323, 1331Slaugenhaupt, S.A., 1958, 1968,2020*
Slavutsky, I., 1334, 1449Sleijfer, D.T., 614Slomski, R., 722Slotnick, R.N., 1137, 1215Slovak, M.L., 619*, 1668Sly, W.S., 1020Smailus, D., 2340Small, K., 2021*Smalley, L., 2562Smalley, S., 863*Smallhorn, J., 941Smeets, B., 405Smeets, D., 1632Smeets, H.J.M., 24, 194*Smeland, E., 1345Smidt-jensen, S., 1266Smirnova, E., 992Smirnova, G.V., 1213Smit, L., 2814Smith, A., 2219, 2386Smith, A.E., Session 51Smith, A.J.K., 517*, 2725Smith, B.F., 518*Smith, D.I., 1722, 2138, 2195,
2198*, 2297Smith, F., 1101*Smith, H., 217Smith, J.R., 1180Smith, K.D., 75, 864*, 2225,2634
Smith, K.H., 2601Smith, M., 863, 2022*, 2301Smith, M.deA.C., 1584
Smith, R.J.H., 2023*Smith, S.H., 2586Smithies, O., Session 9Smith-Sarensen, B., 218, 2803,2813*
Smits, A.P.T., 2005Smits, R., 1865Smoller, D.A., 239Smooker, P.M., 193Smoor, M.A., 984Snabes, M., 1210Snarey, A., 1869Snell, R.G., 1884, 1916, 2088*Snell, T.C., 1898Snoek, M., 594Snover, D.C., 564Snow, C.M., 2444Snyder, H.L., 2169Snyder, P.J., 1081Sobek, I., 409Sobel, E., 294Sobel, R., 1501Sobell, J., 2753*Sobol, H., 2024*Sobrier, M.L., 2455*Soderkvist, P., 305Sofro, A.S.M., 2754*Sohar, E., 1554Sokol, R.J., 1174Sokolov, B.P., 2025*Solaas, M.H., 2755*Solaas, M.K., 2658Solak, M., 1374*Solera, J., 1486Solis, V., 865*Sollazzo, V., 1401, 1418Solomon, E., 2026, 2110, 2206,2218
Solus, J., 2199*Somer, M., 866*Somlo, S., 1869, 2371*Sommer, M.T., 2456*Sommer, S.S., 70, 2632*, 2753,2821
Sonenberg, N., 2450Song, F., 1117Soodyall, H., 2633*, 2635Soreng, L., 1375*SArensen, S.A., 1743, 1765*Soriano, G., 733, 1460, 2756*Soriano-Brucher, H., 2469Sosnoski, D., 2014Sotomaior, V.S., 2859Soto Trejo, H., 450Soukup, S., 1536Sousa, A., 2757*Souza, D.H., 1329Souza, I.R., 2835Soyeur, D., 529Soyka, M., 1094Sozer, A.C., 2871*, 2877Spadaro, M., 1937Spagnolo, A., 2762Spalova, I., 1253Spangler, E.A., 192Sparkes, R., 1585, 1945, 2041Sparr, T., 1107Sparvoli, A.C., 2647Speer, A., 2146Speer, M.C., 78*, 1904, 2012,2368
Speicher, M., 2160Speleman, F., 1534, 1679, 2111Spence, J.E., 1456, 1783Spence, M.A., 1945, 2706Spence, W.C., 1102*
529
Author and Presenter Index
Spencer, E.S., 1923Sperling, K., 1710*, 2275, 2703Spiegel, K., 1082Spiegel, R., 1711*Spielman, R.S., 2711Spielmann, R.C., 577*Spiga, I., 654Spina, E., 1405Spinner, N.B., 938*Spitkovsky, D.M., 2564*Spitsyn, V., 548*Spotila, L.D., 1712*, 2497Spranger, J., 43*Sprecher, D., 2739Springer, L., 366Spritz, R.A., 189*, 525, 2296Spurdle, A., 2872*Spurr, N., 2026*, 2282Squire, J., 2071Sribney, W.M., 2027*Srikumari, C., 1999Srinivasa Murthy, R., 766Srinivasan, M.R., 2758*Srinivas Rao, V., 2855Sriroongrueng, W., 2354Srivastava, M., 2266Staden, R., 238Stajich, J.M., 78, 1904, 2039Stalenhoef, A.F.H., 996Stalker, H.J., 633, 1529*Stallings, R.L., 2124Stamatoyannopoulos, G., Session
71Stambrook, P.J., 1091, 2538Stammer, V., 1547Stampino, L.G., 2561Stanbridge, E.J., 2098, 2301Stanescu, V., 650Stankovics, J., 532Stanley, C.A., 261*Stanley, W.S., 1439, 2089*Stanyon, R., 2641Stark, B., 584Stark-Houck, S.L., 1570, 1612Starr, R.)., 1689Stasiowski, B.A., 1713*Staub, R.W., 2854Stauffer, D., 833Stearn, H., 1876Stedman, H., 518Steed, D.L., 867Steel, G., 2519Steel, K.P., Session 8Steele, D., 1530*Steele, M.W., 757, 1601, 1823*Steen, M-L., 2200*Steensma, Y., 18Stefanescu, D.T., 1344Stefanovich, M., 1944Stefansson, K., 1996Steffenburg, S., 1535Stegnova, T.V., 1103*Steichen-Gersdorf, E., 1376*Steigman, C.K., 868*Stein, C.K., 1628*Stein, J.H.R., 768Steinberg, K.K., 1852, 2737Steiner, R.D., 869*Steinherz, R., 998Steinlein, O., 2028*Steinlin, M., 645Steinman, B., Session 73Steinmann, B., 77Steinmetz, A., 960Stengel-Rutkowski, S., 1234,
1264*
Stenman, U-H., 1847Stenroos, E.S., 1938, 1953Stepanets, A.P., 1837Stephens, K., 2372*Stephenson, C.F., 1377*Stern, H.J., 28, 699, 842, 870*Stetten, G., 1690, 1706, 1714*Stevens, C., 79Stevens, G., 2000Stevenson, R.E., 630, 642, 963,
1104*, 1589, 2015Stewart, C., 2418Stewart, C.S., 1904Stewart, D.A., 2400Stewart, E.A., 2373*Stewart, G.D., 203*, 2507Stewart, J., 1638Stewart, J.M., 819Stewart, L.L., 2670St. George-Hyslop, P.H., 1992,2381
Stibler, H., 187Stieve, J., 1195Stiller, R., 557, 835Stilwell, J.L., 1281, 2457*Stine, O.C., 2091, 2634*Stioui, S., 935St. Jean, P.L., 867*St. John, T., 1542St. Lezin, E., 1866Stocks, J., 2759*Stokland, T., 1345Stoler, J.M., 871*Stoll, C., 537, 1290, 1442,2242*
Stolz, F-M., 2374*Stone, E.M., 513, 1097, 2059,2520
Stone, W.J., 383Stoneking, M., 2635*, 2834,2869
Storto, P.D., 1378*, 1662Storvick, D., 2212Strachan, T., 99, 2375*Strain, L., 1016Strathdee, C.A., 2376*Stratta, R., 557Straub, R.E., 2029*Strausbaugh, L.D., 2456, 2505Strauss, A., 711, 2316, 2377*Strigini, P., 1428Strisciuglio, P., 872*Strom, C., 107, 1278, 2525*Strom, S., 72Strong, L.C., 72, 220, 940, 1892Strong, T., 2814*Strongwater, A., 894Strouboulis, J., 118AStrout, C.L., 2550Strunk, K.M., 525Stubblefield, B.K., 514, 2503Stuger, U., 1320Stul, M., 1387Stunkard, A., 401*Stupca, P., 1228Su, C., 760Su, Y., 2030*, 2062Suarez, B.K., 63*, 1076Subba Rao, Y., 519*Subhadra, M.S., 1851*Subramony, S., 820Suchi, M., 2491*Suchy, S.F., 939*Sudar, D., 2087, 2151Sudhir, K., 746Sugerman, H., 418
Sugita, Y., 2856Sugiura, Y., 873*Sugiyama, R., 2022Suhr, L., 1520Suijkerbuijk, R.F., 1386, 1605Sujansky, E., 874*, 1505, 1541Sujatha, M., 520*Sukernik, R., 2815*Sulik, K., Session 72Sulkes, S., 783Sullivan, B., 1715*Sullivan, J., 2303Sulston, J., 238*, 2126Sultan, C., 751Sumegi, J., 1082, 2098Summar, M.L., 1037, 2031*,2084
Summers, C.G., 564Summers, K.M., 2137Sumner, S., 1686Sun, A.M., 2470, 2481Sun, N-H., 558, 1265*Sun, T-Q., 2529Sun, X.L., 2820Sun, Y., 2876Sundberg, K., 1266*Sundby, S., 2684Sung, C-H., 2378*Super, M., 99, 993Surana, R.B., 1379*, 1483, 1592,
1677Surani, M.A., 241*Surh, L.C., 778, 1043, 1105*Suri, V., 1163Surti, U., 410, 928, 940*, 1530Suryanarayana, A., 1845Suryaprabha, P., 801Susanszky, E., 1267*, 1271Suskov, I., 2816*Suslak, L., 781, 1766*Sutcliffe, J.S., 2005, 2526*Sutera, C.J., 1846Sutherland, G.R., 379*, 2124Suthers, G.K., 17, 2379*Sutphen, J., 533Suttle, D.P., 2458*Suzuki, K., 2446Suzuki, M., 662Suzuki, T., 545, 578*Suzuki, Y., 284*, 578, 1075Svobodova, M., 854Swamy, M., 504Swarna, M., 521*Swaroop, A., 2308, 2459*, 2531Swaroop, M., 2339Swart-van de Berg, M., 890Sweeney, M.G., 1010, 2032*,2427
Sweeny, K., 2836, 2852Sweetman, L., 535, 1217Swergold, G.D., 2460*Swift, M., 1955, 2027, 2385Sylvester, J.E., 165, 1716*, 1893,2436
Syrrou, M., 1489Syvanen, A-C., 46, 2356Szabo, P., 1370, 1717*, 2164Szathmary, E.J.E., 255*Szatrowski, T.P., 586Szemere, G., 1268*Szpirer, C., 1870*, 2374Szpirer, J., 1870
-T-
Tabe, H-., 2527*Tagarelli, A., 1964
Tager, J.M., 436Taggart, R.T., 2090*, 2254Tagle, D.A., 82*, 102, 2204,2210
Tagliabracci, C.E., 2410Tai, J., 1390Taillandier, A., 1849Taillon-Miller, P., 2114, 2185,2339
Tajik, J., 1062Takaesu, N., 916Takahashi, K., 1028Takahashi, N., 506, 2793*Takahashi, R., 2584Takakubo, F., 2416Takebe, H., Session 93Takeshita, K., 627, 798, 875*Takeshita, T., 1531*, 2644, 2772Takeuchi, F., 876*Tallini, G., 2100Talmadge, C., 199Talmud, P., 66, 986Talpos, G., 1322Talukder, G., 2563, 2760*Tam, K.S., 2137Tamai, M., 999Tamaoki, T., 2584Tamayo, G.E., 2761Tamayo, M.L., 2761*Tan, E.C., 2380*Tan, J.A.M.A., 2873*Tan, J.W.O., 2820Tanaka, A., 2446Tanaka, K., 490Tanaka, M., 412Tanaka, Y., 727, 2511Tanci, P., 1317Tandon, J.K., 877*, 2565Taneja, N., 877, 1206, 1229,
2565*Tanese, N., 118Tang, B., 1187Tang, B.K., 544Tang, X., 990Tang, X.D., 2769, 2778Tang, Y., 1124Tangsrud, S.E., 800Tanguay, P., 863Tanguay, R.M., 483Tani, H., 2584Taniwaki, M., 2160Tanke, H.J., 181Tannirandorn, Y., 1249Tanoue, A., 987Tanzer, J., 1323Tanzi, R.E., 1992, 2162, 2189,
2381 *
Tapscott, T., 1920Tardieu, M., 2223Tardo, C., 531Targan, S.R., 2770, 2773Targovnik, H., 662Tariverdian, G., 1269*Tarone, R., 807, 845Taroni, F., 2382*Tarroni, P., 2182Taruscio, D., 223, 414, 2201*Tashian, R.E., 2528, 2751Tasmini, 2754Tassi, R., 1470Tassone, F., 1657Tateno, A., 438, 512Taterka, P., 1824Tatti, M., 526Tauszik, T., 2874*
530
Author and Presenter Index
Tay, J.S.H., 1040, 2746, 2873,2875*
Taylor, A.M.R., 1967, 2604Taylor, C., 1986Taylor, E.W., 1933, 2091'Taylor, M., 294Taylor, R.G., 2530Taylor, R.N., 1204Taylor, S., 2210Taylor, S.A.M., 974, 2348,
2383*, 2599Tazelaar, H., 1062Tchaikovskaya, T., 2782Tease, C., 1951Teboul, M., 1430Tedeschi, B., 1559Tedesco, T.A., 1498Tedseschi, B., 1388Teebi, A.S., 878*Teerenhovi, L., 1333Telej, F., 1421Telenius, H., 2347Telleman, P., 2250Teller, D., 2419Telleria, ).J., 985te Meerman, G.J., 1093, 1926,2033*
Templado, C., 1629*Temtamy, S.A., 624, 715, 879*Tenconi, R., 2762*Tendero, A., 761Tengstrom, C., 1630*ten Kate, L.P., 1093Tenni, R., 1065Teplitz, R.L., 2603*Teramo, K., 1847Tercanli, S., 274, 1225Terrenato, L., 1937, 1993, 2880Terwilliger, J.D., 2034*, 2063Teshima, I., 1723, 1726Tessier, R., 1760Testa, J.R., 1380*Teterina, T.P., 620*Teterwak, U., 1756Tetushkin, E., 2636*Tewfik, A., 700Thakker, N., 99*Thakker, R.V., 1025Tharapel, A.T., 1454, 1725,
1804Tharapel, S.A., 1355, 1381*,
1725The Canadian Collaborative Study
of Predictive Testing forHuntington Disease, 248
The Clinical CytogeneticsLaboratory, 243
The Clinical PelizaeusMerzbacher Disease StudyGroup, 971
The elegans ResearchCommunity, 2126
The European HMSNCollaborative Research Group,1998
The Hereditary DiseaseFoundation CollaborativeResearch Agreement, 298,2210
The Hereditary DiseaseFoundation Huntington DiseaseCollaborative Research Group,82
The Multiple Endocrine NeoplasiaGroup at Bloemfonten, 1025
Theda, C., 487
Theilmann, J., 1807*Theobald, M., 535Theophile, D., 1528Thepot, F., 1079Theriault, A., 1455Therkelsen, A.J., 359Thibault, M-C., 1916, 2878Thibodeau, S., 1062Thick, J.A., 1967, 2604*Thiel, G., 1382*Thierry-Mieg, J., 238Thitivichianlert, A., 387Thomas, D., 278*Thomas, G., 1706, 2130, 2191,
2251Thomas, G.H., 1067Thomas, H., 2110, 2206, 2218Thomas, I.M., 1270*Thomas, I.T., 880*, 1490, 1500Thomas, J., 1392Thomas, K., 238, 2418Thomas, M., 1953Thomas, N.S., 1086, 1106*,
1126Thompson, A.R., 658Thompson, C., 2550Thompson, C.L., 2702Thompson, Jr., J.N., 850, 2817*Thompson, K., 1538Thompson, L., 1347, 1450Thompson, L.M., 2384*Thompson, T., 1943Thomsen, A., 1923Thongtang, O., 1764Thorn, J., 2759Thu, L.T., 793Thuillier, P., 482Tibben, A., 1767*Ticher, A., 2883Tick, D., 957*Tikhonov, V.A., 881*Tikkanen, M., 714, 986Tiller, G.E., 45, 349, 522*, 2031Timakov, V., 2847TimAr, L., 1271*Timberlake, W.E., 2121Timmerman, V., 1998Ting, C-N., 2444Tischfield, J.A., 1091, 2538Tishler, P., 2763*Tjian, R., 118*Tobella, L., 1420Todd, C., 2109, 2125Todd, D., 388Todd, R.D., 1076, 2718Toguchida, J., 2575, 2605*Toi, A., 941, 1526Toji, L.H., 579*, 2081Tokino, T., 604Tokoro, T., 523*Tokunaga, K., 876, 2211, 2876*Tolan, D.R., 2264Tollersrud, O.K., 466Tolmie, J., 1644Tolsma, C., 975Tolun, A., 294, 1987Tomich, J.A., 436Tomilin, N., 2131, 2544Tomioka, S., 68Tomkinson, A.E., 295Tomlinson, G., 882*Tommerup, N., 420*, 767, 1596*Tompkins, B., 2192Tompkinson, G., 1157Tonali, P., 1001Tonelli, L.A., 2871, 2877*
Tong, M.C., 2746Tonini, G.P., 602, 2420Toniolo, D., 374Toniolo Neto, J., 1584Tonks, S., 589Tonlorenzi, R., 96, 2092*, 2259,2294
Tonnesen, T., 2200Tonoki, H., 453Tonomura, A., 1395Toomey, K.E., 28, 788, 883*,
1398, 1452Toone, J., 563*Tops, C.M.J., 609, 2132, 2216Torfs, C., 884*Torhorst, J., 2788Toriello, H.V., 138*, 342*Torresani, T., 645Torrey, E.F., 909Torroni, A., 973, 2610, 2637*Tory, K., 605, 2161Toscano, A., 2032Tosk, J., 979Toso, V., 437Tosteson, T., 2763Toth-Fejel, S., 243, 1718*Tctterman, K., 714Toublanc, J.E., 2341Tout, M.J., 2743Towbin, J.A., 1920, 2220, 2385*Towne, B., 2764*Townsend, S., 535Toyoda, H., 2770Trabace, S., 1937Traboulsi, E.l., 885*Trainor, G., 199Trakhtengroit, A., 1920Tran, C., 1622Tran, L-T., 886*Tran, T.N., 1719*Tranchemontagne, J., 495, 1462Tranebjaerg, L., 821, 1107*Trask, B., 176, 182*, 2203Trauffer, P.M., 887*Traupe, H., 2765*Travis, A., 1867Travis, M., 21Trawoger, R., 1376Treacy, E., 524*, 899, 1502Trefz, F.K., 2432Treiman, L., 2041Tremblay, M.L., 2503Trent, J., 2586Trent, R.J., 2219, 2386*Trese, M.T., 857Trevenen, C., 927Trevor, K.T., 2243*Triche, T.J., 1719Tricoli, J.V., 2606*Trifiro, M., 267Tripathi, R.K., 525*Tristan, M., 2295Troelstra, C., 293Trofatter, J.A., 1880, 2035*,2169
Troiano, R., 1569Tromp, G., 2025Truc, D.B., 793Truchon, J., 2878*Trudel, P., 2202*Trump, B.F., 587Truszczak, B., 1670Tryggvason, K., 24, 194, 382*,2405
Tsai, J., 1631*Tsai, M.Y., 564
Tsalikian, E., 2225Tseng, L-H., 1034, 1108*Tsenghi, C., 1489Tsien, F., 1532*Tsilfidis, C., 404, 778, 2036*,2370
Tsipouras, P., 345, 348*, 1109*,1883
Tsui, L-C., Session 51, 2071,2192, 2261, 2364, 2366, 2814
Tsuji, S., 514, 1071, 1112, 2152,2320, 2521, 2527
Tsukahara, M., 888*Tsukamoto, K., 1946, 2510Tsutsumi, C., 512Tsvetkova, M.N., 2233Tu, L., 471Tuchman, R., 1465Tucker, J.D., 200*Tucker, M.A., 582Tuck-Muller, C.M., 1597*Tuerck, J., 2264Tuerlings, J.H.A.M., 1527Tukun, A., 644Tulinius, M., 228TOmer, L., 644Tuna, M., 1374Tunaoglu, S., 644Tuncer, M., 636Tunnell, S.M., 898Turacli, E., 628Turaeva, S.M., 2715, 2879*Turc-Carel, C.S., 372*Turco, A., 111O*Turina, O.V., 2098Turleau, C., 588, 621*, 1079Turner, A., 968Turner, G., 171*, 1850, 2026Turner, l., 542Turner, S., 2729, 2736Turnpenny, P.E., 889*Turpeinen, U., 1847Tusnady, G., 1267Tuvale, M.K., 724Tveit, K.M., 2567Tyan, D., 2770Tybulewicz, V., 2503Tyler, A., 1768*Tyler-Smith, C., 198Tynan, K.M., 176, 182, 2203*Tzeng, C.C., 1383*Tzingilev, D., 596
-U-
Uchida, I., 363'Uchiyama, T., 438Udayakumar, R., 583Ueoka, Y., 1448Uhl, G.R., 2273Uhrich, S., 1180Uitto, J., 73, 2010, 2387*Ulizzi, L., 2880*Ultmann, M.H., 1440Uluoblu, O., 644Umezawa, Y., 2512Unsworth, N., 1718Upadhyaya, M., 14*, 143, 2012,2037*
Urbano, M.T., 1773Uribe, J.l., 2761Utermann, B., 1436Utermann, G., 427*, 1376,
1436, 2434Uus, E., 1503Uy-Lee, C., 499
531
Author and Presenter Index
Uze, G., 1968Uziel, G., 2382
-V
Vaccarella, C., 759Vaccaro, A.M., 526*Vaezi, S.A., 1471Vahakangas, K., 610Vainzof, M., 2050Vaisanen, M-L., 1198Valada-Filho, H., 2050Valderrama, E., 1444Valdes, J., 82, 102, 2204*Valenti, C., 2420Valentine, J., 625Valenzuela, C.Y., 2655, 2881Valenzuela, M., 1492Valle, D., Session 5, 190, 202,
2153, 2279, 2519Valle, J., 107Valli, M., 1065Valverde, K., 1769*, 1836Van Allen, M.I., 941*, 1526Vanasse, M., 1039, 2018van Baal, S., 125, 2582Van Broeckhoven, C., 964, 1998,2038*
VanCamp, S., 967Vance, J.M., 141*, 1904, 2021,2039*
van de Berg, J., 2451van de Kamp, J.J.P., 763, 890van de Kerkhof, P.C.M., 2765van de Klift, H.M., 609van den Berg, A., 224Van den Berg, D.J., 2388*van den Berg, E., 1384*Vandenberg, P., 2461*Van den Berghe, E., 1387*, 1392Van den Berghe, H., 1387, 1392,
1738van den Engh, G., 182van den Maagdenberg, A.M.J.M.,996
van der Burgt, I., 1632*van der Hout, A.H., 2607*van der Kamp, J.J.P., 1100Vander Laan, D.J., 2254van der Ploeg, M., 180*, 181VanderStoep, J., 2040*van der Valk, M.A., 594van der Veen, A.Y., 224van der Vlies, P., 2607van der Westhuyzen, D.R., 2329van de Wetering, B., 2045Van Dyke, D.L., 1218, 1385*,
1393van Echten, J., 1311, 1386*Van Eerdewegh, P., 63, 2714van Essen, A.J., 1527van Gurp, P.J.M., 2765van Haeringen, A., 763, 890*van Heeren, H., 2517Van Hemel, J.O., 1720*van Heyningen, V., 1643, 2144Vanhoute, F., 527Vanhove, G., 527Van Hove, J., 1533*Van Kirk, V., 1566van Krieken, J.H.J.M., 618Van Maldergem, L., 891*van Melle, E., 1705Vanni, R., 1534*
van Ommen, G.J.B., 18*, 185*,378, 618, 964, 984, 1093,1100, 1556, 1994, 2042,2357, 2389
van Oost, B.A., 194, 378, 972,1985, 2005, 2389
van Osch, L.D., 1985van Rensburg, E.J., 1494Van Roy, N., 1679, 2111van Tol, H.H.M., 1903vanTuinen, P., 2118Van Veldhoven, P.P., 260, 527*van Zandvoort, P., 1985Varawalla, N.Y., 1272*Vardiman, J.W., 2581Vareesangthip, K., 1764Varela, M., 1532Varesco, L., 2218Varga, P., 1787Vargas, F.R., 1683Vargas-Arenas, J., 892*Varghese, M., 569Varshney, S., 1508Vasconcellos, L.C., 2651Vasen, H.F.A., 609Vasen, H.P., 272*Vassart, G., 662Vassault, A., 259, 447Vatsis, K.P., 549*Vaudin, S.A., 993, 1047Vavougios, G., 528*, 2246Vavrova, V., 2703Vayssettes, C., 2119Vaziri, A., 1450Vecoli, C., 2524Vegter-van der Vlis, M., 964,
1100, 1767Veiga, I., 1995Vekemans, M., 1273*, 1421,
1432, 1462, 1502, 1512,1529, 1585, 2002, 2442
VelAzquez, A., 893*Velazquez, F., 2719Velkova, V., 1326Vellek, A., 239Venir, N., 946Venkatraj, V.S., 1962Venkat Raman, R., 657Venta, P.J., 2528*Venter, J.C., 2179, 2392Venter, P.A., 1808*Verderio, E., 2382Vergnaud, A., 1142, 1253Verhage, F., 1767Verjaal, M., 1527Verkerk, A.J.M.H., 378, 2361,2389*
Verlinskaya, D.K., 1523, 1770*Verlinsky, Y., 107*, 1278, 2525Verloes, A., 529*Verma, I.C., 38*, 331*, 775,
776, 1024, 1739, 2488Verma, M., 2422, 2569, 2638*Verma, R.S., 586, 861, 1220,
1346, 1357, 1370, 1409,1563, 1598*, 1717, 2164,2626
Vernier, R., 1160Vernole, P., 1388*, 1559Veropotvelyan, N.P., 942*Veropotvelyan, P.N., 942Verschraegen-Spae, M.R., 1679Verstuyft, J.G., 192Vetrie, D., 1011Vezon, G., 1060Victoria, M.F., 2174
Victorova, T.V., 1599*Vidaud, M., 463Vidyasagar, J.V.S., 824Viegas-Pequignot, E., 2057Vieira, M.M., 580*Vieira-Filho, A.H.G., 2050Vieland, V., 1944Vielvoye, G.J., 616Vigilant, L., 2639*Vignal, A., 2625Vijaya Kumar, T., 1358Vikkula, M., 46Vilain, E., 2341Vilarinho, L., 449Vilchez, J., 1989Vild6sola, C., 847Vilkki, J., 1022Villalba, F., 220Villar, V., 685Villarreal Molina, T., 450Vihia, C., 754Vincent, D., 1889, 1900Vincent, N., 2269Vincent, V., 1752Vine, D., 894*, 1521, 1759Vinney, L., 1453Vintiner, J., 1015Virmani, V., 1292Vishnupriya, S., 657, 895*Viskochil, D., 14Vissing, H., 199Vitale, E., 93, 474Vitale, M., 2122Vits, L., 2046Vivario, M., 529Vlietinck, R.F., Session 85Vnencak-Jones, C.L., 1840,
2390*, 2863Vo, T., 1651, 2267, 2335,
2391*, 2399Vockley, J., 490Vogel, F., 42*, 2028Vogel, W., 1633*Vogelstein, B., 101, 113*, 1991,2193
Vogler, A., 2505Vogler, G.P., 2767*Vogt, P., 2205*Vogt, T.F., 266*Voljavec, A.S., 973Volkov, V., 741Vollmer, M., 1898Vollrath, D., 433Volpato, S., 949Volpini, V., 1111*von Ende, V., 1193von Figura, K., 285*, 2492von Koskull, H., 1847, 1930,
1980von Lindern, M., 125, 2582Vooijs, M., 1283, 1724Voorhoeve, E., 964Voortman, G., 1008Vooys, M., 405Vorechovsky, I., 1965Vorsanova, S.G., 1721*, 1729Vos, J-M.H., 2529*Vugt, J.M.G.v., 1495Vulliamy, T., 1964Vuopala, K., 896*Vuorio, E., 46
WW-
Wachtel, G., -109Wachtel, S., 105, 109*, 2238
Wachtler, F., 1716Wada, Y., 469Wade, R.V., 1456Wadelius, C., 2106Wadey, R., 1518Wadgaonkar, R., 2164Wagener, D.K., 1852*, 2737Waggoner, D.D., 1600*Wagner, Jr., R., 79Wagner, R.M., 1137, 1274*Wagnitz, S., 1871Wagstaff, J., 59, 87, 1860, 2392*Wahlstrom, J., 1535*Wajner, M., 2675Wajntal, A., 787, 1329Wakamatsu, N., 1112*Wakamiya, M., 2484Wakui, K., 1448Wald, N., 1368Wald, N.J., 117*Waldman, F., 217Walker, A.P., 179, 1809*Walker, D.C., 2530*Walker, J., 868Walker, M.E., 1536*Walker, P., 2391Walker, R.G., 249Wall, J., 1113*Wallace, D.C., 31*, 671, 973,
2610, 2637Wallace, M., 14, 2133, 2339,2818*
Wallenburg, J.C., 2556, 2611Wallerstein, D., 897, 920Wallerstein, R., 897*Wallery, J.J., 2817Wallis, L., 2282Walpole, I., 717Walsh, D., 2030Walsh, D.J., 2861Walter, M.A., 2393*Walter, T., 1309Walters, C., 1828Wanders, R.J.A., 128, 263Wang, A-Z., 2768*Wang, B., 1128, 1251, 1275*,
1724Wang, C., 323, 1390Wang, E.T., 2769*, 2778Wang, F., 1351, 2733Wang, G., 2505Wang, L.R., 1049Wang, J.Z., 2394*Wang, M., 990, 1114Wang, N., 1389*, 1722*Wang, P., 953, 1284, 2473Wang, Q., 970, 1124Wang, S., 1049, 1537, 1674Wang, S.j., 1834, 2770*, 2781Wang, S-W., 2230, 2287, 2395*Wang, T., 455, 1114*, 1854Wang, T-R., 1810*Wang, T.Y., 1287Wang, V., 898*Wang, W., 2734Wang, X., 1853*, 2509Wang, X.Q., 2288Wang, Y., 1013, 1537*, 1616,
2462*Wang, Z.H., 2288Wang-Wuu, S., 1390*Wannmacher, C., 2675Wapenaar, M.C., 185Wapner, R.J., 887, 1194, 1276*Warburg, M., 1115*, 2047
532
Author and Presenter Index
Warburton, D., 84*, Session 75,1510, 2096, 2149
Warburton, P.E., 1663, 2640*Ward, B., 1634*, 1691, 1708Ward, D.C., 91, 223, 1722,
1858, 2124, 2163, 2201,2263, 2332, 2392, 2511
Ward, J.R.T., 2206*Ward, L., 2052Ward, R., 905Wargowski, D., 1538*Warner, A., 1828Warner, C.A., 530*Warner, J.P., 1680, 2207*Warnich, L., 2093*Warren, A.C., 2094*Warren, Jr., J.T., 2291Warren, S.T., 374, 378, 379,
Session 77, 1038, 2005, 2152,2159, 2174, 2389, 2521, 2526
Warrington, J.A., 2208*Washington, S.S., 2020, 2209*Wasmuth, J.J., 102, 961, 1516,
1651, 1943, 2168, 2204,2208, 2210*, 2217, 2336,2348, 2384
Watanabe, Y., 876, 2211*Waters, G.D., 232Waters, M.F., 2224Waterston, R., 238, 2126Wathen, T.M., 1701Watkins, C., 897, 920Watkins, P., 2082, 2334Watson, Jr., B., 2576, 2771*Watson, G., 443Watson, J., 1634Watson, P., 1316, 1977Watters, E.A., 208Watters, G.V., 698, 899*Wavrek, D., 883Waye, J.S., 2640Waziri, M., 1325Weatherall, D.J., 386*, 434*Weaver, D.D., 943*Weaver, Jr., R.G., 1490Webber, L.M., 1307Weber, B., 1585, 2271, 2396*Weber, G., 612Weber, J., 2344Weber, J.L., 78, 1924, 1933,
2021, 2045, 2084Weber, M., 900*Weber, M.A., 2871Weber, W., 2788Weber, W.W., 549Webster, M.W., 867Webster, W.D., 943Weeda, G., 293Weeks, D., 2029Weeks, D.E., 64, 2044, 2095*Wei, J.F., 2492*Wei, J.H., 1669Weichselbaum, R.R., 2577Weidinger, S., 680, 2397*Weidmeyer, J., 2671Weier, H-U., 1283, 1635*, 1724Weiffenbach, B., 143, 1918,
2012, 2212*Weigant, J., 181Weigel-DiFranco, C., 9Weiler, S., 436Weinbaum, P., 922, 1178Weinberg, J., 184Weinblatt, V., 1276Weindling, P., 320*Weiner, N., 1444
Weinstat-Saslow, D., 1869, 2371Weinstein, M., 1443Weintraub, L., 531*Weiser, B., 2295Weiss, L., 682Weiss, R.B., 1379Weiss, S., 2883Weissbecker, K., 2041*Weissman, M.M., 1944Weissman, S.M., 2137, 2511Weitz, S., 54Weksberg, R., 638, 941, 1723*Welch, J.P., 1088Weleber, R.G., 810, 1057, 1931,2014
Wells, R.A.W., 2147Wells, Jr., S.A., 1950, 2145Welsh, J.A., 587, 610Welsh, M., Session 51Wen, X.L., 1997Wenger, D., 309, 1539*Wenger, D.A., 286*, 451, 2359Wenger, S.L., 757, 1601*Wenk, R.E., 1540*Wenstrom, K.D., 1238Weremowicz, S., 1391*Wertelecki, W., 1811*Wertz, D.C., 41*Wesby-van Swaaij, E., 1720Wesenberg, F., 1345Wesenberg, R.L., 762Wessels, H., 1303Wessels, J.W., 1556Wessman, M., 2228Westerveld, A., 767, 1209, 2144,
2250, 2585Weston, M.D., 1077, 2155, 2750Westphal, H., 2503Wetering, B.J.M.v.d., 2766*Wethers, D., 1824Wetterberg, L., 1877Wevrick, R., 2213*Wexler, P., 1541*Wexler, S.N., 2029Weyerts, L.K., 1277*Weyland, B., 1255Whaley, L., 298Whaley, L.W., 1727Whaley, W.L., 102, 2348Wheeler, D.A., 2616Whelan, A., 2377Whetsell, L., 622*, 1092, 2495Whitcombe, D.M., 2214*White, B., 1889White, J.J., 2400White, K., 1636*White, M., 107, 1278*, 2418White, P., 1239, 2215*White, R., Session 6, 1316,
1969, 2150Whiteman, D.A.H., 1279*, 1723Whiteside, T.L., 1319, 1378Whitley, C.B., 564*, 577, 1059Whitman, B., 655Whittingham, S., 2733Whyatt, D., 118AWhyte, M.P., 456, 472Whyte, P., 211, 1771Wick, P.A., 2014Wicks, D., 2427Wiebe, V., 2815Wiegant, J., 185Wienberg, J., 1857, 2641*Wienker, T.F., 2047Wieringa, B., 11, 405*Wiersema, J., 1384
Wiese, R., 1870Wiestler, O.D., 231Wiggins, S., 1771*Wigler, M., 98Wigley, F.M., 1597Wiik-Sjostedt, A., 1535Wijker, M., 1990Wijmenga, C., 143, 2012,
2042*, 2607Wijnen, J.T., 2132, 2216*Wijsman, E.M., 1975, 2811Wilcox, E., 79Wilczyrski, J., 1496Wildenauer, D.B., 1094, 2043*Wilder, S., 1018Wilensky, M., 2052Wiley, J., 749Wilfond, B., 1006Wilhelmsen, K.C., 2044*Wilkemeyer, M.F., 532*Wilkerson, C.B., 887Wilkie, P., 2045*Wilkins, I., 689, 1650Wilkins-Haug, L., 944*Wilkinson, D., 2337Willard, H.F., 97, 145*, 1663,
1704, 1974, 2213, 2234,2366, 2640
Willard, H.W., 2307Willems, P.J., 1921, 2046*, 2371Willemse, R., 2582Willems van Dijk, K., 2212Williams, C., 921, 1083Williams, C.A., 907, 933, 1116*,
1549, 2224Williams, D.E., 2468Williams IlIl, J., 1128, 1251,
1275, 1458, 1724*Williams, J.M., 60Williams, J.R., 1134, 1203Williams, M.A.T., 2026Williams, R.R., 164*Williams, S., 1774Williams, S.M., 2642*Williams, T.M., 1090Williams, W.D., 619Williamson, R., 1518, 2310,2463*
Willing, M., 2464*Willms, B., 722Willshaw, H., 1905Willson, T.A., 2360Wilmot, P.L., 1259, 1602*, 1623Wilroy, R.S., 780, 1454, 1725*Wilson, A.C., Session 3, 2614,2639
Wilson, B., 1592Wilson, D., 1458, 1518Wilson, D.l., 901*Wilson, G., 882, 945*Wilson, J.M., 423*, 2494Wilson, M.G., 1581Wilson, P.J., 282, 1042Wilson, R., 238Wilson, R.D., 946*Wilson, W., 533*, 1170, 2177Wilson-Gunn, S., 2339, 2818Wilton, A.N., 1156Wiman, B., 2417Wiman, K.G., 2594Winberg, G., 2098Winderickx, J., 2398*, 2419Winfield, S., 2503Wingard, J., 1367Winking, H., 918Winnard, A.V., 2319, 2443
Winokur, S., 2217*Winqvist, R., 1035, 1198, 2595Winship, I., 79Winsor, E., 941, 1526Winter, R.M., 134*, 341*, 1015Winter, V., 195Winterpacht, A., 1121Wintle, R.F., 1726*Wirschubsky, Z., 2594Wirth, B., 2218*, 2371Wirth, C., 1660Wirtz, M.K., 496, 534*Wiseman, R.W., 305*, 2134Wishnick, M., 826Wisniewski, D., 2267, 2335,2399*
Wisniewski, H.M., 550, 745,1670
Wisniewski, K., 862, 1570Wisniewski, L., 1280*Wisselaar, H.A., 568, 581*Wistow, G., 166*Withers, B., 2335Withers, D.A., 2184, 2608*Witkowski, R., 1382Witoonpanich, P., 1249Witt, D.R., 535*, 1252Wittebol-Post, D.W., 1985Witztum, J., 2485Wlodarska, I., 1387, 1392*Wojcierowski, J., 2465*Wolf, B., 468, 510, 663Wolf, E., 1978Wolf, G., 2525Wolf, J.P., 1258Wolf, M.E., 2588Wolf, P.A., 2667Wolfe, J.H., 518Wolff, D., 1542*Wolff, G., 2003, 2047*Wolff, H.H., 1193Wolford, J.K., 1080Wolman, S.R., 1322, 1340Wolstenholme, J., 816, 1661Wong, H.B., 2873Wong, P., 1580Wong, S., 732Wong, W-Y., 619Wongchanchailert, M., 2354Woo, S.L.C., 2*, 186, 455, 740,
1114, 2462, 2478, 2482Wood, C.M., 2400*Wood, D., 1239, 2818Wood, J., 2869Wood, P.A., 459Wood, S., 2048*, 2110, 2337Woodage, T., 2219*, 2386Woodruff, R.C., 2817, 2819*Woods, C.G., 1582Woods, D., 1859Wooley, T., 2771Woolf, B., 59Wooten, V., 2771Worley, K.C., 2135, 2220*Wormskamp, N., 405Worsham, M.J., 1385, 1393*Worton, R.G., 429, 1911, 2042,2549
Woychik, R., 2562Wray, A., 1628Wright, A.F., 1016Wright, G., 2163Wright, H.H., 625Wright, L.W., 2079Wrogemann, K., 441, 1911Wu, C-W., 2429
533
Author and Prsnter Index
Wu, D., 1447Wu, D-A., 2414Wu, G.Y., 1049, 1117*, 1123Wu, J., 1956Wu, K., 2466*, 2785Wu, L.C., 2403, 2467*Wu, L.L., 164Wu, M., 330*, 601, 2288, 2609Wu, S., 1893Wu, S-)., 570Wu, X., 225, 2493*Wu, Y-Y., 1021Wu, Z., 317Wucher, A., 503Wuepper, K., 592Wulfsberg, E.A., 902*, 1542WOrl, D., 2043Wussler, J.M., 673Wuu, K., 1390, 1854*Wyandt, H., 1394*Wyatt, P.R., 1801, 1812*Wydner, K.L., 1669Wylmotte, R., 1063Wynshaw-Boris, A., 266Wyrobek, A.J., 1281*, 2457
-X-
Xia, J., 1543*, 1665, 2061, 2515Xiao, G-H., 2609*Xiao, H., 1304, 2049*, 2179Xiao, W., 2401*Xie, S-S., 2820*Xie, Y., 647Xin, X., 1447, 1544*Xiong, Y.F., 1856Xiu, Y., 1175Xu, C., 986Xu, D., 1285Xu, J., 2308, 2459Xu, X., 2505Xu, Y., 160, 1502, 1832, 1966,
1971, 2532, 2769, 2778
Y-
Yadvish, K.N., 2342Yaffe, D., 16*Yaffo, A., 1208Yager, R.M., 442Yahav, J., 2551Yamada, K., 1545*Yamagata, Z., 1531, 2644, 2772*Yamaguchi, T., 2605Yamaguchi, Y., 438, 512Yamamoto, M., 1019Yamamoto, T., 523Yamamoto, Y., 690, 903*Yamamura, H., 2688Yamaoka, L.H., 78, 1904, 1992,2039
Yamazaki, K., 572Yan, D., 2531 *Yanagi, H., 567, 1118*Yanagida, M., 318*Yanagisawa, A., 604Yanagisawa, Y., 2856Yandell, D.W., 221 *, 1892,
2553, 2575, 2577, 2605Yang, B-Z., 1119*, 2277Yang, H., 2221*Yang, H.Y., 2770, 2781, 2773*Yang, J., 1124
Yang, M.L., 1120*Yang, P., 2774*Yang, T.P., 2118, 2428Yang-Feng, T.L., 606, 1212,
1338, 1353, 1484, 1503,1655, 1727*
Yao, M., 1122Yao, R., 2281Yao, S.N., 2437, 2494*Yao, X-L., 550*, 1470, 1667Yarom, R., 418Yaspo, M.L., 2119Yasukochi, Y., 2511Yasunami, M., 2244*Yates, J.R.W., 142*, 1680, 2207Yates, P.J., 2861Ye, H.F., 1856Ye, J., 1048, 1114Ye, L., 990, 1537Ye, Z-J., 1048Yeager, A., 561Yeager, M.T., 939Yedwab, G., 1208Yen, P., 2285, 2367, 2402*,2440
Yenamandra, A., 1546*Yeung, C.Y., 2324Yih, M.C., 60Ying, K.L., 1719, 1724Yoda, K., 412Yokoyama, H., 790Yonaha, M., 551*Yoneda, M., 36Yong, S.L., 753, 1154Yoo, H.W., 530Yoon, H-S., 2632, 2821*Yoon, J.S., 1637*Yoon, J.Y., 373Yoshida, A., 2304Yoshida, K., 1075, 2313Yoshida, M.A., 1395*Yoshida, M.C., 1052Yoshimaru, H., 2707Yoshiura, K., 1728*, 2510You, D., 940Youlton, R.R., 1420, 2659,2881*
Young, B.D., 1605Young, D.W., 744Young, K., 789Young, S.R., 1227, 1282*Young, T-L., 600Young, W.H., 1383Younghusband, H.B., 600Youngman, S., 102, 2088Younie, L., 1132Youroukos, S., 1489Yu, C.W., 1547*, 1631Yu, C.Y., 2403*Yu, J., 2532*Yu, L-C., 1283*, 1724, 2285,2367
Yu, M.H., 1548*Yu, M.T., 2096*, 2149Yu, R.K., 2232Yu, S., 379Yu, Y., 1125Yuan, C.C., 225Yuan, L-F., 558, 1048, 1114Yuen, J., 976, 1185, 1831,
1855*, 2679Yuille, M.A.R., 598, 2097*Yuksel, M., 1987
YOksel Apak, M., 1402*, 1406Yune, S.M., 2691Yurov, Y.B., 1639, 1721, 1729*,2197
Yuzbasiyan-Gurkan, V., 947,1871*
-Z-
Zabarovsky, E.R., 2098*, 2579Zabel, B., 930, 1121*, 2142Zablocka, B., 2503Zacchello, F., 654Zachary, C.B., 641Zachau, H.G., 1857Zackai, E.H., 904*, 1507Zackowski, J.L., 1457, 1549*,
1702Zadworny, D., 2080, 2590Zago, M.A., 994Zagursky, R.J., 2078Zahran, F., 715Zatid, K., 2006Zaizov, R., 584Zakharov, S.F., 465Zaki, M.E., 624Zamir, R., 923Zamzam, A., 700Zanjani, E.D., 154*Zappata, S., 2113Zarbo, R.J., 1934Zaret, K., 2430Zaslav, A.L., 1501, 1550*Zasloff, M., 1716Zatterale, A., 1401, 1418Zatz, M., 1735, 2050*Zavala, C., 1560Zavaleta, M.J., 1221Zawislak, S., 1290Zbar, B., 605, 785, 1066, 1122*,
2161Zdzienicka, M.Z., 297*, 2250Zehetner, G., 178, 179Zehnbauer, B., 623*, 1607, 2193Zei, G., 2645, 2882*Zeiger, K., 207Zeinali, S., 1638*Zeitune, M., 1551Zelano, G., 1984Zelante, L., 667, 1703Zelinski, T., 1055Zellers, N., 905*Zemelman, B., 2115Zemer, D., 858, 1554Zeng, F.Y., 2305Zeng, L-Z., 1304Zeng, Y.T., 1087, 1856*, 2305Zengerling, S., 377Zenzes, M.T., 1284*Zer, T., 923Zerba, K., 2775*Zerres, K., 2776*Zeviani, M., 35*, 2178Zhang, A., 1581Zhang, D-S., 2577Zhang, F., 2526Zhang, G-Y., 2404*Zhang, H.R., 2777*Zhang, H.Z., 760Zhang, J., 2102Zhang, J.W., 1123*Zhang, J.Z., 391 *
Zhang, L.M., 1380
Zhang, M., 658, 1699Zhang, Q., 2395Zhang, Q.S., 2769, 2778Zhang, S., 1124*, 1928Zhang, S.L., 2769, 2778*Zhang, S.X., 1125*Zhang, S.Z., 1125, 2769, 2778Zhang, W-M., 558Zhang, X-L., 286, 2359Zhang, X-X., 1048Zhang, Z., 2377Zhao, J-M., 1048Zhao, L., 1337, 1396*Zhao, S-M., 558Zhao, S.Y., 1286Zhao, T.M., 2784Zhao, X., 2573, 2592Zhao, Y.J., 1123Zhen, H.Y., 2779*Zhong, N., 1050Zhong, W., 1447, 1544Zhong, Y.Y., 2851Zhou, B.M., 1853Zhou, J., 326, 2209, 2405*Zhou, J.M., 2474Zhou, L-Y., 1285*Zhou, X.H., 1286*Zhou, X.T., 1287*Zhou, Y., 2114Zhu, C., 1397*Zhu, D., 2051*, 2634Zhu, D.E., 2820Zhu, N., 299Zhu, S.M., 587Zhu, W., 1665Zhu, X.M., 2220, 2385Zhu, Z., 2070Ziegle, J., 2062Zielenski, J., 2261Zielewicz, J., 2465Ziembolewska, Z., 1496Zietkiewicz, E., 1039, 2099*Zimmer, M., 298Zimran, A., 1018Zinn, A.B., 433, 536*, 1701,
2421Zipagan, E., 1366Zis, A.P., 2745Zisovski, N., 1326Zito, J., 1433Zitzelsberger, H.F., 1635Zlotogora, J., 906*, 2255Zober, Y., 463Zoghbi, H.Y., 1897, 2052*,
2065, 2137, 2157Zoll, B., 722Zollino, M., 2349Zonana, J., 1106, 1126*Zonierz, K., 1619Zoossmann-Diskin, A., 2883*Zori, R.T., 708, 907*, 1116,
1457, 2224Zorzato, F., 429Zou, G-Z., 2780*Zrenner, E., 11Zuber, M., 1922Zucchi, I., 373Zullo, S., 2100*Zung, P., 638Zuo, J., 299Zupko, W., 1660Zvereva, S.V., 1473Zwane, E., 1478Zwarthoff, E.C., 1954Zweigbergk, M.v., 719Zyguiska, M., 235*, 2302
534
535
PERMUTED TITLE INDEX
AAl 901 SUBSTITUTION IN A TYPE I
ANTITRYPSIN AS A RESULT OF A POINTANTITRYPSIN NULLWEST ABSENCE OFANTITRYPSIN PDUARTE HETEROGENEITYPROTEINASE INHIBITOR IN DOWN
A1(I) CHAIN OF TYPE I COLLAGEN IN AAll AND B27 /OF HLA ANTIGENSAll COLLAGEN CHAIN PRODUCES RECURRENTA2 RECEPTORS IN ABSTINENT ALCOHOLICSA2(Q) GLY 922 /SERINE SUBSTITUTION FORA3 AND A5 CHAINS OF COLLAGEN IV AS /OFAS CHAINS OF COLLAGEN IV AS THE /AND
GENE LEADING TO CLINICALLYA5(IV) CHAIN AND FURTHER /IV COLLAGEN
COLLAGEN GENE OF THREE /IN THEABDOMINAL AORTIC ANEURYSM ASSOCIATION
CALCIFICATIONS THE USE OFABERRANT C MYC EXPRESSION AND /WITH
SPLICING OF PHENYLALANINEABERRATION /MOSAICISM FOR CHROMOSOMAL
IN A UTERINE LEIOMYOMAIN LYMPHOCYTES IN PARENTS
ABERRATIN /OF FETAL CHROMOSOME/OF NUMERICAL CHROMOSOMEAND MUTATIONS IN MAN ANDASSOCIATE WITH THEBY COMPETITIVE IN SITU /21IN 542 MENTALLY RETARDEDIN A LEIOMYOSARCOMA OFIN ARTHROGRYPOSISIN CIGARETTE SMOKERSIN CULTURED LYMPHOCYTESIN HUMAN BREAST CANCERIN HUMAN D G GROUP /ARMIN NON MALIGNANT CELLSIN PERIPHERAL BLOODIN TUMOR CELLS /CHROMOSOMEIN WORKERS EXPOSED TOINDUCED BY AFLATOXIN B1NONRANDOMLY DISTRIBUTEDWITH RESPECT TO MATERNAL
ABL GENE IS JOINED WITH 5 BCR IN SOMEABNORMAL CHILD WITH A COMBINATION OF
CHROMOSOMAL SEGREGATION INCONCEPTUSES (TERATOTHANASIA)EARS MENTAL RETARDATIONHEMOGLOBINS IN THE TRIBAL /OFKARYOTYPE /THE NORMAL ANDKARYOTYPE BIOCHEMICAL /WITHKARYOTYPES /REGISTRY OFMATURATION OF PROSAPOSINMIDTRIMESTER ULTRASONOGRAPHYOUTCOME /INCREASED RISK FORPHENOTYPE ASSOCIATED WITH ANPHENOTYPE BY TRANSFER OF /THEPHENYLALANINE METABOLISM INSEGREGATION OF /DUE TOSEX CHROMOSOME COMPLEMENTSULTRASOUND FINDINGS /INX AND Y CHROMOSOMES
ABNORMALITES/AND CHROMOSOME/ANTERIOR CHAMBER EYE/HUMAN SPERM CHROMOSOMEAN CYTOGENETIC/OF FETAL CHROMOSOME/SCREENING OF GONOSOMAL/STRUCTURAL CHROMOSOMAL/STRUCTURAL CHROMOSOME/WITH OCULOMOTOR/WITH SEX CHROMOSOME/WITH SEX CHROMOSOMEAN INDICATION FORAND ABSENCE OF P53AND DUODENAL ATRESIAAND GALACTOSEMIA /DUCTASSOCIATION OF KINGBY FLUORESCENT IN SITUCAUSING BIRTH DEFECTSDIAGNOSED PRENATALLYDUE TO ABNORMALIN 902 CASES OF
10652326232627971595534592446517
1054383383194
240510118671182918
22801570136411361614128328161597164416301362152425371531259515371312135216161599130114491523259716321554103710
271714451479358495112912471457875
242688
145512441085757
149416292431823148012181588514213168512731325927832
126717081279124888
1270
IN A PATIENT WITHIN A RARE CASE OF GIANTIN ACUTE MYELOBLASTICIN CHILDHOOD ACUTEIN CHILDREN WITH ACUTEIN CHOLESTEROL /DISEASEIN EPENDYMOMAS ANDIN INTERPHASE CELLSIN LEUKEMIA DIAGNOSEDIN PATIENTS TREATEDIN PATIENTS WITH ENDIN PROLYMPHOCYTICIN PROSTATIC CANCERIN SPONTANEOUS ABORTIONSIN SPONTANEOUSLYIN THE BRAINS OF HPRTIN TRANSSEXUAL MALESIN TWO FETUSES WITHKLIPPEL TRENAUNAYMICROMELIA AND MILDOF CHROMOSOME 1 AND 11OF CHROMOSOME 12 INOF CHROMOSOME 18 /OFOF COLLAGEN TYPE IIIOF FETAL MICROSCOPIC /BYOF MITOCHONDRIAL IRONOF THE BRAIN IN THEOF THE EXTERNAL EAR AREUSING FLUORESCENCE IN
ASNORMALITIESIMENTAL RETARDATIONABNORMALITY /OF FETAL CYTOGENETIC
ASSOCIATED WITH CUTANEOUSAT 28 WEEKS GESTATIONIN BAHRAIN 6 YEAR STUDYIN PATIENTS WITH ELEVATEDIN PRENATAL DIAGNOSES
ABO ANTIGEN AND SERUM ANTIBODY TITERSBLOOD GROUPS /DERMATOGLYPHICS ANDBLOOD SYSTEM /INTERACTION WITH THE
ABORIGINAL POPULATIONS /THREE CANADIANABORTION /CAUSES OF SPONTANEOUS
/COUNSELING IN SPONTANEOUS/MOSAICISM IN SPONTANEOUSIS THIS CHROMOSOMAL ANOMALY
ABORTIONS /DEFECTS IN SPONTANEOUSAIN 902 CASES OF RECURRENTAIN SPONTANEOUS/OF HUMAN SPONTANEOUSGROUPS AT RISK FOR /REPEATEDIN QATARI POPULATION
ABORTUSES /A STUDY ON 1089 INDUCEDWITH ABNORMAL KARYOTYPE
ABRUPT CHANGE IN SURNAMES /REGIONS OFABSENT CORPUS CALLOSUM IRIS COLOBOMAS
IN WOLMAN DISEASE SHOWS ITPATELLAE AND DIAPHRAGMATIC
ABSTINENT ALCOHOLICS NORMAL CONTROLSABUSE OF GENETICS /DISEASE AND THEACADIAN KINDREDS /1A IN FIVE FRENCH
POPULATION CLINICAL ANDACATALASEMIA /GENE EXPRESSION ANDACCEPTABILITY OF PRENATAL DIAGNOSISACCEPTOR OF ORNITHINE /AT A SPLICEACCESSORY ECTOPIC CERVICAL THYMUSACCIDENT/BYELORUSSIA AFTER CHERNOBYL
/CONNECTION WITH CHERNOBYL/EFFECTS OF THE CHERNOBYL/OF THE CHERNOBYL REACTOR
ACCOMPLISH DIAGNOSIS OF THE MEIOTICACCURACY /X SYNDROME DETERMINATION OF
AND REPRODUCIBILITY OF /THEOF FAMILY HISTORY DATA ONOF PCR ANALYSIS FOR SINGLE
ACETABULAR DYSPLASIA IN SEX /ANDACETALDEHYDE INDUCED LIVER DAMAGE IN
TOXICITY AND THE ROLE OFACETYLATION POLYMORPHISM AND ITS /NACETYLATOR PHENOTYPE AND CONGENITALACETYCHOLINE RECEPTOR SUBUNITSACETYLCHOUNESTERASE BAND AT /POSITIVE
TESTS IN THEACETYLTRANSFERASE AT THE NATI AND /NACHANG ETHNIC GROUP A MINORITY /E INACHE TESTS IN PRENATAL DIAGNOSIS /AND
15081365135813461326798
136013061303136713021366130036314384781206152664188813501334156735011744821433724
1704879112913531145139911371159575
185126512829365366364936S75127036391611671400119914792882879
2248640517181719582023244818252802834
26992782281636016541259252427232525881504
2410545537
2182127493954918561165
ACHONDROPLASIA /FELINE MODEL FORAND PSEUDOACHONDROPLASIA
ACID /INDUCED BY RETINOIC/PRESENCE AND ABSENCE OF RETINOICA GLUCOSIDASE ACTIVITY /NORMALAND CHOLESTEROL IN NEU LAXOVAB GLUCOSIDASE FUNCTION /OFBETA GALACTOSIDASE CDNA SEQUENCEDISORDERS IN MENTALLY RETARDEDEMBRYOPATHY /IN HUMAN RETINOICIN PRIMARY GENERALIZED ANDINDUCED CDNA FROM A HUMANLIPASE GENE FAMILY /BELONGS TO ANON DIMETHOATE INDUCED SISTEROXIDATION DEFECTS PROSPECTS FOROXIDATION DISORDERS OVERVIEW ANDPHOSPHATASE AND HEMOGLOBIN INPHOSPHATASE GENE /HUMAN PROSTATICRECEPTOR GENE AND MAPPING OF THESTORAGE DISORDER /A FREE SIALICSUBSTITUTION IN SRY CAN LEAD TOTRANSPORT DISORDERS (CONDITIONS
ACIDEMIA (CBL F) AND LYSOSOMAL/RESPONSIBLE FOR ISOVALERICTYPE 1 /DIAGNOSIS OF GLUTARIC
ACIDEEAMOCYSTINURIA DUE TOACIDIC KERATIN /OF A 40K TYPE 1
PHOSPHOLIPID CONTAINING /INTOACIDOSIS AND STROKE LIKE EPISODES
AND STROKE LIKE EPISODESAND STROKE LIKE EPISODES
ACIDS /OF PROTEINS AND NUCLEIC/PLASMA AND URINE ORGANICEVIDENCE THAT MANY OF THE AMINOFOR GENE MAPPING DIAGNOSTICSIN FACTOR IX FUNCTION AS SPACERIN X ADRENOLEUKODYSTROPHY /FATTY
ACIDURIA /CBIC TYPE OF METHYLMALONIC/THERAPY OF MUT METHYLMALONICWITH NORMAL 3
ACRANIA A MANIFESTATION OF ADAMSACROCENTRIC CHROMOSOMES ANVOLVINGACROCENTRICS CHROMOSOMES IN RELATIONACRODYSOSTOSS /INHERITANCE OFACROFACIAL DYSOSTOSIS A CASE REPORT
DYSOSTOSIS SYNDROME IN AACROMEGALOID FACIAL APPEARANCEACTIVATED NEUTRAL PROTEASE IN /CALCIUMACTIVATING PROTEINS /BY GTPASEACTIVATION AND OXIDATION OF FATTY
IN NEUROBLASTOMA /RAS GENEOF ERB B2 DIRECTLY CAUSESOF PLATELETS IN /AN IN VIVO
ACTIVATOR INHIBITOR 1 LEVELSINHIBITOR 1 PROMOTER SHOWSPROTEINS GENE RESULT IN TWOPROTEINS STRUCTURE FUNCTION
ACTIVATORS AND THE BASAL INITIATIONCO ACTIVATORS AND THE
ACTIVE AND ATTENUATED VIRUSES CANAND INACTIVE X CHROMOSOMES /THERATHER THAN REACTIVE GENETICSITE HOMOLOGY WITH LYSOZYME
ACUTE INTERMITTENT PORPHYRIA /WITHINTERMITTENT PROPHYRIA /OFLEUKEMIA /IN PATIENTS WITHLEUKEMIA BEFORE AND AT /WITHLEUKEMIAS AN T(l 1;19)LYMPHOBLASTIC LEUKEMIALYMPHOBLASTIC LEUKEMIA /WITHLYMPHOBLASTIC LEUKEMIA IN ALYMPHOCYTIC LEUKEMIA (ALL L2)LYMPHOCYTIC LEUKEMIA /MARROW INMYELOBLASTIC LEUKEMIA PATIENTSMYELOGENOUS LEUKEMIA AN ANMYELOGENOUS LEUKEMIA /WITHMYELOID LEUKEMIA /OF T(8;21) INMYELOMONOCYTIC LEUKEMIA TO /INNONLYMPHOCYTIC LEUKEMIA /INNONLYMPHOCYTIC LEUKEMIA SUB
ACYL COA DEHYDROGENASE ACTIVITY /CHAINCOA DEHYDROGENASE DEFICIENCYCOA DEHYDROGENASE DEFICIENCYCOA DEHYDROGENASE DEFICIENCY
This index was produced by a computerized permutation process that creates anentry for every significant term (key word) in the title of an abstract. Key wordsappear alphabetically in bold type, followed by the text to provide subject context.If space permits, the ending word in each title is followed by a slash and then bythe word or words that precede the key word. Abstract numbers appear at theend of each index line. Key words in the title of a paper for which no abstractwas supplied are referenced by session (S) number.
80948
24201289529913
2545451519924477228822482543262259
27542331190720131190261476490481508
268452643797710172518263
263292
263251653153212177791602122286965679766773112
516602
2572872241724172359286118118
1371242820852810441008132813441323132013261324136913451358137013961342170925821346459265475498
Permuted Title Index
COA DEHYDROGENASE DEFICIENCYCOA DEHYDROGENASE DEFICIENCYCOA DEHYDROGENASE DEFICIENCYCOA DEHYDROGENASE DEFICIENCYCOA DEHYDROGENASE DEFICIENCY ANDCOA DEHYDROGENASE DEFICIENCY INCOA DEHYDROGENASE MUTANT ALLELECOA DEHYDROGENATION DISORDERCOA OXIDASE A NOVEL PEROXISOMALPEPTIDE HYDROLASE GENE /THE RAT
ACYLPEPTIDE HYDROLASE IS FREQUENTLYACYLTRANSFERASE LOCUS ON SERUM LEVELSADA AND ADDITIONAL MARKERS ON /WITH
DEFICIENCY AND CANCER /THERAPY FORADAMS OLIVER SYNDROME /OFADAPTIVE RESPONSE IN LYMPHOCYTES FROM
RESPONSE TO LOW DOSE OFADDUCTED THUMBS SYNDROME FURTHER /ANDADDUCTS ON HUMAN CHROMOSOMES /DNAADENO ASSOCIATED VIRAL VECTOR
ASSOCIATED VIRUS MEDIATEDADENOCARCINOMA /GENE IN HUMAN PROSTATE
/IN BARRETT'S/IN PRIMARY GASTRIC
ADENOCARCINOMAS /IN EIGHT PRIMARY LUNG/IN OVARIAN SEROUS
ADENOMATOUS POLYPOSIS BY LINKAGEPOLYPOSIS COLI /FAMILIALPOLYPOSIS COLI GENE /THEPOLYPOSIS GENE /FAMILIALPOLYPOSIS IN 16 FAMILIESPOLYPOSIS LOCUS (5021
ADENOSINE A2 RECEPTORS IN ABSTINENTDEAMINASE IN HUMAN /OF HUMAN
ADENOVIRUS MEDIATED DIRECT GENEADH GENE COMPLEX AND MULTIPLE /IN THE
GENE IS LOCATED IN THE ADH GENEADH5 AND RELATED PSEUDOGENES /GENEADHERENCE OF HUMAN ERYTHROCYTESADHERING AMNIOTIC FLUID CELLS INADIPOSITY IN AN INDIAN POPULATION /OFADJUNCT TO LINKAGE ANALYSIS AND RFLPADJUSTMENT ON MSAFP SCREENING FOR
ON SCREENING FOR DOWNTO THE BIRTH OF A CHILD
ADMIXED POPULATIONS /ASSOCIATIONS INADMIXTURE AMONG THE SINHALESE AND /AND
MODELS /THE TWO LOCUS VERSUSADOLESCENT OSTEOSARCOMA /CHILDHOOD ANDADOPTION WORKERS IN GENETICS /TRAININGADP RIBOSYL ATION /INVERSION FROM POLYADRENAL HYPERPLASIA /BY CONGENITAL
HYPERPLASIA BY DNA RFLPHYPOPLASIA CONGENITA LOCI /AND
ADRENOLEUKODYSTROPHY /FATTY ACIDS IN X/OF X LINKEDAND ITS VARIANTSASSOCIATED COLORPATIENTS
ADULT GM2 GANGUOSIDOSIS AMONG JEWSMALES /WITH GC PHENOTYPE INONSET DISORDERS LOW ACCEPTANCEPATIENTS WITH GM1 GANGLIOSIDOSISPOLYCYSTIC KIDNEY DISEASE /FORPOLYCYSTIC KIDNEY DISEASE /OFPRESENTING WITH CEREBRAL PALSYTWINS /AND SENILE DEMENTIA INWITH 49 XYYYY KARYOTYPEWITH PROFOUND BIOTINIDASE
ADULTS IS DETERMINED IN PART BY A /INMEDICAL AND CULTURAL /FOR DEAFWITH SPINA BIFIDA /FOR
ADYSPLASIA WITH MULLERIAN ANOMALIES AAETHIOPS /THE AFRICAN GREEN MONKEY (CAFST TO HUMAN CHROMOSOME 3PTER 3P25.1AFAFP AND ACHE TESTS IN PRENATAL
MEASUREMENTS /RACE ON MSAFP ANDAFFECTEDS ONLY /SCREENING USINGAFFECTIVE DISORDER /LINKED TO BIPOLAR
DISORDER IN THE OLD ORDERILLNESS /ANALYSIS OF BIPOLAR
AFLATOXIN B1 IN RAT BONE MARROW CELLSAFP ALBUMIN PREALBUMIN AND TOTAL
AND UE3 /THAN 35 YEARS OF AGE HCGESTRIOL AND HCG SCREENING FORTEST IN PRENATAL REVEALING OF /THE
AFRICA /AND DNA VARIATION IN SOUTHERN/EDUCATION IN GENETICS INA FIRM DIAGNOSIS OF SPECIFICRESULTS AND EXPERIENCES /SOUTHWITH A VERY HIGH PREVALENCE OF
AFRICAN AMERICAN CYSTIC FIBROSIS /ANDAMERICANS BY PCR OF DRIEDBLACKS EXCLUSION OF CANDIDATEGREEN MONKEY (C AETHIOPS) /THEHYPERLIPIDEMICS FOR FAMILIALIMMUNOGENETIC AND RED CELLPOPULATION /DIGIT IN THE SOUTHPOPULATIONS /DNA INPOPULATIONS /EVOLUTION OF WESTPOPULATIONS /IN SOUTHERNPOPULATIONS /IN SOUTHERNRURAL AREA /IN A SOUTHTRADITIONAL HERBAL MEDICINES
AFROABORIGINAL POPULATIONS OF
11192277231623779751959754975272297257926901962S9177914732542737134324922477260625711299133613381876591609
21321051101517
2484S9119731973228449911732713275311691203176027582875190672
177625736541108222051686413021902320
32685211451176410481530
6815105107528
1737639678
210411651224S32194019882029130191218441847183725832723
17922827279827432000678103626186692639263426332635180825572839
AG M MICROSATELLITE REFLECTS THETO GG TRANSITION AT A SPLICE
AGAROSE GELS /POLYMORPHISMS ONAGE /ASSOCIATED WITH YOUNG MATERNAL
/FOR DOWN SYNDROME USING MSAFP AND/OF SYSTOLIC BLOOD PRESSURE WITH/RATE IN ADVANCING MATERNAL/WITH RESPECT TO MATERNAL30 /PRENATAL DIAGNOSIS AFTER35 /CONSIDERATIONS IN WOMEN UNDER35 AND OLDER /SYNDROME IN WOMEN35 AND OLDER /SYNDROME IN WOMENAND DOWN SYNDROME A STUDY OF 522AND LATE ONSET ALZHEIMER DISEASEAND NONTRISOMIC CYTOGENETICAND THREE BIOCHEMICAL MARKERSAT MENOPAUSE A TWIN STUDYAT ONSET AS A COVARIATE /USINGAT ONSET FOR FAMILIAL OVARIANAT ONSET OF HUNTINGTON DISEASEDEPENDENCE OF FETAL CHROMOSOMALDEPENDENCE OF GUSTATORY HABITSEFFECT /FAMILIES IS THERE ANFREQUENCY OF PREGNANCY LOSS ANDGROUPS OF HUMAN BLOOD LYMPHOCYTESHCG AFP AND UE3 /THAN 35 YEARS OFOF ONSET /METABOLISM AND THEOF ONSET DISTRIBUTIONS FROM /OFOF ONSET IN FAMILIAL AMYLOID /OFOF ONSET IN MACHADO JOSEPH DISEASEOF SIX IN HAIKOU /UNDER THEON THE CONTRIBUTION OF THE /OFRELATED NONDISJUNCTION RELEVANCERELATED RISKS AND PRENATALSEX RATIO AND HYPERHAPLOIDY /SPERMSUGGESTS MECHANISM OF GENETIC
AGE! /PARENT SUPPORT GROUPS COME OFAGED TWINS HDL CHOLESTEROL /OF SAMEAGENESIS /DIAGNOSIS OF BILATERAL RENAL
OF CORPUS CALLOSUM /WITHWITH TRACHEOESOPHAGEAL /RENAL
AGENT IN PATIENTS UNDERGOINGAGENTS /EXPOSED TO GENOTOXIC
OF THE FANCONI ANEMIA LIKEAGGREGATION AND TRANSMISSION OF
OF AMYOTROPHIC LATERALOF AND MULTIVARIATEOF BLOOD PRESSURE IN ANOF INSULIN DEPENDENTOF LEISHMANIA DONOVANIOF STROKE /OF FAMILIALOF SYMPTOMS /FAMILIAL
AGING /C2 POLYMORPHISM IN/FOR ONCOGENESIS ANDAND SENILE DEMENTIA IN ADULTAT ELEVATED TEMPERATURES AS AON CELL CYCLE KINETICS AND X /OF
AGOUTI LOCUS /LETHAL MUTATIONS AT THEAGRANULOCYTOSIS TREATED WITH /KOSTMANNAGRESTIS /IN THE FIELD VOLE MICROTUSAICARDI SYNDROME AND GOLTZ SYNDROMEAIDS PATHOGENESIS /HIV 1 VARIATION INAll IN MACROPHAGE KILLING FUNCTIONSAIMED AT CLONING THE X CHROMOSOMALALABAMA AND BETWEEN THE SOUTHEASTERN
U.S.A AND UPPSALA COUNTYALAGILLE SYNDROME MOLECULAR ANALYSIS
SYNDROME PHENOTYPE /WITH THEALAND ISLAND EYE DISEASE /ANALYSIS OF
ISLAND EYE DISEASE /ANDISLAND EYE DISEASE/INCOMPLETE
ALAR INDENTATIONS A DOMINANTLY /NASALPLATE IN HUMAN RETINOIC ACID
ALBINISM /ANALYSIS OF X LINKED OCULAR/AROUND X LINKED OCULAR/IN TYPE IA OCULOCUTANEOUSIN SOUTHERN AFRICAN BLACKS
ALBINO MUTATIONS DEFINE FUNCTIONALALBIPUNCTATUS UTILIZING PCR COUPLEDALBUMIN PREALBUMIN AND TOTAL PROTEINALCOHOL DEHYDROGENASE GENE ADH5 AND
DEHYDROGENASE MULTIGENEDRINKING BEHAVIOR AND THE /THEINDUCTION OF CHROMOSOME [THESENSITIVITY ACETALDEHYDE
ALCOHOUCS /LIVER DAMAGE IN CHRONIC/RULED OUT IN 45NORMAL CONTROLS ANDTHEIR FIRST DEGREE /IN
ALCOHOLISM /WITH MULTIGENERATIONALAND ALLELES OF THE HUMANIN A CANADIAN OUTPATIENT
ALDEHYDE DEHYDROGENASE /OF CYTOSOLICDEHYDROGENASE 2 ISOZYME /INDEHYDROGENASE GENE /STOMACH
ALDOLASE B GENE FROM AN INDIVIDUALALDRICH SYNDROME GENE ON XP BETWEENALIGARH /FIRST COUSIN MARRIAGES IN
/IN A NORTH INDIAN HOSPITALALIVE BIRTH FROM CHILDLESS MARRIAGESALK PRE MRNA OF DROSOPHILA /OF THE MLCALKAUNE PHOSPHATASE AND CALCIUM /OF
PHOSPHATASE BIOCHEMICALPHOSPHATASE GENE IN SEVERELY
ALLAN HERNDON SYNDROME CONFIRMATION
280028022789936120327291204152311461201116912501474266712481215275519705822660126828741474121825421844233
26612757544
27792775409
1781159426601755399117919009271251255822502713270427392720266326512744276326942546
68250815312239619171014482295243120652844267116645331905712810663924
2051201423182000525
2523912
22842619271627162410504
109451749351710762725241027162304226419121164140312362438895456472642
ALLEGED FATHER WAS UNAVAILABLE FORALLELE /ACYL COA DEHYDROGENASE MUTANT
/1 COMMONLY DUE TO COLlAl NULL/NEW MUTATIONS AND A MARCO POLO/TO CARRY A CLASSICAL TAY SACHSACCOUNTS FOR THE HIGH /MUTANTASSOCIATION BETWEEN THE /STRONGDISCRIMINATION USING INTERNALEFFECTS INFLUENCES THE RISE OFFREQUENCIES AT THE /ANDFREQUENCIES WITHIN THE BLACKFREQUENCY DISTRIBUTION ANDFREQUENCY DISTRIBUTIONS AMONGLOSS DETECTION IN TUMOR SAMPLESLOSS DURING CARCINOGENESIS INLOSS FROM CHROMOSOMES 5 AND 7LOSS IN FAMILIAL AND SPORADICLOSSES REVEALS THE PRESENCE OFOF THE B HEXOSAMINIDASE A /DNOF THE INSULIN GENE IN TYPE IIRAISING APOLIPOPROTEIN B /OF ANSHARING AND GENETIC DISTANCESPECIFIC DIFFERENTIAL BINDINGSPECIFIC PCR /OF CDF508 BY
ALLELES /DIFFERENT NORMAL BACKGROUND/IN BRAZILIAN CYSTIC FIBROSIS/M5 AND M6 ALPHA ANTITRYPSIN/OF PRODUCTION OF NEWAND CORONARY ARTERY DISEASEDETERMINE LIPOPROTEIN(A)FROM AN INDIVIDUAL WITH /PRIONIN BULGARIAN CLASSICAL /AND 4IN THE CAJUN POPULATIONIN U.A.E /OF B THALASSEMIAINTERGENIC CONVERSION BETWEENLIPOPROTEIN(A) LEVELS AND THEOF THE HUMAN DOPAMINE D2 /ANDREGIONS OF ABRUPT CHANGE INRESULTING FROM GENE MUTATIONSWITH REFERENCE TO CYSTIC
ALLELIC ASSOCIATION OF HUMAN DOPAMINEEFFECTS ON SODIUM LITHIUMLOSS IN THE MULTIPLELOSSES ON 3P IN SPORADICMODEL TO EXPLAIN UNUSUALTO THE ADENOMATOUS POLYPOSISVARIATIONS IN MONOAMINE
ALLELOTYPE STUDIES OF BREAST CANCERALLELOTYPING OF MALE GERM CELL TUMORSALLOANTIBODIES /MEMBRANE ALPORT.ALLOGENEIC BONE MARROW TRANSPLANTATION
SWINE CLASS II GENES IN /OFALLOTYPES GM AND KM IN CHINESE ANDALPHA 1 ANTICHYMOTRYPSIN GENE /IN THE
1 ANTITRYPSIN HAPTOGLOBIN AND1 ANTITRYPSIN VARIANTS BY /HUMAN3 BETA 4 AND ALPHA 5 NEURONAL5 NEURONAL ACETYLCHOLINE /4 ANDANTITRYPSIN ALLELES /M5 AND M6DELETIONS /DETECT (SEA) DOUBLEFETOPROTEIN IN DOWN SYNDROME ANFETOPROTEIN LEVELS IN NONLETHALGENE /TRANSFORMING GROWTH FACTORGLOBIN GENE DELETIONS /OF SINGLEGLOBIN VARIANTS AMONG CHINESERECEPTOR GENE ON HUMANSATELLITE CLONES FROM THESATELLITE DNA /EVOLUTION OFSATELLITE DNA /IRREGULARITIES INSATELLITE DNA FAMILIES ONSATELLITE DNA IN THE /OFSATELLITE DNA ON THE STABILITYSATELLITE DNA PROBES FOR HUMANSATELLITE DNA PROBES IN /USE OFSATELLITE SUPRACHROMOSOMAL /NEWTHALASSEMIA 72 BETA THALASSEMIATHALASSEMIA BY DUAL RESTRICTIONTHALASSEMIA IN TAIWAN /OFTHALASSEMIA IN THE DRAVIDIANTO NONSYNDROMIC CLEFT LIP ANDWITH CLEFT LIP AND PALATE
ALPHA1 ANTICHYMOTRYPSIN GENE /OF THETHALASSEMIA MAJORS OUTCOME OF
ALPHOID REPETITIVE SEQUENCE FAMILIESSEQUENCES TO ISOLATE YEAST
ALPORT ALLOANTIBODIES /MEMBRANESYNDROME /CONTAINS MUTATIONS INSYNDROME /DIFFERENT SUBTYPES OFSYNDROME /LINKAGE STUDIES OFSYNDROME /MOLECULAR GENETICS OFSYNDROME /THREE PATIENTS WITHSYNDROME CHARACTERIZING PARTSYNDROME IDENTIFICATION OF A3SYNDROME LINKAGE TO NINE X
ALPP ON CHROMOSOME 2 FIRST REPORT OFALTAIANS /POPULATION GENETICS OF THEALTER GENE EXPRESSIONS ALTERATION OFALU ALU RECOMBINATION
BANDING BY FLUORESCENCE IN SITU /4CLUSTERS LOCALIZATION IN UNSTABLEELEMENT MEDIATED PCR /SORTING ANDMAPPING OF HUMAN GENOME ALUPCR /PROBES GENERATED BY INTERPCR AMPLIFICATION /HYBRIDS USINGPCR GENERATION OF HUMAN /INTER
536
2877975
246422461067489
23532789272911142844285428281317305
258160313731059722
27242837241710992797286323972800714
243423901027270927992627427107628822797273210942736595
260727766092303302611383160724902733680867
2073218221822397183912058511015976267919682213264016392234172916461635122716941831112010342873101322422411118521202145383
2405194381382
101123623831923
792850257625491656213116052131224721081649
Permuted Title Index
PCR PROBES FOR ISOLATION OF HUMANPRIMERS THAT ALLOW SPECIFIC ANDRECOMBINATION /ALURNA TRANSCRIPTS IN HUMAN /OFSEQUENCES AND THE EVOLUTION OF
ALUI GIEMSA OF CHROMOSOME 19 /BYALUMINUM IN CELLS CHROMOSOMES AND /OFALVEOLAR RHABDOMYOSARCOMA ASSOCIATEDALZHEIMER DISEASE /21 LOCI IN FAMILIAL
DISEASE /AND NONFAMILIALDISEASE /FEATURE OFDISEASE /GENE IN EARLY ONSETDISEASE /GENE IN FAMILIALDISEASE /JAPANESE FAMILIALDISEASE /MARKER FORDISEASE A LATE ONSET MOSAICDISEASE AN EXAMPLE OF /ONSETDISEASE ELDERLY AND YOUNGDISEASE GENE AND THE /THEDISEASE IN JAPAN /FAMILIALDISEASE PATIENTS IN /AND
AMBIGUOUS GENITALIA NEWBORNS BY PCRAMELOGENIN IS EXPRESSED FROM BOTH THEAMERICA /AMONG FAMILIES IN LATIN
/AMONG POPULATIONS IN NORTH/DIAGNOSIS COUNSELING IN NORTH/OF BIRTH DEFECTS IN LATINTESTING MODELS OF POPULATION
AMERICAN (U.S.A.) FAMILIES /WITHINCAUCASIAN AND AFRICAN /NORTHCYSTIC FIBROSIS PATIENTSHISPANIC POPULATIONS USINGMATERNAL PHENYLKETONURIA
AMERICANS (U.S.A.) /AND NATIVE/RECEPTOR LOCUS IN MEXICANBY PCR OF DRIED BLOODOF FRENCH CANADIAN ANCESTRYOF THE SOUTHWEST (U.S.A.)
AMERICAS /AND THE PEOPLING OF THEAMERINDIAN DEMES BASED ON BLOOD
MITOCHONDRIAL DNA ANALYSISAMERINDIANS /HAPLOTYPE DISTRIBUTION IN
FROM BRAZIL /AND GUARANIAMINO ACID DISORDERS IN MENTALLY
ACID SUBSTITUTION IN SRY CANACIDS EVIDENCE THAT MANY OF THEACIDS IN FACTOR IX FUNCTION AS
AMINOACID SUBSTITUTION IN THE HUMANAMINOACIDOPATHIES IN MENTALLY /OFAMINOBUTYRIC ACID RECEPTOR GENE ANDAMINOLEVUUNATE DEHYDRATASE HAS TWOAMINOTRANSFERASE GENE IN GYRATE
GENE IN TYROSINEMIAGENE OF PATIENTS /DGENE RESULTS IN ANMODULATION BYPOLYMORPHISMRELATED AND OTHER XRELATED SEQUENCES AT
AMISH /DISORDER IN THE OLD ORDERAMMONIA AND UREA AND INCREASE INAMNIOCENTESES /DIAGNOSIS OF 1303
/IN EARLYWHAT ARE THE REAL RISKS
AMNIOCENTESIS /BY MID TRIMESTERNERSUS MID TRIMESTERA RETROSPECTIVE /EARLYAFTER ELEVATED MSAFPAND COMPARISON WITH CVSAND CORDOCENTESIS /TOAND THEIR CONCERNS /OFASSOCIATION WITH FETALBY HISPANIC PATIENTS ATBY RECULTIVATING THE /INCLINICAL AND /EARLYCOMPLEMENTED WITH INCOMPLICATIONS IN /EARLYFOLLOWING PRENATALFOR EVALUATION OFFOR PRENATAL DIAGNOSISPROSPECTIVE FOLLOW UPQUESTIONNAIRE FOR /POST
AMNIOCYTE CULTURE METHOD /WITH IN SITUAMNIOCYTES CONSTANT FREQUENCY IN 10
IN RELATION TO CALCIUM ANDAMNIOTIC FLUID AND FETAL BLOOD A /ON
FLUID CELL CULTURES /INFLUID CELLS IN ANENCEPHALYFLUID DURING SAMPLING /OF THEFLUID GLYCINE /ENZYME ANDFLUID MOSAICISM DOES NOTFLUID SAMPLES ACHIEVED BY /INFLUID SPECIMENS PROCESSED /IN
AMP DEAMINASE /ON HUMAN ERYTHROCYTEDEAMINASE DEFICIENCY IN CAUCASIANS
AMPLIFICATION /BY PCR MEDIATED DNA/HYBRIDS USING ALU PCR/REGION BY EXONAND ANALYSIS OF HLAAND CHROMOSOME LP /N MYCAND DEAMPLIFICATIONAND EFFICIENT CLONINGAND LOSS OF TUMORAND SEQUENCING OF LARGEAT CHROMOSOME 11Q13 IN
23212516254924542625159855037019922811807
229023811071745
15042667158420577398451175236726962854389
272228651893279827982824212
28672801274317882676255
28422637256
285951911902632263224554801907240910575072519280224501945193121531988477122016131180920
124116311201
61115117441274114316211232121212621742117212261252175812121187445911
1221117312665631423126612284914891627210823832617584
245825102172505604
BY PCR REVEALS MULTIPLEIN CANCER /AND GENEIN DUCHENNE AND BECKERIN JAPANESE POPULATIONIN TUMORS OF /SEQUENCEIS THE METHOD OF CHOICEOF CODING SEQUENCES INOF COINCIDENT SEQUENCESOF GC RICH DNA USINGOF HUMAN GENOMIC DNA BYOF MICRODISSECTEDOF NUCLEAR RDNA DURINGOF PROTO ONCOGENE C NEUOF THE CYSTIC FIBROSISOF TWO MICROSATELLITEOF VNTR LOCI BY THE PCROF YEAST ARTIFICIAL /PCROF ZFY AND SRY SPECIFICREFRACTORY MUTATIONREFRACTORY MUTATION
AMIIPUFIED BY PCR ELIMINATION OF /GENESCDNAS /SEQUENCING OF THE PCRDNA FRAGMENTS FOR DETECTIONDOMAIN IN NEUROBLASTOMASDYSTROPHIN SEQUENCES /TWOIN MULTIPLEX /OF 14 EXONSIN SITU HYBRIDIZATION OFMATERIAL /OF PCRYEAST ARTIFICIAL CHROMOSOME
AMYlC IN PAROTID GLAND OF TRANSGENICAMYCTROPHIC LATERAL SCLEROSISAMYLASE GENE AMY1C IN PAROTID GLANDAMYLOID ANGIOPATHY /CYSTATIN C
POLYNEUROPATHY I /IN FAMILIALPRECURSOR PROTEIN GENE IN /THEPRECURSOR PROTEIN LOCUS BY
AMYLOIDOSIS (DUTCH) BY SINGLE /WITH/ASSOCIATED WITH CARDIACAS A PARACRINOPATHY
AMYLOIDOTIC POLYNEUROPATHY BYAMYOTROPHIC LATERAL SCLEROSIS
LATERAL SCLEROSIS /OFLATERAL SCLEROSIS TO
AN2 AND FSHB /WAGR REGION GENE BETWEENANAL ATRESIA CARDIAC DEFECTS TRACHEOANALOGS TO DETECT SINGLE BASEANALYZER FOR NEWBORN SCREENINGANAPHASE LAGGING IN MOTHERS OFANAPLASTIC LARGE CELL LYMPHOMAANCESTORS /CANADIANS SEARCH FOR COMMONANCESTRAL POPULATIONS /ROUTES OF THE
TELOMERE TELOMERE FUSION /ANANCESTRY PUBLIC HEALTH ISSUES INANCHORED SINGLE SITE CLEAVAGE OF THEANCIENT AND MODERN DNA SEQUENCES /FROM
BONES /RECOVERY OF DNA FROMHUMANS /IN CONTEMPORARY ANDMONGOLOID MIGRATIONS /OFPERUVIAN MUMMIES /D4S175 IN
ANDHRA PRADESH INDIA /POPULATION FROMPRADESH INDIA /POPULATION OFPRADESH SOUTH INDIA /PARDHIS OFPRADESH TRIBES /IN
ANDROGEN INSENSITIVITY SYNDROMERECEPTOR GENE DEFECT IN XRECEPTOR MUTATIONS THATRECEPTOR STUDY IN ONE CASE
ANEMBRYONIC PREGNANCY /PROTEINS INANEMIA /A CANDIDATE GENE FOR FANCONI
/GLYCOPHORIN A LOCUS IN FANCONI/HETEROGENEITY IN FANCONIAND ATAXIA TELANGIECTASIAAND ITS CORRECTION IN VITROCELLS /REPAIR DEFECT OF FANCONIDEFECT BY GENE TRANSFERIN AN INFANT WITH RING /ANDLIKE CHINESE HAMSTER CELLLINKAGE ANALYSIS WITH ADA ANDLYMPHOBLASTS /LOCUS IN FANCONIPATIENTS /TO FANCONIPATIENTS IN VIVO /ON FANCONIPATIENTS IN VIVO HYPEROXIA AREGISTRY A NEED FOR PREANEMICTHE CININNATI COMPREHENSIVEWITH SIX MARKERS ON CHROMOSOME
ANENCEPHALY /AMNIOTIC FLUID CELLS INCHANGES OVER 17 YEARS IN
ANEUPLOID DIRECTED INTRAUTERINEFETUSES /DETECTION OFINDUCTION IN MOUSE BONE
ANEUPLOIDY /FETAL MALFORMATIONS ANDAND COMPARISON OF XAT PREGNANCY TERMINATIONBUT NOT FOR MOSAICISMDETECTION IN HUMAN SPERMIN HUMAN GAMETES /OFIN MAN /PAIRING ANDIN NEWBORNS BY INTERPHASEIN TWIN GESTATIONS /RISK OFIN ULTRASONOGRAPHICALLY /OFIN UNCULTURED FETAL CELLSLEVELS IN HUMAN /OFRISK SPECIFICATION BYUSING QUANTITATIVE PCR
ANEURYSM ASSOCIATION WITH ALPHA 1
209936910402313258610732612205
253025162053128925961210988252225261685993104725132305279321931087103320962517216024441910244410262757107122449649607435781938270480
2241816
207818431591133126622876214717882074315
2502262226102617734
27172866285544195
2677519191874253523761609296
227522741398225019622559152214011418696177419651173121111742761853127485
1163162211841587157816361146119511183
12251069867
ANEUSOMIES /OF AUTOSOMAL SEGMENTALANEUSOMY /INVOLVED IN SEGMENTAL
IN PROBANDS WITH A /SEGMENTALOF 15Q11Q13 IN THE PRADER
ANGELMAN AND PRADER WILLI SYNDROMESAND PRADER WILLI SYNDROMESAND PRADER WILLI SYNDROMESSYNDROME /ANALYSIS INSYNDROME /DISOMY INSYNDROME /NATURAL HISTORY OFSYNDROME IN A PATIENT /OFSYNDROME PATIENTS WITH ANDSYNDROMES /PRADER WILLI ANDSYNDROMES /PRADER WILLI ANDSYNDROMES IS SYNTENIC TO THE
ANGELMAN/PRADER WILLI REGION OF HUMANANGIOGENIN AND LIVER GLYCOGEN /FORANGIOGRAPHICALLY DOCUMENTED CORONARYANGKIPATHY /CYSTATIN C AMYLOIDANGLO AND HISPANIC ETHNIC GROUPS INANHYDRASE A POSSIBLE NEW /CARBONIC
11 DEFICIENCY SYNDROME11 STRUCTURAL GENE /CARBONIC
ANHYDRIDE /EXPOSED TO PIROMELLITICANIMAL MODEL /DEFICIENCIES IN A LARGE
MODEL FOR INHERITED CATARACTSMODEL FOR RETINITIS PIGMENTOSAMODEL OF WILSON DISEASE I /NEWMODEL OF WILSON DISEASE Il /NEWMODELS /IN MICE AND POSSIBLE
ANIMALS BY GENE ENGINEERED FIBROBLASTSANION EXCHANGE HIGH PERFORMANCE /USING
GENERATION AN IN VIVOANIRIDIA /IN AUTOSOMAL DOMINANT
EVIDENCE FOR INVOLVEMENT OFANKYLOSING APONDYLITIS /OFANLL /OF THE T(6;9) TRANSLOCATION INANNEAUNG IN CHROMOSOME /OF SIMULATEDANNEXIN VII GENE /OF THE HUMAN SYNEXINANOMAUES /DYSPLASIA IN SEX CHROMOSOME
/MANAGEMENT OF GENITOURINARY/OF FETAL CHROMOSOMAL/PREGNANCIES WITH FETAL US/REGISTRIES OF CONGENTIAL/TUMOR AND GENITOURINARYA FAMILY CASE REPORTA FRENCH SURVEY /CHROMOSOMALA NEW AUTOSOMAL RECESSIVEA NEW DOMINANTLY INHERITEDAN UPDATE ON THE ORALAND AUTOSOMAL DOMINANTAND FACIAL DYSMORPHOLOGYAND NORMAL GROWTH HORMONECAUSED BY CONGENITALDELINEATION OF DIFFERENTDELIVERED FOLLOWING FIRSTEAR ANOMALIES VERTEBRALIN A POPULATION REFERREDIN AFFECTED AND RELATIVESIN CHINA (II) /CHROMOSOMALIN FETO PLACENTALIN HEMIFACIAL MICROSOMIAIN THREE CASES OF TRISOMYMOUSE MODELS /CRANIOFACIALREPORTING AND EDUCATIONRESULTS IN ITS FIRST TWOSYNDROME /INSTABILITY FACIALVERTEBRAL DEFECTS AND /EARWITH DE NOVO APPARENTLY
ANOMALIES/MENTAL RETARDATION SYNDROMEANOMALY /OF REGULATING GENES FOR THIS
/THORACIC FUSION KLIPPEL FEILAND ASSOCIATED SYSTEMICASSOCIATED WITH YOUNGPRENATAL DIAGNOSIS MAY MODIFYSHORT LIMBED DWARFISM ANDSYNDROME WITH ASSOCIATED
ANONYMOUS DNA MARKERS ON HUMAN /I TODNA PROBES USING GC CLAMPEDMARKER D19S63 SHOWS LINKAGE
ANOPHTHALMIA IN ITALY /CLINICALANTEMORTEM DIAGNOSIS BY MAGNETICANTENATAL DETECTION OF FETAL /FOR
DIAGNOSIS OF RECURRENTSCREENING FOR NEURAL TUBE
ANTERIOR CHAMBER EYE ABNORMALITIESMENINGOCELE TESTING LINKAGE
ANTHROPOMETRIC CRANIOFACIAL PATTERNMEASUREMENTS IN /FORSTANDARDS FOR PRADER
ANTI GLOMERULAR BASEMENT MEMBRANE /FORZETA WILL RELIABLY DETECT (SEA)
ANTIBODIES /ANTINEUTROPHIL CYTOPLASMICAND ITS APPLICATION ONIN PATIENTS WITH SYSTEMICIN THE STUDY OF HUMAN
ANTIBODY TECHNIQUE ON HISTONE /BY BRDUTITERS IN DUODENAL ULCERS
ANTICENTROMERE ANTIBODIES AND ITS /OFANTIBODIES IN PATIENTS
ANTICHYMOTRYPSIN GENE /IN THE ALPHA 1GENE /OF THE ALPHA1
ANTICIPATION IN MYOTONIC DYSTROPHYOF AGE OF ONSET IN /AND
ANTICIPATORY GUIDANCE IN THE COMMON
537
146456
16645987
18682224154915581707481116
59145918602392197971410262689275110201020159924782268799438512186824745658721960767
2734125
21212266881274126894135522063917997208263428928361407698653112817666812154311618421555341
27302756644817146864614688328859361178903721
20312059187527628991614887117
1494195362970994838318392773161615972143163357516161597680
241124072757174
Permuted Title Index
ANTIDIURETIC HORMONE SECRETIONANTIGEN AND MULLERIAN INHIBITING
AND NASCENT POLYPEPTIDE INAND SERUM ANTIBODY TITERS INCENP B AND CENTROMERICGENE MAPS NEAR THE /SURFACEGROUP (X/Y) POLYMORPHISM /B
ANTIGENS 1 AND 2 GENES /PEMPHIGOIDAll AND B27 /OF HLABY INTERFERON GAMMA IS /MHCTYPING IN PATIENTS WITH /HLA
ANTIMULLERIAN HORMONE DEFICIENCY IN AANTIMUTAGENIC EFFECT OF ASCORBIC ACIDANTINEOPLASIC FLUORO URACIL ALTERSANTINEUTROPHL CYTOPLASMIC ANTIBODIESANIPROUFERATIVE PROTEIN PROHIBITINANTISESE RAS GENE MAMMALIAN /ANDANTITRYPSIN ALLELES /M5 AND M6 ALPHA
AS A RESULT OF A POINT /AlDEFICIENCY ADENOVIRUS /A 1HAPTOGLOBIN AND TYPE IIINULLWEST ABSENCE OF /AlPDUARTE HETEROGENEITY OFVARIANTS BY DENATURING /1
ANXIETY A STUDY OF PRENATAL DIAGNOSISAO NAGAS NAGALAND INDIA /AMONG THE
NAGAS NAGALAND INDIA /STUDIES INAORTIC ANEURYSM ASSOCIATION WITHAPC REGION /PHYSICAL MAPPING OF THEAPE CDNA ENCODING THE MAJOR HUMAN /OF
EVOLUTION THROUGH RRNA GENES /ANDAPES /GENE HYPERVARIABILITY IN GREATAPHASIA SHUFFLING GAIT AND ADDUCTEDAPHIDICOUN AND METHOTREXATE IN HUMAN
IN INDIVIDUALS AFFECTEDINDUCED PULVERIZATION OF
APLASIA AND COMPLEX BRACHYDACTYLYAPNEA /RELATIONSHIP TO INFANTILE SLEEP
FAMILIAL AGGREGATION OF SYMPTOMSAPO B 3 VNTR IN HUMANS AND NONHUMAN
TRAITS NARIANCE OF NINE LIPID ANDAPO(A) ALLELES DETERMINEAPOAI CIII GENE REGION /RFLPS IN THEAPOLIPOPROTEIN A 1 LOCUS IN EMBRYONIC
A 1 PREVENTS POLYGENICA DEFICIENCY WITHA I GENE CAUSES /IN THEA IV AND LIPOPROTEINB 100 /DEFECTIVEB ANTIGEN GROUP (X/Y)B GENE 3HYPERVARIABLEB GENE IN INDIVIDUALSB GENE VNTR SITE /THEB GENE WITH CORONARYB LEVELS IN A SAMPLEC2 POLYMORPHISM INCII EXONIC (C2Kl9T)E POLYMORPHISM ON /OFE POLYMORPHISM TO THEE3 LEIDEN IN AN /WITH
APOUPOPROTEIN(A) ALLELESGENE STRUCTURE INISOFORM PHENOTYPES
APONDYLTIS /OF ANKYLOSINGAPP GENE CODON 717 MISSENSE MUTATION
GENE IN EARLY ONSET ALZHEIMER /THEGENE IN FAMILIAL ALZHEIMER DISEASE
APPEARANCE /AND DISTINCT FACIALSYNDROME (MIM- 102150)
APPLE PEEL BOWEL SYNDROME /OFAPRT DEFICIENCY /MUTATIONAL BASIS OF
GENE /MUTATIONS IN THE HUMANAPURINIC ENDONUCLEASE A MEMBER OF AARAB COMMUNITY /IN ISRAELI
KINDRED FROM ISRAEL IS CAUSED BYPATIENTS IN ISRAEL /IN JEWISH ANDPATIENTS WITH PHENYLKETONURIA /IN
ARABIAN DUCHENNE MUSCULAR DYSTROPHYARABINOSIDE CYTOSINE IN LYMPHOCYTESARCHIVAL CHINESE ESOPHAGEAL CANCER /INARCITECTURE /OF FETAL MICROSCOPICARGENTINIAN PATIENTS /AMONG GERMAN ANDARGINASE All IN MACROPHAGE KILLING /OFARGININO SUCCINATE SYNTHETASE LOCUSARM /A JUNCTION WITH THE CHROMOSOME
/EUCHROMATIC Y CHROMOSOME LONG/THE PROXIMAL X CHROMOSOME SHORT120 AND RAT CHROMOSOME 7ABERRATIONS IN HUMAN D G GROUPBREAKPOINT OF CHROMOSOME 16 /THE PINHERITED FROM AN ASYMPTOMATICMARKERS /RELATED AND OTHER X SHORTOF CHROMOSOME 1 MAKES DNA /SHORTOF CHROMOSOME 11 AND CHROMOSOME 17OF CHROMOSOME 17 /PROXIMAL SHORTOF CHROMOSOME 17 /PROXIMAL SHORTOF CHROMOSOME 20 /OF THE LONGOF CHROMOSOME 22 /OF THE LONGOF CHROMOSOME 4 ANALYZED /THE LONGOF CHROMOSOME 5 /LOCI ON THE LONGOF CHROMOSOME 5 /MAP OF THE SHORTOF CHROMOSOME 8 /OF THE SHORTOF CHROMOSOME 9 /OF THE LONGOF CHROMOSOME 9 [TYPE TO THE LONGOF CHROMOSOME 9 KARYOTYPE /LONG
659105459575412
2372986
2387592
21031349891
2543155727732400259223972326S9186723262797207317522749286886722062270165
2624737
155913521297847
274827632631277524342404246319211181118266910369867146666
2746272426944712689277599642767
5672734281122902381903667
11811091253822701746998
2551740958138858711742344243121402213217622601870153717091498193119352016199821391462148116702208217715851512598
1529
OF HUMAN CHROMOSOME 11 CONTAININGOF THE HUMAN X CHROMOSOME /LONGOF THE HUMAN Y CHROMOSOME /LONGOF THE X CHROMOSOME CONTAINS ATRANSLOCATION (9P22P 90220) IN A
ARRAY OF DROSOPHILA /THE HISTONEARRAYED CDNA LIBRARIES /USINGARSACS GENE FROM LINKAGE TO HUMAN /THEARTERIES ASSOCIATED WITH /OF THEARTERY DISEASE /DOCUMENTED CORONARY
DISEASE IN FINNISH PATIENTSDISEASE IN THE CHINESE
ARTHRIS AND AUTOIMMUNE THYROIDIN JAPANESE /OF RHEUMATOID
ARTHROGRYPOSIS ABSENT PATELLAE ANDAND MENTAL RETARDATIONIN FINLAND /LETHALMULTIPLEX CONGENITA /IN
ARTIFACT /STUDIES TRUE INCREASE ORARTIFACTS /ELIMINATION OF HETERODUPLEXARTIFKICAL CHROMOSOME AND CDNA CLONES
CHROMOSOME AT D13S31 /YEASTCHROMOSOME BASED MAPPINGCHROMOSOME CLONES ANDCHROMOSOME CLONES FROMCHROMOSOME CLONES IN THECHROMOSOME CLONING /YEASTCHROMOSOME CLONING ANDCHROMOSOME CLONING INCHROMOSOME CLONING OFCHROMOSOME CONTIG /A YEASTCHROMOSOME CONTIG /YEASTCHROMOSOME CONTIG AROUNDCHROMOSOME CONTIG AT THECHROMOSOME CONTIG PROXIMALCHROMOSOME END FRAGMENTSCHROMOSOME LIBRARY /YEASTCHROMOSOME LIBRARY FROMCHROMOSOME RECOMBINATIONCHROMOSOME TECHNOLOGY TOCHROMOSOMES /22 USING YEASTCHROMOSOMES /AS YEASTCHROMOSOMES /IN YEASTCHROMOSOMES /IN YEASTCHROMOSOMES /IN YEASTCHROMOSOMES /OF YEASTCHROMOSOMES /OF YEASTCHROMOSOMES /USING YEASTCHROMOSOMES /WITH YEASTCHROMOSOMES A PARADIGM FORCHROMOSOMES AND COSMIDSCHROMOSOMES CONTAININGCHROMOSOMES CONTAINING DNACHROMOSOMES CONTIG AROUNDCHROMOSOMES DNA INSERTCHROMOSOMES FROM THE /YEASTCHROMOSOMES FROM THE HLACHROMOSOMES IN XP21 /YEASTCHROMOSOMES NEAR THE /YEASTCHROMOSOMES ON HUMAN /YEASTCHROMOSOMES PHYSICAL /YEAST
ARYL HYDROCARBON HYDROXYLASE INARYLSULFATASE A DEFICIENCY /LEADING TO
A GENES IN BONE MARROWASBESTOS EXPOSURE AND THE ABSENCE OFASCITIC RAUCHER LEUKEMIA VIRUS /ANDASCORBIC ACID ON DIMETHOATE INDUCEDASHKENAZI /THE SEPHARDIC ORIGIN OF
JEWISH AND OTHER POPULATIONSJEWS/IN
ASHKENAZIC JEWS /ON CHROMOSOME 9034 INASIA /SCREENING IN SOUTHEAST
AND MULTIPLE MIGRATION ROUTES OFFAMILIAL ISOLATE /ENRICHED MIDDLE
ASIAN BLACK CAUCASIAN AND HISPANICBLACK CAUCASIAN AND HISPANICBLACK CAUCASIAN HISPANIC AND /INMITOCHONDRIAL DNA ANALYSISORIGIN POPULATION GENETIC /SOUTH
ASIANS /ORIGIN OF THALASSEMIA GENES INASO REVERSE DOT BLOT /BY MEANS OFASPRTYLGLUCOSANNIDASE PRECURSOR INASPARTYLGLUCOSAMURIA /GENETICS OF
DEFECT IN THEIN DIFFERENTPATIENTS
ASSAY /USING A RECOMBINATION BASEDFOR LINKAGE ANALYSIS ANDIMPLICATIONS FOR ONCOGENESISIN THE MONITORING OF /BRDURDOF CVS GLYCINE CLEAVAGE ENZYMEVARIANCE /SYNDROME THE IMPACT OF
ASSEMBLY DEFECT IN ZELLWEGER SYNDROMEASSORTATIVE MATING /DISEASE LOCI AND
MATING ON LINKAGE /ANDASSORTMENT AND RELIABILITY OF DNAASSUMED KARYOTYPE OF THE ZYGOTE ANDASSYMETRIC LIMB HYPERTROPHY WITH ANDASTHMA /OF PATIENTS WITH BRONCHIAL
AND KIDNEY DISEASES /TOSUBTYPE /ASTHMATIC FAMILIES BY
ASTHMATIC FAMILIES BY ASTHMA SUBTYPEASTROCYTOMA IN A NEONATE WITH THE /ANASTROCYTOMAS /PATTERN IN MALIGNANTASYMPTOMATIC ADULT WITH PROFOUND
21842118210520151347264223302004705714714
2746266387664014308961524116825132168237337319502160206521932185179
2306102204
2389101
2159207521022167
1820572162
5049203
2158200252621892204202185
21351682378
27852112211422202145215618591294285
2492610134125432826
423292353387
287619472836285228672610
661070184946645846623564662507978254625585631828505
2027189911031264641741
27527897896821332510
MOSAIC MOTHER /FROM ANASYNCHRONOUS REPLICATION OF THE /THEATAXIA /EFFORTS FOR SPINOCEREBELLAR
/MELLITUS AND CEREBELLARAND SPASTIC DIPLEGIAAND SPASTIC PARAPLEGIA /WITHGENE IS TIGHTLY LINKED TOIN A SPANISH POPULATIONIS PROBABLY DUE TO A MUTATIONLOCUS BY ANALYSIS OFLOCUS TO A 6 CM SUBREGION OFMENTAL DEFICIENCY PARTIALOF CHARLEVOIX SAGUENAY /SPASTICREGION AT 9Q13021.1TELANGIECTASIA GENE(S) TO A CMTELANGIECTASIA GROUP D CELLSTELANGIECTASIA IN ITALY DATATELANGIECTASIA IS FLANKED BYTELANGIECTASIA LOCUS /NEAR THETELANGIECTASIA LYMPHOBLASTSTELANGIECTASIA PATIENT WITH ATELANGIECTASIA USING BIVARIATEWITHIN AMERICAN (U.S.A.)
ATELOSTEOGENESIS TYPE II SONOGRAPHICATHEROSCLEROSIS /LP(A) GENE AND
/THE GENETICS OFIN TRANSGENIC MICE
ATHEROSCLEROTIC DISEASE /ETIOLOGY OFATLANTA AND SOUTHWEST OHIO 1974 1989
DOES COCAINE PLAY A ROLEATLANTOAXIAL INSTABILITY IN THEATOMIC BOMB SURVIVORS /IN CHILDREN OF
STATION CATASTROPHE /CHERNOBYLATRESIA AND ASSOCIATED ANOMALIES
AND TRACHEOESOPHAGEAL FISTULACARDIAC DEFECTS TRACHEO /ANALRENAL DEFECTS AND RADIAL LIMBRESULTING IN NORMAL PULMONARY
ATRIAL NATRIURETIC FACTOR GENE IN [THETACHYCARDIA AND APPARENT /WITH
ATRIOVENTRICULAR HEART BLOCK IN DOWNATROPHIES /FOR THE SPINAL MUSCULAR
/OF THE SPINAL MUSCULAR/ONSET SPINAL MUSCULAR
ATROPHY /DOMINANT OLIVOPONTOCEREBELLAR/IN AN EXON DELETION IN GYRATE/PEDIGREES IN SPINAL MUSCULAR/REGION FOR SPINAL MUSCULAR/SPINAL AND BULBAR MUSCULAR/THE GENE FOR SPINAL MUSCULARAMONG FINNS AND OTHERS /GYRATECONFIRMATION OF CLOSE LINKAGEFROM THE NETHERLANDS /MUSCULARGENE WOBBLER MAPS CLOSE TOIN FINLAND /SPINAL MUSCULARLOCUS /OF THE SPINAL MUSCULARLOCUS /OF THE SPINAL MUSCULARLOCUS /TO THE SPINAL MUSCULARNEW SYNDROME /AND CEREBELLAROF THE CHOROID AND RETINAREGION ENRICHING THE REGIONSYNDROME /AND OPTICUPDATE ON MOLECULAR GENETICSUSING PCR DENATURING GRADIENTUSING POLYMORPHIC DNA PROBES
ATTENUATED VIRUSES CAN CAUSE MEIOTICATTITUDES AND REASONING OF M S /OF THE
OF THAI FAMILIES TOWARDTOWARD THALASSEMIA /CONSUMER
ATYPICAL PHENOTYPES /X PATIENTS WITHAUDITORY BRAIN STEM RESPONSES IN THE
TISSUES /IN HEARING FROMAUSTRAUA /GENETIC EDUCATION IN
/OF HEMOPHILIA A IN SOUTHAUSTRALIAN PROGRAM /RESULTS FROM ANAUTISM /SMALL MARKER CHROMOSOMES IN
AND 47 XX + INV DUP (15)AND TUBEROUS SCLEROSIS /OFIN A CHILEAN POPULATION /AND
AUTISTIC PROBANDS /FAMILY MEMBERS OFAUTOIMMUNE DISEASE /AND EXPRESSION IN
THYROID DISEASE IN FAMILIESAUTOLOGISTIC MODEL TO ACCOUNT FORAUTOLOGOUS BONE MARROW TRANSPLANTATIONAUTOMATED AND RAPID SEQUENCING OF
DETECTION OF NON CDF508GENOTYPING OF HIGHLYPROBE MAPPING BY /SEMI
AUTOMATIC ASSESSMENT OF THE QUALITYCONSTRUCTION OF GENETIC /FOR
AUTOMATION OF A METHOD FORAUTONOMOUS REGION /IN NINGXIA HUIAUTOPHAGY /MYOPATHY WITH EXCESSIVEAUTORADIOGRAPHS /OF SOUTHERN BLOTAUTOSOMAL CHROMOSOMAL TRANSLOCATION
DISORDER /PROBABLY RECESSIVEDISORDERS NEW MUTATION /ANDDOMINANT /ANALYSIS INDOMINANT ANIRIDIA /INDOMINANT DISEASES MIMIC /OFDOMINANT DISORDER /SEIZURESDOMINANT FORM OF LIMB /OF ANDOMINANT INHERITANCE /ANDDOMINANT INHERITANCE OFDOMINANT POLYCYSTIC KIDNEY
538
14981557215750219879832052198982081
2001645
20042178294
2301265419671955677260416091893794162163192161
26862702894506
2806653
264681681692710377811463194312391885187328022776214695
1886S4
2018109318642687210121122332668
25192218866S5
105712231371182117641855151148426
32828121749145115218631492625425266326431367249711052062208716182060577
278018875861468769
280818731960203476178892832226
Permuted Title Index
DOMINANT POLYCYSTIC KIDNEYDOMINANT POLYCYSTIC KIDNEYDOMINANT POLYCYSTIC KIDNEYDOMINANT POLYCYSTIC KIDNEYDOMINANT POLYCYSTIC KIDNEYDOMINANT RETINITIS /INDOMINANT RETINITIS fINDOMINANT RETINITIS /WITHDOMINANT RETINITIS /WITHDOMINANT TRAIT WITH /LIMITEDDOMINANT TRANSMISSIONDOMINANTLY INHERITED BONEINHERITANCE /TO X LINKED ANDINVERSIONS /PERICENTRICLOCUS UNDERLYING BIPOLAR /ANRECESSIVE ECTODERMAL /A NEWRECESSIVE FORM /OF THERECESSIVE HYDROTICRECESSIVE INHERITANCE /WITHRECESSIVE INHERITANCE /WITHRECESSIVE MULTIPLE /NEWRECESSIVE PHENOTYPE /A NEWRECESSIVE SENSORINEURALRECESSIVE SPASTIC ATAXIA OFRECESSIVE SYNDROME /A NEWRECESSIVE SYNDROME /XI ANRECESSIVE SYNDROME OF /ANRECESSIVE SYNDROME OR A /NEWSEGMENTAL ANEUSOMIES /OF
AUTOSOME TRANSLOCATION IN A GIRL WITHAUTOSOMES /22 AND OTHER HUMANAVAILABIITY SAMPLING ON MTDNA /OFAVERAGE COMPUTER /DYSMORPHOLOGY TO ANAVIAN V MAF ONCOGENE PRODUCT /TO THEAXIAL MESODERMAL DYSPLASIA SPECTRUMAXIS SPECIFICATION AND CNS DEVELOPMENTAXONAL TRANSPORT /BY RETROGRADEAZF LOCUS THE USE OF INTERVAL 6 AND 7AZOOSPERMA FACTOR A MALE FERTILITY
FACTOR TO THE DISTAL /THE
249998111019022371
72378
899922377817388021515198881278064883984987-9720788
20048828468178141464643
21302869136
24598593112489910
22052176
B
B+ THALASSEMIA PROMOTER MUTATION ON /AB.S.S.R /SYSTEM HEREDITARY DISEASES INB1 GAMMA AMINOBUTYRIC ACID RECEPTORGENE IN EMBRYONIC STEM CELLSIN RAT BONE MARROW CELLS IN VIVOVARIANT /A LATE INFANTILE TAY SACHSVARIANT OF GM2 GANGLIOSIDOSIS /WITH
B12 /LYSOSOMAL TRANSPORT OF VITAMINB2 DIRECTLY CAUSES MALIGNANCY IN /ERBB27 /OF HLA ANTIGENS All ANDB3 SUBUNIT GENE (GABRB3) TO THEBABIES FROM SAME FATHER AND TWO /TWO
WITH MICROGNATHIA AND OTHER /OFBABOONS/ON SERUM LEVELS OF HDL C INBACTERIAL EXPRESSION OF HUMANBACTERIOPHAGE CLONES FROM THE /ANDBAHRAIN 6 YEAR STUDY /ABNORMALITY INBALANCED 2;18 TRANSLOCATION AND /A
AUTOSOMAL CHROMOSOMALCHROMOSOME REARRANGEMENTSCHROMOSOME REARRANGEMENTSCOMPLEX FIVE BREAK 1OF ARECIPROCAL TRANSLOCATION /AROBERTSONIAN TRANSLOCATION TT(13;21) /WITH AN APPARENTLYT(6P;13Q) CHROMOSOMETRANSLOCATION /WITH X;3TRANSLOCATIONS /10 INTRANSLOCATIONS AND MENTALX AUTOSOME TRANSLOCATION INX/AUTOSOME TRANSLOCATION
BALB/CBYJ MOUSE /POLYPEPTIDE IN THEBAND 11 P15.5 /MAP OF HUMAN CHROMOSOME
17P11.2 /TYPE IA GENE IN DISTAL1 P36 EMERGENCE OF TWO /OF3 IN JAPANESE BRAZILIANS3P13 /BREAKPOINTS IN CHROMOSOMAL3P21.1 /WITHIN HUMAN CHROMOSOMAL3P21.1 /WITHIN HUMAN CHROMOSOMALAT AMNIOCENTESIS ASSOCIATIONFLAVORS /MAP TO CHROMOSOMEIN TWO FAMIUES /9QH + VARIANTLP36 IN OVARIAN SEROUS ANVOLVING015 Q21 OF CHROMOSOME S WITH /TO024 OF CHROMOSOME 16 /GENE TOSCORING /THREE YEARS OF QUALITYSHARING AMONG INDIVIDUALS INSPECIFIC PAINTING FLUORESCENCEXQ28 /WITHIN THE G6PD CLUSTER OF
BANDED METAPHASES /OF THE QUALITY OF GBANDING AND PAIRING PATTERN OF HUMAN
BY FLUORESCENCE IN SITU /4 ALUFOR ELECTRON MICROSCOPYINCLUDING FRAGILE X SCREENINGPATTERNS USING FLUORESCENCETECHNIQUE /CHROMOSOMEVARIANTS ON HUMAN METAPHASE
BANDS /OF GIEMSA AND REVERSE
242327281907243513014941059476
2572592
2392747112
26902323200813992002146884
1247163211701230660
14211472118814096431457459
21421952153826291722213821951274411151313382171217218042871172819641618420165620851630200162016111657
BANGKOK THAILAND /HOSPITALBANK /OF HUMAN PROTEIN CDNA
AND CELL REPOSITORY /ITALY DATABANKING EXPERIENCE FOR MULTIPLE /DNA
FOR GENETIC ANALYSIS FROM ABAR CODES BY FLUORESCENCE IN SITUBARGUISIMETO VENEZUELA /OF NTDS INBARRET'S ADENOCARCINOMA /INBARRIER TRANSPORT OF PROTEIN FROMBASAL CELL CARCINOMAS OF THE SKIN /IN
CELL NEVUS SYNDROME /INCELL NEVUS SYNDROME IN CHINESEINITIATION COMPLEX MECHANISMS
BASE DIFFERENCES /TO DETECT SINGLEIN FACIAL GROWTH RABBIT MODELINSERTION OF JEWISH INFANTILEMUTATIONS IN HPRT CDNA USING THEPAIRS FROM A POLYMORPHIC /SITE 20SEQUENCES IN THE CENTROMERIC /OF
BASEMENT MEMBRANE ALPORT /GLOMERULARBASES ON DETECTION OF POINT MUTATIONSBASHKIR POPULATION /FIBROSIS GENE INBASIC/LEUCNE ZIPPER MOTIF HOMOLOGOUSBATTEN DISEASE GENE CLN3BAYESIAN EVALUATION OF THEBCL 1 LOCI /NEOPLASIA TYPE 1 AND
1 ONCOGENE FROM HUMAN CHROMOSOME2 /1 HAS SIGNIFICANT HOMOLOGY TO
BCL2 GENE IN HUMAN MULTIPLE MYELOMABCR IN SOME PATIENTS WITH /WITH 5BECKER MUSCULAR DYSTROPHIES /AND
MUSCULAR DYSTROPHY A /ANDMUSCULAR DYSTROPHY BY /ANDMUSCULAR DYSTROPHY FAMILIESMUSCULAR DYSTROPHY PATIENTSMUSCULAR DYSTROPHY PATIENTSMUSCULAR DYSTROPHY PATIENTS INMUSCULAR DYSTROPHY WITH /ANDPATIENTS /FROM DUCHENNE AND
BECKER'S ALLELIC MODEL TO EXPLAINBECKWITH WIEDEMANN SYNDROME /IN THE
WIEDEMANN SYNDROME /SPORADICWIEDEMANN SYNDROME AND /FORWIEDEMANN SYNDROME AND /THEWIEDEMANN SYNDROME SUPPORT
BEHAVIOR AND BRAIN IMAGING /GENETICSAND THE ALCOHOL INDUCTION OFDEPENDING ON THE SEX OF THEIN 32 MENINGIOMAS /ANDIN WOMEN GENETICALLY /HEALTH
BEHAVIORAL CHANGES IN OLDER /ANDGENETICS AND FUNCTIONSPROBLEMS ASSOCIATED WITH A
BEHMEL SYNDROME /THE SIMPSON GOLABIBELGIUM (1971 1990) /20 YEAR STUDY INBELL SYNDROME IN AN IRANIAN FAMILYBENIGN FAMILIAL NEONATAL CONVULSIONS
FAMILIAL NEONATAL SEIZURESMAMMARY PATHOLOGIES
BERARDINELLI SEIP SYNDROME ANDBETA /SCREENING THE USE OF FREE
4 AND ALPHA 5 NEURONAL /ALPHA 3ALLELE OF THE INSULIN GENE IN /OFGALACTOSIDASE CDNA SEQUENCE OF 2GALACTOSIDASE DEFICIENCY /INGLOBIN DOMAIN [THEGLOBIN GENE BY DENATURING /IN THEGLUCURONIDASE DEFICIENCY NVllHEXOSAMINIDASE ACTIVE SITETHALASSEMIA /DIAGNOSIS OFTHALASSEMIA AND 306 NORMAL /72THALASSEMIA IN NORTH INDIA /OFTHALASSEMIA IN SOUTHERN THAILANDTHALASSEMIA/HEMOGLOBIN E DISEASE
BFF BY ISOELECTRIC FOCUSING AN /OFBIAS IN GENETIC EPIDEMIOLOGICALBIASES IN TWIN RESEARCH /PRENATALBIFUNCTIONAL ENZYME DEFICIENCYBIHAR INDIA /A MUSLIM COMMUNITY FROM
INDIA /TRIBES OF RAJMAHAL HILLSBILATERAL ABSENCE OF THE VAS DEFERENS
CONGENITAL HALLUX VIRUSNASAL ALAR INDENTATIONS ARENAL AGENESIS /DIAGNOSIS OF
BILIARY ATRESIA AND ASSOCIATEDCIRRHOSIS /AND PRIMARY
BIUNEAL PEDIGREES FOR LINKAGE /OFBINARY SCORING /EXPERIMENTS BASED ONBINDING AND CAUSES LARON DWARFISM
AND PROPER MITOTIC SEGREGATIONAND TRANSIENT EUTHYROIDDOMAINS /PROLINE RICH AND DNAFACTOR 1 MAPPED TO HUMANOF TRANSCRIPTION FACTORS /DNAPROTEIN GENE AND RELATEDPROTEIN GROUP SPECIFIC /DPROTEIN OF E COLI /OF CYSTINEPROTEINS DURING DEVELOPMENTTO HEPG2 NUCLEAR EXTRACTS AND
BIOASSAY UTILIZING AN INDUCIBLE /NEWBIOCHEMICAL ABNORMALITIES IN THE
AND CLINICAL FINDINGSAND MOLECULAR /CLINICALAND MOLECULAR GENETICS OFASPECTS OF EMBRYOLETHALITY
12492512235417862737184
26802571955
258320031359118
2078931
24462813959
222838310072317245919722006218426082589167425971098205010231046989
2292104011231029277676790
2181767159619572716115313101733554121
1535735
147514718337611308891310
21827224511075336
251724735281272183110242354793
283869
S85487
282228331067476631179653542
2683212124551663853
22881867254022762262448120
241712914784874984931479
CHARACTERISTICS OF /ANDCONSEQUENCES OF GENETICEVIDENCE FOR AN /ANDHETEROGENEITY ANDMARKERS /AGE AND THREEMARKERS /OF GENETIC ANDSCREENING FOR DOWNSCREENING FOR DOWNSCREENING FOR DOWN /OFSCREENING FOR DOWN /SERUMSCREENING OF A FAMILY /ANDSTUDIES IN 14 PORTUGUESESTUDIES OF HEXOSAMINIDASESTUDIES ON HUMAN /ANDSTUDY OF COLLAGENVARIATION IN SOME CASTEVARIATION IN THE GARHWAL
BIOCHEMISTRY TO PRENATAL PROGNOSIS OFBIOETHICAL CONSIDERATION ON GENETICBIOGENESIS OF PEROXISOMESBIOLOGICAL DETERMINANTS OF BLOOD /AND
ROLE OF HUMAN CHROMOSOMALBIOLOGY AND COUNSELING /FOR DETECTION
AND GENETICS OF DIZYGOTICAND PATHOGENESIS /MOLECULARAND TREATMENT /MOLECULARCLASSES /USE IN HIGH SCHOOLEDUCATION IN THE NATION'S
BIOMEDICAL SCIENCES /THE DIVISION OFBIOMEK 1000 WORKSTATION /USING THEBIOPSY /DYSTROPHY BY FETAL MUSCLE
AN ALTERNATIVE TO /PLACENTALCONTRACTURE TESTING ASSIGNMENTUSING MALTOSE AS A SUBSTRATE
BIOSYNTHESIS IN FIBROBLASTS AND /ANDBIOSYNTHETIC PATHWAY AMINOLEVULINATEBIOTIN /TRANSPORT AND RECYCLING OFBIOTINIDASE DEFICIENCY /WITH PROFOUND
DEFICIENCY A COMPARISONBIOTINYLATED DNA PROBE /X CENTROMERE
PCR PROBES /WITHY SPECIFIC DNA PROBE /BY
BIPLAR AFFECTIVE DISORDER /LINKED TOAFFECTIVE DISORDER IN THE OLDAFFECTIVE ILLNESS /ANALYSIS OFDISORDER /IN FAMILIES WITHILLNESS /LINKAGE STUDIES OF
BIRTH /FOR ZYGOSITY DIAGNOSIS ATA 20 YEAR STUDY IN BELGIUM /ATCOHORT /SYSTEM (VACARES) 1987DEFECTS /ABNORMALITIES CAUSINGDEFECTS FOR SOCIETAL DECISIONDEFECTS IN LATIN AMERICA /OFDEFECTS INCIDENCE IN FETUSES /OFDEFECTS OF 37,954 PERINATAL /ONDEFECTS RATES IN JEFFERSONDEFECTS REGISTRY IN INDIAFROM CHILDLESS MARRIAGES DUE TOOF A CHILD WITH CONGENITAL /THEOF A VNTR SIZE AND SEQUENCEOF CONGENITAL MALFORMATIONS ATWEIGHT /ASSOCIATED WITHWEIGHT OF OFFSPRING BORN AFTER
BIRTHS WITH DOWN SYNDROME IN /REDUCINGBIVARIATE BRDU HOECHST FLOW CYTOMETRY
PHENOTYPE UNDER COMPLEX /ABLACK AND WHITE POPULATIONS OF /THE
CAUCASIAN AND HISPANIC RACIALCAUCASIAN AND HISPANIC RACIALCAUCASIAN HISPANIC AND NATIVEHAIR DYE /OF A PERMANENT
BLACKFOOT DISEASE ENDEMIC AREA INBLACKS AND MONGOLOIDS /POPULATION
EXCLUSION OF CANDIDATE LOCIBLADDER TUMORS USING FLUORESCENCE INBLASTS IN A CASE OF KOSTMANNBLEOMYCIN A STUDY IN TWINS /TO
AND ARABINOSIDE CYTOSINE INBLEPHAROPtUMOSIS SYNDROME /OF THE OHDOBLINDED STUDY /RESULTS FROM A LARGEBLINDNESS (NORRIE DISEASE) (EPISKOPI
MAY BE LINKED WITH G /NIGHTPHENOTYPE /STATIONARY NIGHTPROXIMAL TO DXS7 /NIGHT
BLIZZARD SYNDROME /STUDY OF JOHANSONBLOCK IN DOWN SYNDROME /HEARTBLOOD /AMERICANS BY PCR OF DRIED
/CHROMOSOME ANALYSIS FROM CORD/INDIVIDUALITY OF HUMANA PROBLEM FOR DETECTION BIOLOGYAFP ALBUMIN PREALBUMIN AND /CORDBRAIN BARRIER TRANSPORT OF [THEBY CORDOCENTESIS /AND IN FETALBY PCR MAY ALSO LEAD TO FALSEDONORS OF THE INDONESIAN RED /INENZYMES IN THE CENTRAL REGIONFREQUENCIES MEASURED BY THE PCRGROUP A AND B GENE ENCODEDGROUP IN MALFORMED NEWBORNS ANDGROUPS /DERMATOGLYPHICS AND ASOGROUPS AND PROTEIN ELECTROMORPHSGROUPS IN RELATION TO ASTHMALYMPHOCYTES /AGE GROUPS OF HUMANLYMPHOCYTES /IMRNA IN PERIPHERALLYMPHOCYTES INDUCED BY
539
50645615854421215766307S643093081025837494491450287028329291739131
27071579911400264279178039417822125120711511911574513
240947951046816981656167619401988202920911879S851475273012791813272226992780267177612361760263126882880127126861609271428442836285228672560138328232000164261913391388763111
204719288101878723146327431495285391191295512851060275428451131572
2655185128422752254210891352
Permuted Title Index
LYMPHOCYTES TO G2 PHASE X /OFMITOCHONDRIAL DNA IN KEARNS /INPLASMA OF WOMEN AT HIGH RISK /BYPRESSURE AND BODY MASS INDEX /OFPRESSURE IN AN INDIAN POPULATIONPRESSURE IN THE AFRICAN GREENPRESSURE IN TWINSPRESSURE WITH AGE /OF SYSTOLICPROSPECTS FOR NONINVASIVESPECIMENS /DRIED FILTER PAPERSPOT SAMPLES COLLECTED ON /DRIEDSPOTS /BY DIRECT PCR OF GUTHRIESYSTEM /INTERACTION WITH THE ABO
BLOOD/SKIN MOSAICISM FOR CHROMOSOMALBLOOM SYNDROME /CARCINOMA IN
SYNDROME /DNA LIGASE DEFECT INSYNDROME CELLS /OF
BLOT /BY MEANS OF ASO REVERSE DOTANALYSIS AND FLUORSCENT IN SITUAND PCR TECHNIQUES /BY SOUTHERNAUTORADIOGRAPHS /OF SOUTHERNHYBRIDIZATION /OF REVERSE DOT
BLOTS /USING DENATURING GRADIENT GELBLOTrlNG AND PCR /USING SOUTHERN
IN THE STUDY OF MENKESBLUE LIGHT PHOTOTHERAPY AND VITAMIN EBODY COMPOSITION MEASURED USING /OF
MASS INDEX /OF BLOOD PRESSURE ANDMEASUREMENTS ON NEONATES FROMSTALK ANOMALY PRENATAL DIAGNOSIS
BOHEMIA AND MORAVIA HYPOTHESIS ON THEBOMB SURVIVORS /IN CHILDREN OF ATOMICBOMBAY PHENOTYPE /CHEMOTAXIS ANDBONE AND SOFT TISSUE SARCOMAS /WITH
AND SOFT TISSUE TUMORS /OFCT FINDINGS /HAND AND TEMPORALDISORDER /DOMINANTLY INHERITEDDYSPLASIA ASSOCIATED WITH /OF ALESIONS PATHOGENIC DIAGNOSTICMARROW BY TRIPTERYGIUM /IN MOUSEMARROW CELLS BY BIOTINYLATED YMARROW CELLS IN VIVO AND THEIRMARROW CELLS USING A REPLICATIONMARROW CELLS USING RECOMBINANTMARROW CULTURES FOR CHROMOSOMALMARROW FINDINGS IN 15 PATIENTSMARROW IN ACUTE LYMPHOCYTICMARROW TRANSPLANT FORMARROW TRANSPLANT STUDIESMARROW TRANSPLANTATIONMARROW TRANSPLANTATIONMARROW TRANSPLANTATION AIN UTEROMARROW TRANSPLANTATION /VI BYMARROW TRANSPLANTATION FOR /OFMARROW TRANSPLANTATION IN CANINEMARROW TRANSPLANTATION TO /AFTERMARROWS WITH NORMAL OR UNCERTAIN
BONES /RECOVERY OF DNA FROM ANCIENTAND ABSENCE OF TALUS AND /CARPAL
BONY FRAGILITY /BRACHYSYNDACTYLY ANDBOUNDARY CLONES CONTAIN TWO NEW GENES
OF THE PSEUDOAUTOSOMAL REGIONBOVINE RAT MOUSE AND CHICKEN REVEALS
TISSUES IMPROVE LIFE QUALITYBOW MOUTH PROGNATHISM ABNORMAL EARSBOWEL DISEASE /FORMS OF INFLAMMATORY
SYNDROME /OF APPLE PEELBOY BORN TO CONSANGUINEOUS PARENTS
WITH A SUBTLE DELETION (15CEN /AWITH LEUKEMOID REACTION AND /IN AWITH MULTIPLE ANOMALIES AND /IN AWITH X LINKED RECESSIVE /OF A
BOYS WITH ABNORMAL SEX CHROMOSOMEWITH PROGERIA AND A WOMAN WITH
BP IN FRAME DELETION OF THE /3BRACHMANN DE LANGE SYNDROME /CASE OFBRACHYDACTYLY /APLASIA AND COMPLEXBRACHYSYNDACTYLY AND BONY FRAGILITYBRAIN /CDNA CLONES EXPRESSED IN HUMAN
/INJECTION EXTRACTED FROM FETUS/OF THE DYSTROPHIN GENE IN THEBARRIER TRANSPORT OF PROTEINCANAVAN DISEASE /DEGENERATION OFCDNAS /LOCALIZATION OF 60DISEASE /IN CHRONIC HEART ANDDISORDER /POSSIBLE IN THIS FATALIMAGING /GENETICS BEHAVIOR ANDIN THE 18Q2 MONOSOMY SYNDROMEMORPHOMETRY IN USHER SYNDROMEPARENCHYMA INDUCED BY PLASMA /TOSPECIFIC CDNA ENCODING A NEW /ASTEM RESPONSES IN THE /AUDITORYTUMOR REGISTRY /FAMILIALTUMORS /OF MALIGNANT PEDIATRIC
BRAINS OF HPRT DEFICIENT MICE /IN THEBRANCH /RED CROSS YOGYAKARTABRANCHED CHAIN FATTY ACYL COA OXIDASEBRANCHIO OTO RENAL DYSPLASIA SYNDROMEBRAZIL /AND GUARANI AMERINDIANS FROM
/FOR MENTALLY HANDICAPPED IN/IN A PEDIATRIC HOSPITAL INNINE YEAR REPORT FROM A /IN
BRAZILIAN CYSTIC FIBROSIS ALLELES /INISOLATED COMMUNITY /IN APATIENTS /STUDY ON 26
269599515772707272067826932729
6011021186184026511570597295168918491867958586111320691110571156826492707116411782703506688
2605371796738933130518531676130124922490163813091345564166813671607154561156
24731522216
2502738705
219520342612950710
2770118189114541321140790214559504491496847705
252725332050955573
21796711935195714338509552380484615219478275452771828591617777
267528632835707
PATIENTS /STUDY ON 26POPULATION BLACKS AND /THE
BRAZILIANS /BAND 3 IN JAPANESEBRDU ANTIBODY TECHNIOUE ON HISTONE /BY
HOECHST FLOW CYTOMETRY /BIVARIATEINDUCED COMMON FRAGILE SITES IN
BRDURD ASSAY IN THE MONITORING OFBREAK REARRANGEMENT IN A MOTHER ANDBREAKAGE BY BLEOMYCIN AND ARABINOSIDE
SYNDROMES /MODELS FOR HUMANBREAKPOINT CLONING IN THE ABSENCE OF
CLUSTER REGION IN AN ACUTECLUSTER REGION IS TIGHTLYCLUSTER REGION WITHIN A MALIGNANT SCHWANNOMAIN A PATIENT WITH RAPP /14IN A PATIENT WITH RETTOF CHROMOSOME 16 INVERSION
BREAKPOINTS /4 CHROMOSOMES WITH 6/AND DISTRIBUTION OF/BY CLONING TRANSLOCATIONAND POSSIBLE LOCATIONS OFAPPLICATION OF A HIGHASSOCIATED WITH THE /OFIN A HETEROZYGOUS /OF THEIN CHROMOSOMAL BAND 3P13OF 11Q13 ARE CLOSELYON 11Q23 AND 12023 /WITHON CHROMOSOME 16
BREAST AND OVARIAN CANCER /C NEU INCANCER /ABERRATIONS IN HUMANCANCER /AND SPORADIC OVARIANCANCER /FAMILY HISTORIES OFCANCER /GENETICS OF HUMANCANCER /OF EARLY ONSET FAMILIALCANCER /PREDISPOSED TOCANCER /PREDISPOSITION TOCANCER /SUFFERING FAMILIALCANCER EVIDENCE FOR 17Q LINKAGECANCER IN A SWEDISH POPULATIONCANCER IN THE CANCER AND /OFCANCER INVESTIGATION OF ALLELECANCER OVARIAN CANCER /OFCANCER PATIENTS /CHROMOSOMES INCANCER USING LOCUS SPECIFICCARCINOMAS /AND 17Q IN HUMANCARCINOMAS USING CONSTANTOVARIAN CANCER LOCUS ON
BRITAIN AND THE UNITED STATES /INBRMSH COLUMBIA NATIVE KINDRED /IN A
FAMILIES /11Q22 23 IN 45BRITTANY /MUTATION IN SOUTHBROMODEOXYURIDINE LABELING INBRONCHIAL ASTHMA /OF PATIENTS WITHBROTHER AND SISTER /PROBLEMS IN A
AND SISTER /TRISOMY 5P INBUDAPEST /IN THE MALE POPULATION OFBULBAR MUSCULAR ATROPHY /SPINAL ANDBULGARIAN CLASSICAL PHENYLKETONURIABULLOSA /DYSTROPHIC EPIDERMOLYSIS
SIMPLEX /WITH EPIDERMOLYSISSIMPLEX MUTATION MAPS TOTO THE TYPE VII COLLAGEN GENE
BULLOUS DYSTROPHY TO XQ24 OTER /OFPEMPHIGOID ANTIGENS 1 AND 2
BURKITT LYMPHOMAS /P53 MUTATIONS INBUTYRYLCHOLINESTERASE /OF HUMAN SERUMBYELORUSSIA AFTER CHERNOBYL ACCIDENTBYELORUSSIAN CHILDREN POPULATIONS /OF
8312823262916331609156425581632138829737013702005S772600166620651709140684124
13131620767444172213871329185
25962595603608127
202417331754596
202660727713733021297217
25672181977319190919672712160874180015391166
951027192722572010
73199023872594546
26992806
C
C AETHIOPS /THE AFRICAN GREEN MONKEYAMYLOID ANGIOPATHY /CYSTATINAND CELL DISEASE /DISEASE TYPEAND CELL DISEASE /DISEASE TYPEAND OTHER FAMILY 2 CYSTATINS MAP TOELEGANS /GERMLINE PROLIFERATION INFOS AND C RAS ONCOGENE HOMOLOGS INFOS EXPRESSION IN HUMAN OVARIAN /ANDIN BABOONS /ON SERUM LEVELS OF HDLKIT (MAST/STEM CELL GROWTH FACTORKIT GENE COMPLEX /FACTOR RECEPTORMYC AND C FOS EXPRESSION IN HUMANMYC C FOS AND C RAS ONCOGENEMYC EXPRESSION AND PROLONGEDNEU IN BREAST AND OVARIAN CANCERRAS ONCOGENE HOMOLOGS IN DIFFERENTTO T MUTATION AT A MSPI SITE OF THE
C2 POLYMORPHISM IN AGINGC2Kl9T AND INTRONIC SEQUENCE /EXONICC4 GENE AND ITS EXPRESSION /HUMAN LDH
PROMOTER /OF THE HUMAN COMPLEMENTRELATED GENES IS RARE COMPARED TO
C4A AND C4B IN THE MAJOR /COMPONENTGENES /CARRYING DUPLICATED
C4B IN THE MAJOR HISTOCOMPATIBILITYCA DINUCLEOTIDE REPEATED SEQUENCES ON
N DINUCLEOTIDE REPEATS IN THEPOLYMORPHISMS IN A DELETION PRONEPOLYMORPHISMS IN THE HUMAN /AMONG
6781026627798
2183324256924132690189
229624132569918
25962569559
26944711286246726272403221124032166
82978983
REPEAT MARKER DXS548 FOR PRENATALCA3 AND MOUSE STRAIN CAR 2 /THE HUMANCA476 CONTAINS TWO HTF ISLANDS ANDCABRAL CHILDREN'S HOSPITAL /REIDCAENORHABDITIS ELEGANS /GENOME MAP OF
ELEGANS /GENOME OFCAFE AU LAIT SPOTS /WITH MULTIPLECAFFEINE CONNECTION AGE OF ONSET INCAJUN POPULATION /ALLELES IN THECALCANEUS A NEW AUTOSOMAL DOMINANTLYCALCIFICATIONS THE USE OF DNACALCITONIN GENE HYPERMETHYLATION INCALCIUM ACTIVATED NEUTRAL PROTEASE IN
AND CALCIUM DEPENDENT /TOCHANNEL SUBUNITS IN HUMANSDEPENDENT PARAMETERS /ANDLEVELS WITH REFRACTIVE ERROR
CALCYCUN GENE EXPRESSION INCAUFORNIA MEDICAL CENTER /OF SOUTHERNCALLOSUM /WITH AGENESIS OF CORPUS
IRIS COLOBOMAS AND (CORPUSCALPAINS IN SKELETAL MUSCLE OF /OFCALPASTATIN GENE TO BAND Q15 021 OFCAMP INDUCIBLE CHLORIDE CONDUCTANCECAMPOMELIC DYSPLASIA OF THE LONG /INCAMPTODACTYLY HYPOPLASTIC CARPAL (WITH
SYNDROME TYPECANADIAN ABORIGINAL POPULATIONS /THREE
ANCESTRY PUBLIC HEALTHCOLLABORATIVE STUDY OF /THEFAMILIES /TO D5S39 IN FRENCHMYOTONIC DYSTROPHY /A FRENCHOUTPATIENT POPULATION (IN APHENYLKETONURIA MUTATION INPOPULATION WHICH HAS AN
CANADIANS /DISEASE MUTATIONS IN FRENCH/DNA POLYMORPHISM IN FRENCH/LIPID METABOLISM IN FRENCHSEARCH FOR COMMON ANCESTORS
CANAVAN DISEASE /DEGENERATION OF BRAINCANCER (LYNCH SYNDROME) FAMILIES
/130 AND XP IN HUMAN OVARIAN/A COMMON STEP IN HUMAN/ABERRATIONS IN HUMAN BREAST/ABNORMALITIES IN PROSTATIC/AND GENE AMPLIFICATION IN/AND SPORADIC OVARIAN BREAST/AT ONSET FOR FAMILIAL OVARIAN/BY LOSS OF HETEROZYGOSITY IN/C NEU IN BREAST AND OVARIAN/CELL CARCINOMA AND UTERUS/CONSIDERATION OF COLORECTAL/COUNSELING AND FAMILIAL/EXPRESSION IN HUMAN OVARIAN/EXPRESSION IN SMALL CELL LUNG/FAMILY HISTORIES OF BREAST/GENETICS OF HUMAN BREAST/HETEROZYGOSITY IN ESOPHAGEAL/IMPORTANCE OF FAMILIAL/IN ARCHIVAL CHINESE ESOPHAGEAL/OF EARLY ONSET FAMILIAL BREAST/OF ENVIRONMENTALLY INDUCED/ONCOGENESIS OF PRIMARY OVARIAN/PREDISPOSED TO BREAST/PREDISPOSITION TO BREAST/RAS ONCOGENE IN HUMAN OVARIAN/RELATION TO FAMILY HISTORY OF/SUFFERING FAMILIAL BREAST/THERAPY FOR ADA DEFICIENCY ANDAND A VARIABLE NUMBER OF POLYPSAND OTHER CANDIDATE GENESAND POLYPS /EXAMPLE OF COLONAND STEROID HORMONE STUDY (THEAND TOXICITY /RISK OF HUMANCELL LINE ENCODES A PROTEINCLUSTERS AMONG FIRST DEGREECYTOGENETICS AN OVERVIEWEVIDENCE FOR 170 LINKAGEHEPATOCELLULAR CARCINOMA RENALHLA ASSOCIATIONS IN PATIENTSIN 221 HIGH RISK CHINESEIN A SWEDISH POPULATION /BREASTIN THE CANCER AND STEROIDIN THE NETHERLANDS UNDERINVESTIGATION OF ALLELE LOSSESLOCUS ON CHROMOSOME 17 /OVARIANOVARIAN CANCER HEPATOCELLULARPATIENTS /CHROMOSOMES IN BREASTPRONENESS /TO DNA REPAIR ANDSPECIFIC TRANSLOCATIONS BY INSUSCEPTIBILITY GENES IN THE /OFUSING LOCUS SPECIFIC PROBESVICTIMS INCLUDING RADON ANDWITH A CONSISTENT REDUCTION OF
CANCERATION OF BASAL CELL NEVUS /ONCANCERS /EXPRESSION IN HUMAN
/ORAL CAVITY AND HEAD AND NECKDO NOT HAVE SIGNIFICANTLY
CANDIDATE FIBRILLIN GENE FOR MARFANFOR A JUNCTION WITH THE /7FOR HYA AND SPY FROM THE /AFOR THE MEN2 GENE /AGENE /A HUNTINGTON DISEASEGENE (IN THE ABSENCE OF AGENE ANALYSIS OF FUNDUS
540
103825282297733
2126238742544
27097381182617731445
2180445895242011431900879486
2171236482373868528291788177120182036272527122840228928785152662573600606S6325951300369603582244
2596302272269
2413224608127
2609273587
20242726257217331754593
2695596S91599101S5827742822882710367
20263025906016072772721373197730212978453685942176102241359258058359293
2213234323472391370
2523
Permuted Title Index
GENE FOR FANCONI ANEMIA /AGENE FOR KALLMANN SYNDROMEGENE FOR LOWE SYNDROMEGENE FOR MARFAN SYNDROME /AGENE FOR MULTIPLE ENDOCRINEGENE FOR THE HUMAN /OF AGENE GENE ORGANIZATION ANDGENE IMPLICATED IN HUMANGENE LOCI IN TOURETTE /OFGENES /CANCER AND OTHERGENES AND ANONYMOUS DNA /INGENES FOR HERITABLEGENES FOR MYOTONIC DYSTROPHYGENES FOR THE X LINKED EYEGENETIC LOCI IN /OFHUNTINGTON DISEASE GENE /ALOCI CHROMOSOMAL REGIONS /OFREGION AMONG NEW MUTANTSREGION AND PROGRESS TOWARDREGION BY EXON AMPLIFICATIONREGION FOR THE HUNTINGTON /AREGION FOR THE HUNTINGTON /AREGIONS ON CHROMOSOMES 50REGIONS ON HUMAN /OF
CANINE COPPER TOXICOSIS /ON INHERITEDDYSTROPHIN MRNA IN GOLDEN /THEHOMOLOGS OF SYNTENIC HUMAN ANDMUCOPOLYSACCHARIDOSIS VII /INMUSCLE PHOSPHOFRUCTOKINASE /OF
CAR 2 POLYMORPHISMS /AND MOUSE STRAINCARIBAMATE COMPOUNDS /ANDCARBAMYL PHOSPHATE SYNTHETASE TYPECARBOHYDRATE DEFICIENT GLYCOPROTEINCARBONIC ANHYDRASE I A POSSIBLE NEW
ANHYDRASE II DEFICIENCY /THEANHYDRASE II STRUCTURAL GENE
CARBOXYLATE REDUCTASE BY /PYRROLINE 5CARBOXYMETHYL L CYSTEINE AND PRIMARYCARBOXYPEPTIDASE TO THE DISTAL /HUMANCARCINOGENESIS /FACTORS INVOLVED IN
AND TUMOR INVERSIONIN MICE /LOSS DURING
CARCINOMA /3P IN SPORADIC RENAL CELL/ALTERATIONS IN PROSTATE/DECREASED IN RENAL CELL/IN HUMAN TRANSITIONAL CELL/OF CERVIX ON ENDOMETRIAL/OF ONCOGENES IN HUMAN LUNG/OF PRIMARY HEPATOCELLULAR/PATIENTS WITH COLORECTAL/WITH PRIMARY HEPATOCELLULARAND UTERUS CANCER /CELLBY FLUORESCENT IN SITUCELL LINE BY INTRODUCTIONCELLS /HUMAN HEPATOCELLULARCELLS /IN HUMAN EMBRYONALCELLS /OF EMBRYONALGENE AND PART OF 180 AS THEIN BLOOM SYNDROMEIN FIVE KINDREDS /COLORECTALIN SITU IS SIMILAR FOR ALLIN SITU OF THE TESTIS /OFIS NOT LINKED TO CHROMOSOMEOF CERVIX ON ENDOMETRIALRENAL CELL CARCINOMA ANDSTUDIES INVOLVING SOMATIC
CARCINOMAS /AND 170 IN HUMAN BREAST/OF 14 SMALL CELL LUNG/OF RENAL CELL/THE 90 CASES OF ESOPHAGEALOF THE HEAD AND NECK /CELLOF THE HEAD AND NECK /CELLOF THE HEAD AND NECK AOF THE HEAD AND NECK AREOF THE LUNG /SOUAMOUS CELLOF THE SKIN /IN BASAL CELLUSING CONSTANT DENATURANT
CARDIAC AMYLOIDOSIS /ASSOCIATED WITHDEFECTS TRACHEO OESOPHAGEALDISEASE /MSAFP DUE TO FETALHISTOLOGY IN TRISOMY 21ULTRASOUND AND CARDIOLOGY
CARDIOLOGY /CARDIAC ULTRASOUND ANDCARDIOMYOMATHY /IN FAMILIAL DILATED
AND RENAL /NEONATALAND WITH MITOCHONDRIALMOLECULAR /DILATEDTO CHROMOSOME 14QL IN
CARDIOPATHY A NEW DISORDER DUE TO ACARDIOVASCULAR MALFORMATION HIGHER
MALFORMATIONSMALFORMATIONS NEW /OFPATHOLOGY /AND
CAREY SYNDROME /NEW CASE TORIELLOCARNfl1NE PALMITOYLTRANSFERASE /OF
PALMITOYLTRANSFERASE B /OFPALMITOYLTRANSFERASE TYPE 2
CAROLINA MACULAR DYSTROPHY AN /NORTHCARPAL BONES AND ABSENCE OF TALUS ANDCARRIER /DEPENDING ON THE SEX OF THE
DETECTION AND PROSPECTS OFDETECTION BY MEANS OF RFLPDETECTION IN DUCHENNE ANDDETECTION OF FRAGILE X USINGFREOUENCY IN WISCONSIN USING
187422942352
94234023422267
102072101
2059351228725312064233520002348102
238322712396203020201871967
18612473518
2528539
2031187
27511020102022795421462S93257330526071340257925775851313226513901397302132213952429245422431991597199161413181888585302
25992567138013846041319138513941393131525832189608161235934275275106253633
2385192035
2650232
26681730755
2382536535
2021738
115310461021102314871006
SCREENING AND PRENATALSCREENING FOR CYSTIC FIBROSISTESTING ASSESSING GENETIC 10
CARRIERSI(6.16) TRANSLOCATION IN MALECOMPARISON OF TWO SCREENINGDETECTION AMONG HEATLABILEIN HIS FAMILY /OF EXON 8 ANDOF CHROMOSOME ABERRATIONS /INOF COMPLEX GLYCEROL KINASEOF PHENYLKETONURIA MUTATIONSOF THE MURINE RB(6.16) /INWITH RECIPROCAL CHROMOSOMAL
CARTILAGE DEFECTS IN THE HUMAN /OFHAIR HYPOPLASIA /GROWTH IN
CASE /RETARDATION REPORT OF SECONDALSO FOUND TO BE 180 BY DNAAND REVIEW OF THE LITERATUREFOR POSTPONING TESTING /THEMANAGEMENT A FUSION OF OLD ANDOF A MICRODELETION DEL /13 AOF ANGELMAN SYNDROME IN A /SUBTLEOF BOTH SYNDROMES WITH XP22.3 IAOF BRACHMANN DE LANGE SYNDROMEOF CURRARINO TRIAD /ISSUES INOF FRYNS SYNDROME ASSOCIATEDOF GIANT CELL OSTEOGENIC SARCOMAOF HUMAN CHIMERISM IN AOF KOSTMANN AGRANULOCYTOSIS /IN AOF MILLER (POSTAXIAL ACROFACIALOF MOSAIC TRISOMY 5 /REPORT OF AOF PARTIAL TRISOMY 2031 2035OF PARTIAL TRISOMY 80 ANDOF PATTERSON DAVID SYNDROME /OF AOF RESOLVED FETAL HYDROPS /AOF TETRASOMY 12P /DIAGNOSEDOF THE OHDO BLEPHAROPHIMOSISOF THE SMITH LEMLI OPITZ SYNDROMEOF Y POLYPLOIDY /AREPORT /ACROFACIAL DYSOSTOSIS AREPORT IANOMALIES A FAMILYREPORT /MOSAIC TRISOMY 15 AREPORTS UNUSUAL CYTOGENETICSTUDIES ON UNUSUAL VARIANT 9STUDY OF JOHANSON BLIZZARD /ATORIELLO CAREY SYNDROME /NEWWHERE THE ALLEGED FATHER WAS IAWITH 14P+ MARKER CHROMOSOME /THEWITH 17011.2 DNA MARKERS ANALYSIS
CASES/A NEUROCRISTOPATHY REPORT OF 17/AN EGYPTIAN SAMPLE OF FRAGILE X/BY TRANSABDOMINAL ROUTE 1700/CHROMOSOMES INVOLVED IN 2148/CYTOGENETIC EVALUATION OF 500/DIAGNOSIS OF CYSTIC HYGROMA 23/DYSOSTOSIS REPORT OF 13/IN 10 YEARS AND 26,000/IN 9 FAMILIES AND 16 SPORADIC/IN PRENATALLY DETECTED/OF 1575 GENETIC COUNSELING/PATELLA SYNDROME STUDY OF 37/PROSPECTIVE FOLLOW UP OF 604/REAL RISKS EXPERIENCE WITH 2556/TYPE 2 PATIENTS AND SPORADIC/ULNA COMPLEX AN ANALYSIS OF 491/UTERINE SARCOMAS A STUDY OF 12A PRACTICAL APPROACH /OF TEN NEWAFFECTED BY INCOMPLETELYAN INDICATOR OF GENETIC /INDEXAND SUCCESSFUL PRENATAL /TWO NEWCOMPARED TO COMPLICATIONS INFROM INDIA /REPORT OF TWOOF CHILDHOOD KI 1 POSITIVEOF CONFINED PLACENTAL MOSAICISMOF ESOPHAGEAL CARCINOMAS /THE 90OF GASTROSCHISIS IN A LARGEOF HYDROCEPHALUS ASSOCIATEDOF MACERATED INTRAUTERINE FETALOF NON HODGKIN LYMPHOMA /IN FOUROF PENTASOMY X (49,XXXXX) /TWOOF RECURRENT ABORTIONS /IN 902OF TRANSABDOMINAL CVS /150OF TRISOMY 9P ARISING FROM AOF X LINKED DISEASES /SPORADICSCREENED FOR THE FRAGILE X /685THROUGH MSAFP PROGRAM /OF INDEXTO THE EIGHT PREVIOUSLY REPORTEDWITH INFANTILE MARFAN SYNDROMEWITH OVERLAPPING FEATURES /NEWWITH SPECIAL EMPHASIS ON
CASTE POPULATIONS OF CHAMBA HIMACHALCATALASE GENE EXPRESSION AND /MURINECATALOGUE OF HUMAN CHROMOSOMALCATALONIANS FROM THE EBRO DELTA /INCATALYTIC DOMAIN OF THE TYPE 1CATARACT/GENETIC STUDY OF CONGENITAL
AND MENTAL RETARDATION INENRICHED MIDDLE ASIA /OF
CATARACTS /ANIMAL MODEL FOR INHERITEDIN INDIA /AND CONGENITAL
CATASTROPHE /CHERNOBYL ATOMIC STATIONCATEGORIZING BIRTH DEFECTS FORCATESPIN E AND RENIN ON CHROMOSOME 1CATHEPSIN E /ANALYSIS OF GASTRICCATHOLIC HOSPITAL MORE LIKELY TO /AT ACAUCASIAN AND AFRICAN AMERICAN CYSTIC
112018481836158318304616901523687
242615521757477657101690153618221805647748
14481496176115201365937619797
12311406140271192214127637511427656639148215401461723755
28771544635815822125312751232114269511876761718760746125211802585235133514672791271053512628561331935604884939114913331527127012621555111116121183874727771636
2870244815432674
96700890194722682664280618132148225417422798
AND HISPANIC RACIAL GROUPSAND HISPANIC RACIAL GROUPSHISPANIC AND NATIVE /BLACKPOPULATIONS /OF VARIOUS
CAUCASIANS /DEAMINASE DEFICIENCY INCAUDAL DYSGENESIS /INHERITANCE OFCAUSAL HETEROGENEITY IN ISOLATEDCAUSATIVE GENE IN NAIL PATELLA /AS THECAVITY, AND HEAD AND NECK CANCERS /ORALCBIC TYPE OF METHYLMALONIC ACIDURIACBL F AND LYSOSOMAL TRANSPORT OFCBLC FORM /METABOLISM OF THECC ESSENTIAL FOR DEVELOPMENT /PRODUCTCD1 PYRROLINE 5 CARBOXYLATE REDUCTASECD508 MUTATION FROM SINGLE CELLSCDF508 ANALYSIS IIN WISCONSIN USING
BY ALLELE SPECIFIC PCR /OFCYSTIC FIBROSIS MUTATIONS /NON
CDNA A CANDIDATE GENE FOR MARFANAND GENOMIC CLONE PROBESAND INITIAL STUDIES IN ZELLWEGERBANK /OF HUMAN PROTEINCHARACTERIZATION USING ARRAYEDCLONE THAT CAN PARTIALLY CORRECTCLONES /ARTIFICIAL CHROMOSOME ANDCLONES CORRESPONDING TO LOCI /OFCLONES EXPRESSED IN HUMAN BRAINCLONES TO HUMAN CHROMOSOMES 5CLONES WHICH COMPLEMENT /OFCLONING AND SEQUENCING OF SERUMCLONING MAPPING AND EXPRESSIONENCODING A NEW MEMBER OF THEENCODING THE MAJOR HUMAN /OF APEFROM A HUMAN ESOPHAGEAL CANCERFROM THE HUNTINGTON DISEASE /OF AIN ANIMALS BY GENE ENGINEERED /IXIN THAT REGION /ISOLATION OF AINTO PRIMARY HEPATOCYTES OF THELIBRARIES /AND MEDULLA OBLONGATALIBRARIES /USING ARRAYEDPROBES AND PCR IS RELATIVELY LOWPROBES ENCODING GLUTARYL COASEQUENCE OF 2 ADULT PATIENTSSURVEYING OF CANDIDATE GENES FORUSING PROBES GENERATED BY INTERUSING THE PCR IN COMBINATIONWHOSE GENE MAPS TO HUMAN
CDNAS /LOCALIZATION OF 60 BRAIN/OF HUMAN PROTAMINE 1 AND 2/SEQUENCING OF THE PCR AMPLIFIEDENCODED BY HUMAN CHROMOSOME 21ENCODED BY LARGE GENOMIC REGIONSFOR TYPE PROCOLLAGEN FROM /OFOF ALTERNATIVE TRANSCRIPTS /ANDUSING YEAST ARTIFICIAL /SPECIFIC
CEUAC DISEASE PATIENTS AINCELL (DNA) BANKING FOR GENETIC
ABO ANTIGEN AND SERUM ANTIBODYACID PHOSPHATASE AND HEMOGLOBINANEMIA THE CININNATI /OF SICKLECARCINOMA /3P IN SPORADIC RENALCARCINOMA /DECREASED IN RENALCARCINOMA AIN HUMAN TRANSITIONALCARCINOMA AND UTERUS CANCERCARCINOMAS /OF RENALCARCINOMAS OF THE HEAD AND NECKCARCINOMAS OF THE HEAD AND NECKCARCINOMAS OF THE HEAD AND NECKCARCINOMAS OF THE LUNG /SQUAMOUSCARCINOMAS OF THE SKIN AIN BASALCENTER EXPERIENCE /SICKLECONTAMINATION IN AMNIOCYTESCONTAMINATION IN AMNIOTIC FLUIDCULTURES /IN AMNIOTIC FLUIDCYCLE AND IN GENE EXPRESSION /THECYCLE DEPENDENT DNA REPAIR /FOR ACYCLE DEPENDENT EXPRESSION OFCYCLE KINETICS AND X RAY INDUCEDCYCLE REGULATED PROTEIN KINASE /ADISEASE /DISEASE TYPE C AND IDISEASE /DISEASE TYPE C AND IDISEASE /MINOR ELEMENTS IN SICKLEDISEASE AND OTHER INHERITEDDISEASE IN THE WESTERN REGION OFENZYME AND SERUM PROTEIN /REDFACTOR LOCI MAY BE INVOLVED INFUSION STRATEGY /KINASE GENE BYGROWTH FACTOR RECEPTOR (C KIT)GROWTH FACTOR RECEPTOR PROTOGROWTH IN A HUMAN RENAL /OFHYBRID DNAS /FROM SOMATICHYBRID MAPPING PANEL FOR THEHYBRID PANEL /REDUCED SOMATICHYBRIDIZATION MICROCELL MEDIATEDHYBRIDS AIN HUMAN RODENT SOMATICHYBRIDS AND COSMIDS FOR ANALYSISHYBRIDS CARRYING FRAGMENTS OFHYBRIDS CONTAINING A GENOMICIN VIVO /IN MURINE HEMATOPOIETICLEUKEMIA /NEW TRANSLOCATION IN TLEUKEMIA IN AN ATAXIA /OF TLEUKEMIA MCL 1 HAS SIGNIFICANT /iLEUKODYSTROPHY /INFANCY GLOBOIDLINE /EPISOMAL COSMID IN A HUMANLINE /HUMAN CHOLANGIOCARCINOMA
541
28362852286723024898082301996583531476508
240022791210100610991105
941123190
25122330227521682299252718972388543
225923802270228823832474208824722333233010982322451
22872247281322582179245723052281201
2497243220214492737575
275417742607257925773021384131913851394131525831774118712281221409807
258415312128627798
2127250418272866256624662296189
1395205
21392136189125011722213223212471135726042589862
16461378
Permuted Title Index
LINE /IN A CHOLANGIOCARCINOMALINE /IN A MAUGNANT SCHWANNOMALINE /PATIENT MOSAIC FOR A NORMALLINE ARE SIMILAR TO THOSE IN /3T3LINE BY INTRODUCTION OF A #3PLINE BY PCR IN A PATIENT WITHLINE DERIVED FROM A MALIGNANT /ALINE ENCODES A PROTEIN /CANCERLINE EXPRESSING CYTOCHROME P450LINE OF THYMIDINE KINASE GENE BYLINE RESOURCE FOR THE UNITEDLINE WITH TRISOMY 10 IN A /MOSAICLINEAGE /OF NON FOLLICLE CENTERLINES /ORIGIN OF SV40 TRANSFORMEDLINES/STUDIES OF ZELLWEGERLINES AND DURING NEURONALLINES ARISING FROM BLACKFOOTLINES FROM HUMANS /LYMPHOBLASTOIDLINES FROM SUBJECTS AFFECTED BYLUNG CANCER /EXPRESSION IN SMALLLUNG CARCINOMAS /OF 14 SMALLLYMPHOMA /ANAPLASTIC LARGELYMPHOMA /AND EXTRANODAL LARGEMATURATION GENE TO THE Y /LEYDIGMEMBRANE BAND 3 IN JAPANESE /REDMEMBRANE GLYCOPROTEIN GENE PCIMULTIPLE FLASK/COLONY AMNIOTICMUTANT V H4 IS CORRECTED AFTERMUTANTS AS MODELS FOR HUMANNEVUS SYNDROME /IN BASALNEVUS SYNDROME IN CHINESE /BASALNUCLEI FIBROBLASTS MALEOSTEOGENIC SARCOMA /CASE OF GIANTPOLYMORPHISM IN TURKEY /REDPOLYMORPHISMS ARE ASSOCIATED /REDPROLYMPHOCYTIC LEUKEMIA /IN BRECEPTOR B JUNCTIONAL DIVERSITYRECEPTOR GENES /IN TRECEPTOR GENES IN MULTIPLE /AND TREPOSITORY /ITALY DATA BANK ANDSAMPLING INFUSION OF THE UTERUSSCREENING AND TREATMENT PROGRAMSSURFACE MARKERS IN FIRST DEGREETRANSPLANTATION /IN UTERO STEMTRANSPLANTATION AND GENE THERAPYTUMOR BREAKPOINTS IN CHROMOSOMALTUMORS /ALLELOTYPING OF MALE GERMTUMORS /OF EXTRAGONADAL GERMTUMORS OF THE TESTIS /ALL GERMTYPE SPECIFIC AND HYPOXIAYIELD IN AMNIOTIC FLUID SAMPLES
CELLMEDIATED CHROMOSOME TRANSFER OF ACELLS /A 1 LOCUS IN EMBRYONIC STEM
/A EXPRESSED IN COS/ACTIVITY IN MURINE HEPATOMA/81 GENE IN EMBRYONIC STEM/BY RECULTIVATING THE OLD/CHROMOSOME ABERRATIONS IN TUMOR/ENCAPSULATED NONAUTOLOGOUS/EXPRESSION IN HUMAN HEPATOMA/HUMAN HEPATOCELLULAR CARCINOMA/IN HUMAN EMBRYONAL CARCINOMA/IN MOUSE EMBRYONIC STEM/INDUCED MUTATIONS IN MAMMALIAN/ISOMERASE IN TROPHOBLAST/LEUKEMIA VIRUS TRANSFORMED/LEVEL IN HUMAN NORMAL AND TUMOR/METHOTREXATE IN HUMAN EMBRYONIC/MISMATCH REPAIR IN HUMAN/OF BLOOM SYNDROME/OF EMBRYONAL CARCINOMA/OF MUTAGENIZED HUMAN SOMATIC/OF THE RAT EMBRYONAL/OF THE SRY GENE IN COS/REARRANGEMENT IN MAMMALIAN/REPAIR DEFECT OF FANCONI ANEMIA/REPAIR PATHWAYS IN HUMANAGAINST DNA DAMAGE /PIGMENTOSUMAND CELLS FROM NIEMANN PICK /3T3APPLICATION TO HEMOPHILIA A ANDAPPLICATIONS TOWARD GENETICARE THE FUNCTIONS OF IONICBY A DOUBLE LABELING /NORMALBY BIOTINYLATED Y SPECIFIC DNABY MICRO CELLMEDIATED /GROUP DCHROMOSOMES AND GENES /INDERIVATION AND PROPERTIES /STEMDERIVED FROM CHILDREN SUFFERINGFROM DOWN SYNDROME AND /INFROM DUCHENNE AND BECKERFROM FINNISH /PRECURSOR INFROM NIEMANN PICK DISEASE TYPEFROM NIEMANN PICK DISEASE TYPEFROM PATIENTS WITH HEMATOLOGICIN ANENCEPHALY /AMNIOTIC FLUIDIN MATERNAL BLOOD FREQUENCIESIN MATERNAL BLOOD PROSPECTS FORIN SEX MISMATCHED BONE MARROWIN THE MATERNAL CIRCULATIONIN THE MATERNAL CIRCULATIONIN VITRO /RIDOMILL ON HUMANIN VIVO AND THEIR SUPRESSION BYISOLATED FROM FIRST TRIMESTERISOLATION AND ENZYMATICNEW RESULTS FROM A LARGE /FETAL
166226001439798139510322232226825472466205412091387579143524201383143850022413801331618
23492629130714232250297
2003135921531365283026181304224027841917265412871796625155424172261113116142453126623012463283
24772435162116162470242524292454249325341269134113541559254416892243280713142393255622752412253962725251210256413371676230155029
13128451029466627798
130611731131
601668109115
2561130112941635111
OF PATIENTS WITH BRONCHIAL /THEOVEREXPRESSING CUZN SUPEROXIDEREDUCES THE LIFESPAN OF /SOMATICTO PRODUCE A MOUSE MODEL OFUSING A REPLICATION DEFECTIVEUSING PCR /SOMATIC AND SPERMUSING RECOMBINANT CYTOKINESUSING RECOMBINANT RETROVIRALWITH CONFLUENCED CULTURE SYSTEMWITH MONOSOMY 7 IN PATIENTS /OFWITHOUT MTDNA A SYSTEM FOR THE
CELLULAR BASIS OF SEX DETERMINATIONMODELS OF MITOCHONDRIAL
CENP B AND CENTROMERIC SATELLITE DNASCENTERS /SERVICES BY CYSTIC FIBROSISCENTRAL NERVOUS SYSTEM AND
NERVOUS SYSTEM MALFORMATIONSNERVOUS SYSTEM MANIFESTATIONSREGION (VILLA CLARA) OF CUBA
CENTROMERE ANTIGEN CENP B AND /A HUMANBIOTINYLATED DNA PROBE /XOF CHROMOSOME 1 /MAP AT THEOF CHROMOSOME 21 TO/THEOF CHROMOSOME 4 /NEAR THEOF CHROMOSOME 7 CANDIDATEPROTEIN BINDING AND PROPER
CENTROMERES /SEGREGATION ANDIN THE METAPHASE
CENTROMERIC A SATELLITE DNA SEQUENCESCHROMOSOME 14 BREAKPOINTHETEROCHROMATIN /IN THEPROBES ARE USEFUL INREGION OF HUMAN /AND THEREGIONS /DNA FROM HUMANSATELLITE DNA PROBESSATELLITE DNAS /CENP B AND
CENTROMETRIC INSTABILITY FACIALCEPH PEDIGREES /LINKAGE STUDIES USINGCEREBELLAR ATAXIA /MELLITUS AND
ATROPHY NEW SYNDROME /ANDCDNA CLONES TO HUMAN iHUMAN
CEREBRAL A V MALFORMATION/1 AND AHEMORRHAGE WITH AMYLOIDOSISPALSY /ADULT PRESENTING WITH
CEREBROSPINAL FLUID /PLASMA ANDCEREVISIAE /IN SACCHAROMYCESCEROID LIPOFUSCINOSIS (BATTEN /ONSET
LIPOFUSCINOSIS TO THE SHORTCERULOPLASMIN LACKS OXIDASE ACTIVITY
METABOLISM IN LONG /ANDCERVICAL AND THORACIC FUSION KLIPPEL
INSTABILITY IN CHILDREN WITHSPINE FORAMEN MAGNUM AND /THETHYMUS WITH LIP PSEUDOCLEFTS
CERVIX ON ENDOMETRIAL CARCINOMA /OFCFTR /AND FUNCTIONAL ANALYSIS OF
/HUMAN DNA SEQUENCES RELATED TO/STRUCTURAL ANALYSIS OFAND CHLORIDE CHANNEL /FIBROSISGENE /OF LARGE DELETIONS IN THEGENE /POLYMORPHISMS WITHIN THEGENE ANALYSIS IN PRENATAL /ANDGENE BY DENATURING GRADIENT GELGENE MUTATIONS IN BOHEMIA AND /OFGENES /NORMAL AND MUTANT HUMANMUTATIONS IN A LARGE SAMPLE OFMUTATIONS IN CHICAGO AREA CYSTIC
CHAIN 3 HYDROXYACYL COA DEHYDROGENASEACYL COA DEHYDROGENASE /LONGACYL COA DEHYDROGENASE /MEDIUMACYL COA DEHYDROGENASE /MEDIUMACYL COA DEHYDROGENASE /MEDIUMACYL COA DEHYDROGENASE /MEDIUMACYL COA DEHYDROGENASE /MEDIUMACYL COA DEHYDROGENASE /MEDIUMACYL COA DEHYDROGENASE /MEDIUMACYL COA DEHYDROGENASE /MEDIUMACYL COA DEHYDROGENASE ACTIVITYACYL COA DEHYDROGENASE MUTANTAND FURTHER CHARACTERIZATION OFDYSFUNCTION IN DISEASEENZYME DEFICIENCIES IN MANFATTY ACID TRANSPORT DISORDERSFATTY ACYL COA OXIDASE A NOVELGENE ORGANIZATION POLYMORPHISMIS LOCATED ON CHROMOSOME 12(021LOCUS IN CONJUNCTION WITH HLA /BOF TYPE COLLAGEN IN A /A1(I)PRODUCES RECURRENT LETHALPROMOTER REGIONS /FACTOR A AND B
CHAINS IN THE COMPUTER PROGRAM /MARKOVOF COLLAGEN IV AS THE TARGET
CHAMBA HIMACHAL PRADESH INDIA /OFCHAMER EYE ABNORMALmES /ANTERIORCHARACTERISTIC CARDIAC HISTOLOGY IN
FACIAL GESTALT IN /ACHARACTERIZED BY AN UNSTABLE REGION
BY MONOMERIC /FAMILYCHARACTERIZING MARKERS ANEUPLOIDY BUT
PART OF THE UNKNOWN 5THE PROMOTER OF A
CHARCOT MARIE TOOTH DISEASE /OFMARIE TOOTH DISEASE /OFMARIE TOOTH DISEASE ON /LINKEDMARIE TOOTH DISEASE TYPE 1
741 MARIE TOOTH DISEASE TYPE 1A2229 MARIE TOOTH SYNDROME2819 MARIE TOOTH TYPE 1 FAMILIES2503 MARIE TOOTH TYPE 1A GENE IN2492 CHARGE ASSOCIATION FURTHER EVIDENCE440 CHARLEVOIX SAGUENAY EXCLUSION OF THE2468 CHD DEATHS /RISK FAMILIES AVOID EARLY2490 CHEICAL MISMATCH CLEAVAGE INCLUDING1575 MISMATCH CLEAVAGE OF 14 /BY1396 CHEMICALS/OF GENOTOXIC EFFECTS OF191 AND TO IDENTIFY EFFECTS OF431 CHMILUMINESCENT DETECTION OF36 CHEMOTAXIS AND BOMBAY PHENOTYPE
412 CHERNOBYL ACCIDENT /BYELORUSSIA AFTER1769 ACCIDENT/CONNECTION WITH842 ACCIDENT /EFFECTS OF THE868 ATOMIC STATION CATASTROPHE616 DISASTER /OF THE2845 REACTOR ACCIDENT /OF THE412 CHICAGO AREA CYSTIC FIBROSIS FAMILIES1698 CHICKEN REVEALS HIGHLY CONSERVED DNA2199 CHICKENS AS A MODEL SYSTEM /USING1654 WITH RESISTANCE TO A HERPES1907 CHILD /AT RISK FOR HAVING AN AFFECTED2213 /WITHOUT A PREVIOUSLY AFFECTED1663 ASSOCIATED WITH SOLUBLE318 BY IN SITU HYBRIDIZATION /IN A1580 OF A WOMAN WITH KEARNS SAYRE /A1858 WITH 46,XY DEL 3P23P24.12 /IN A1666 WITH A COMBINATION OF HIGH2228 WITH CONGENITAL MALFORMATION /A1622 WITH DUP 12023 OTER DUE TO /IN A2057 WITH MILD CLINICAL FEATURES AND1682 CHILDHOOD /GONADOBLASTOMA IN EARLY1666 ACUTE LYMPHOBLASTIC LEUKEMIA412 ACUTE NONLYMPHOCYTIC /N644 AND ADOLESCENT OSTEOSARCOMA1901 DEAFNESS ON NEWFOUNDLAND'S502 EPILEPSY ASSOCIATED WITH /OF668 KI 1 POSmVE ANAPLASTIC /OF1897 ONSET SPINAL MUSCULAR /OF732 ONSET SPINAL MUSCULAR /THE964 CIDLESS MARRIAGES DUE TO FETAL /FROM1530 CHILDREN /CONGENITAL MALFORMATION IN572 /IN MENTALLY RETARDED
2279 /IN MENTALLY RETARDED1972 /IN SECONDARY MALNOURISHED1935 /OF NTD IN TURKISH512 /SYNDROME IN FIVE SPANISH438 ANDA FURTHER 12% HAD/OF THE832 AND IN FETAL BLOOD BY699 ASCERTAINED CLINICALLY AND744 ATTENDING SPECIAL SCHOOLS IN834 CONCORDANT FOR MULTIPLE /AND585 DYING SUDDENLY WITHOUT /FROMS51 FOR GENETIC DISORDERS /OF2366 IN TAIWAN /RETARDED SCHOOLS51 OF ATOMIC BOMB SURVIVORS /INS51 OF HIGH AND LOW SOCIO /OF1014 POPULATIONS FALLEN VICTIMS988 PRESENTING WITH MULTIPLE1004 SUFFERING FROM DIFFERENT985 UNDER THE AGE OF SIX IN2703 WITH ACUTE LYMPHOBLASTIC /IN2364 WITH CLEFT PALATE /IN463 WITH DOWN SYNDROME /IN1829 WITH SEX CHROMOSOME263 CHILDREN'S HOSPITAL /REID CABRAL
2316 CHILE /ANALYSIS OF FACIAL CLEFTING IN195 /ECONOMIC STRATA IN SANTIAGO265 /OF SINGLE GENE DEFECTS IN475 CHLEAN POPULATION /AND AUTISM IN A498 CHIMERIC MICE WITH GLUCOCEREBROSIDASE975 CHMERISM /DIAGNOSIS OF 46,XX/46,XY1119 IN A STILLBORN FETUS /HUMAN2277 CHIPANZEE /AMONG HUMAN AND2377 AND HUMAN BUT DIFFER IN /IN459 AND ORANGUTAN /OF MAN975 CHINA (II) /CHROMOSOMAL ANOMALIES IN
2405 /AND PRENATAL DIAGNOSIS IN SOUTHS1o /CLEFT PALATE IN SHANGHAI503 /EDUCATION IN GENETICS IN261 /GENERAL POPULATION OF SICHUAN527 /GROUP A MINORITY NATIONALITY IN425 /IN FIVE PROVINCES OF SOUTH
2164 /LISU NATIONALIES OF SICHUAN100 /PRENATAL DIAGNOSTIC PROGRAM IN534 /STATE FARMS IN HAINAN PROVINCE446 /STORAGE DISEASES IN NORTH
2415 AND THEIR APPLICATION TO /NORTH2788 BY PCR /MUTATIONS IN HUNAN333 CARRIER DETECTION BY MEANS OF
2870 TWO NEW MUTATIONS AND A MARCO1494 CHINESE /ARTERY DISEASE IN THE934 /OF A GLOBIN GENE IN773 /OF WILSON DISEASE IN379 AND MALAY PATIENTS WITH /KM IN1694 BY THE PCR /DEFICIENCY OF A1622 DUCHENNE MUSCULAR DYSTROPHY2362 ESOPHAGEAL CANCER /IN ARCHIVAL2399 FAMILIES /IN 221 HIGH RISK141 FAMILIES /NEVUS SYNDROME IN
1922 HAMSTER CELL MUTANT V H4 IS2007 LAOTIANS AND FILIPINOS /AMONG2039 CHLORIDE CHANNEL /FIBROSIS CFTR AND
542
1958196119981952682
2004164
26141033254725622518688269927822816280627963601829261220802590186018411553171722882716321760132914566721320134672
7297581331268718851236128848051966483869223
128546823
274211199511854506
28812806742131227791326956699213733803
2881265914922503145093726152626172915433912706330
277818561117276912652768558111428201021224627461125990273323241087587601135922502679SS1
Permuted Title Index
CONDUCTANCE IN TRANSFECTEDCHOLANGIOCARCINOMA CELL LINE /HUMAN
CELL LINE AN ACHOLESTEROL /OF SAME AGED TWINS HDL
ESTERASE ABSENT IN WOLMANESTERIFICATION IN NIEMANNIN NEU LAXOVA SYNDROMELEVELS OF KOREAN TWINSMETABOLISM IN THE 3T3 /N
CHOUNERGIC ENZYMES IN NONSPECIFICCHOUNESTERASE PHENOTYPING /OF SERUM
VARIANTS WiTH /OF SERUMCHONDROCYTE CULTURE IN IDENTIFYING ACHONDRODYSPLASIA /A PHENOTYPE OF A
PUNCTATA DUE TO ANPUNCTATA REPORT OF A
CHONDRODYSPLASIAS /IN THE HUMANCHOREA IN A PATIENT WITH WOLFCHORION CONFINED OR FETAL REPORT OF A
TYPE ON COGNITIVE AND /OFVILLUS SAMPLING /STUDIES OF
CHORIONIC VILLI BIOPSY USING MALTOSEVILLUS TROPHOBLAST AND /IN
CHORIORETINAL DYSTROPHY CHOROIDEREMIACHOROID AND RETINA /ATROPHY OF THE
PLEXUS CYSTS INDICATIVE OFCHOROIDEREMIA /CHORIORETINAL DYSTROPHY
GENE AND MUTATIONMOLECULAR DELETION /AND
CHROMATID DAMAGE IN CELLS FROM DOWNEXCHANGE AND CHROMOSOMEEXCHANGE DETERMINATIONEXCHANGE FREQUENCY INEXCHANGE IN MALNUTRITIONEXCHANGES /OF SISTEREXCHANGES AND HUMAN /SISTEREXCHANGES IN CERTAIN ETHNICEXCHANGES IN HUMAN /SISTEREXCHANGES IN MOUSE TUMORINTERCROSSINGS AND FRAGILE
CHROMATIN MAPPING A STRATEGY FORMATERIAL /OR DELETION OF
CHROMATOGRAPHY/PERFORMANCE LIQUID/PERFORMANCE LIQUID
CHROMOSOMAL ABERRATION /MOSAICISM FORABERRATIONS AND MUTATIONSABERRATIONS ASSOCIATEABERRATIONS INABERRATIONS IN 542ABERRATIONS IN A /CLONALABERRATIONS IN CIGARETTEABERRATIONS IN PERIPHERALABNORMALITIES /STRUCTURALABNORMALITIES BY /OFABNORMALITIES INABNORMALITIES INABNORMALITIES INABNORMALITIES INABNORMALITIES INABNORMALITIES IN /NOVELABNORMALITIES IN /OFABNORMALITIES IN 902ABNORMALITY IN BAHRAIN 6ALTERATIONS INDUCED BYAND METABOLIC SCREENINGANOMALIES /OF FETALANOMALIES A FRENCH SURVEYANOMALIES IN CHINA (II)ANOMALY ASSOCIATED WITHASSIGNMENT OF HUMAN TYPEBAND 3P13 /BREAKPOINTS INBAND 3P21.1 /WITHIN HUMANBAND 3P21.1 /WITHIN HUMANBAR CODES BY FLUORESCENCEBREAKAGE BY BLEOMYCIN ANDBREAKPOINT IN A PATIENT /XBREAKPOINTS AND POSSIBLECHANGES IN MULTIPLEDEFECTS IN SPONTANEOUS /OFDISORDERS /DIAGNOSIS OFDISORDERS /FOR FETALDISORDERS /IN THE COMMONDNA /FOR MICRODISSECTEDDNA FROM A 46,XX TRUE fINERROR INFLUENCE PHENOTYPEEVENT /A POSSIBLE PRIMARYFRAGILE SITES ASSOCIATEDFRAGILE SITES EXPRESSIONGENES IN MAMMALIAN /OF YHETEROZYGOSITY IN /LOSS OFIN SITU SUPPRESSION /BYINSTABILITY DISORDERINSTABILITY IN CLASSICALINSTABILITY IN FIRST /ONLOAD /ESTIMATION OFLOCALIZATION ANDLOCALIZATION AND ANALYSISLOCALIZATION OF 60 BRAINLOCALIZATION OF HUMAN /ANDLOCALIZATION OF SIMPLELOCALIZATION OF THE GENESMARKERS /HUMAN AND MURINEMARKERS IN THE DETECTIONMATERIAL /MICRODISSECTEDMOSAICISM IN CVS FETAL
236413781662399
2248523913
2691798520580539474
246190290247
24421231921S1557412642342251912802342
111086845130216041568158625651196284325431341631
2071161956557015702816159715241630136225371352121817081206130013061346136013663631270139925631854126817991543936
2387172221382195184
138820651313759S7516151155174
251023951411139414051390433
260921601436677139716062308221421792282169621821861415
2053914
MOSAICISMS ON AMNIOTIC /OFMUTABILITY /CHANGES OFORIGIN /OF DIFFERENTPATTERN /A GIRL WITH XO/XXPATTERN FROM A 46,XYPSEUDOMOSAICISM INO HETEROCHROMATIN REGIONSO HETEROMORPHISMS IN TWOREARRANGEMENT RESPONSIBLEREARRANGEMENTS /OF COMPLEXREARRANGEMENTS /SPECIFICREGION 4Q35 /MAP OFREGION 8024 LINKED TOREGIONS AND OVER 60% OFRFLP MARKERS IN FOURTEENSEGREGATION IN /ABNORMALSTUDIES /CULTURES FORTRANSLOCATION /AUTOSOMALTRANSLOCATION 14;16TRANSLOCATION EXPERIENCESVARIANTS AFTER X RAY ANDVARIANTS USING SPECIAL
CHROMOSOMALLY INTEGRATED SINGLE COPYCHROMOSOME /ANALYSIS OF THE HUMAN X
/DISORDER SHOWING LOSS OF Y/FACTOR MAPPING ON Y/FROM A DERIVATIVE X;9/GENE FOR PERLECAN TO MOUSE/GENETIC DEFECT ON THE X/IN PART BY A GENE ON THE X/INDUCTION OF THE FRAGILE X/INSERTED INTO A MOUSE/LONG ARM OF THE HUMAN X/LONG ARM OF THE HUMAN Y/MAP OF THE MOUSE X/MATURATION GENE TO THE Y/OF AN INACTIVE DERIVATIVE/OF FRAGILE X AND A MARKER/OF THE INACTIVE X/ON THE INACTIVE HUMAN X/RANGE MAPPING OF THE X/REGION OF THE HUMAN Y/SXR REGION OF THE MOUSE Y/THE CASE WITH 14P+ MARKER/WITH A SINGLE GIANT MARKER/WITH AN ADDITIONAL MARKER1 /MAP AT THE CENTROMERE OF1 AND 11 RELATED TO /OF1 MAKES DNA DIAGNOSTICS /OF1 MAPPING ADDITIONAL /HUMAN1 USING TWO COLOR /RENIN ON10 /HUMAN HEXOKINASE 1 ON10 /PERICENTRIC REGION OF10 AND 12 ARE BOTH MEMBERS10 IN BALANCED /RATE OF10 MARKERS LINKED TO /TO10 PERICENTROMERIC MARKERS10 SPECIFIC ALPHOID /USING11 (11012 013) /i REGION OF11 /CLOSE TO ERBB ON MOUSE11 AND CHROMOSOME 17 /OF11 CONTAINING THE MULTIPLE11 IN THREE PATIENTS WITH11 IN UREMIC /1 REGION OF11 IRRADIATION REDUCED11 SYNDROME /WITH RING11 YEAST ARTIFICIAL /OF A11P12 P14 /PHYSICAL MAP OF11P13 WILMS TUMOR LOCUS WT1110 /WITH MARKERS OF110 MARKERS NEAR THE /OF11013 /ONCOGENE FROM HUMAN11Q13 IN THE 90 CASES OF11022 23 IN 45 BRITISH /ON11023 /TO A CM INTERVAL ON12 /MUTATION MAPS TO12 IN MYELODYSPLASTIC /OF12(021 024) /IS LOCATED ON13 /INVERSION OF13 A CASE OF A /DISEASE AND13 AND 17 IN HUMAN /LOCI ON13 CLONES AND THEIR /OF13 LACK OF A DISTINCT /RING13 MAPPING REAGENTS /HUMAN14 /PHOSPHORYLASE ON14 /TERMINAL DELETIONS OF14 BREAKPOINT IN A PATIENT14 IRS PCR /HYBRIDS FROM14 SUGGESTED BY 0TO140L IN A DIVERSE U.S.A FTO15 /1 RELATED LOCUS ON15 /WILLI REGION OF HUMAN15 /WITH A MARKER150 SPECIFIC PROBES TO THE16 /BREAKPOINTS ON16 /GAMMA IS ENCODED BY16 /GENE MAPS TO HUMAN16 /GENE TO BAND 024 OF16 /LINKAGE MAPS OF HUMAN16 INVERSION IN ACUTE /OF16P AND 160 MAY EXPLAIN16P CONTAINING THE PKD117 /OF CHROMOSOME 11 AND17 /OVARIAN CANCER LOCUS ON17 /PROXIMAL SHORT ARM OF
911280517148251386122115792823157214082228221225912000192315541638146811531757255516282536179
13561665155518902293
751623413
211821051951234916591688155724522109198
234315441377140421991350193522022148213520082234118819821888214520901864201621841723595
213613982102196126
1986195526086041967294
2010133421641477647
25932116141622091979172616662165207719202328239215351718185
2103225821722124170915561869201619771998
17 /PROXIMAL SHORT ARM OF17 /THE PKD1 GENE AND MOUSE17 COSMID LIBRARY USING /A17 LOCI /AND LINKAGE TO17 USING RADIATION REDUCED17P13 IN MILLER DIEKER /OF17021 /CLONING OF HUMAN18 /BY TRANSFER OF HUMAN18 /OF ABNORMALITIES OF18 /RECOMBINATION MAP OF18 HOMOLOGIES WITH HUMAN18 IN OVARIAN EPITHELIAL19 /BY ALUI GIEMSA OF19 /CONTIG MAP OF HUMAN19 /FINGER GENES ON HUMAN19 BY FLUORESCENCE IN SITU19 COSMID CONTIG MAP USING19 DNA MARKERS LINKED TO19 IN 15 SYSTEMATICALLY19 STRATEGIES AND RESULTS190 /DISTANCES ON HUMAN190 /TROPONIN T GENE ON19013.3 /A 350 KB REGION OF19013.3 WHICH CONTAINS THE1P36 COMMONLY DELETED IN10 /LOCUS ON HUMAN10 /USHER TYPE II REGION ON10 MARKERS /UNLINKED TO2 AN ANCESTRAL TELOMERE2 FIRST REPORT OF THE /ON20 /KINDRED LINKED TO20 /OF THE LONG ARM OF20 FTO POLYMORPHIC LOCI ON20 /TWO DIFFERENT LOCI ON20 AND POSSIBLE ASSIGNMENT20 CLONING AND ISOLATION20P DELETION /WITH A200 /ADDITIONAL MARKERS ON200 /WITH SIX MARKERS ON21 /AS LINKAGE MARKERS FOR21 /FAMILIES ON HUMAN21 /HYBRID MAP OF HUMAN21 /LATERAL SCLEROSIS TO21 /NEW COSMIDS FOR HUMAN21 /OF DOWN SYNDROME ON21 /RECEPTOR GENE ON HUMAN21 /REGION OF HUMAN21 ABERRATIONS BY /OF21 AND DOWN SYNDROME /OF21 BY PULSED FIELD GEL /OF21 DERIVED FROM HER MOTHER21 DOES NOT PREDISPOSE OF21 IN DOWN SYNDROME21 IN MEIOTIC PROPHASE21 MARKERS AND OTHER /OF21 SPECIFIC SEQUENCE /OF21 SPECIFIC YEAST21 STUDY OF FIVE PATIENTS21 THAT CAUSES DOWN /OF21 TO ACCOMPLISH DIAGNOSIS21 USING VARIOUS METHODS21022.3 SPECIFIC PROBE SET22 /EWING TRANSLOCATION ON22 /NOT1 LINKING CLONES ON22 /OF THE LONG ARM OF22 /REPEATED SEQUENCES ON22 /TO MAPPING OF HUMAN22 /TYPE 2 LOCUS ON22 AND OTHER HUMAN /HUMAN22 AND RAPID /FOR PAINTING22 BY SCREENING CHROMOSOME22 ENRICHED LIBRARIES22 IN NEURINOMAS OF /OF22 PROBE SPECIFIC FOR22 RESPONSIBLE FOR /ON22 TUMOR SUPPRESSOR GENE /A22 USING YEAST ARTIFICIAL22 WITH FURTHER /ON22011 012 MARKERS /OF EIGHT2P AND 11P MARKERS IN /OF20/ DNA MARKERS ON HUMAN3 /PCR BASED MARKERS FOR3 Nil COLLAGEN GENE ON3 BY SOUTHERN BLOT /MOUSE3 ENCODES A TUMOR /HUMAN3 SEQUENCES PRESENT WITHIN3P ORDERED BY FLUORESCENT3PTER 3P25.1 /AF8T TO HUMAN4 (023025) AND MOUSE4 /A PHYSICAL MAP OF HUMAN4 /GENE REGION OF HUMAN4 /NEAR THE CENTROMERE OF4 ALU BANDING BY /OF HUMAN4 ANALYZED CYTOGENETICALLY4 AND ISO (4P),ISO 4(0) /OF4 VARIANT THROUGH THREE4 YIELD A SINGLE LINKAGE4P DELETIONS AND /OF40 /MUSCULAR DYSTROPHY TO40 MARKERS IN RELATION TO4OTER IN TWO FAMILIES /ONTO5 /LOCI ON THE LONG ARM OF5 /MAP OF THE SHORT ARM OF5 CRI DU CHAT DELETION /FOR5 HARBORING THE FAMILIAL
543
21391889215119612150
582306875156721881863257415982203227218252
19842043176
210723682036237022152134215510772147
798331462
7421831462237416641962196520942120S8980
20821528196820571644416211913241707415420193821892167143021061654228116342083219114812166199
2169213016492251225125851649901
1391216220351954196020311978
73186725882198216121041867218523841907165616701582954
197116511904203711322208217711762132
Permuted Title Index
MARKERS/OF 75 2216WITH FLUORESCENCE IN /OF 2171
50/HOMOLOGIES WITH HUMAN 18635Q/MUSCULAR DYSTROPHY TO 786/BY THE TRANSFER OF HUMAN 26016/OF THE DMD LIKE LOCUS ON 23796 AT THE HLA LINKAGE GROUP 21976 THUS EXCLUDING A /FROM 19296P /MAPPING OF SCAl ON 19936P /TO A 6 CM SUBREGION OF 20016P/TOTHEMHCON 19327/ARM 120 AND RAT 18707/PROXIMAL REGION OF MOUSE 18607/WITH MATERNAL DISOMY FOR 17127 AND THE HUMAN MYOTONIC S867 CANDIDATE FOR A JUNCTION 22137 DERIVED MARKER /LOSS OF 1396702232 REGION /THE HUMAN 21928/LINKAGE MAP OF 20488/OF THE SHORT ARM OF 15859/FROM A MARKED HUMAN 21499/FROM LINKAGE TO HUMAN 20049/MEDIATED TRANSFER OF 25689/OFTHE LONG ARM OF 15129/TYPE TO THE LONG ARM OF 5989 BY FLUORESCENCE IN SITU 22019 IN BASAL CELL CARCINOMAS 25839 KARYOTYPE PHENOTYPE /OF 15299 MARKERS TO FRIEDREICH 18939P INVOLVEMENT IN MELANOMA 2239034 IN ASHKENAZIC JEWS /ON 2353A GENOME STRATEGY TO /X 2174ABERRATION IN A UTERINE/A 1364ABERRATIONS /OF FETAL 1614ABERRATIONS /OF NUMERICAL 1283ABERRATIONS IN CULTURED 1531ABERRATIONS IN NON 1312ABERRATIONS IN TUMOR CELLS 1616ABERRATIONS IN WORKERS /OF 1599ABERRATIONS INDUCED BY 1301ABERRATIONS NONRANDOMLY 1449ABERRATIONS WITH RESPECT 1523ABNORMALITIES /AND 757ABNORMALITIES /HUMAN SPERM 1629ABNORMALITIES /OF FETAL 1823ABNORMALITIES /STRUCTURAL 1588ABNORMALITIES /WITH SEX 213ABNORMALITIES /WITH SEX 1685ABNORMALITIES CAUSING /OF 1279ABNORMALITIES IN /NONRANDOM 1438ABNORMALITIES IN A PATIENT 1508ABNORMALITIES IN ACUTE /OF 1358ABNORMALITIES IN CHILDREN 1326ABNORMALITIES IN LEUKEMIA 1303ABNORMALITIES IN PATIENTS 1302ABNORMALITIES IN PATIENTS 1367ABNORMALITIES USING /OF 1704ALTERATIONS IN PERIPHERAL 2716ANALYSES OF PLEURAL 1374ANALYSIS /HIGH RESOLUTION 1505ANALYSIS /HIGH RESOLUTION 1541ANALYSIS AMONG 155,223 /AND 2768ANALYSIS AND IN SITU 1632ANALYSIS FROM CORD BLOOD 1495AND CDNA CLONES /ARTIFICIAL 2168AND LOCALIZATION OF THE AT 2301ANEUPLOIDY AND COMPARISON 85ANEUPLOIDY USING /OF SEX 1069ANOMALIES /DYSPLASIA IN SEX 881ARM /A JUNCTION WITH THE 2213ARM 120 AND RAT CHROMOSOME 1870AT D13S31 TIGHTLY LINKED 2373BAND 11 P15.5 /MAP OF HUMAN 2142BAND FLAVORS /MAP TO 411BAND SPECIFIC PAINTING 1728BANDING FOR ELECTRON /NEW 2085BANDING PATTERNS USING 200BANDING TECHNIQUE 1620BASED MAPPING OF XQ24 28 373BREAKPOINTS APPLICATION OF 1620BY COMPARATIVE MAPPING OF 2205BY CYTOGENETIC TECHNIQUES 1667BY FLUORESCENCE IN SITU 1719BY IN SITU HYBRIDIZATION 1700CENTROMERES IN THE /OF 1580CLONES AND IDENTIFICATION 1950CLONES FROM HUMAN 2160CLONES IN THE EFFORTS 2065CLONING /YEAST ARTIFICIAL 2193CLONING AND CONSTRUCTION 2185CLONING IN GENOME ANALYSIS 179CLONING OF HUMAN 2306COMPLEMENTS /ABNORMAL SEX 1455COMPLEMENTS AND CHROMOSOME 83COMPLEMENTS OF SUGARBEET 1548CONDENSATION TECHNIQUE AN 1320CONTAINS A HIGH /OF THE X 2015CONTIG /A YEAST ARTIFICIAL 102CONTIG AROUND THE FRAGILE 2389CONTIG AT THE FAMILIAL 101CONTIG CONTAINING THE 204CONTIG PROXIMAL TO THE 2159COUNTING RATIO AND 2236DAMAGE INDUCED BY A 1681DIAGNOSIS AND ITS IMPACT 2686
DIAGNOSIS IN DENMARK 1970DNA REPAIR AND IMMUNOLOGICEND FRAGMENTS /ARTIFICIALER 7 CHANGES AS A POSSIBLEERRORS/WITH THREEEVOLUTION RECONSTRUCTED BYFRAGILITY AND AUTISM IN AFRAGMENTATION AND GENOMEFUNCTIONAL FEATURES MAP TOGENETIC MAPS FROM /OF XHOMOLOGIES AND GENES WHICHHYBRIDS /FROM SINGLE HUMANIDENTIFIED BY IN SITU /XIMPRINTING IN MAN FROM /FORIN A CHOLANGIOCARCINOMAIN AN INFANT UTILIZINGIN PRENATAL DIAGNOSIS BYIN RETT SYNDROME /OF THE XIN THE ETIOLOGY OF 46,XX/YINACTIVATION /OF HUMAN XINACTIVATION AND /XINACTIVATION/REACTIVATIONINCLUDING PROBABLY A /RINGINSERTED INTO A MOUSEINSTABILITY IN THE FAMMMINSTABILITY SYNDROMES /THEINSTABILITY SYNDROMES OFINVERSION /WITH AIRREGULARITIES IN TURKEYLESIONS IN HUMAN SPERM /OFLIBRARY [YEAST ARTIFICIALLIBRARY FROM SORTEDLINKED DISORDER AND WITH /XLINKED FAMILIAL EXUDATIVELONG ARM /EUCHROMATIC YLP DELETIONS IN /ANDMAP LENGTH /ESTIMATION OFMAPPING /CHROMOSOMES FOR XMARKERS BY FLUORESCENT INMICRODISSECTION AND PCRMICRODISSECTION PCR /USINGMORPHOLOGY /GENE CONTENT TOMOSAICISM IN RETT SYNDROMEOF MEN WITH IDIOPATHIC /YORGANIZATION RELATIONSHIPPCR AND MICROCLONING /YPLOIDY IN BLADDER TUMORSPOLYMORPHISMS IN INFERTILEPROBE P49A DETECTS COMPLEXREACTIVATION IN HUMAN /XREARRANGEMENT /OF A COMPLEXREARRANGEMENT/T(6P;130)REARRANGEMENTS /AT RISK FORREARRANGEMENTS AND EXTRAREARRANGEMENTS BY /SUBTLEREARRANGEMENTS DETECTEDREARRANGEMENTS FREQUENTLYRECOMBINATION /ARTIFICIALRECONSTRUCTION EXPERIMENTSREGION /DISSECTED DEFINEDREGION /GIEDION SYNDROMEREGION /OF THE PRADER WILLIREGION /THE PRADER WILLIREGION SPECIFIC LIBRARIESREGIONS /IN UNSTABLEREGIONS INVOLVED IN /OFREPLICATION BY BRDU /OFREPORT OF A FAMILIAL CASERESEARCH IN A REFERREDRESPONSIBLE FOR IN VITRORESULTING FROM A FAMILIALSEGREGATION AND CENTROMERESSELECTION IN HYPODIPLOIDSHORT ARM /THE PROXIMAL XSPECIFIC CDNA CLONES /OF XSPECIFIC CDNA USING PROBESSPECIFIC DNA LIBRARIESSPECIFIC DNA LIBRARIESSPECIFIC DNA LIBRARY /BY ASPECIFIC DNA PROBES /BYSPECIFIC DNA PROBES /TOSPECIFIC LIBRARY /WITHSPECIFIC POLYMORPHISMS /YSPECIFIC PROBES /ANDSPECIFIC PROBES /TOSPECIFIC PROBES BY DIGITALSPECIFIC PROBES FOR /OFSPECIFIC PROBES IN /YSPECIFIC PROBES IN A GIRLSPECIFIC REPETITIVE /OFSPECIFIC REPETITIVE /XSTATUS OF UNFERTILIZEDSUBBANDS /PROBES WITHINTECHNOLOGY TO FIND NEWTELOMERESTRANSFER AND INTERPHASETRANSFER AND X RAY HYBRIDTRANSFER OF A SINGLETRANSLOCATION /UNBALANCEDTRANSLOCATION IN CHRONICTRANSLOCATION INHERITEDVIA MICROCELL FUSION /A #3PWALKING AND THEWITH Y CHROMOSOME SPECIFICX AND 11 /WITH MARKERS FROM
359183820751314143426411492249841185
S292081169824216621546172422232225145166015711369413131625541574124326771566210221672416857
2176584
207621221189253220701643783
2205164320611642156028721389142214211167
84167912471338
1821211728197
238622992070213156
163315367341689158931816242260252722471677171515421721170816442826
831667169712831693165312811658128420662057236208918912301701135116011395213816532038
X BY FLUORESCENCE IN SITUCHROMOSOMES /22 USING YEAST ARTIFICIAL
/ABNORMAL X AND Y/AS YEAST ARTIFICIAL/DNA ADDUCTS ON HUMAN/FROM BOTH THE X AND Y/FROM FLOW SORTED HUMAN/INHUMAN DGGROUP/IN THE STUDY OF HUMAN/IN YEAST ARTIFICIAL/IN YEAST ARTIFICIAL/IN YEAST ARTIFICIAL/INVOLVING ACROCENTRIC/MARKERS DERIVED FROM SEX/OF MAMMALIAN/OF TERMINAL REARRANGED/OF X Y TRANSLOCATION/OF YEAST ARTIFICIAL/OF YEAST ARTIFICIAL/ON HISTONE DEPLETED/ON HUMAN METAPHASE/ON THE MOUSE AND HUMAN X/PRONUCLEI AND METAPHASE/THE ACTIVE AND INACTIVE X/USING YEAST ARTIFICIAL/WITH YEAST ARTIFICIAL130 AND XP IN HUMAN /ON19 AND 21 LOCI IN /OF2 13 AND 21/ON HUMAN20AND21 IN ABOY WITH21 AND 18 BY FLUORESCENCE5 AND 10 /GENETIC MAPS FOR5 AND 16 /CLONES TO HUMAN5 AND 7 IN MALIGNANT /FROM5Q AND110 /REGIONS ON6 AND 15 AND DETAILED6P AND 130 RESULTING FROM8/OF SECOND GENE ON HUMAN8 10 AND 12/FOR HUMAN9AND11 /FOR LOCI ONA NEW TOOL FOR CHROMOSOMEA PARADIGM FOR MAPPINGAND COSMIDS APPLICATIONSAND GENES /IN CELLSAND OUTCOME OF PREGNANCIESAND SNURPOSOMES RNAAT INTERPHASE AS REVEALEDBY CHROMOSOME SPECIFICBY IN SITU NICK /THE HUMANBY PCR MEDIATED DNA /HUMANCONSTRUCTION /FROM SORTEDCONTAINING DNA FROM HUMANCONTAINING HUMANCONTIG AROUND THE FRAGILEDNA INSERT USING AFOR HYPERVARIABLE DNAFOR X CHROMOSOME MAPPINGFROM 23 NON JEWISH /SACHSFROM THE HLA COMPLEXFROM THE VICINITY OF THEIDENTIFIED AT PRENATALIN 4000 JAPANESE /INV(9)IN AUTISM /SMALL MARKERIN BREAST CANCER PATIENTSIN MYELOPROLIFERATIVEIN PATIENTS WITH TURNERIN PRENATAL DIAGNOSIS AIN RECONSTRUCTIONS OF /OFIN RELATION TO GENETICIN SPERM OF MEN /OFIN XP21 SURROUNDING THEIN YEAST ARTIFICIALINVOLVED IN 2148 CASESISOLATED IN /IN HUMANNEAR THE MULTIPLEOF MAN CHIMPANZEE AND /THEON HUMAN CHROMOSOMES 21PHYSICAL LINKAGE OF ZFYPRESENTATION OF TEN NEWRESULTS IN CENTROMERERESULTS IN THE FORMATIONREVEALED BY TAOI DIGESTIONSPECIAL PROBE POOL /AND YSTUDIES IN HUMAN EMBRYOSUSING FLOW SORTING ANDUSING FLOW SORTING AND /
USING RADIATION HYBRIDSUSING RADIATION HYBRIDSUSING SHOT GUN PCR /HUMANWITH 6 BREAKPOINTS /4X 4 5 AND 16 AND THE /ON
CHRONDRODYSPLASIA PUNCTATA IN ANCHRONIC ALCOHOLICS /LIVER DAMAGE IN
HEART AND BRAIN DISEASE /INHEPATITIS B VIRUS INFECTIONHEPATORENAL TYROSINEMIALYMPHOCYTIC LEUKEMIA BY /12 INMYELOGENOUS LEUKEMIA /INMYELOGENOUS LEUKEMIA /INMYELOGENOUS LEUKEMIA IWITHMYELOGENOUS LEUKEMIA PATIENTSMYELOID LEUKEMIA /INMYELOID LEUKEMIA AND IN /INRENAL FAILURE /WITH END STAGESPINAL MUSCULAR ATROPHY /OF
544
21292162108550
1343236724991537214349203
215816021699S131655144120025261633161124212153242821892204606199220201407215621631897258120301502142123141635142
249820218555014913171640172116521627216716822135378
278521942122106721142112
8415451451129713721725116221411222407222049
12752096214517292156185914671663139615632515168416051605158
2040177
14061858045046717728931355132716491379586
135161713022018
Permuted Title Index
CHRYSENE DNA ADDUCTS ON HUMAN /OFCHULALONGKORN HOSPITAL BANGKOK /ATCMYLOMICRONEMIA AND THEIR CLINICALCIGARETTE SMOKERS /ABERRATIONS IN
SMOKERS AND NONSMOKERS /OFCU EXONIC (C2K19T) AND INTRONICCMI GENE REGION /RFLPS IN THE APOAICININNATI COMPREHENSIVE SICKLE CELLCINNAMON A DROSOPHILA MODEL FOR A /OF
RATS /ACTIVITY IN LONG EVANSRATS /IN LONG EVANS
CIRCULATING BLASTS IN A CASE OFFACTOR IX FROM /OFRETICULOCYTES PROSPECTS
CIRCULATION /CELLS IN THE MATERNAL/FROM MATERNALISOLATION BY /THE MATERNAL
CIRRHOSIS /AND PRIMARY BILIARYCIS EFFECT OF A B+ THALASSEMIA
REGULATORY ELEMENTS INVOLVED INCLADISTICS TO THE LDL RECEPTOR GENECLADOGENESIS OF COLOMBIAN AMERINDIANCLAMPED DENATURING GRADIENT GEL /GC
DENATURING GRADIENT GEL /GCGRADIENT GEL ELECTROPHORESIS
CLASPED THUMB AND MENTAL RETARDATIONCLASSES /USE IN HIGH SCHOOL BIOLOGYCLASSICAL AND LOW RADIOSENSITIVITY /IN
FORM ON 90 /LOCUS AS THEMETHODS FOR MEASURING /ANDNEUROFIBROMATOSIS /CAUSESPHENYLKETONURIA /BULGARIANPHENYLKETONURIA IN SOUTHERNTAY SACHS ALLELE /TO CARRY ATURCOT SYNDROME GENE IS NOTTYPE OF MAPLE SYRUP URINE /A
CLASTOGENIC REPAIR ACTIVITIES OF /OFCLEAVAGE ENZYME AND AMNIOTIC FLUID
INCLUDING A MISSENSEOF 14 EXONS AMPLIFIED INOF THE MOUSE GENOME /SITESIGNAL 1 PROTEIN MOLECULAR
CLEFT LIP AND PALATE /ALPHA WITHLIP AND PALATE /ANALYSIS OFLIP AND PALATE /MALFORMATIONSLIP AND PALATE /PATIENTS WITHLIP AND PALATE /STUDIES OFLIP AND PALATE /TO NONSYNDROMICLIP AND PALATE ASSOCIATION ANDLIP WITH OR WITHOUT CLEFT /OFLIP WITH OR WITHOUT CLEFT /OFPALATE /IN CHILDREN WITHPALATE AND MICROGNATHIA IN TWOPALATE IN A BRITISH COLUMBIAPALATE IN NORTHERN INDIAPALATE IN SHANGHAI CHINA
CLEFTING IN CHILE /ANALYSIS OF FACIALSYNDROMES /UPDATE OF
CLINIC FOR MARFAN SYNDROMEIN HONG KONG /COUNSELING
CUNICAL AND BIOCHEMICALAND CYTOGENETIC EVALUATIONAND CYTOGENETIC OBSERVATIONSAND GENETIC CHARACTERISTICSAND GENETIC HETEROGENEITYAND GENETIC HETEROGENEITY OFAND GENETICAL STUDY ON 26 /lAND HISTOLOGIC FINDINGS INAND HISTORICAL SIGNIFICANCEAND LINKAGE STUDIES OFANOPHTHALMIA IN ITALYAPPLICATION /AND ITSAPPLICATION IN DUCHENNE /ITSAPPLICATION OF GENE TRANSFERASPECTS MOLECULAR BIOLOGYBIOCHEMICAL AND MOLECULARCOMPARISONS /NOR VARIANTSCONSEQUENCES /22011 AND ITSCONSEQUENCES /DISEASE AND ITSCORRELATION /ANALYSIS ANDCYTOGENETIC AND MOLECULARCYTOGENETICS AND MOLECULARCYTOGENETICS LABORATORY /THECYTOGENETICS OF HUMAN SOLIDDELINEATION BASED ON A LARGEDELINEATION OF INTERSTITIALDIAGNOSIS IN THE MEDICALEPIDEMIOLOGY AND EVALUATIONEXPRESSION NARIABILITY INEXPRESSION AT THE PEPD LOCUSEXPRESSION OF HEREDITARYFEATURES AND A NORMAL CVSFEATURES OF DOWN SYNDROMEFINDINGS /BIOCHEMICAL ANDFINDINGS IN PATIENTS WITHFINDINGS SUGGESTING ANFOLLOW UP OF 45 CASES OFGENETICAL AND TOMOGRAPHICGENETICS /SYSTEM INHETEROGENEITY AND NATURAL /2HETEROGENEITY IN A FAMILYIMPORTANCE OF FAMILIAL CANCERLABORATORY BY COLOR PCR ANDMANIFESTATIONS OF GAUCHERMOLECULAR GENETIC AND
13431249470
25371294471
240417742312512438619
24882541115110109542
24232438268228421097205925201925178067782016801084102722801067609
10581575563
281410332074230922422774775
236969
1013101526782706956762
1909267827068033401787178550812328021934202319228311506470381
2762545
10812479279498120015181994778
145814191610372737
1505733604858
23276841456418487
96989357077506768052731113553227
OBSERVATION OF THE NERVE /ANDPHENOTYPE OF SINGLE GENE /THEPHENOTYPES /ASSOCIATION WITHPROFILES ACCOUNT FOR THE RP2PROGNOSIS IN PRENATALLY /ANDREINVESTIGATION AND LINKAGERELEVANCE /AND THEIRRELEVANCE /DIAGNOSTIC ANDSIGNIFICANCE AND /FREQUENCYSTUDY OF TYPE 2TERATOLOGY /META ANALYSIS INUSE OF FLUORESCENT IN SITUVARIABILITY OF STICKLER
CLINICALLY AND BY NEWBORN SCREENINGDIFFERENT SUBTYPES OF /TOHETEROGENEOUS FORM OF /IN AINSIGNIFICANT /SIGNIFICANTSIGNIFICANT CORRELATION /ORSUSPECTED TRIPLOIDY /OF
CUNODACTYLY AN OBJECTIVE ASSESSMENTCLN3 /(BATTEN DISEASE) GENECLOACA IN LANGER GIEDION SYNDROMECLONAL CHROMOSOMAL ABERRATIONS IN A
EVOLUTION IN CHRONICEVOLUTION OF T CELL LEUKEMIALOSS AND SUBSEQUENT CLONALORIGIN OF GASTRIC CARCINOMA
CLONE CONTAINING THE GENE FOR PROTEININ CHRONIC MYELOGENOUS LEUKEMIALIBRARIES FROM FLOW SORTEDMAP AT THE CENTROMERE OFPOOLING SCHEMES /MAP USINGPROBES /CDNA AND GENOMICTHAT CAN PARTIALLY CORRECT THE
CLONED AS YEAST ARTIFICIAL CHROMOSOMESFRAGMENTS OF FLOW SORTED /FROMFRAGMENTS USING TRANSPOSONSGENES BY LINKAGE ANALYSIS /OFIN YEAST ARTIFICIAL CHROMOSOMESYEAST 06 METHYLGUANINE/04 /OF A
CLONES /ARTIFICIAL CHROMOSOME AND CDNA/PROBES AND HTF SPECIFIC/WITHIN 7000 RECOMBINANTAND IDENTIFICATION OF NEWAND THEIR APPLICATION TO /13CONTAIN TWO NEW GENES WITHINCONTAINING CPG ISLANDS AT XQ24CORRESPONDING TO LOCI WITHINEXPRESSED IN HUMAN BRAIN /CDNAFOR GLUTATHIONE REDUCTASEFROM A CHROMOSOME 17 COSMID /OFFROM HUMAN FOREBRAIN AND /THEFROM HUMAN ONCOGENES BYFROM SOMATIC CELL HYBRIDSFROM THE CENTROMERE OFFROM THE PERICENTRIC REGION OFIN THE EFFORTS AIMED ATON CHROMOSOME 22 /NOT1 LINKINGON HUMAN CHROMOSOME X BYTO HUMAN CHROMOSOMES 5 AND 16USING COT 1 DNA NEW COSMIDSWHICH COMPLEMENT SENSITIVITY
CLONING /DISEASE GENES BY POSITIONAL/YEAST ARTIFICIAL CHROMOSOMEAND ANALYSIS OF THE CANDIDATEAND CHARACTERIZATION OFAND CHARACTERIZATION OF AAND CHARACTERIZATION OF THEAND CHARACTERIZATION OF THEAND CHROMOSOMAL ASSIGNMENT OFAND CHROMOSOMAL LOCALIZATIONAND CONSTRUCTION OF AAND IDENTIFICATION OF AAND ISOLATION OF POTENTIAL /20AND PHYSICAL MAPPING OF AAND SEQUENCING OF SERUM /CDNAEFFORTS FOR SPINOCEREBELLARFOR MICRODISSECTED /EFFICIENTGENES INVOLVED IN HEARINGHUMAN CD1 PYRROLINE 5IN GENOME ANALYSIS OF THEIN THE ABSENCE OF A CANDIDATEIN THE XP22.3 REGION /OVERLAPMAPPING AND EXPRESSION /CDNAOF A HUMAN 3 METHYLADENINEOF A PAIR OF DUPLICATED GENESOF CORRECTING DNA SEQUENCESOF HUMAN CHROMOSOME 17021OF HUMAN LDH C4 GENE AND ITSOF LEUKEMIA ASSOCIATED /THEOF PORK AND HUMAN CDNA PROBESOF SBY A CANDIDATE FOR HYAOF THE FERRIC REDUCTASE GENEOF THE FRAGILE X LOCUS IN THEOF THE HUMAN ALCOHOLOF THE LYSOSOMAL CHOLESTEROLSTRATEGY /WALKING AND JUMPINGTHE MYOTONIC DYSTROPHY GENETHE X CHROMOSOMAL BREAKPOINTTRANSCRIPTION AND /MOLECULARTRANSLOCATION BREAKPOINTS /BYWHERE IT'S BEEN AND WHERE
CLONINGS /GENE MAMMALIAN EXPRESSIONCLOSURE OF THE CHROMOSOME 19 COSMIDCLOVERLEAF SKULL (TYPE II) A NEW /WITH
2533434
10011939171820471915130584
22912931282906468194534758
1135142687119721507136213272604132725992334586177
219952
11232275
50212225051948215824012168S772198195021162195215222992527453
21512333216023212213200820652191212918972082238821742193
9394
2294190
2386238722822185227223742128543
21572510
262279179370
2092225922582403227423061286185
232223432363373
228422482785404
20652309124421
259252
900
CLOVIS COLONIZATION OF THE NEW WORLDCLUSTER COSMIDS AND NOT1 BOUNDARY
OF BABIES WITH MICROGNATHIAOF BAND XQ28 /WITHIN THE G6PDOF VITAMIN D DEPENDENT /OF APHENYLALANINE HYDROXYLASEREGION IN AN ACUTE /BREAKPOINTREGION IS TIGHTLY LINKED TOREGION WITH GENETIC LINKAGE
CLUSTERED AT XQ22.3 Q24 /SEQUENCECLUSTERING OF ABNORMAL HEMOGLOBINS IN
OF MANIFESTATIONS OF VONCLUSTERS AMONG FIRST DEGREE RELATIVES
LOCALIZATION IN UNSTABLE /ALUOF BIRTH DEFECTS IN LATIN
CM INTERVAL ON CHROMOSOME 11023 /TO AOF HUMAN DNA SURROUNDING THE /20SUBREGION OF CHROMOSOME 6P /TO A 6
CMT 1A LOCUS WITHIN 17P11.2 ITYPE 1CNS DEVELOPMENT /SPECIFICATION ANDCO ACTIVATORS AND THE BASALCOA DEHYDROGENASE /ENCODING GLUTARYL
DEHYDROGENASE ACTIVITY ANTIGENDEHYDROGENASE DEFICIENCY /ACYLDEHYDROGENASE DEFICIENCY /ACYLDEHYDROGENASE DEFICIENCY /ACYLDEHYDROGENASE DEFICIENCY /ACYLDEHYDROGENASE DEFICIENCY /ACYLDEHYDROGENASE DEFICIENCY AND /ACYLDEHYDROGENASE DEFICIENCY FROMDEHYDROGENASE DEFICIENCY FROMDEHYDROGENASE DEFICIENCY IN EUROPEDEHYDROGENASE DEFICIENCY PLASMADEHYDROGENASE MUTANT ALLELE /ACYLDEHYDROGENASE RESPONSIBLE FORDEHYDROGENATION DISORDER /ACYLHYDRATASE ACTIVITYLYASE INITIAL MOLECULARMUTASE ACTIVITY IN HUMAN PLACENTAMUTASE DEFICIENCY /METHYLMALONYLMUTASE FOR CHARACTERIZATIONOXIDASE A NOVEL PEROXISOMAL /ACYL
COAGULATION STUDIES (F7R) /AND NORMALCOAST /ON NEWFOUNDLAND'S SOUTHCOCAINE PLAY A ROLE /ATLANTA DOESCOCHLEA /OF G PROTEINS IN HUMANCOCHRAN METHODS OF META ANALYSIS INCOCKAYNE SYNDROME /PIGMENTOSUM ANDCODE FOR GENETICISTS /A SPECIAL ETHICS
OF ETHICS FOR HUMAN GENETICISTSOF ETHICS THE NATIONAL SOCIETY
CODES BY FLUORESCENCE IN SITU /BARCODING DNA SEQUENCES /OF ENOLASE
FOR THE HUMAN ALPHA 3 BETA 4FOR VENTRICULAR MYOSIN /GENEHUMAN GLYCOSYLASPARAGINASEITS APPLICATIONS FOR SYNDROMEREGION SUBSTITUTIONS IN T CELLSEQUENCES IN THE CYSTIC /OF
CODON 200 OF THE PRP GENE /MUTATION AT347 MUTATION OF THE RHODOPSIN370 OF HUMAN GLUCOCEREBROSIDASE373 OF FVIII GENE CAUSING /AT41 42 (TTCT) DELETION LEADING574 OF TYPE II COLLAGEN IN /AT717 MISSENSE MUTATION IS RARE
COEXISTENCE OF TRANSLOCATION 14;18COEXISTENT MOLAR PREGNANCY AND LIVECOFACTOR DEFECT AN UNDERRECOGNIZED
DEFICIENCY /MODEL FOR A HUMANCOGNITIVE AGING AND SENILE DEMENTIA
AND PERSONALITY FACTORS INCOHORT /SYSTEM (VACARES) 1987 BIRTHCOINCIDENT SEQUENCES FROM SOMATIC /OFCOINCIDENTAL FAMILIAL PARACENTRIC /ACOLIAl /IN A TYPE PROCOLLAGEN GENE
COL1A2 AND COL3A1 ARE NOTGENE OF TYPE COLLAGEN /IN THENULL ALLELE /I COMMONLY DUE TO
COL1A2 AND COL3A1 ARE NOT LINKED TOMOLECULAR AND PHENOTYPIC
COL2A1 GENE /DYSPLASIA ANALYSIS OF THEIN TRANSGENIC MICE PRODUCESMETABOLISM /INBORN ERRORS OFMOLECULAR AND PHENOTYPIC
COL3A1 ARE NOT LINKED TO EHLERS /ANDCOL4A5 GENE ITHE UNKNOWN 5 HALF OF THE
WHICH CONTAINS MUTATIONS INCOLCEMID ON HUMAN SPERM CHROMOSOME /OFCOLCHICINE TREATED FAMILIAL /OFCOLI /FAMILIAL ADENOMATOUS POLYPOSIS
/OF CYSTINE BINDING PROTEIN OF EGENE ITHE ADENOMATOUS POLYPOSIS
COLIC /A COMMON CAUSE OF INFANTCOLITIS EVIDENCE FROM A SUBCLINICALCOLLABORATION /NEW HAVEN AND ROCHESTER
/OF AN INTERNATIONAL/OF AN INTERNATIONAL
COLLABORATIVE LINKAGE STUDY OF GILLESSTUDY /PHENYLKETONURIASTUDY OF LINKAGE /ON ASTUDY OF PREDICTIVESTUDY ON PRENATAL
COLLAGEN/BIOCHEMICAL STUDY OF/HAPTOGLOBIN AND TYPE III
545
26372195112
1964725
288313702005S7716582717231
271021312722294
214020012039311118
2322459265475498
227723169751119237719526397549049712174885705115325271500729
2702233812932934241
1814184
2638218221642355140
278426121000999436
27941049474
2811133311544392312
68921
2730205
17481065202534724642025348
11212461
45349
20252362240516291554591448609457
27731941188320121924212193717711234450867
Permuted Title Index
/IN THE COLIAl GENE OF TYPEAS GENE LEADING TO /TYPE IVA5(IV) CHAIN AND FURTHER /IVAND BULLOUS PEMPHIGOID NIlAND CARBAMYL PHOSPHATE /1ICHAIN PRODUCES RECURRENT /AllFROM TWO PATIENTS OF THE /IGENE OF THREE PATIENTS WITHGENE ON CHROMOSOME 3 N/lGENES /EXPRESSION OFGENES COLlAl COL1A2 ANDIN A CLINICALLY /OF TYPE IIN HYPOCHODROGENESIS /TYPE 11IV AS THE TARGET FOR ANTI /OFPROCESSING DEFECTS ANDPRODUCES LETHAL /OF TYPE II
TYPE III /ABNORMALITIES OFCOLLAGENASE GENE AND THEIR USE IN /THECOLLAGENS /IN GENE FOR FIBRILLARCOLLINS SYNDROME IN A CHILD WITH
SYNDROME LOCUS TO 5031.3COLLOBORATIVE STUDY /FROM THE GERMANCOLOBOMAS AND CONNECTIVE TISSUE /IRISCOLOCAIZED ON HUMAN CHROMOSOME ARMCOLOMBIA /RICKETS IN A RURAL AREA OF
GENETIC AND HISTORICAL /OFWITH SPECIAL EMPHASIS ON /IN
COLOMBIAN AMERINDIAN DEMES BASED ONCOLON CANCER (LYNCH SYNDROME)
CANCER AND A VARIABLE NUMBER OFCANCER AND POLYPS /EXAMPLE OF
COLONIZATION OF THE NEW WORLD /CLOVISOF THE PACIFIC /OF THE
COLONY STIMULATING FACTOR CYTOKINESTIMULATING FACTOR RECEPTOR
COLOR FLUORESCENCE IN SITU /BY TWOFLUORESCENCE IN SITU /USING TWOIN A GENETIC ISOLATE /OF SKINPCR AND AN IMPROVED METHOD OFVISION CHANGES AND DNAVISION DEFECTS /HUMAN RED/GREENVISION DEFICIENCIES AMONG /GENEVISION DEFICIENCY /FOR RED GREEN
COLORADO /IN THE SAN LUIS VALLEY/IN THE SAN LUIS VALLEY
COLORECTAL CANCER /CONSIDERATION OFCANCER AND OTHER CANDIDATECARCINOMA /PATIENTS WITHCARCINOMA GENE AND PART OFCARCINOMA IN FIVE KINDREDSTUMORIGENESIS /UNDERLYINGTUMORS /13 AND 17 IN HUMAN
COLUMBIA NATIVE KINDRED /IN A BRITISHCOMBALAMIN METABOLISM OF THE CBLC FORMCOMBINATION OF HIGH RESOLUTION /WITH A
OF TRADITIONALSTRATEGIES /OPTIMAL LOCUSWITH CONSTANT DENATURANT
COMBINED HYPERLIPIDEMIA /FOR FAMILIALPCR WALKING AND JUMPING /A
COMMERCIAL LABORATORY /FROM ALABORATORY /FROM A
COMMNUNITY MIYAMA /IN THE ISOLATEDCOMMON ALLELIC LOSSES ON 3P IN /OF
ANCESTORS /CANADIANS SEARCH FORCAUSE FOR CLASSICAL /THE MOSTCAUSE OF INFANT COLIC /ACHROMOSOMAL DISORDERS /IN THECYSTIC FIBROSIS MUTATIONS /FOURDISEASE HAVING COMPLEX ETIOLOGYDISEASES USING PCR /ANALYSIS OFFEATURE OF THE CHROMOSOMEFRAGILE SITE AT 3P14 AND (THEFRAGILE SITE FRA(X)(027.2)FRAGILE SITES ARE DEPENDENT ONFRAGILE SITES IN UNTREATED NONFRAGILE SITES IN YQ12 /INDUCEDLITHUANIAN MUTATION CAUSINGMEDIUM CHAIN ACYL COA /OF THEPOLYMORPHISM IN THEREGION OF DELETION IN LUNG /THESTEP IN HUMAN CANCER /ATO PATIENTS EITHER WITHUNDERREPORTED DOMINANT SYNDROME
COMMUNITIES AT POTENTIAL INCREASEDCOMPARATIVE EPIDEMIOLOGY OF DOWN
HOMOLOGY MODELING OFMAPPING OF MICRODELETIONSMAPPING OF MOUSERETROSPECTIVE STUDY /ASTUDY OF PCR AND
COMPARISONS /NOR VARIANTS CLINICALOF SIX VNTR LOCI IN THREE
COMPENSATION /DETERMINATION AND DOSAGECOMPETITIVE IN SITU EXPRESSION WITHCOMPETITOR IN SEQUENCE TAGGED SITESCOMPLEMENT
C4 PROMOTER /OF THE HUMANCOMPONENT C4A AND C4B INRECEPTOR ON HUMAN /OFSENSITIVITY TO GAMMA (WHICH
COMPLEMENTARY DNA /NUCLEAR RNACOMPLEMENTATION ANALYSIS AMONG THE
BETWEEN CYSTINURIAIN SACCHAROMYCES /BY
347194
240523872031446496
101173
3532025534474383S73522350192744
827193312648791870725
283927612842600599S582637257619
2360215321482764111321902419886
223126692689272101
139019911991113
25931909508163214552062281327242785103027402857260726622280457174
104727384262554170516121375136315642329975
2417224S63473782178826972472205S861177415120028292236164421001454246724032858238825216274622279
OF ATAXIA /FUNCTIONALOF BLOOM SYNDROME
COMPLEMENTED WITH IN SITU AMNIOCYTECOMPLEMENTS /ABNORMAL SEX CHROMOSOME
AND CHROMOSOME SPECIFICOF SUGARBEET PLANTS
COMPLETE ATRIOVENTRICULAR HEART BLOCKDELETION OF THE PLP GENE INFAMILIAL EVALUATION AINGENETIC MAP /LOCUS AGAINST AGENOMIC SEQUENCE OF 180 KBLONG RANGE RESTRICTION MAP /AMOLECULAR NOSOLOGY /TOWARD AOR MOSAIC TRISOMY 21 IN /WITHPRIMARY STRUCTURE OF THESWEDISH POPULATION SAMPLE AS
COMPLEX /BY DNA RFLP ANALYSIS OF HLA/CHROMOSOMES FROM THE HLA/FACTOR RECEPTOR (C KIT) GENE/THE MAJOR HISTOCOMPATIBILITY/WAGRAN ANALYSIS OF 491 CASES /ULNAAND MULTIPLE PSEUDOGENES AREAND T CELL RECEPTOR GENES INBRACHYDACTYLY /APLASIA ANDCHROMOSOMAL REARRANGEMENTS /OFCHROMOSOME REARRANGEMENT /OF ACONGENITAL HEART DISEASE IN ADISORDERS /LINKAGE ANALYSIS OFDOUBLE TRANSLOCATION /PATERNALETIOLOGY /DISEASE HAVINGETIOLOGY /DISEASES WITHFIVE BREAK REARRANGEMENT IN AFOUR WAY TRANSLOCATION /NOVOGENES /HISTOCOMPATIBILITYGENETIC LOCUS /SUGGESTS AGENOMIC REARRANGEMENT IN /TOGLYCEROL KINASE DEFICIENCY /OF(NADH DEHYDROGENASE)MECHANISMS OF TRANSCRIPTIONALMETHYLATION PATTERN /EXHIBIT AMODES OF INHERITANCE /UNDERPATTERNS OF LINKAGEPHENOTYPES /EPIDEMIOLOGY OFPROBES IN IDENTIFYING THEPVUII HAPLOTYPES /P49A DETECTSSEGREGATION ANALYSISSEGREGATION ANALYSIS OFSEGREGATION ANALYSIS OF CLEFT
COMPONENT /PROTEIN GROUP SPECIFICC4A AND C4B IN THE MAJOR
COMPONENTS IN ETIOLOGY OF /OF GENETICIN TWINS /DIETARY INTAKEOF BODY COMPOSITIONOF HUMAN SATELLITE DNA
COMPOSITION MEASURED USING UNDERWATERSTUDIES WITH MONOZYGOTIC
COMPOSITIONAL MAP OF THE HUMANCOMPOUND HETEROZYGOSITY OF B GLOBINCOMPOUNDS /AND CARBAMATECOMPREHENSIVE GENETICS SERVICES
NATIONAL GENETICS /OFSICKLE CELL CENTER
COMPULSIVE DISORDER IN A MEXICANCOMPUTED TOMOGRAPHY IN RETT SYNDROMECOMPUTER /DYSMORPHOLOGY TO AN AVERAGE
ASSISTED DETERMINATION OFASSISTED DETERMINATION OFASSISTED DIFFERENTIATION OFPACKAGE FOR MULTIPOINT /APROGRAM DISEASES (IN THEPROGRAM FOR AUTOMATIC /SYSTEMPROGRAM TO PERFORM A /HOMAGESYSTEMS IN DYSMORPHOLOGYVIDEODISK PROGRAM AND TEXT
COMPUTER/LASER VIDEODISK SYSTEM FOR /ACOMPUTERIZED DATABASE OF CALL /UPDATE
IMAGE ANALYSIS OF BRAINCOMPUTERS IN DYSMORPHOLOGY THE LONDON
IN SYNDROMOLOGY (THE USE OFIN THE DIAGNOSIS OF LETHAL
CONCENTRATION IN PLASMA /DENSITY ANDOF GENES CAUSING MENTAL
CONCENTRATIONS CYTOGENETIC /MSAFPCONCEPT /AND FUNCTIONS SYSTEMS
AS A PATHOGENETIC DIAGNOSISOF SOMATIC MUTATIONAL DISEASE
CONCEPTS IN PRENATAL DIAGNOSIS /NEWCONCEPTUSES (TERATOTHANASIA) AND THECONCERTED ACTION ON HERITABLECONCORDANT FOR MULTIPLE SCLEROSISCONCURRENCE OF HUMAN VITAMIN DCONDENSATION TECHNIQUE AN ALTERNATIVECONDITIONAL MUTATION IN THE TESTIS
XY SEX INVERSION /LEAD TOCONDUCTANCE IN TRANSFECTED (CHLORIDECONE DEGENERATION TO XP11 REGION
GUIDANCE IN DROSOPHILA FASCICLINCONFIDENTIALITY IN GENETIC TESTING
IN GENETIC TESTINGCONFIRMATION BY A CHROMOSOME SPECIFIC
BY PCR /CYTOMETRY ANDOF A MOSAIC CELL LINEOF A NEW SYNDROMEOF A SUSPECTED DELETION
230116891212145583
15481463108314172063257513613511219240510051108211422962403S1423519731917847140814221413196314062738270163215472621231
2556687513118
2436271423362657211728722648803
277422622403272627672649169626492759225610705391809S3017742719683136
2064207214642040278820601970138137133
1793850134135139
243420151201121859292S53103354274289113202341119023647033253940
154210912098341516
OF CLOSE LINKAGE TOOF CYSTIC FIBROSIS IN AOF CYTOGENETIC FINDINGSOF LINKAGE OFOF PDGFA LOCALIZATION TOOF PRENATALLY DIAGNOSEDOF THE PHENOTYPEUSING FLUORESCENT IN
CONFLUENCED CULTURE SYSTEM /CELLS WITHCONFORMATION POLYMORPHISM ANALYSIS
POLYMORPHISM ANALYSISPOLYMORPHISM ANALYSIS OFPOLYMORPHISM METHOD
CONFORMATIONAL POLYMORPHISM /STRANDEDCONGENITA /DYSPLASIA
/IN ARTHROGRYPOSIS MULTIPLEXAND ESTIMATION OFLOCI /AND ADRENAL HYPOPLASIA
CONGENITAL ABNORMALITIES ASSOCIATIONABNORMALITIES/MENTALABSENCE OF THE THYROID /ANDADRENAL HYPERPLASIA /BYADRENAL HYPERPLASIA BY DNAANOMALIES IN A POPULATIONANOMALIES REPORTING ANDANOMALIES RESULTS IN ITSANOMALIES/MENTAL /MULTIPLEATAXIA MENTAL DEFICIENCYBILATERAL ABSENCE OF THECARDIOVASCULAR /RISK OFCARDIOVASCULAR /RISKS OFCATARACT /GENETIC STUDY OFCATARACTS IN INDIA /ANDCOMPLETE ATRIOVENTRICULARCRANIOFACIAL MALFORMATIONSDEAF MUTES HELD AMONG /ONDEFECTS /OF MULTIPLEDIAPHRAGMATIC HERNIA NOTERYTHROPOIETIC PORPHYRIAGLAUCOMA /OF PRIMARYGLAUCOMA FROM TURKEYHALLUX VIRUS WITHHEART ANOMALIES EARHEART DEFECTS IN TRISOMY 8HEART DISEASE /ANDHEART DISEASE AND TURNERHEART DISEASE IN A PATIENTHIP DISLOCATION ANDHYPOPARATHYROIDISM WITH /OFLACTASE DEFICIENCY /IN THEMALFORMATION /A CHILD WITHMALFORMATION IN CHILDRENMALFORMATIONS /ANDMALFORMATIONS /AND FETALMALFORMATIONS /WITHMALFORMATIONS AND /OFMALFORMATIONS AT A /OFMALFORMATIONS IN A FEMALEMALFORMATIONS REGISTERMENTAL RETARDATION AND /OFMUSCULAR DYSTROPHY IN TWOMYOPATHIES THE KING /BYNEPHROSIS /IN NONLETHALNEPHROSIS DETECTION OFNEPHROTIC SYNDROME /INSPONDYLOEPIPHYSEALSTATIONARY NIGHT BLINDNESSSTATIONARY NIGHT BLINDNESSSTATIONARY NIGHT BLINDNESS
CONGENITALLY MISSING TEETH AND SEVERECONGENTIAL ANOMALIES /REGISTRIES OFCONJOINED TWINS /THE PATHOGENESIS OFCONJUGATED TRIENES /INCREASEDCONJUNCTION WITH HLA CLASS II GENESCONNECTIVE TISSUE DISORDERS /HERITABLE
TISSUE DISORDERS /HERITABLETISSUE DYSPLASIA /ANDTISSUES TOWARD A COMPLETE
CONSANGUINEOUS PARENTS (BOY BORN TOCONSANGUINITY AND FOUNDER EFFECT AS ACONSECUTIVE LIVEBIRTHS IN EASTERN /OF
PREGNANCIES WITH COMPLETECONSENSUS CRITERIA FOR DIAGNOSIS OF
SEQUENCES /TO SPLICE SITESURVEY /AND INTERNATIONAL
CONSENT REPRODUCTIVE GENETIC SERVICESCONSEQUENCE OF TRANSLOCATIONSCONSEQUENCES /22011 AND ITS CLINICAL
/ASSESSING GENETIC 10 AND/DISEASE AND ITS CLINICALFOR ONCOGENESIS /AND ITSOF GENETIC HETEROGENEITYOF THE CHERNOBYL DISASTER
CONSERVATION OF AMINO ACIDS EVIDENCEOF ENOLASE CODING DNAOF NRS 1 A NOVEL HUMANOF SYNTENY IN MICE AND
CONSERVED DNA SEGMENTS WITHIN THEDNA SEQUENCES /HIGHLYMRNA SEQUENCE WHICH /NOVELSEQUENCES /BY THREE HIGHLYSEQUENCES FROM THE PROXIMAL
CONSORTIUM /OF THE INTERNATIONAL/THE WAARDENBURG SYNDROMETO STUDY VALUE OF BONE /A
546
20181102944190421111163642165015759649842290280411055221524802222012678797886541108666
27302756646645106232
2650700
26641463775
277718371192530764628747817149971114141413881736509176012885371290696726
2688147294927688216988511183116011218101878192884135594344310035235487935189117462760121965524961739174016021518183619942578456279626322638230818682457261224451865226014379156
Permuted Title Index
CONSTANT DENATURANT GEL /GENE USINGDENATURANT GEL /USINGDENATURANT GEL /WITHFREQUENCY IN 10 YEARS AND
IIItoUIDONAL CYTOGENETICHETEROMORPHISM OFREARRANGEMENT INRING CHROMOSOME 21
CONSTIT lVE HETEROCHROMATION DURINGCONSTRICTION REGIONS OF HUMANCONSTRUCTS IN EBV BASED EXPRESSION
TO MOTOR NEURONS BY /GENECONSUMER ATTITUDES TOWARD THALASSEMIACONTANATION IN AMNIOCYTES CONSTANT
IN AMNIOTIC FLUID /CELLCONTEMPORARY AND ANCIENT HUMANS /INCONTIG /A YEAST ARTIFICIAL CHROMOSOME
AROUND THE FRAGILE SITE FRAXAAROUND THE FRAGILE SITE FRAXAAT THE FAMILIAL ADENOMATOUSCONTAINING THE HUMAN IDS GENEMAP OF HUMAN CHROMOSOME 19MAP OVER A 600 KB REGIONMAP USING CLONE POOLING SCHEMESMAP WITH THE CYTOGENETIC ANDPROXIMAL TO THE FRAGILE X SITE
CONTIGUOUS A CASE OF BOTH SYNDROMESGENE /HETEROGENEITY OR AGENE DELETION SYNDROMEREGIONS OF MAMMALIAN /LARGE
CONTRACTURE TESTING ASSIGNMENT INCONTRACTURES AND TECHNICAL DIFFICULTYCONTRASTING EXPRESSION PATTERNS OFCONTREUTION OF A SINGLE GENE WITH
OF BIOCHEMISTRY TOOF IMPRINTING TO THEOF POPULATION BASED TWINOF THE APOLIPOPROTEIN ETO COGNITIVE AGING ANDTO PHYSICAL MAPPING IN
CONVENTIONAL CYTOGENETIC AND /BYCONVERSION /READILY CAPABLE OF GENE
BETWEEN MURINE C4 RELATEDEVENT /EVIDENCE FOR A GENEEVENTS INVOLVING THE /GENE
CONVERT DNA SEQUENCE VARIATION INTOCONVULSIONS IN A NEWFOUNDLAND KINDREDCOPING STYLE ON RISK PERCEPTION ANDCOPPER AND CERULOPLASMIN METABOLISM /l
BLOTTING IN THE STUDY OFTOXICOSIS /ON INHERITED CANINE
COPY GENES /PROBES OF SINGLEHSV 1 TK GENE /INTEGRATED SINGLENUMBER /IN MITOCHONDRIAL DNAOF THE HUMAN RHODOPSIN GENE
CORD BLOOD /CHROMOSOME ANALYSIS FROMBLOOD AFP ALBUMIN PREALBUMIN ANDINTEGRITY WITH REVIEW OF THE /AND
CORDOCENTESIS /AND IN FETAL BLOOD BY/TO AMNIOCENTESIS AND
CORNEAL DYSTROPHY TYPE I /IN LATTICECORONARY ARTERY DISEASE /DOCUMENTED
ARTERY DISEASE IN FINNISHARTERY DISEASE IN THE CHINESEHEART DISEASE /THE PREMATUREHEART DISEASE /THE RISK FOR
CORPUS CALLOSUM /WITH AGENESIS OFCALLOSUM IRIS COLOBOMAS AND
COS CELLS /A EXPRESSED INCELLS /OF THE SRY GENE IN
COSENZA ITALY /IN THE PROVINCE OFCOSIUD AND BACTERIOPHAGE CLONES FROM
CA476 CONTAINS TWO HTF ISLANDSCLONE CONTAINING THE GENE FORCLONES CONTAINING CPG ISLANDSCLONES FROM SOMATIC CELL /HUMANCLONES ON HUMAN CHROMOSOME XCONTIG MAP OF HUMAN CHROMOSOMECONTIG MAP USING CLONE POOLINGCONTIG MAP WITH THE /OF THEIN A HUMAN CELL LINE /EPISOMALLIBRARY USING FLUORESCENCE INPROBE /HYBRIDIZATION WITH AWALK OF 460 KB IN A CANDIDATEWALKING IN ADJACENT REGIONSYEAST ARTIFICIAL CHROMOSOME
COSMIDS AND NOT1 BOUNDARY CLONESAPPLICATIONS TO REGIONAL /ANDFOR ANALYSIS OF RENAL CELLFOR HUMAN CHROMOSOME 21 /NEW
COST BENEFIT OF NEWBORN SICKLE CELLCOST/BENEFIT CONSIDERATIONS ANDCOSTA RICA /DISEASE IN A SMALL TOWN INCOT 1 DNA NEW COSMIDS FOR HUMAN /USINGCOUMARIN METABOLISM /STUDY OFCOUNSELING /APPROACH TO GENETIC
/FOR DETECTION BIOLOGY AND/FOR GENETIC SCREENING AND/FOR TRISOMY 8 AND GENETIC/IMPLICATIONS FOR GENETIC/INFORMATION FOR GENETIC/THAN REACTIVE GENETICNERSUS MEDICAL GENETICSAND FAMILIAL CANCERAND FETAL KARYOTYPING
280321828131187135313791707132417101563247624891855118712282622102378
2389101204
22032133
52212421591448743144349
19111128930
273692989402
277568
21461671261126272375221025288331733438571
187120852536
347991495912744128511511055714714
274611184271900879283
239327272008229723342152232121292203
5221241646215115162396211321682195185
1722208217961528652082540
156191120912021747226208
17812691273
AND FOLLOW UP COUNSELINGAND INTERNATIONAL /GENETICAND PRESYMPTOMATIC ANDAND SOCIAL PROBLEMSBASED ON COMPARISON OF /FORCASES /OF 1575 GENETICCHALLENGE /PATIENT GENETICCLINIC IN HONG KONGDILEMMA /A TRUE GENETICDILEMMA /PATIENT GENETICEFFECTIVENESS AND /GENETICEFFICACY IN MULTICULTURALFOR ADULTS WITH SPINAFOR DEAF ADULTS MEDICALFOR ORNITHINE /PRENATALFOR PARENTS HAVING G 6 PDIN A NORTH INDIAN HOSPITALIN ABNORMAL ULTRASOUNDIN FAMILIES WITH THE XIN JAPANESE FAMILIES WITHIN KUWAIT /AND GENETICIN NEUROMUSCULAR DISEASESIN NOONAN SYNDROME /GENETICIN NORTH AMERICA /DIAGNOSISIN PREDICTIVE TESTING FORIN RETINITIS PIGMENTOSAIN SPONTANEOUS ABORTIONIN SPORADIC CASES OF XISSUES AND LONG TERMISSUES FOLLOWING DIAGNOSISISSUES IN CASE OF /GENETICLINKED GENES /IN GENETICOF CARRIERS WITH /GENETICOF DISEASES WITH HIGHON PATIENT ANXIETY A STUDYON REPRODUCTIVE CHOICES OFTRAINING AN ASSESSMENT OFWITH DNA POLYMORPHISMS
COUNSELOR IN A SCREENING PROGRAM FORSTRESS AND INSTITUTIONAL
COUNSELORS 22 YEARS EXPERIENCE WITH AEXPERIENCE /OF GENETICREGARDING ETHICAL ISSUES
COUNTERTRANSPORT TO PREDICTINGCOUNTRIES /IMMIGRANTS FROM THIRD WORLD
/SERVICES IN DEVELOPINGIMPLICATIONS FOR GENETIC
COUNTRY /HOSPITAL OF A DEVELOPINGCOUNTY ALABAMA U.S.A AND UPPSALA
SWEDEN /U.S.A AND UPPSALAUNIVERSITY OF SOUTHERN /ANGELES
COUPLED RESTRICTION DIGESTS /PCRCOUPLES /POLYMORPHISMS IN INFERTILE
WHO HAVE TERMINATED A /FORWITH A TRISOMIC CHILD /INWITH MULTIPLE SPONTANEOUS /OFWITH REPEATED ABORTIONSWITHOUT A PREVIOUSLY AFFECTED
COURSE AND EARLY DIAGNOSTIC /UNUSUALOF MEDIUM CHAIN ACYL COA
COURTROOM ISSUES AND CONCERNS IN THECOUSIN MARRIAGES IN ALIGARH /FIRSTCOUSINS AFFECTED WITH THE PRADERCOVARIANCES ON THE EVALUATION OF RISKCOVARIATE /USING AGE AT ONSET AS ACOWDEN DISEASE A NEW PHAKOMATOSIS /INCPG DINUCLEOTIDES AND GERM LINE /AT
ISLAND /T AND IDENTIFICATION OF AISLAND 5 OF THE FACTOR Vil GENEISLAND ENRICHED LIBRARY FORISLANDS AND ASSOCIATED /MULTIPLEISLANDS AT XQ24 XQ28 LOCUSRICH ISLAND AND PHYSICAL MAP OFRICH ISLAND FROM A REGION OF /OF ASEQUENCES ON THE HUMAN /OF
CRANIAL BASE IN FACIAL GROWTH RABBITSCLEROSIS REPORT OF A PATIENT
CRANIOFACIAL ANOMALIES AN UPDATE ONANOMALIES MOUSE MODELSDEVELOPMENTDIGITAL ANOMALY SYNDROMEDYSMORPHISM ABSENT /WITHMALFORMATION /SYNDROME OFMALFORMATIONS AND SEVEREMALFORMATIONS CLEFT LIPPATTERN PROFILES IN DOWNSYNDROMES /NONCLEFTING
CRANIOFRONTONASAL DYSOSTOSIS REPORTDYSPLASIA IN A GIRL
CRANIOSYNOSTOSIS /RABBIT MODEL FORIN NEONATES WITHSYNDROME UPDATE
CREST /FOR INVOLVEMENT OF THE NEURALCREUTZFELDT JAKOB DISEASE /IN FAMILIAL
JAKOB DISEASE AND CONTROLSJAKOB DISEASE CARRYING AJAKOB DISEASE IS /FAMILIAL
CRI DU CHAT DELETION /FOR CHROMOSOME 5DU CHAT SYNDROME (5P15.2) USING
CRIMINAL INVESTIGATIONS INVOLVING /INCRITICAL DELETION INTERVAL PARENTAL
REGION FOR PALLISTER KILLIANREGION FOR THE 18Q SYNDROMEREGION FOR THE TRISOMY 18REGION IN DIGEORGE SYNDROME
173817391764177012417601246178511621080175617581737
2812371778140312441743101917361735176338917381016366
1111114111791761200617571005175218501762675174917841779181418212736174018031747178926712671114325231560176615531400116718418934753141164145927381970616106823342154237423962152212323701652931796342341S72721879870800775629343695774931905339682
2291239010001003117621682861170214371672169586
REGION RESPONSIBLE FOR THECROSS HOMOLOGY BETWEEN CHROMOSOME 16P
REACTIVE PROTEIN IN CLOSEYOGYAKARTA BRANCH /RED
CROSSED RENAL ECTOPIA AND PELVIC /WITHCROSSUNKING AGENTS OF THE FANCONICROUZON SYNDROME /IN A FAMILY WITH
SYNDROME A FAMILY WITH THREECRYPTIC SPLICE SITE FOUND IN THE PLP
TRANSLOCATIONS BY IN SITU /ANDCRYSTALLINS NEW FUNCTIONS PRECEDECSF LEVELS OF GLUTAMATERGIC ANDCT FINDINGS /HAND AND TEMPORAL BONECUBA /CENTRAL REGION (VILLA CLARA) OF
/DISEASE IN THE WESTERN REGION OF/DISEASES BY DNA ANALYSIS IN/DISEASES CONTROL PROGRAM IN
CULTURAL AND BIOLOGICAL DETERMINANTSIMPLICATIONS /MEDICAL AND
CULTURE /LYMPHOCYTES IN LONG TERMAND ROBOTIC HARVESTING /SITUAND SHOW LITTLE INTRATUMOR /INCYTOGENETIC ANALYSIS OF CVSIN IDENTIFYING A SERINE FORMETHOD /WITH IN SITU AMNIOCYTESYSTEM /CELLS WITH CONFLUENCED
CULTURED CELLS FROM DUCHENNE ANDFIBROBLASTS /LEVELS INHUMAN KERATINOCYTES WITH /OFLYMPHOCYTES FROM PATIENTS /IN
CULTURES /IN AMNIOTIC FLUID CELL/IN HUMAN LYMPHOCYTEAS A METHODOLOGY FORFOR CHROMOSOMAL STUDIESIN VITRO /IN HUMAN LYMPHOCYTE
CUPID BOW MOUTH PROGNATHISM ABNORMALCURRARINO TRIAD /ISSUES IN CASE OFCURRENT CLASSIFICATION OF THESE /AND A
PRACTICES AND SUGGESTIONS FORPROGNOSTIC MOLECULAR
CURRICULUM DEVELOPMENT /FORCUT BY RESTRICTION ENDONUCLEASESCUTANEOUS MALIGNANT /ASSOCIATED WITH
SKELETAL INVOLVEMENT THESKELETAL SYNDROME [THE FACIOVASCULAR ABNORMALmES
CUTOFF FOR PRENATAL DIAGNOSIS OF /RISKCUZN SUPEROXIDE DISMUTASE ACTIVITY TOCUZNSOD MICE DISPLAY CLINICALCVS (MINISTRY OF SCIENCE AND /AFTER
/150 CASES OF TRANSABDOMINAL/AMNIOCENTESIS AND COMPARISON WITH/CULTURE CYTOGENETIC ANALYSIS OF/DIFFICULTY OF TRANSCERVICAL/FOLLOW UP PREGNANCIES AFTER/FOLLOWING FIRST TRIMESTER/PATIENTS UNDERGOING TRANSCERVICAL/THE TRANSABDOMINAL APPROACH FOR/TRANSABDOMINAL AND TRANSCERVICALA FURTHER DELINEATION OF THEAN ANALYSIS OF INCIDENCE AND /INAND FETAL TISSUE OF TWIN GESTATIONAND MIDTRIMESTER OLIGOHYDRAMNIOSBY TRANSABDOMINAL ROUTE 1700 CASESFETAL DEVELOPMENT AND PREGNANCYFIVE YEARS OF INDIAN EXPERIENCESGLYCINE CLEAVAGE ENZYME AND /OFIN THE EVALUATION OF SEVEREIS PREFERRED TO EXCLUSIVEMOSAICISM CHORION CONFINED ORMOSAICISM FOR TRISOMY 8 ANDPRECEDING MULTI FETAL PREGNANCYRESULT /FEATURES AND A NORMAL
CYCLE /INHERITED DEFECT OF THE KREBSAND IN GENE EXPRESSION /THE CELLDEPENDENT DNA REPAIR DEFICIENCYDEPENDENT EXPRESSION OF THEKINETICS AND X RAY INDUCED /CELLREGULATED PROTEIN KINASE /A CELL
CYCLIZATION OF RANDOM PRIMINGCYCLOBUTANE PYRIMIDINE DIMER FORMATIONCYCLOPHOSPHAWDE IN TURKISH PATIENTSCYP17 GENE CAUSES 17A HYDROXYLASE /THECYP2D6 GENOTYPES ASSOCIATED WITH
PHENOTYPE ASSIGNMENT BYPOLYMORPHISM /GENETICS OF THE
CYP2DPS ON CHROMOSOME 22 WITH /LOCUSCYSTATHONNE B SYNTHASE DEFICIENCY
B SYNTHASE RAPID METHODCYSTATIN C AMYLOID ANGIOPATHY
C AND OTHER FAMILY 2CYSTATINS MAP TO TWO DIFFERENT LOCI /2CYSTEINE AND PRIMARY BILIARY CIRRHOSIS
FOR GLYCINE SUBSTITUTION ATCYSTIC FIBROSIS /A DIAGNOSIS OF
FIBROSIS /ELEVATED INCIDENCE OFFIBROSIS /GENETICS ANDFIBROSIS /NOT ASSOCIATED WITHFIBROSIS /PRENATAL DIAGNOSIS OFFIBROSIS /SCREENING FORFIBROSIS /SCREENING FORFIBROSIS [TO HEMOPHILIA A ANDFIBROSIS /WITH REFERENCE TOFIBROSIS ALLELES /IN BRAZILIANFIBROSIS AMONG PREGNANT WOMEN
547
1727155623322754150822501447840
23581673166520796
28451827250417912707
281624122813931278474121215751029501
2476153112212543160816382809710
1761902176210961762252813536486466411823222941812341262
61127811281254112
125111381256119512751641115012539141147563115211301231120212761456447409807
258415312128251425405381045551541S9320352300232310262183218354253411822840
6887
100425118422525273228631848
Permuted Title Index
FIBROSIS AND A 1 ANTITRYPSINFIBROSIS CARRIER FREQUENCY INFIBROSIS CARRIER TESTINGFIBROSIS CD508 MUTATION FROMFIBROSIS CENTERS /SERVICES BYFIBROSIS CFTR AND CHLORIDEFIBROSIS EXPERIENCES FROM A /OFFIBROSIS FAMILIES /13 NORWEGIANFIBROSIS FAMILIES /CHICAGO AREAFIBROSIS GENE /FUNCTION OF THEFIBROSIS GENE /WITHIN THEFIBROSIS GENE CARRIERS /OFFIBROSIS GENE FROM HUMAN /THEFIBROSIS GENE IN BASHKIR ITHEFIBROSIS GENE IN JEWISH ANDFIBROSIS GENE MUTATIONS /OFFIBROSIS GENE MUTATIONS INFIBROSIS GENOTYPING BY DIRECTFIBROSIS IN A NEWBORN /OFFIBROSIS IN LENINGRAD /OFFIBROSIS IN NATIVE AMERICANSFIBROSIS IN THE CLINICAL /OFFIBROSIS IN U.S.A COUPLES /FORFIBROSIS LOCUS /GENE AND THEFIBROSIS MICRODELETION /F508FIBROSIS MUTATION G542X INFIBROSIS MUTATIONS /FOUR COMMONFIBROSIS MUTATIONS /THREE NOVELFIBROSIS MUTATIONS AMONG /OFFIBROSIS MUTATIONS BY CHEMICALFIBROSIS MUTATIONS BY MEANS OFFIBROSIS MUTATIONS IN FAMILIESFIBROSIS MUTATIONS IN HIGH ANDFIBROSIS MUTATIONS IN ITALYFIBROSIS MUTATIONS IN SPAIN /OFFIBROSIS MUTATIONS IN TORONTOFIBROSIS MUTATIONS USINGFIBROSIS MUTATIONS USING AFIBROSIS MUTATIONS USING PCRFIBROSIS PATIENTS /IN ITALIANFIBROSIS PATIENTS HAVEFIBROSIS PATIENTS IN FRANCE /OFHYGROMA /POSTERIOR NUCHALHYGROMA 23 CASES /DIAGNOSIS OFHYGROMA BY PRENATAL STUDIES /OFHYGROMA WITH A DE NOVO /AND
CYSTINE BINDING PROTEIN OF E COLI /OFCYSTINURIA PHENOTYPES /BETWEENCYSTS INDICATIVE OF TRISOMY 18 /PLEXUSCYTOCHEMISTRY OF PEROXISOMES /ANDCYTOCHROME B MUTATIONS ASSOCIATED /DNA
P 450 DEBRISOQUINE LOCUSP450 GENES APPLICATION IN
CYTOGENETIC ABERRATION IN LYMPHOCYTESABNORMALITIES /INABNORMALITIES AND ABSENCEABNORMALITIES DIAGNOSEDABNORMALmES IN A RAREABNORMALITY /OF FETALABNORMALITY ASSOCIATEDABNORMALITY IN PATIENTSALTERATIONS IN SIXANALYSES OF INTERPHASEANALYSIS AND IN SITUANALYSIS OF ALPHAANALYSIS OF CHROMOSOMEANALYSIS OF CVS CULTUREANALYSIS OF TWO NEWAND DNA PROBES ANALYSISAND FLUORESCENCE IN SITUAND GENETIC LINKAGE MAPSAND IMMUNOPHENOTYPICAND IN SITU HYBRIDIZATIONAND MOLECULARAND MOLECULAR ANALYSES OFAND MOLECULAR ANALYSIS INAND MOLECULAR ANALYSIS OFAND MOLECULAR ANALYSIS OFAND MOLECULAR DELINEATIONAND MOLECULAR EVALUATIONAND MOLECULAR GENETICAND MOLECULAR GENETICAND MOLECULAR IN SITUAND MOLECULAR STUDIES INAND MOLECULAR STUDIES OFAND MOLECULAR STUDIES OFAND MOLECULAR STUDIES ONANOMALIES IN FETOBONE MARROW FINDINGS INCHARACTERIZATION OFCHARACTERIZATION OF ACHARACTERIZATION OF ACHARACTERIZATION OF A NEWCLASSIFICATION OFCLASSIFICATION OF RENALCONFIRMATION USINGCONSIDERATIONS IN WOMENDATA ON 200 U.S.ADIAGNOSIS OF THE FRAGILEEVALUATION OF 500 CASESEVALUATION OF A KINDREDEVALUATION OF COEXISTENTEVIDENCE FOR A CELL CYCLEEVIDENCE FOR ENHANCEDFINDINGS /PATHOLOGIES
S911006183612101769S511030110718292418100918302612231725512798106
1840110227412676111318412883109222451047231123442814184928409701078107422611106993997985
27984637041142116893844846212801299732035254711362431325124813651129135311371319163515811729170412781383107913772124134516836231713154913821641147014581380167117031465
57916167511611309162813641662137813111384165012011381125912321459115480712041308
FINDINGS ASSOCIATED WITHFINDINGS BY FLUORESCENCEFINDINGS IN HUMAN SPERMHETEROGENEITY IN T(11 ;19)IDENTIFICATION OF HUMANIDENTIFICATION OF PARTIALINVESTIGATION OF 115 MALEINVESTIGATION OF COUPLESINVESTIGATIONS IN THEMARKER FOR ALZHEIMERMODEL /ORIGIN OF MAN AOBSERVATIONS ON EIGHT /ANDPHYSICAL AND CLASSICALPROFICIENCY TESTING INPROFILE OF UTERINEPROFILES IN HUMAN ORALRESPONSE OF BLOODRESULTS /OR UNCERTAINSTUDIES IN A HIGH RISKSTUDIES IN PATIENTS WITHSTUDIES IN PATIENTS WITHSTUDIES OF HUMAN OOCYTESTUDIES OF MALIGNANTSTUDIES OF WAARDENBURGSTUDIES OF ZELLWEGER CELLSTUDY /HYPOXYGENATION ASTUDY /IN VIVO HYPEROXIA ASTUDY IN PRIMARY GASTRICSTUDY OF 1575 GENETICSTUDY OF 56 CASES OFSTUDY OF A 21P+ VARIANTSTUDY OF MICROINJECTEDSTUDY OF SHORT ARMSTUDY ON THE CASE WITHTECHNIQUE FOR GENOME /NEWTECHNIQUES AND /BYTECHNIQUES AND IN SITUTEST OF BYELORUSSIAN
CYTOGENETICAL AND MOLECULAR /NEWDNA REPARATIONAL AND
CYTOGENETICALLY AND MOLECULARLYNORMAL PARENTS /21 INSTABLE IN CULTURE AND
CYTOGENETICS /ANALYZED BY MOLECULAR/AND FUNCTIONAL/BY MOLECULAR/MAPPING AND DIAGNOSTICA STRATEGY FOR MAPPINGAN OVERVIEW /CANCERAND BEHAVIOR IN 32AND MOLECULAR STUDIES INAND MOLECULAR STUDIES INDEMONSTRATES /INTERPHASEEVALUATION OF 4800 CVSFOR MONITORING PATIENTSIMPROVED PRENATALIN CHILDHOOD ACUTEIN HUMAN BREAST CANCERIN THE DOMINICAN REPUBLICLABORATORY PERIMETERSOF 22 SQUAMOUS CELLOF 226 BONE LESIONSOF BONE AND SOFT TISSUEOF GENE AMPLIFICATIONOF HUMAN SOLID TUMORSOF LOW GRADE GLIOMASVERSUS PHENOTYPIC
CYTOKINE THERAPY /STIMULATING FACTORCYTOKINES /CELLS USING RECOMBINANTCYTOMEGALOVIRUS DNA AS A PLACENTALCYTOMETRIC DIAGNOSIS OF CLINICALLYCYTOMETRY /BIVARIATE BRDU HOECHST FLOW
AND CONFIRMATION BY PCRAND FLUORESCENCE IN SITU
CYTONECTIN /CHARACTERIZATION OFCYTOPLASMIC ANTIBODIES /ANTINEUTROPHILCYTOSINE IN LYMPHOCYTES OFCYTOSOUC ALDEHYDE DEHYDROGENASE /OFCYTOSTATIC TREATMENT /DURING THE
15409443621323172116861525140027967452620802168018041335583
26952161410132814891240219105214351401141812997601149144712581537154416371667145528061615741167012191393185792
2641183
2089367131012291419131811471607111
132021714601610138513053712458372129816916192468113314261609109183
22492773138824101344
D
D AMINOTRANSFERASE GENE OF PATIENTSAMINOTRANSFERASE RELATED SEQUENCESBINDING PROTEIN GROUP SPECIFICCELLS BY MICRO CELLMEDIATED /GROUPDEFICIENCY /OF PROLIDASE (PEPTIDASEDEPENDENCY TYPE IN NORTHEASTERNDEPENDENT RICKETS IN A RURAL AREAG GROUP CHROMOSOMES /IN HUMANGENE TO THE REGION 11Q22.3 23.1 /ATMELANOGASTER GENE PRODUCT CC /OF THERESISTANT RICKETS TOTAL NITAMIN
D10S97 TIGHTLY LINKED TO MULTIPLED1153B5SMY/D113S5 ON CHROMOSOME /AND011S424 AND D11S385/STMY/D11S35 OND13S31 /LOCUS AND THE CLOSE MARKER
TIGHTLY LINKED TO THE WILSOND14S13 VNTR LOCI AMONG ASIAN BLACK015S10 IN PRADER WILLI SYNDROME /LOCUSD166S5 D17S79 AND D20S15 VNTR LOCI
2519215322622301987269872515372301240089119561967196719262373285222192836
D17S79 AND D20S15 VNTR LOCI AMONGD19S63 SHOWS LINKAGE DISEQUILIBRIUMD1S7 D2S44 AND D14S13 VNTR LOCI AMONGDIS80 DETECTED BY THE PCR NNTR LOCUS02 RECEPTOR AS A MODIFYING GENE IN
RECEPTOR DNA POLYMORPHISM RULEDRECEPTOR LOCUS STUDIES OF /DOPAMINE
020S15 VNTR LOCI AMONG ASIAN BLACKD21S1 REGION ON CHROMOSOME 21 STUDY022S68 IN LINKAGE STUDIES USINGD2S44 AND D14S13 VNTR LOCI AMONG /D1S7D3 RECEPTOR GENE (VDR) ARE04 DOPAMINE RECEPTOR MAPS TO DISTALD04139 D16S85 D17S79 AND D20S15 VNTR04175 IN ANCIENT PERUVIAN MUMMIESD4843 /SYNDROME 2MB DISTAL TOD5S39 IN FRENCH CANADIAN FAMILIES /TO68S109 IN ITALY /SCA1 AND D6o89 ANDD0689 AND D6S109 IN ITALY /SCA1 AND
ON 6P IN A FAMILY WHERE CLOSEDAMAGE /PIGMENTOSUM CELLS AGAINST DNA
AND REPAIR IN THE DOMAIN OFIN CELLS FROM DOWN SYNDROMEIN CHRONIC ALCOHOLICS /LIVERIN CHRONIC HEART AND BRAIN /DNAIN MALE MICE /CAN CAUSE MEIOTICINDUCED BY A REPLICATION
DAMAGING FACTORS IN ETIOLOGY OFDANDY WALKER MALFORMATION IN A FAMILYDANISH FAMILIES /MARKERS IN FOURTEENDATA /ONSET DISTRIBUTIONS FROM FAMILY
AND MUSCLE BIOPSY CONTRACTUREAT THE X LINKED HYDROCEPHALUSBANK AND CELL REPOSITORY /ITALYFOR ANGIOGENIN AND LIVER /LINKAGEFOR THE LONG QT(ROMANO WARD)FROM A TUMOR REGISTRY /USINGFROM THE GERMAN COLLOBORATIVEOBTAINED BY PRENATAL DIAGNOSTICSON 200 U.S.A VETERANS WITHON SEIZURE DISORDERS /HISTORYTHE ENCYCLOPEDIA OF THE MOUSEVALIDATE THE USE OF DNA TYPING
DATABASE /THE LONDON DYSMORPHOLOGYFOR A GENETICS RESEARCHOF CALL MANAGEMENT
DAVID SYNDROME (PSEUDOLEPRECHAUNISM)DE LA TOURETTE SYNDROME /OF GILLES
LA TOURETTE SYNDROME SEGREGATIONLANGE SYNDROME /CASE OF BRACHMANNNOVO APPARENTLY BALANCED AUTOSOMALNOVO BALANCED CHROMOSOMENOVO COMPLEX FOUR WAY TRANSLOCATIONNOVO DUPLICATION OF THE LONG ARMNOVO DUPLICATIONS USING CHROMOSOMENOVO MINUTE MARKER CHROMOSOME BY /ANOVO MUTATION IN MAN /ORIGIN OFNOVO MUTATIONS IN UNSELECTED /FORNOVO POINT MUTATION CAUSING HUMANNOVO RECIPROCAL TRANSLOCATIONNOVO T(14Q21Q) BY FLUORESCENT IN /ANOVO T(22;22)(P1 1QI1) /WITH ANOVO TRANSLOCATION /TRISOMY 7Q IN ANOVO TRANSLOCATION BETWEENNOVO TYR206CYS MUTATION IN THENOVO UNBALANCED TRANSLOCATION /A
DEAF ADULTS MEDICAL AND CULTURAL /FORCHILDREN ATTENDING SPECIALMUTES HELD AMONG 87,521 HAIKOU
DEAFNESS /GENETICS OF X LINKED/IMPLICATIONS OF GENETIC/IN THE STUDY OF HEREDITARY/LINKAGE STUDY FOR PRELINGUAL/STUDIES OF EARLY ONSETAND CHOROIDEREMIA MOLECULARAND CONGENITAL ABSENCE OFIN A FEMALE WITHIN AN INSTITUTIONALIZED /OFIN CAMPOMELIC DYSPLASIA OFON NEWFOUNDLAND'S SOUTH COASTSYNDROME /FACIES MIXED
DEAMINASE /ON HUMAN ERYTHROCYTE AMPDEFICIENCY IN CAUCASIANSGENE IN SWEDISH PATIENTSGENE WITH SCHIZOPHRENIAIN HUMAN HEMATOPOIETIC
DEAMPUFICATION /AMPLIFICATION ANDDEATH /OF MACERATED INTRAUTERINE FETAL
IN NEUROFIBROMATOSIS 1 PATIENTSSYNDROME AN ANALYSIS OF POSTSYNDROME AND ITS RELATIONSHIPSYNDROME PATIENTS /SUDDEN INFANT
DEATHS /RISK FAMILIES AVOID EARLY CHDDESRISOQUINE HYDROXYLATION (CYP2D6)
LOCUS (CYP2DP8) ON /P 450DEBRISOOUINE/SPARTEINE IN JAPANESE /OFDECALVANS /FOLLICULARIS SPINULOSADEEP ORBITS SHORT PHILTRUM SYNDROMEDEFECT /AND SEVERE OSSIFICATION
/AS A DEVELOPMENTAL FIELD/ASSOCIATION WITH DNA REPAIRAN UNDERRECOGNIZED INBORNBY GENE TRANSFER MOLECULARFAMILIES /RISK IN LEFT FLOWIN B THAL GENE DIRECT /SPLICING
548
283618752852231397910941076283614301901285218701903283626171727201819371937205225392570845504671
1371168112886891923266119111959265419792197600126412681381272318982506134
20791793711192427661496148884
1547167016771700406
28072375132116349381686150297214702823
27772425S8
199922
10867881452276182372988349148910442011248424581149830975
27482377164541
20355511985716650889816439227426502305
Permuted Title Index
IN BLOOM SYNDROME /DNA LIGASEIN FAMILIAL DILATED /THE GENEIN FANCONI ANEMIA AND ITSIN HOMOCYSTINURIA DUE TOIN SALLA DISEASE A FREE SIALICIN SIBLINGS WITH THE ALAGILLEIN THE INTRACELLULAR TRANSPORTIN TYPE COLLAGEN FROM TWOIN X LINKED SPINAL AND BULBARIN XP A IDENTIFICATION OFIN ZELLWEGER SYNDROME /ASSEMBLYOF FANCONI ANEMIA CELLS /REPAIROF THE KREBS CYCLE /INHERITEDON THE X CHROMOSOME /GENETICWITH ANTERIOR MENINGOCELE
DEFECTS /ABNORMALITIES CAUSING BIRTH/ASSOCIATED TRACHEOBRONCHIAL/HCG AND FETAL VENTRAL WALL/HUMAN RED/GREEN COLOR VISION/NEURAL TUBE OR VENTRAL WALL/OF MULTIPLE CONGENITAL/OF THE SEARCH FOR MOLECULARANAL ATRESIA CARDIAC DEFECTSAND DOWN SYNDROME /NEURAL TUBEAND PHENOTYPIC CORRELATIONSAND RADIAL DYSPLASIAAND RADIAL LIMB DEFECTS WITHAT MULTIPLE LOCI ONE OF WHICHCAUSING /GENEFOR SOCIETAL DECISION MAKINGIN CHILE /OF SINGLE GENEIN KARNATAKA INDIA EVIDENCEIN LATIN AMERICA /OF BIRTHIN SPONTANEOUS ABORTIONSIN THE HUMAN CHONDRODYSPLASIASIN TRISOMY 8 MOSAICISM /HEARTIN XERODERMA PIGMENTOSUM ANDINCIDENCE IN FETUSES ANDOF 37,954 PERINATAL INFANTSOF FACTOR IX IN 64 HEMOPHILIAPROSPECTS FOR SCREENINGRATES IN JEFFERSON COUNTYREGISTRY IN INDIA PRELIMINARYTRACHEO OESOPHAGEAL FISTULAEUNDERLYING CHYLOMICRONEMIAWITH HYDROCEPHALUS /LIMB
DEFERENS /BILATERAL ABSENCE OF THE VASDEFICIENCIES AMONG VIETNAMESE STUDENTS
IN A LARGE ANIMAL MODELIN MAN /CHAIN ENZYMEMOLECULAR BIOLOGY AND
DEFICIENCY /ACYL COA DEHYDROGENASE/ACYL COA DEHYDROGENASE/ACYL COA DEHYDROGENASE/ACYL COA DEHYDROGENASE/ACYL COA DEHYDROGENASE/CAUSES 17A HYDROXYLASE/CYSTATHIONINE B SYNTHASE/DIETOTHERAPY IN FUMARASE/FOR RED GREEN COLOR VISION/HABITUS AND LAMININ/IN BETA GALACTOSIDASE/IN RELATION TO ITS/IN THE CONGENITAL LACTASE/LEADING TO ARYLSULFATASE A/METHYLMALONYL COA MUTASE/MODEL FOR A HUMAN COFACTOR/MUTATIONAL BASIS OF APRT/OF COMPLEX GLYCEROL KINASE/OF HUMAN B GALACTOSIDASE/OF PROLIDASE (PEPTIDASE D)/PALMITOYLTRANSFERASE/SEPARATE PROBANDS WITH LPL/TO PHOSPHORYLASE B KINASENIl (BETA GLUCURONIDASE/WITH PROFOUND BIOTINIDASEA COMPARISON OF CHILDRENA POSSIBLE CAUSE OF FETALA RARE INHERITED DEFECT OFADENOVIRUS MEDIATED DIRECTAND CANCER /THERAPY FOR ADAAND ITS DISTRIBUTION INAND SUDDEN INFANT DEATHAND WHITE MATTER DISEASE AASSOCIATED WITH NEONATAL /BBIOCHEMICAL AND CLINICALEVIDENCE FOR A GENEFROM CHILDREN DYINGFROM SUDDEN INFANT DEATHHETEROZYGOSITYIDENTIFICATION OF NATURALIDENTIFIED BY NEWBORNIN A TURKISH BOY BORN TOIN ALDEHYDE DEHYDROGENASEIN CAUCASIANS /DEAMINASEIN EUROPE /DEHYDROGENASEIS A POINT MUTATIONNEONATES /HAVING G 6 PDOF A CHINESE BY THE PCRPARTIAL HYPOTHALAMICPLASMA AND URINE ORGANICPOSSIBLE DIAGNOSTIC /REPAIRSYNDROME /ANHYDRASE IITHERMOLABILITY OF RESIDUALTWO NEW CASES AND [TYPE 2
2951062296
2300201353346649695
2314505
2275447
229319531279721
182624191137183748
816117S7381781679
23561813265918452722S7547
1499293
26992780658262
2671776816470816106886
2478503264265475498
2277231610452300562
2231106110752414509285511
23121091687284987
2382470846
24735104681158447S91S912735975645536487
2375111923771237193
1832891
271648919551817782324645263807
1020501535
WITH MULTIPLEWITH THE PREMATURE /A
DEFICIT HYPERACTIVITY DISORDERDEFORMATION PATELLA SUBLUXATION ANDDEFORMING OSTEOGENESIS IMPERFECTADEFORMITY GENE IN LIMB AND KIDNEY
HYPOTONIA AND SEVERE MENTALDEGENERATION /WITH TAPETOCHOROIDAL
OF BRAIN CANAVAN DISEASEOF THE RETINA AND GROWTHTOXP1i REGION/CONE
DEGREE FAMILY MEMBERS OF AUTISTICOF POLYMORPHISM OF THE HUMANOF SEQUENCE SIMILARITY TO THERELATIVES AND UNRELATED /FIRSTRELATIVES OF EPILEPTIC PROBANDSRELATIVES OF INDEX CASES ANRELATIVES OF PATIENTS WITH
DEHYDRATASE HAS TWO TRANSCRIPTIONALDEHYDROGENASE /ENCODING GLUTARYL COA
/OF CYTOSOLIC ALDEHYDE2 ISOZYME DETERMINE THEACTIVITY AND /l (NADHACTIVITY ANTIGEN ANDDEFICIENCIES MOLECULARDEFICIENCY /ACYL COADEFICIENCY /ACYL COADEFICIENCY /ACYL COADEFICIENCY /ACYL COADEFICIENCY /ACYL COADEFICIENCY A RAREDEFICIENCY AND SUDDENDEFICIENCY FROM /COADEFICIENCY FROM SUDDENDEFICIENCY IN EUROPEDEFICIENCY OF A CHINESEDEFICIENCY PLASMA ANDDEFICIENCY WITHElA SUBUNITS /PYRUVATEGENE /STOMACH ALDEHYDEGENE ADH5 AND RELATEDLOCUS /PHOSPHOGLUCONATEMULTIGENE FAMILY AS AMUTANT ALLELE /ACYL COARESPONSIBLE FOR /COA
DEHYDROGENATION DISORDER SUBSTRATEDEL (13)(Q32.3Q33.2) WITH POTENTIAL
(4) (P14P16) /IN AN INFANT WITH(6) /PRENATAL DIAGNOSIS OF INV3P23P24.12 /IN A CHILD WITH 46,XY
DEL(17 (P11.2)) DELINEATION OF THEDEL(21X021Q22.1) /210 DELETIONDEL(5) IN ONE EXTENDED FAMILY /AND RECDEL(X) (P22.2) /IN A GIRL WITHDEL11Pi5 IN A FAMILY /RECURRENCE OFDELAYED PUBERTY /SHORT STATURE ANDDELETION (15CEN QLL.2) DUE TO A 45,X,
(20Q) MAY NOT BE ASSOCIATED/BOTH SYNDROMES WITH XP22.3/FOR CHROMOSOME 5 CRI DU CHAT/PATIENTS WITH A 10KB/SYNDROME ASSOCIATION WITH 80/WITH A CHROMOSOME 20P3P25 SYNDROME /OF THEANALYSIS /MOLECULARANALYSIS IN THE 3P SYNDROMEANALYSIS IN X LINKEDAND 200 TRISOMY UNBALANCEDAND IN SITU MAPPING OF THEAND RECURRENT POINT /NOVELASSOCIATED WITH AN INVERTEDCAUSING WOLF HIRSCHHORNCHARACTERIZATION AND /FORDEL(21)(021022.1) /210DETECTED PRENATALLY BY /4PHOT SPOT /THE DYSTROPHIN GENEIDENTIFIED IN ONE MILDLY /20IN A PATIENT WITH THEIN BLOOD MITOCHONDRIAL DNAIN DUCHENNE MUSCULAR /OFIN FRENCH CANADIANS SEARCHIN GYRATE ATROPHY /IN AN EXONIN LUNG CANCER WITH A /OFIN MITOCHONDRIAL DNA LEADINGIN PATIENTS WITH VON /DNAIN THE DYSTROPHIN GENE OFIN THE LDL RECEPTOR GENE ONINTERVAL PARENTAL ORIGIN ANDLEADING TO B THALASSEMIA BYMAP AND AZF LOCUS THE USE OFMUTANTS /FROM GLOBIN GENEMUTATION IN AN EYE LENSOF 4P16 BY FLUORESCENT INOF 60 IN EIGHT PRIMARY LUNGOF 60 IS INVOLVED INOF 70 IN SQUAMOUS CELLOF 8P23.1 MINIMAL DYSMORPHICOF CHROMATIN MATERIAL /OROF CHROMOSOME 22 IN /PARTIALOF EXON 8 AND CARRIERS IN /AOF IMMUNOGLOBULIN (IGHG1)OF THE CEN D21S1 REGION ON /AOF THE LONG ARM OFOF THE LONG ARM OF /TERMINALOF THE PHENYLALANINE /FRAME
482111867377062626687011
573769703625
23602297493877
2710139724092322241027165134592642654754982277231644797511192377195
2324263482241623042284192826199754904976478041503827170214651453774
157216531454136814481176268215071664106610867851106749
21769941585148817181465166123571484171199511242662280222411151028235151517021049910337
22681516133625981394150016192585690
2815143015121481449
OF THE PLP GENE IN A FAMILYOF VON WILLEBRAND FACTOROF YQ IN A PATIENT WITHPATTERNS IN FORTY GREEKPRONE REGION OF DYSTROPHIN /ARESULTING FROM A DE NOVO /60SCREENING METHOD FOR /INITIALSYNDROME /CONTIGUOUS GENESYNDROME /INTERSTITIAL 180XQ24 IN A WOMAN WITH
DELETIONAL ALPHA THALASSEMIA IN THEREGION FOR THE PRADER
DELETIONS (1)(P36.3) AND THE/DETECT (SEA) DOUBLE ALPHA/OF SINGLE ALPHA GLOBIN GENE/XP22.31Q THE ROLE OF HIGHAND CRYPTIC TRANSLOCATIONSAND INTRAGENIC RFLPS BY PCRAND MUTATIONS OF THE GENEAND REARRANGEMENTS /4PDETECTED BY CDNA PROBES ANDHAVE SIMILAR PHENOTYPES /13IN CHINESE DUCHENNEIN NEGATIVE /DYSTROPHYIN NEUROBLASTOMA TUMORS /LPIN THE CFTR GENE /OF LARGEIN THE DYSTROPHIN GENE ANDIN THE DYSTROPHIN GENE OF AOF BAND 1P36 EMERGENCE OFOF CHROMOSOME 14 /TERMINALOF CHROMOSOMES 20 AND 21 INOR INSERTIONS IN THE /LARGEUSING PCR BASED /OF 4PWITHIN THE DYSTROPHIN GENE
DEUBERATE HETERODUPLEX FORMATION ANDDEUMIITATION OF THE REGION OF COMMONDELTA /IN CATALONIANS FROM THE EBRO
/THREE PATIENTS WITH 1677F 508 FREQUENCY IN EUROPEAN /OF
DELTAF508 IN EUROPE /OF G551D ANDDEMENTIA (MEMBRANOUS LIPODYSTROPHY
AND PARKINSON DISEASEIN ADULT TWINS /AND SENILE
DEMES BASED ON BLOOD GROUPS ANDDEMETHYLATION INDUCED REACTIVATION OFDEMISE /FINDINGS AFTER FETALDEMOGRAPHIC FINDINGS IN CHROMOSOME
FINDINGS IN MONOGENIC ANDDEMOGRAPHY OF THE MULTIETHNIC /GENETICDENATURANT GEL ELECTROPHORESIS
GEL ELECTROPHORESISGEL ELECTROPHORESIS
DENATURING GRADIENT ELECTROPHORESISGRADIENT GELGRADIENT GEL /BYGRADIENT GEL /CFTR GENE BYGRADIENT GEL /GC CLAMPEDGRADIENT GEL /GC CLAMPEDGRADIENT GEL /GENE BYGRADIENT GEL /HHAI RFLPS BYGRADIENT GEL /USE OFGRADIENT GEL /USINGGRADIENT GEL /USINGGRADIENT GEL /USING PCRGRADIENT GEL NARIANTS BYGRADIENT GEL BLOTS /USING
DENDROGRAMS AND GENETIC STRUCTUREDENMARK /AMONG PREGNANT WOMEN IN
1970 1989 A TWENTY YEAR /INDENOVO TRANSLOCATION /DETECTION OF ADENSITOMETRY OF SOUTHERN BLOT /BYDENSITY AND CONCENTRATION IN PLASMA
GRADIENT SEPARATED AMNIOCYTESGRIDDING OF GENOMIC LIBRARIES
DENTAL ANOMALIES IN AFFECTED ANDDEOXYADENYLATE ANTIBODIES IN THE /OFDEFARTMENT AT ROBERT REID CABRAL
OF A SECOND LEVEL GENERALDEPENDENCE IN ANALYSIS OF FAMILIAL
OF FETAL CHROMOSOMAL /AGEOF GUSTATORY HABITS /AGE
DEPENDENCY TYPE I IN NORTHEASTERN /DDEPENDENT AND INDEPENDENT DNA
DIABETES MELLITUS /INSULINDIABETES MELLITUS /INSULINDIABETES MELLITUS RISK ANDIABETICS /IN INSULINDNA REPAIR DEFICIENCY /CYCLEENZYMES AND RESPONSES OFEXPRESSION OF THE /CYCLEON DNA REPLICATION /AREPARAMETERS /AND CALCIUMPENETRANCES OF AUTOSOMALRICKETS IN A RURAL AREA OFTRANSCRIPTION OF THE
DEPLETED CHROMOSOMES /ON HISTONEDEPRESSION AND BEHAVIORAL CHANGES INDEPRESSIVE ILLNESS WITH MARKERS FROMDEREGULATED IN LYMPHOID NEOPLASIAS /ISDERIVATIVE CHROMOSOME /OF AN INACTIVE
X;9 CHROMOSOME /FROM ADERIVATIVES OF THE RHOMBENCEPHALIC /OFDERMATOGLYPHIC LIP PRINT AND GENETICDERMATOGLYPHICS AND ABO BLOOD GROUPS
549
1083444
167822929781470989144314251420287318601541183997655
150516731040591
16511098111610878105841014100110801538172614072348961
2346279226072674962174727038732704
68284224521691267726652847218
28032813279227934639851097205925172652588437100810572073206928641848359953586
2434445
212581221437331789264312682874269824122663271127082670807212725841375445
2034725
24561633554
203822516591555924700
1851
Permuted Title Index
IN FEMALES WITHON TEN AND HAND /ON
DERSIMIONIAN LAIRD COCHRAN METHODS OFDESMOSOMAL AND INTERMEDIATE FILAMENTDETACHMENTS IN THE SMITH MAGENISDETERMINATIONS OF VNTR MARKERS /WEIGHT
PRENATAL CYTOGENETICSDETRIMENTAL RECESSIVES IN HUMAN /OFDEVELOPED FROM CLONED FRAGMENTS OF
NATIONS ITO GENETIC SERVICESDEVELOPMENT /AND EMBRYONIC GROWTH AND
/AND GENETICS OF ERYTHROID/B GLOBIN SWITCHING DURING/BINDING PROTEINS DURING/CRANIOFACIAL/FOR CURRICULUM/GENES IN MAMMALIAN/IN NORMAL PULMONARY/PRODUCT CC ESSENTIAL FOR/RETINAL STRUCTURE AND/SPECIFICATION AND CNS/THE STUDY OF EMBRYO FETALAND APPLICATION OF AAND DISEASE /HOMEOSTASISAND DISTRIBUTION OFAND PREGNANCY OUTCOME TWOAND TYPING OF /FOR THEBY NONRADIOACTIVE IN SITUIN TRISOMY 18 AND TRISOMYOF A HUMAN VIRAL BASEDOF A RELATIONAL DATABASEOF AN INFORMATION SYSTEMOF GENETIC SERVICES IN AOF GENETICS SERVICES FROMOF HUMAN TWINS /GROWTH ANDOF LABORATORY GUIDELINESOF MULTIPLEXOF POLYMORPHIC DNA PROBESOF SYNTHETIC MOLECULARLYOF THE HUMAN SKELETON
DEVELOPMENTAL ANOMALIES IN HEMIFACIALCONTROL OF HUMAN FETALDISORDER /AS PERVASIVEDYSLEXIA /GENETICS OFFIELD DEFECT /AS AOUTCOME IN INFANTS WITHOUTCOME OFREGULATION OF GENES /THERETARDATION AND ASIGNIFICANCE AND
DEVELOPMENTS IN REGRESSIVE MODELSDEXTROMETHORPHAN METABOLISM AND THEDF508 MUTATION IN 13 NORWEGIAN CYSTICDIABETES /HLA LINKED GENES IN TYPE I
MELLITUS /GENE IN TYPE IIMELLITUS /INSULIN DEPENDENTMELLITUS AND CEREBELLARMELLITUS AS A HUMAN TERATOGENMELLITUS RHEUMATOIDMELLITUS RISK AN /DEPENDENTOF THE YOUNG TO POLYMORPHIC
DIABETIC EMBRYOPATHY WITH ADIABETICS /IN INSULIN DEPENDENTDIAGNOSES /ABNORMALITY IN PRENATALDIAGNOSIS /A PREGNANCY AFTER PRENATAL
/AMNIOCENTESIS FOR PRENATAL/AND ACHE TESTS IN PRENATAL/AND PREIMPLANTATION GENETIC/AND SUCCESSFUL PRENATAL/APPLICATION TO PRENATAL/CONCEPT AS A PATHOGENETIC/DYSMORPHOLOGY APPROACHES TO/FOR NONINVASIVE PRENATAL/HYBRIDIZATION IN PRENATAL/IN UTERO FOR PRENATAL/NEW CONCEPTS IN PRENATAL/OF WOMEN WHO HAVE PRENATAL/PSEUDOMOSAICISM IN PRENATAL/STUDY OF HEMOPHILIA A GENEA COMPARATIVE RETROSPECTIVEA COMPARISON OF COMMUNITYA TRUE GENETIC COUNSELINGAFTER AGE 30/PRENATALAFTER CVS (MINISTRY OFAND CHROMOSOME ABNORMALITIESAND GENETIC COUNSELING INAND INCIDENCE AT BIRTH A 20AND ITS IMPACT UPONAND LEARNING ABOUT SYNDROMESAND MANAGEMENT OF /PRENATALAND MANAGEMENT OF WILSONAND MSAFP LEVELS IN EARLYAND PERINATAL MANIFESTATIONAND PRENATAL DIAGNOSIS OFAND THERAPY OF MUTAT BIRTH /FOR ZYGOSITYBY FLUORESCENCE IN SITUBY MAGNETIC RESONANCECOUNSELING IN NORTH AMERICAEXPERIENCE IN ECUADORFOR HEREDITARY CEREBRAL /DNAFOR TRISOMY 21 AFTERFREOUENCY CLINICAL /PRENATALIN DENMARK 1970 1989 A
IN DUCHENNE MUSCULAR
5856361293224314432524169128412122
371296S71118A120S7217624339272400
10311908552453178091453
2230214
2529207918111808S302721180710472501200930842
2240748199788976817502437773241S582331107S32722
2711502674
26632708
74174826701159176612261165107535111485913860
1719114S53175316261050117717811162114612347571735147526861332749479261148558532S8517248993891625964182584359978
IN FINNISH DUCHENNE ANDIN HONG KONG /AND PRENATALIN PATIENTS WITH CONGENITALIN POLAND /OF PRENATALIN SOUTH CHINA /AND PRENATALIN THE FEDERAL REPUBLIC OFIN THE MEDICAL GENETICSMAY MODIFY REPORTEDOF 1303 AMNIOCENTESESOF 3 METHYLGLUTACONICOF 46,XX/46,XY CHIMERISMOF A GENETIC DISEASE OROF A RAPIDLY PROGRESSIVEOF A RINGCHROMOSOME (20)OF ALPHA THALASSEMIA BYOF AN ISOCHROMOSOME 18POF ANEUPLOIDY IN NEWBORNSOF APPLE PEEL BOWEL SYNDROMEOF AUTOSOMAL DOMINANT /THEOF BETA THALASSEMIAOF BILATERAL RENAL AGENESISOF CHROMOSOMAL ANOMALIES AOF CHROMOSOMAL DISORDERSOF CHROMOSOMAL MOSAICISMSOF CHROMOSOME ABNORMALITIESOF CLINICALLY SUSPECTEDOF COMPLEX CHROMOSOMALOF CONGENITAL ADRENALOF CYSTIC FIBROSISOF CYSTIC FIBROSIS /AOF CYSTIC FIBROSIS /PRENATALOF CYSTIC HYGROMA 23 CASESOF DANDY WALKER /OF PRENATALOF DOWN SYNDROME IN MAINEOF DUCHENNE MUSCULAROF DUCHENNE MUSCULAR /GENEOF DUCHENNE/BECKER MUSCULAROF DYSMORPHOLOGY A CASEOF FAMILIAL ADENOMATOUSOF FAMILIAL ADENOMATOUSOF FANCONI ANEMIA AND /RAPIDOF FETAL CHROMOSOMEOF FRAGILE X SYNDROMEOF FRAGILE X SYNDROME /THEOF FRAGILE X SYNDROME ANDOF FRASER SYNDROME /PRENATALOF FRYN SYNDROME CONGENITALOF GENETIC DISEASEOF GLUTARIC ACIDEMIA TYPE 1OF HUNTINGTON DISEASE /OFOF HYPOCHONDROPLASIAOF INV DEL (6) /PRENATALOF LEBER HEREDITARY OPTICOF LETHAL DISORDERS AIN THEOF LYSOSOMAL STORAGEOF MALIGNANT HYPERTHERMIAOF MEDIUM CHAIN ACYL COAOF MITOCHONDRIAL /GENETICOF MUCOLIPIDOSES II AND IIIOF NEUROFIBROMATOSIS TYPE 1OF NON KETOTIC /PRENATALOF NUMERICAL CHROMOSOMEOF OTO PALATAL DIGITALOF POMPE DISEASE (TYPE IIOF PRADER WILLI SYNDROMEOF PRADER WILLI SYNDROMEOF RECURRENT MECONIUMOF SEX CHROMOSOME /MOLECULAROF SICKLE CELL ANEMIA THEOF SICKLE CELL DISEASE ANDOF SPECIFIC GENETIC /A FIRMOF SPINAL MUSCULAR ATROPHYOF SPONGY DEGENERATION OFOF STROKE DUE TO HEREDITARYOF THE FRAGILE X SYNDROMEOF THE MEIOTIC STAGE OFOF THE PREIMPLANTATIONOF THE SKELETAL DYSPLASIASOF TRIOSE PHOSPHATEOF TRIPLOIDY /IN PRENATALOF WILSON DISEASE IN CHINESEOF X LINKED /FIRST PRENATALOF X LINKED /PRENATALPATIENTS /STUDY OF PRENATALTECHNIQUES AND OUTCOMETHE FIRST FIVE YEARSUSING FETAL CELLS IN THEVALUE OF THE AFP TEST IN
DIAGNOSTIC AND CLINICAL RELEVANCEAPPLICATIONS /SYNDROME ANDASSESSMENT HAS BEEN /YEARSCODING ITS APPLICATIONSCYTOGENETICS /MAPPING ANDDIFFICULTIES /AND EARLYDNA MARKERS FOR THE /OFFEATURE OF ALZHEIMERMARKER FOR NORRIE DISEASEMETHOD FOR FAMILIALPROBLEM OF A BONE Ill THEPROGRAM IN CHINA /PRENATALSERVICES LOCAL IMPACTSERVICES PROVINCIAL IMPACTSYSTEM IN CLINICAL GENETICSTECHNOLOGY /DNATEST FOR
104638869617563911802733117812201217145066612771519112016501636118111101272117917991615911127914261408110810301182100411426891134120711231096723
1051187616091823119819081038652119262
481174589715031073139558
10121119101044274256312839335746551056887106917742504
23122357310261259165412101260126992399012639681752S83116115
18371305377231401838931894807194557893312651801181275051
577
TESTING OF THE SPINALTOOL /A NEW PRENATAL
DIAGNOSTICS AND FUNCTIONAL /MAPPINGFOR MYELIN PROTEOLIPIDOF CYSTIC FIBROSIS IN THEON MATERNAL AGE /PRENATALPOSSIBLE IN THIS FATAL
DIAPHRAGMATIC EVENTRATION A NEW /ANDHERNIA /ASSOCIATION FORHERNIA NOT AMENABLE TO,
DIASTROPHIC DYSPLASIA LOCUS /THEDICENTRIC YP /STUDIES IN DIFFERENTDIET RESPONSIVE PSYCHIATRIC PROBLEMSDIETARY INTAKE COMPONENTS IN TWINSDIETOTHERAPY IN FUMARASE DEFICIENCYDIFFERENTIAL BINDING TO HEPG2 NUCLEAR
DISTRIBUTION OFMATURATION OF SEGREGANTSSEX DEPENDENTTERMINATION OF PRIMER
DIFFERENTIATED LIPOSARCOMA WITH ADIFFERENTIATING GENETICS AND EUGENICSDIFFERENTIATION AND ADMIXTURE AMONG
INDUCED BY RETINOICOF AUTOSOMAL /ASSISTEDOF EMBRYONALOF HUMAN RACESOF PRIMARY ANDOF THE MYOGENIC /AND
DIFFUSION OF HEALTH CARE TECHNOLOGIESDIGEORGE LOCUS ON CHROMOSOME 22 /THE
SYNDROME /CRITICAL REGION INSYNDROME /STUDIES OF
DIGEST LIBRARIES FROM FLOW SORTEDDIGESTION /BY RESTRICTION ENZYME
/ELECTROPHORESIS AFTER NRUI/REVEALED BY TAQI
DIGESTS /PCR COUPLED RESTRICTIONDIGIT IN THE SOUTH AFRICAN POPULATIONDIGITAL ANOMALY SYNDROME WITH
IMAGE ANALYSIS /ANDIMAGE PROCESSING /PROBES BYIMAGING /LABELED PROBES ANDIMAGING MICROSCOPY /WITHSYNDROME TYPE I AND Il /FACIALSYNDROME TYPE II THE /PALATALSYNDROMES /ON THE ORAL FACIALSYNDROMES TO LUMP OR TO SPLIT
DIHYDROPTERDINE REDUCTASE DEFICIENCYDIHYDROPYRIDINE SENSITIVE CALCIUM /OFDIHYDROXYVITAMINE D3 RECEPTOR GENEDILATED CARDIOMYOPATHY /IN FAMILIAL
CARDIOMYOPATHY MOLECULARDINER FORMATION /PYRIMIDINEDIMERIC SUPRACHROMOSOMAL SUBFAMILYDIMETHOATE INDUCED SISTER CHROMATIDDINUCLEOTIDE POLYMORPHISM OF THE
REPEAT AT THE CYTOCHROMEREPEAT POLYMORPHISM INREPEAT POLYMORPHISM IN /AREPEAT POLYMORPHISMS /OFREPEATED SEQUENCES ON /CAREPEATS AS LINKAGE /OFREPEATS IN THE /(CA)N
DINUCLEOTIDES AND GERM LINE MOSAICISMDIPEPTIDASE GENE TO BAND 024 OF /RENALDIPHALLUS AND ASSOCIATED ANOMALIESDIPLEGIA /ATAXIA AND SPASTICDIRECTED FRAMESHIFT MISMATCH REPAIR
INTRAUTERINE GROWTHMUTAGENESIS /MEDIATED SITE
DIRECTIONS /SOME FUTUREDISASTER /OF THE CHERNOBYLDISCORDANT FOR RED GREEN COLOR VISION
MZ TWIN STUDY /APHENOTYPES IN SIBLINGS
DISEASE (PELIZAEUS MERZBACHER DISEASE)(TYPE II GLYCOGEN STORAGE/(PELIZAEUS MERZBACHER/21 LOCI IN FAMILIAL ALZHEIMER/A MOUSE MODEL OF GAUCHER/ANALYSIS OF ALAND ISLAND EYE/AND ALAND ISLAND EYE/AND CONGENITAL HEART/AND EXPRESSION IN AUTOIMMUNE/AND MANAGEMENT OF WILSON/AND NONFAMILIAL ALZHEIMER/AND ROLE IN LYSOSOMAL/AT RISK FOR HUNTINGTON/CAUSES PELIZAEUS MERZBACHER/CHAIN DYSFUNCTION IN/CONCEPT OF SOMATIC MUTATIONAL/DEGENERATION OF BRAIN CANAVAN/DEMENTIA AND PARKINSON/DIAGNOSIS OF GENETIC/DIAGNOSTIC MARKER FOR NORRIE/DISEASE TYPE C AND CELL/DISEASE TYPE C AND CELL/DOCUMENTED CORONARY ARTERY/DOMINANT POLYCYSTIC KIDNEY/DOMINANT POLYCYSTIC KIDNEY/EPISKOPI BLINDNESS (NORRIE/ETIOLOGY OF ATHEROSCLEROTIC/FEATURE OF ALZHEIMER/FOR ADULT POLYCYSTIC KIDNEY
550
1239119492
11011113126819356401520119219181683554
2767562
24171587155220349741377181828752420146422432636156332618029018657
2499100762115632523669721
21511697
912087831933342633193
21801870106223852540223425432005203519831882
532166209482
106821721468198725441174997S27279622319091440971574971199225031905712711425947
2811286227972S1o292573
270462
1945627798714249
23712047161807
1764
Permuted Title Index
/FOR TWO LOCUS MODELS OF/FOR TYPE IIB VON WILLEBRAND/FORMS OF INFLAMMATORY BOWEL/GENE IN EARLY ONSET ALZHEIMER/GENE IN FAMILIAL ALZHEIMER/HEREDITARY KIDNEY/HOMEOSTASIS DEVELOPMENT AND/HOMOCYSTINURIA AND VASCULAR/IMPLICATION FOR HUNTINGTON/IN A PATIENT WITH GAUCHER/IN CHRONIC HEART AND BRAIN/IN FAMIUAL CREUTZFELDT JAKOB/IN FAMIUES WITH HUNTINGTON/IN JAPANESE GAUCHER/IN PATIENTS WITH THYROID/IN PELIZAEUS MERZBACHER/IN THE STUDY OF MENKESAIN TYPE 1 GAUCHER/INCREASED RISK FOR GENETIC/JAPANESE FAMILIAL ALZHEIMER/MARKER FOR ALZHEIMER/MILD PRESENTATION OF GAUCHER/MINOR ELEMENTS IN SICKLE CELL/MSAFP DUE TO FETAL CARDIAC/OF ADULT POLYCYSTIC KIDNEY/OF CHARCOT MARIE TOOTH/OF CHARCOT MARIE TOOTH/OF ENZYME THERAPY IN GAUCHER/OF JEWISH INFANTILE TAY SACHS/OF ONSET IN MACHADO JOSEPH/OF THE DNA TEST OF HUNTINGTON/RESPONSIBLE FOR HUNTINGTON/STUDIES AND THERAPY OF FABRY/STUDIES IN MACHADO JOSEPH/TESTING FOR HUNTINGTON/TESTING FOR HUNTINGTON/TESTING FOR HUNTINGTON/TESTING FOR HUNTINGTON[TESTING FOR HUNTINGTON[TESTING IN HUNTINGTON/TESTING IN HUNTINGTON/THE EXPERIENCE OF HUNTINGTON[THE PREMATURE CORONARY HEART[THE RISK FOR CORONARY HEART[THEIR APPLICATION TO WILSON/TO THE TREATMENT OF GAUCHER/TRANSPLANTATION FOR METABOLIC/TYPE OF MAPLE SYRUP URINENARIANT OF VON WILLEBRANDNULNERABILITY TO PARKINSONIWITH PELIZAEUS MERZBACHER/WITH PELIZAEUS MERZBACHER/WITH THE X LINKED FABRY/X LINKED LYMPHOPROLIFERATIVE/X LINKED LYMPHOPROLIFERATIVE1 /CAUSED BY POLYCYSTIC KIDNEYA FREE SIALIC ACID STORAGEA LATE ONSET MOSAIC FORM OFA NEW PHAKOMATOSIS /IN COWDENA NEW SYNDROME /WHITE MATTERA WORLD WIDE PERSPECTIVEABNORMALITIES IN CHOLESTEROLALLELES IN THE CAJUN /SACHSAN EXAMPLE OF GENETICANALYSIS /IN HUMAN GENETICAND ADULT GM2 GANGLIOSIDOSISAND CHROMOSOME 13 A CASE OF AAND CONTROLS /JAKOBAND DOWN SYNDROME /KIDNEYAND HLA DP /BETWEEN HODGKINAND IN THEIR SIBS /HUNTINGTONAND ITS CLINICAL CONSEQUENCESAND MALIGNANT LYMPHOMA ANDAND NF 2 NON HIPPEL LINDAUAND OTHER INHERITED DISEASESAND PATERNAL AGE SUGGESTSAND THE ABUSE OF GENETICSAND TURNER SYNDROME /HEARTANTEMORTEM DIAGNOSIS BY /SPATZBY DNA POLYMORPHISM ANALYSISBY ENZYME REPLACEMENT THERAPYCANDIDATE GENE /A HUNTINGTONCANDIDATE GENE GENECANDIDATE REGION BY EXONCARRYING A MUTATION AT CODONCHARACTERIZATION OF MUTANTCLINICAL ASPECTS MOLECULARCOMPLEMENTATION ANALYSIS /PICKCORRECTION OF THE ABNORMALCORRELATION BETWEEN /URINEEFFICACY OF ENZYME /GAUCHERELDERLY AND YOUNG INDIVIDUALSENDEMIC AREA IN TAIWANFIBROBLASTS BY RETROVIRALGENE IA CANDIDATE HUNTINGTONGENE /CLOSE TO THE HUNTINGTONGENE /FOR THE HUNTINGTONGENE /FOR THE HUNTINGTONGENE AND THE CENTROMERICGENE ASSOCIATIONS IN ADMIXEDGENE BY A NEW MAPPINGGENE CANDIDATE REGION AMONGGENE CANDIDATE REGION ANDGENE CLN3 /(BATTENGENE REGION OF HUMAN
27181068277022902381380453
23232442560671
2291211
2315547
110157155717881071745436
212712351048141
1922556
24465441100299
24751889210966173217711807175117682481118427
21162486157
1058444
23031083235817439681263998
20131504616645300798
270926672532
3647
23901444589
176519941349303
25042660181714148991122553
239122672383100028327962787552455515841383249123352399227123962057275820882348102
19722384
GENE UNLIKELY /THE HUNTINGTONGENES BY POSITIONAL CLONINGHAVING COMPLEX ETIOLOGYCOPPER AND CERULOPLASMIN
11 SERUM CERULOPLASMIN LACKSIN A PATIENT WITH 48,XXXXIN A SMALL TOWN IN COSTA RICAIN A THREE GENERATION FAMILYIN AN UZBEKI JEWISH AND AIN CHINA TWO NEW MUTATIONSIN CHINESE /OF WILSONIN CHORIONIC VILLI BIOPSYIN FAMILIES /THYROIDIN FINNISH PATIENTS WITHIN ICELAND /POLYCYSTIC KIDNEYIN ITALIAN FAMILIES USINGIN JAPAN /FAMILIAL ALZHEIMERIN NEW ENGLAND FRANCO /SACHSIN NORTH EAST SCOTLANDIN THE ASHKENAZI JEWISH ANDIN THE CHINESE /ARTERYIN THE INDIANA KINDREDIN THE NETHERLANDS /HUNTINGTONIN THE WESTERN REGION OF CUBAIN VIETNAM /EINDICATIONS AT INTEGRATEDIS ASSOCIATED WITH THREELINKAGE ANALYSIS OF CANDIDATELINKAGE RELATIONSHIPS /JOSEPHLOCI AND ASSORTATIVE MATINGLOCUS /A PUTATIVE PAGETLOCUS /HEMOCHROMATOSISLOCUS /LINKED TO THE WILSONLOCUS AND THE CLOSE MARKERLOCUS FOR THE SPINAL MUSCULARLOCUS ON XP11.3 /OF THE NORRIELOCUS TO 13033.1 /OF ONEMOLECULAR ANALYSIS OF ACID BMUTATIONS IN FRENCH CANADIANSNEW INFORMATION FOR GENETICON PROXIMAL XQ /MARIE TOOTHONE GENERATION ASSESSMENTOR ENVIRONMENTAL RISK /GENETICORIENTED NATIONAL GENETICSORIENTED NATIONAL HEALTHOUTCOME OF 136 AT RISKPATIENTS /IN CELIACPATIENTS IN RELATION TO DNAREGION (4P16.3) /HUNTINGTONREGION /IN THE HUNTINGTONREGION /THE HUNTINGTONREGION WITH YEAST ARTIFICIALREGISTRY /LYMPHOPROLIFERATIVERELATIONSHIP OF GENOTYPE TOSHOWS IT BELONGS TO AN ACIDTHE CASE FOR POSTPONINGTHE PHYSICAL MAP /HUNTINGTONTHE RELATIONSHIP BETWEENTHE VALUE OF PSYCHOMETRICTHROUGH A PREDICTIVE TESTINGTYPE 1 (CMT IA) LOCUS WITHINTYPE IA IN FIVE FRENCH /TOOTHTYPE C AND CELL DISEASETYPE C AND CELL DISEASETYPE MOLECULAR AND /GAUCHERUSING GLUCOCEREBROSIDASEUSING RECOMBINANT HUMANWHERE WE ARE /OF GENETICWITH IDIOPATHIC /PARKINSONWITH MARKERS ON 40 RESULTS OFWITH NORMAL ACID A /POMPEWITH RIGIDITY AND VERY EARLYXi GSD XI AN AUTOSOMAL
DISEASE/INCOMPLETE CONGENITAL /EYEDISEASES /ANALYSIS OF MITOCHONDRIAL
/AS DEMONSTRATED IN HUMAN/COUNSELING IN NEUROMUSCULAR/GENES FOR MULTIFACTORIAL/GENES FOR THE X LINKED EYE/IN ANALYSIS OF FAMILIAL/IN MONOGENIC AND POLYGENIC/IN THE COMPUTER PROGRAM/MITOCHONDRIAL DNA/MODELS OF MITOCHONDRIAL/MOSAICISM IN X LINKED/OF IMPRINTING FOR HUMAN/OF POLYCYSTIC KIDNEY/RELATED TO VARIOUS MALIGNANT/SPORADIC CASES OF X LINKED/TO ASTHMA AND KIDNEY/TO MULTIFACTORIAL TRAITS AND/TRANSPLANTATION FOR STORAGEA FORMULATION ASSUMING ANBASIS FOR PLANNING ANDBY DNA ANALYSIS IN CUBACONTROL PROGRAM IN CUBAIN A PEDIATRIC DEPARTMENT OFIN A PEDIATRIC HOSPITAL ININ B.S.S.R /SYSTEM HEREDITARYIN DIFFERENT POPULATIONS OFIN GENERAL POPULATION OFIN GENERAL POPULATIONS OFIN NORTH CHINA /STORAGEIN POPULATIONS OF TURKMEN SSRIN UZBEKISTAN /HEREDITARY
18842174273843851214138651490998
2246990574
2663714190211107391788860
4274618961767182779317861003202019952027192921172373192619432196647
25452289226
2007207666S30150301144984582
2336221022041082
31224818222982331738174520391958627798837552
248342233
20125297918468101912871735S322531264326652788
3236
1191245384135011112752S95156
2786149
250417911789777
2728965
27782769558
27152692
MIMIC LINKAGE TO THEUSING PCR /ANALYSIS OF COMMONWITH COMPLEX ETIOLOGYWITH HIGH MUTATIONAL /OF
DISEOUIUBRIA AMONG CA POLYMORPHISMSDISEOUlUBRIUM /OF LINKAGE AND LINKAGE
BETWEEN SCAl AND DoS89BETWEEN THE MYOTONICIN THE FRENCH /LINKAGEIN THE HUNTINGTONMAKE A TELOMERIC SITEWITH MYOTONIC /LINKAGEWITHIN THE G6PD
DISJUNCTION IN MEIOSIS /HAZARDOUS FORDISLOCATION AND ACETABULAR DYSPLASIADISUTASE ACTIVITY TO OXYGEN FREE
PHENOTYPES /SUPEROXIDEDISODIUM IN THE TREATMENT OFDOMY FOR CHROMOSOME 7 /WITH MATERNAL
IN ANGELMAN SYNDROMEIN PRADER WILLI SYNDROMEIN SPORADIC BECKWITH WIEDEMANNOF CHROMOSOME 4 AND ISO
DISORDER (PSEUDO POMPE DISEASE) WITH/A FREE SIALIC ACID STORAGE/AS PERVASIVE DEVELOPMENTAL/CHROMOSOMAL INSTABILITY/DEFICIT HYPERACTIVITY/DOMINANTLY INHERITED BONE/IN FAMILIES WITH BIPOLAR/LINKAGE ANALYSIS OF PANIC/LINKED TO BIPOLAR AFFECTIVE/NEW VARIANT OF PEROXISOMAL/POSSIBLE IN THIS FATAL BRAIN/PROBABLY RECESSIVE AUTOSOMAL/SEIZURES AUTOSOMAL DOMINANTAND WITH SPERM SPECIFIC GENEDUE TO A POINT MUTATION OFIN A MEXICAN POPULATIONIN THE OLD ORDER AMISHOF COMBALAMIN METABOLISM OFSHOWING LOSS OF Y CHROMOSOMESUBSTRATE OXIDATION ANDWITH MARKED VARIABILITY IN
DISORDERS (CONDITIONS NOT /TRANSPORT/AND 7 IN MALIGNANT MYELOID/AND IN OTHER GENETIC/AS OBSERVED IN HUMAN/CLASSIFICATION OF THESE/DIAGNOSIS OF CHROMOSOMAL/DIFFERENT LYSOSOMAL/FOR FETAL CHROMOSOMAL/GENE IN NEUROPSYCHIATRIC/HERITABLE CONNECTIVE TISSUE/HISTORY DATA ON SEIZURE/IN MYELOPROLIFERATIVE/IN THE COMMON CHROMOSOMAL/IN THE DIAGNOSIS OF LETHAL/INTO THE GENETICS OF MOOD/LINKAGE ANALYSIS OF COMPLEX/MALFORMATIONS AND INHERITED/MORBIDITY RISKS IN MOOD/OF CHILDREN FOR GENETIC/PHENOTYPE OF SINGLE GENE/TO TWO MITOCHONDRIALA RESEARCH AND PATIENTAN UPDATE /PEROXISOMALAND THE FINNISH POPULATIONASSOCIATED WITH ANAT INCREASED RISK OFIN MENTALLY RETARDED /ACIDIN SECONDARY MALNOURISHEDIN THE PREGNANT PATIENTLOW ACCEPTANCE RATE INNEW MUTATION SELECTIONOF CONNECTIVE TISSUESOF LYSOSOMAL MEMBRANEOF PUBERTY /HAPLOTYPES INORGANIZATION AND OBJECTIVESOVERVIEW AND INTRODUCTIONTHE EXPERIENCE OF /ONSET
DISPLAY CLINICAL FEATURES OF DOWNINFLUENCED BY ENVIRONMENTALLITTLE HOMOLOGY AT THE /BUT
DISPLAYING X LINKED RECESSIVE /FAMILYDISPLAYS OF GENOMIC DATA THE /GRAPHICDISRUPTION OF SUPPRESSOR GENE
OF THE TRANSFORMING GROWTHDISSECTED DEFINED CHROMOSOME REGIONDISSECTION OF THE FOLDING AND /GENETICDISSEMNATION OF MUTANT ALLELES WITHDISSIMILARMES/SIMILARITIES ANDDISTAL II P /DOPAMINE RECEPTOR MAPS TO
15011013 A DIFFERENCE BETWEENBAND 17P11.2 /TYPE IA GENE INDELETION OF YQ IN A PATIENTEUCHROMATIC LONG ARM OF THEEUCHROMATIC Y CHROMOSOME LONGSEGMENT OF THE LONG ARM OF [THETO D4S43 /SYNDROME 2MBXP THAT ESCAPES X INACTIVATION
DISTANCES ON HUMAN CHROMOSOME 190DISTINCT BRDU INDUCED COMMON FRAGILE
FACIAL APPEARANCE /ANDHAND AND TEMPORAL BONE CT
551
2034426270100598319491937191628482336184187519641136681
2229155395717121558159390
1582529
20137481436673738
2091194419404541935769761
241635
271919885081356497858261
2581484289902161523591155979352
27231372174139122
1963726
2745951434
2781784128
510642325196641246211
2808351281665354259248418548
22346891898258724351728S462732260190387
195216782105217614621727240221071564903796
Permuted Title Index
PATTERNS OF NUCLEOTIDE /THEPOSTAXIAL POLYDACTYLYSYNDROME /13 LACK OF A
DISTINCTIVE FACIES IN TWO SIBLINGSDISTRIBUTION /AND THEIR POPULATION
AMONG FAMILIES IN LATINAND CHARACTERIZATION OFAND INCIDENCE OFAND METHYLATION OF CPGIN AMERINDIANS /HAPLOTYPEIN ITALY /GEOGRAPHICALIN MONGOLIA /AND ITSOF A (TG)N(AG)MOF ANEUPLOIDY IN /OF THEOF ANEUPLOIDY IN HUMANOF BREAKPOINTS /ANDOF EDUCATIONAL MATERIALSOF MHC HAPLOTYPES INOF TAY SACHS DISEASE /ANDOF THE DUFFY BLOOD GROUPOF TYROSINASE GENE /AND
DISTRIBUTIONS AMONG HUMAN RACIALFROM FAMILY DATA /ONSETIN PARENTS AND CHILDRENOF CYSTIC FIBROSIS GENEOF PHYSICAL AND /X ONOF PLASMA LIPOPROTEIN(A)
DISTRIBUTIVE PAIRING AND ANEUPLOIDYDISTURBANCES (OLIVER AND MAC FARLANE
IN THE CELL CYCLE AND INDIVERSE POPULATIONS OF LUNG CANCER
U.S.A POPULATION /140L IN ADIVERSITY /CELL RECEPTOR B JUNCTIONAL
/FOR ESTABLISHING GENETICAND GENETIC COUNSELINGAND GENETIC DISTANCE AMONG
DIVISION OF BIOMEDICAL SCIENCES /THEOF TRIPLOID EMBRYOS THE /OF
DIZYGOTIC TWINNING /AND GENETICS OFDlD LIKE LOCUS ON CHROMOSOME 6 /OF THEDN ALLELE OF THE B HEXOSAMINIDASE ADNA /BY AN UNSTABLE REGION OF
/EVOLUTION OF ALPHA SATELLITE/FOR DETECTION OF VARIATION IN/FOR MICRODISSECTED CHROMOSOMAL/GENE IN A 1 MB CONTEXT OF XQ28/IRREGULARITIES IN ALPHA SATELLITE/NUCLEAR RNA COMPLEMENTARY/OF DNA METHYLATION IN GENOMIC/POLYMORPHIC LOCI IN HUMAN/TRANSFECTION OF NORMAL HUMANADDUCTS ON HUMAN CHROMOSOMESAMPLIFICATION /BY PCR MEDIATEDAMPLIFICATION OF TWO /MULTIPLEXANALYSES AND FLUORESCENCE IN SITUANALYSIS CONFIRMS THE GENETICANALYSIS DUE TO MISDIAGNOSIS OFANALYSIS IN CRIMINAL /USE OFANALYSIS IN CUBA /DISEASES BYANALYSIS IN THE DIAGNOSIS OFANALYSIS REVEALS GENETICANALYSIS TO ESTABLISH A DIAGNOSISAND CYTOGENETIC EVALUATION OFAND GENE CONTENT TO CHROMOSOME /OFAND GENETIC COUNSELING INAND PROTEINS FROM PERUVIAN MUMMIESAND QUANTITATION OF HETEROPLASMYAND RNA IN MITOCHONDRIALAND THE DISPERSAL OF EARLY HUMANSAND THE SPREAD OF MODERN PEOPLEAS A PLACENTAL MARKER FOR FETALBANKING EXPERIENCE FOR MULTIPLEBANKING FOR GENETIC ANALYSISBINDING DOMAINS /PROLINE RICH ANDBINDING OF TRANSCRIPTION FACTORSBY PCR /OF HUMAN GENOMICCAN BE AN EFFICIENT COMPETITOR INCHANGES AT LOCI ON CHROMOSOME 13CLONED AS YEAST ARTIFICIALCONTROL REGION SEQUENCE VARIATIONCOPY NUMBER /IN MITOCHONDRIALCROSSLINKING AGENTS OF THE /TOCYTOCHROME B MUTATIONS ASSOCIATEDDAMAGE /PIGMENTOSUM CELLS AGAINSTDAMAGE IN CHRONIC HEART AND BRAINDELETION IN PATIENTS WITH VONDIAGNOSIS FOR HEREDITARY CEREBRALDIAGNOSTIC TECHNOLOGYDIAGNOSTICS POSSIBLE IN THISDISEASE RELATIONSHIP OF GENOTYPEDISEASES /MITOCHONDRIALELEMENTS IN SOMATIC CELLS REDUCESEXCISION REPAIR PATHWAYS IN HUMANEXIST IN CHIMPANZEE AND HUMAN BUTEXTRACTION FROM FORMALIN FIXED /OFFAMILIES /OF HUMAN SATELLITEFAMILIES ON CHROMOSOME 10 AND 12FINGERPRINTING IN PARENTAGEFINGERPRINTING IN VERIFICATION OFFINGERPRINTS /OF SIMILARITY OFFRAGMENTS FOR DETECTION OFFRAGMENTS FROM 5011.2 13.3 USINGFROM A 46,XX TRUE HERMAPHRODITEFROM ANCIENT BONES /RECOVERY OFFROM DRIED FILTER PAPER BLOOD /OF
26218921416792253
26962854270116522562882273528001195158784
1780287627092655231828282661274227982700
671578769409610192022402630176228621782159040023791059379
26402793251020416392521244920992250134316279881690263718242861250410732610118211541643101956643724272614168
11331786273722882540251621002593
502635
3422509732539671102896451
19353132
281924122626108116962234274057964
2793211023952502
FROM HUMAN CENTROMERIC REGIONSFROM PATIENTS WITH CLEFT LIP ANDFROM SINGLE HUMAN CHROMOSOME /OFGENE FAMILY /SAME MITOCHONDRIALGENOTYPING ASSORTMENT ANDGENOTYPING OF CATARACT ENRICHEDGLYCOSYLASE CDNA WHOSE GENE MAPSHAVE A BEGINNING AND AN ENDIN AFRICAN POPULATIONSIN KEARNS SAYRE SYNDROMEIN MATERNAL BLOOD BY PCR MAY ALSOIN THE CHROMOSOMES OF MANIN THE COURTROOM ISSUES AND /OFINSERT USING A COMBINED PCRINTEGRATION LEADING TO COMPLEXINTO SIMIAN CHROMOSOMES RESULTSISOLATED FROM HUMAN HAIR SHAFTSLEADING TO THE KEARNS SAYRELIBRARIES /CHROMOSOME SPECIFICLIBRARIES /CHROMOSOME SPECIFICLIBRARIES AND FLUORESCENT IN SITULIBRARY /BY A CHROMOSOME SPECIFICLIGASE DEFECT IN BLOOM SYNDROMELINKAGE ANALYSES /TRIMETHOPRIM ANDLOCI /USING HYPERVARIABLEMARKER STUDIES OF POSSIBLE GENEMARKERS /OVARIAN TERATOMAS USINGMARKERS ANALYSIS /WITH 17011.2MARKERS BY EXPLORING /CONTENT OFMARKERS FOR THE FRAGILE X SYNDROMEMARKERS LINKED TO MYOTONIC /19MARKERS OF X028 /SEVEN POLYMORPHICMARKERS ON 150 RESULTS OF AN /10MARKERS ON HUMAN CHROMOSOME 20MARKERS PROGRESS IN MULTIPLEXINGMARKERS RN1 AND VK23 USED IN THEMETHYLATION /MOLAR PREGNANCY ANDMETHYLATION IN GENOMIC DNA /OFMETHYLATION IN THE ANGELMAN ANDNEW COSMIDS FOR HUMAN CHROMOSOMEON THE STABILITY OF AN EPISOMALPOLYMORPHISM ANALYSIS /DISEASE BYPOLYMORPHISM AND HOMINOIDPOLYMORPHISM IN FRENCH CANADIANSPOLYMORPHISM IN KOREAPOLYMORPHISM IN SITES CLOSELY /OFPOLYMORPHISM RULED OUT IN 45POLYMORPHISMS (XBAI AND ECORI) OFPOLYMORPHISMS /COUNSELING WITHPOLYMORPHISMS DETECTED WITH GCPOLYMORPHISMS IN BASAL CELL NEVUSPOLYMORPHISMS IN EUROPEAN ANDPOLYMORPHISMS IN SOUTHERN AFRICANPOLYMORPHISMS IN THE /BETWEENPOLYMORPHISMS USEFUL FOR LINKAGEPOLYMORPHISMS WITHIN THE HUMANPREFERENTIALLY INTEGRATES INTOPREPARED BY SALT VERSUS /OFPROBE /X CENTROMERE BIOTINYLATEDPROBE HYBRIDIZED IN SITU /SPECIFICPROBES /AND Y SPECIFIC A SATELLITEPROBES /BY CHROMOSOME SPECIFICPROBES /CENTROMERIC SATELLITEPROBES /HYPERVARIABLE MULTILOCUSPROBES /IN SITU HYBRIDIZATION WITHPROBES /TO CHROMOSOME SPECIFICPROBES /WITH SATELLITEPROBES ANALYSIS /CYTOGENETIC ANDPROBES FOR CYTOGENETIC ANALYSESPROBES FOR HUMAN CHROMOSOMES 8 10PROBES FOR IN SITU HYBRIDIZATIONPROBES FROM HUMAN TRANSCRIBEDPROBES IN PRENATAL AND PERINATALPROBES IN THE VICINITY OF THE /NEWPROBES OF THE 5012 014 REGIONPROBES USED AS RFLP MARKERS FORPROBES USING GC CLAMPED /ANONYMOUSPROBES WITHIN SELECTED SUBREGIONSPROFILE AND PATERNITY /OF AREARRANGEMENTS IN TWO PATIENTSREGIONS /FOR HYPERVARIABLEREPAIR AND CANCER PRONENESS /TOREPAIR AND IMMUNOLOGIC ANALYSISREPAIR DEFECT /ASSOCIATION WITHREPAIR DEFECT IN XP A /FORREPAIR DEFECT OF FANCONI ANEMIAREPAIR DEFICIENCY POSSIBLEREPAIR ENZYMES /OF A FAMILY OFREPAIR EVOLUTION AND ITSREPAIR GENE ERCC 1 /OF THE MURINEREPAIR IN NORMAL AND UVC REPAIRREPAIR METHYLTRANSFERASE GENEREPARATIONAL AND IMMUNOLOGICALREPARATIVE PROCESSES INREPLICATION /ARE DEPENDENT ONRFLP ANALYSIS OF HLA COMPLEX /BYRFLPS IN THE APOAI CIII GENE /BYRNA AND PROTEIN LEVELS /1 AT THESAMPLES DELIBERATE HETERODUPLEXSCREENING OF SOUTH AFRICANSEGMENTS WITHIN THE UNTRANSLATEDSEQUENCE AMPLIFICATION IN TUMORSSEQUENCE DIFFERENCES INSEQUENCE HYBRIDIZATION TO
1102 SEQUENCE POLYMORPHISMS IN HUMAN
168223692081
331103194722582640263999510601729314
278525561663250011151677171517061542295
148728242210410635
20931894198419591883203120621908928
24492224208216461122167
28782846231710942746675
2520200319162633
662059196817052508169816761725172116662871128117081704107916351635199
25011227210112232630205920582877244721948451838816231422758072270257823252564240174181313751108240428182792103624572586262221992069
SEQUENCE VARIATION BY PCR OF /FORSEQUENCE VARIATION INTO SITES CUTSEQUENCES /CLONING OF CORRECTINGSEQUENCES /FROM ANCIENT AND MODERNSEQUENCES /HIGHLY CONSERVEDSEQUENCES /OF ENOLASE CODINGSEQUENCES AT 2021 AND 9013SEQUENCES REGULATING CELL TYPESEQUENCES RELATED TO CFTR /HUMANSEQUENCES TO INTERPHASE CELL /OFSEQUENCING IN A FAMILY WITH BISTRANDS OF THE PRION PROTEIN GENESURROUNDING THE ARGININO /OF HUMANTEST OF HUNTINGTON DISEASE /OF THETESTING FOR HUNTINGTON DISEASE INTESTS IN FORENSIC PRACTICE /OFTO A CHILD OF A WOMAN WITH KEARNSTRANSFECTION /STUDIED BYTYPING WITH POLYMORPHIC TRIMERICUSING DENATURING GRADIENT GELUSING THE HOT PCR METHOD /GC RICHVARIATION IN SOUTHERN AFRICA /ANDVARIATION IN THE HUMAN SPECIES /OFVARIATIONS IN XQ28 /CHANGES AND
DNAS /CENP B AND CENTROMERIC SATELLITE/FROM SOMATIC CELL HYBRIDFROM DISSECTED DEFINED /USING
DNF15S2 WITH A HIGH DEGREE OF /LOCUSDOCTOR RELATIONSHIP ETHICAL AND LEGALDOG MODEL WITH NO SOMATIC REVERSIONDOMAIN /THE BETA GLOBIN
IN NEUROBLASTOMAS USING YEASTOF THE HUMAN MYC ONCOGENE /THEOF THE TYPE 1 /CATALYTICOF TYPE II COLLAGEN PRODUCES
DOMAINS /PROLINE RICH AND DNA BINDINGOF THE SPHINGOLIPID ACTIVATOR
DOMINANT ANIRIDIA /IN AUTOSOMALCONDITIONS /PENETRANTDISEASES MIMIC LINKAGE TODISORDER /SEIZURES AUTOSOMALDYSTROPHIC EPIDERMOLYSIS /OFFORM OF LIMB GIRDLE MUSCULARHEREDITARY MOTOR AND SENSORYINHERITANCE /AND AUTOSOMALINHERITANCE OF ACRODYSOSTOSISINHERITANCE OF CAUDAL /WITHINHERITANCE OF EXTENSIVEOLIVOPONTOCEREBELLAR ATROPHYOSTEOGENESIS IMPERFECTA WITHPERIODIC PARALYSIS /OFPOLYCYSTIC KIDNEY DISEASEPOLYCYSTIC KIDNEY DISEASEPOLYCYSTIC KIDNEY DISEASEPOLYCYSTIC KIDNEY DISEASE INPOLYCYSTIC KIDNEY DISEASE INPOLYCYSTIC KIDNEY DISEASE INPSEUDOHYPOPARATHYROIDISMRETINITIS PIGMENTOSARETINITIS PIGMENTOSARETINITIS PIGMENTOSARETINITIS PIGMENTOSARETINITIS PIGMENTOSA ANDSELECTABLE MARKERS IN HUMANSYNDROME /UNDERREPORTEDTRAIT WITH VARIABLETRANSMISSION /AUTOSOMALVARIANT OF VON WILLEBRAND /A
DOMINANTLY INHERITED BONE DISORDERINHERITED SYNDROME /A NEWINHERITED TRAIT /A
DOMINICAN REPUBLIC /IN THESURVEILLANCE OF CONGENITAL
DONOR LYMPHOCYTES ACOUIRE MMCSITE /MUTATION IN A MRNA SPLICE
DONORS OF THE INDONESIAN RED CROSSDONOVANI INFECTION AND THE /LEISHMANIADOMMINE D2 RECEPTOR AS A MODIFYING
D2 RECEPTOR DNA POLYMORPHISMD2 RECEPTOR LOCUS STUDIES OFRECEPTOR MAPS TO DISTAL lI P
DOSAGE COMPENSATION /DETERMINATION ANDDOSE OF XRAYS IN DIFFERENT AGE GROUPS
RATE MODULATED MICROWAVE AND /LOWDOT BLOT /BY MEANS OF ASO REVERSE
BLOT HYBRIDIZATION /OF REVERSEDOUBLE ALPHA DELETIONS /DETECT (SEA)
FAMILIAL GENETICS ABNORMALITYISOCHROMOSOME Y IDENTIFIED BYLABELING FLUORESCENT IN SITU /AMINUTE CHROMOSOMES INMINUTES HARBORING THE MOUSERECOMBINATION WITHIN THE CENTRANSLOCATION INVOLVING 4
DOWN REFERRED FOR GENETIC COUNSELINGSYNDROME /AND FROM PATIENTS WITHSYNDROME /CHROMOSOME 21 INSYNDROME /CLINICAL FEATURES OFSYNDROME /FROM PATIENTS WITHSYNDROME /HEART BLOCK INSYNDROME /IMPLICATIONS FORSYNDROME /IN CHILDREN WITHSYNDROME /KIDNEY DISEASE ANDSYNDROME /NEURAL TUBE DEFECTS ANDSYNDROME /OF CHROMOSOME 21 AND
552
279225282274315261226381858245323662153105922982140110017671103228
2406250620692530258312
2190412205172822971816464336
21932570
98522
228823591960279120347617378
1914892869808832187310652394226249
237199811101902824
78
9992378
92096782
2237781444738826663146027561522232627542651979109410761903223625422576184911131839115914761337137213611687140614031473415418153114634196991444117416
Permuted Title Index
SYNDROME /ONSET MOSAIC FORM OFSYNDROME /ORIGIN OF MIXOPLOIDSYNDROME /PATTERN PROFILES INSYNDROME /PHENOTYPIC FEATURES OFSYNDROME /SCREENING FORSYNDROME /SCREENING FORSYNDROME /SCREENING FORSYNDROME /SCREENING FORSYNDROME /THE RISK OF FETALSYNDROME A STUDY OF 522 /AGE ANDSYNDROME AN UPDATED STUDY /INSYNDROME AND ALZHEIMER DISEASESYNDROME BE DETECTED BY AINSYNDROME DETECTION /SCREENING FORSYNDROME FAMILIES AINHIBITOR INSYNDROME IN A SURVEY OF /OFSYNDROME IN A THIRD WORLDSYNDROME IN LIBYASYNDROME IN MAINE 1980 TO 1989SYNDROME IN METROPOLITAN ATLANTASYNDROME IN MONGOLIASYNDROME IN ONE PATIENT /CAUSESSYNDROME IN RELATION TO INSULINSYNDROME IN TWO HIGHLY /OFSYNDROME IN TWO SIBLINGS BY TWOSYNDROME IN WOMEN AGE 35 AND /FORSYNDROME IN WOMEN AGE 35 AND /FORSYNDROME IN WOMEN LESS THAN 35SYNDROME ON CHROMOSOME 21 /OFSYNDROME PRELIMINARY RESULTS /FORSYNDROME PRENATAL DIAGNOSIS ANDSYNDROME PROSPECTIVES OF GENETICSYNDROME REGISTER IN ENGLAND ANDSYNDROME SCREENING THE USE OFSYNDROME SCREENING USING MSAFPSYNDROME SCREENING WITH MSAFPSYNDROME STATISTICALLY /WITHSYNDROME THE IMPACT OF ASSAY /FORSYNDROME USING MSAFP AND AGE /FORSYNDROME WITH MATERNAL AGE AND
DOWNSTREAM OF A GLOBIN GENE IN CHINESEDP /BETWEEN HODGKIN DISEASE AND HLADOAl AND D4S175 IN ANCIENT PERUVIANDRAVIDIAN INDIANS IN SINGAPORE AIN THEDRD4 THE D4 DOPAMINE RECEPTOR MAPS TODREIFUSS MUSCULAR DYSTROPHY LOCUS
MUSCULAR DYSTROPHY WITHDRIED BLOOD /AMERICANS BY PCR OF
BLOOD SPOT SAMPLES COLLECTED ONFILTER PAPER BLOOD SPECIMENS
DRIFT IN A BRAZILIAN ISOLATED /GENETICDRINKING BEHAVIOR AND THE ALCOHOLDROSOPHILA /OF PATTERNING GENES IN
/OF THE MLC ALK PRE MRNA OF/THE HISTONE ARRAY OFFASCICLIN II FUNCTIONS ASGENOME /PHYSICAL MAP OF THEMELANOGASTER /H2A GENE INMELANOGASTER /LIFESPAN OFMODEL FOR A HUMAN COFACTOR
DRUG METABOLIZING ENZYMES RELEVANCEDUAL RESTRICTION ENZYME ANALYSIS /BYDUCHENNE AND BECKER MUSCULAR /FINNISH
AND BECKER MUSCULAR /GREEKAND BECKER MUSCULAR /INAND BECKER MUSCULAR /INAND BECKER MUSCULAR /WITHAND BECKER PATIENTS /FROMMUSCULAR DYSTROPHY /INMUSCULAR DYSTROPHY /INMUSCULAR DYSTROPHY /INMUSCULAR DYSTROPHY /WITHMUSCULAR DYSTROPHY AND /FORMUSCULAR DYSTROPHY AND /OFMUSCULAR DYSTROPHY BY /INMUSCULAR DYSTROPHY BY. FETALMUSCULAR DYSTROPHY CAUSED BYMUSCULAR DYSTROPHY DELETIONSMUSCULAR DYSTROPHY FAMILIESMUSCULAR DYSTROPHY FAMILIESMUSCULAR DYSTROPHY GENE /THEMUSCULAR DYSTROPHY GENE /THEMUSCULAR DYSTROPHY GENE BYMUSCULAR DYSTROPHY IN A WIREMUSCULAR DYSTROPHY IN JAPANMUSCULAR DYSTROPHY IN NORTHMUSCULAR DYSTROPHY KOBE /OFMUSCULAR DYSTROPHY PATIENTMUSCULAR DYSTROPHY PATIENT /AMUSCULAR DYSTROPHY PATIENTSMUSCULAR DYSTROPHY PATIENTSMUSCULAR DYSTROPHY PATIENTSMUSCULAR DYSTROPHY/MDX /OFTYPE MUSCULAR DYSTROPHY /OF
DUCHENNE/BECKER DYSTROPHY AND ALANDMUSCULAR DYSTROPHY /OF
DUCT ABNORMALITIES AND GALACTOSEMIADUFFY BLOOD GROUP IN MALFORMED /OF THEDUODENAL ATRESIA RESULTING IN NORMAL
ULCERS /ANTIBODY TITERS INDUP (15) KARYOTYPE /AND 47 XX + INV
12023 OTER DUE TO MATERNAL /WITHDUP(12XQ13 OTER) IN TWO T(14;18)DUP(5) AND REC DEL(5) IN ONE EXTENDEDDUPLICATED C4A GENES /CARRYING
15041428629417307308309S6411271474120584518359421595276014781750113426861497210614422697155111691250184415281749147576635731012331140758
1828120312151125589
2617287319032207781
27431186110228352716S6924382642325239
2456281923124281120104622921023104010981029108110882319486989112311241207254981095897816S718
46417941021235169010807318291087
197957121096632
2655927575
15211329139214532211
GENES RP1 AND RP2 LOCATEDDUPLICATION /FUNCTIONS PRECEDE GENE
OF 3 EXONS IN A PATIENTOF 30 VIA SPREADING OF XOF 8P23 PTER IN AN ADULTOF LO22 32 A KARYOTYPIC /AOF THE LONG ARM OFOF THE LONG ARM OF /NOVOOF THE MITOCHONDRIALOF THE SHORT ARM OFON THE SHORT ARM /DUE TO AOR DELETION OF CHROMATINRESULTING IN DUCHENNE
DUPLICATIONS /TRANSLOCATIONS ANDAND FEATURES OF /WITH I1 PUSING CHROMOSOME /DE NOVO
DUTCH BY SINGLE STRANDEDDWARFISM /BINDING AND CAUSES LARON
/PATIENTS WITH LARONAND DISTINCT FACIAL /LIMBEDDEFECTIVE NEUTROPHIL /LIMBEDWITH DYSMORPHIC FACE /LIMB
DXS148 AND DXS7 /GENE ON XP BETWEENDXS369 AT XQ27 /RETARDATION LINKED TODXS52 IN A FRAGILE X NEGATIVE FAMILYDXS548 FOR PRENATAL DIAGNOSIS OFDXS7 /GENE ON XP BETWEEN DXS146 AND
/NIGHT BLINDNESS PROXIMAL TODYE /OF A PERMANENT BLACK HAIRDYING SUDDENLY WITHOUT EXPLANATION BYDYNAMICS OF BIRTH DEFECTS INCIDENCEDYSAUTONOMIA /ANALYSIS IN FAMILIALDYSSETALIPOPROTEINEMIA ASSOCIATEDDYSFUNCTION IN DISEASE /CHAINDYSGENESIS /AND 46,XY PURE GONADAL
/FAMILIAL SACRAL/FEMALE WITH MIXED GONADAL/IN X LINKED GONADAL/INHERITANCE OF CAUDALAND HERMAPHRODITES /GONADALAND PALATAL FEATURESIN 46,XX INDIVIDUALS
DYSKERATOSIS CONGENITA AND ESTIMATIONDYSLEXIA /GENETICS OF DEVELOPMENTAL
SUBTYPES GENETICS BEHAVIORDYSMEGAKARYOPOIESIS /SYNDROME ANDDYSMORPHIC FACE OMPHALOCELE AND /WITH
FACE SHORT STATUREFEATURES /SPASMS ANDFEATURES AND SEVERE GROWTHFEATURES IN PATIENTS WITHFEATURES SLIGHT MENTALNEWBORNS WITH A RECIPROCALSUBTYPES OF ATTENTION
DYSMORPHISM ABSENT CORPUS CALLOSUMDYSMORPHOLOGY /ANOMALIES AND FACIAL
A CASE STUDY OF /OFAPPROACHES TO DIAGNOSISDATABASE /THE LONDONIN 250 PREGNANCIES WITHTHE LONDON /COMPUTERS INTO AN AVERAGE COMPUTERTO HOUSESTAFF [TEACHING
DYSMYEUNATING DISEASE (PELIZAEUSDYSIYEUNATION AND LONG TERM /BETWEENDYSORGANOGENESIS /AND RENALDYSOSTOSIS A CASE REPORT /ACROFACIAL
AND ECTRODACTYLY ANREPORT OF 13 CASESSYNDROME IN A TURKISH
DYSPLASIA (RIBBING TYPE) WITH/AND CONNECTIVE TISSUE/DEFECTS AND RADIAL/EVALUATION OF DYSSEGMENTAL/HYDROTIC ECTODERNAL/HYPOHIDROTIC ECTODERMALANALYSIS OF A FAMILYANALYSIS OF THE COL2A1 GENEASSOCIATED WITH MULTIPLECLINICAL GENETICAL ANDCONGENITAIN A GIRL WITH DEL(X)IN ROBERTS SYNDROMEIN SEX CHROMOSOME ANOMALIESLOCUS /ECTODERMALLOCUS /THE DIASTROPHICOF THE ARTERIES ASSOCIATEDOF THE LONG LIMBED TYPE ASPECTRUM CONCEPT AS ASWEAT PORE AND LINKAGESYNDROME /ECTODERMALSYNDROME A CAUSE OF /RENALURETHRAL VALVES AND /RENALVARIED PRESENTATIONWITH CAMPTODACTYLYWITH CLOVERLEAF SKULL (TYPE
DYSPLASIAS /DIAGNOSIS OF THE SKELETAL/NOMENCLATURE OF SKELETAL/OF THE NONLETHAL SKELETAL/TWO FETUSES WITH SKELETAL
DYSSEGMENTAL DYSPLASIA /EVALUATION OFDYSTONIA GENE AND LOCI ON CHROMOSOME
PARKINSONISM /(X LINKEDPARKINSONISM SYNDROME LOCUS
DYSTROPHIC EPIDERMOLYSIS BULLOSA
2403166
2549154215301520152916705021585149816191088170617231677964
24559699036886501912194619801038191218782560111926991880996S1022388801386197680812291466780802199719571366650890852736638150016016738798367231381349411341361379715245366568196957977628798177306481106634
112193370752277486188111261918705823859904812718917878738900126043
1731526730
2353204419491927
EPIDERMOLYSIS BULLOSA TODYSTROPHIES /AND BECKER MUSCULAR
/IN PROGRESSING MUSCULARDYSTROPHIN /A DELETION PRONE REGION OF
/OF SMOOTH MUSCLEASSOCIATED GLYCOPROTEINSCDNA AND GENOMIC CLONECROSS REACTIVE PROTEIN INGENE /AT XP21 LINKED TO THEGENE /BY THE 3 END OF THEGENE /IN THE HUMANGENE /MAP OF THE HUMANGENE AND ASSOCIATION WITHGENE DELETION HOT SPOT /THEGENE IN NONMUSCLE CULTUREDGENE IN THE BRAIN /OF THEGENE IN THREE SAUDI /IN THEGENE MICROHETEROGENEITIESGENE MUTATIONS BY ANALYSISGENE OF A DUCHENNE /IN THEGENE OF DUCHENNE MUSCULARGENE RESULTING FROM [THEHOMOLOGOUS /MINIGENES ANDIN MDX TRANSGENIC MICEISOFORMS ANDMRNA IN GOLDEN RETRIEVERMRNA IN PERIPHERAL BLOODMRNA PRECURSOR DUE TO ANPROTEIN AND PCR BASED GENESEQUENCES /TWO AMPLIFIED
DYSTROPHY /ANTICIPATION IN MYOTONIC/GENES FOR MYOTONIC/GOLDEN RETRIEVER MUSCULAR/IN DUCHENNE MUSCULAR/IN DUCHENNE MUSCULAR/IN DUCHENNE MUSCULAR/MUSCULAR/MYOTONIC/OF DUCHENNE TYPE MUSCULAR/WITH DUCHENNE MUSCULARA SUSCEPTIBILITY LOCUS FORAN EXCLUSION MAP USINGAND ALAND ISLAND EYE DISEASEAND BECKER MUSCULARAND BECKER MUSCULARAND CLOSELY LINKED MARKERSBY FETAL MUSCLE BIOPSYBY MULTIPLEX PCR /MUSCULARBY QUANTITATIVE MULTIPLEXCAUSED BY INTRACHROMOSOMALCHOROIDEREMIA /CHORIORETINALDELETIONS IN NEGATIVEFAMILIES /BECKER MUSCULARFAMILIES BY SOUTHERN BLOTFAMILIES REVEALS NO LINKAGEFAMILIES USING CA /MUSCULARGENE /CLONING THE MYOTONICGENE /CONTAINS THE MYOTONICGENE /THE DUCHENNE MUSCULARGENE /THE DUCHENNE MUSCULARGENE AT 4Q35 4QTER /MUSCULARGENE BY HOMOLOGOUS YEASTGENE IN MONOZYGOTIC TWINSGENE IS CONTAINED WITHIN AGENE ON 4Q35 LINKAGEGENE REGION /HUMAN MYOTONICGENE REGION /OF THE MYOTONICILLUSTRATING SOME OF THEIN A WIRE HAIRED FOXIN ITALY AND SPAIN /MYOTONICIN JAPAN /DUCHENNE MUSCULARIN NORTH CHINA CARRIERIN THE SPANISH POPULATIONIN TWO MALE SIBS A NEWKOBE /OF DUCHENNE MUSCULARLOCUS /DREIFUSS MUSCULARLOCUS /MAP OF THE MYOTONICLOCUS AND FOUR DNA /MYOTONICLOCUS ON 4Q35LOCUS ON THE SUBTELOMERICMULTIGENERATIONAL MOLECULAROBSERVATIONS ON THEPATIENT GENETIC COUNSELINGPATIENT WITH A DELETION OFPATIENTS /BECKER MUSCULARPATIENTS /BECKER MUSCULARPATIENTS /DUCHENNE MUSCULARPATIENTS /DUCHENNE MUSCULARPATIENTS AND THEIR FAMILIESPATIENTS IN SINGAPOREPATIENTS USING TWO /MUSCULARPOPULATION SUGGESTS THETO CHROMOSOME 4Q /MUSCULARTO CHROMOSOME 5 /MUSCULARTO XQ24 QTER /OF BULLOUSTYPE I /IN LATTICE CORNEALWITH ATRIAL TACHYCARDIA ANDWITH DYSTROPHIN CDNA AND
DYSTROPHY/IDX MUTATIONS /MUSCULAR
E /AN EXPRESSIONS OF HEMOGLOBIN/ANALYSIS OF GASTRIC CATHEPSIN
553
731098813978
244320
11232332753
22699832256100123571029205095810331089108023512346
172480
1596710892351109610872407228796710811088231920372115795486
20502021712989112328481207112410232549234281010469582848978404
237016S7
221718
22222036143S8640510434641984179410211875821
2351220723101916196620427784031080690989
229273182910961040108720361904
78199010557811123
19
10722254
Permuted Title Index
AND RENIN ON CHROMOSOME 1 USING TWOCOLI /OF CYSTINE BINDING PROTEIN OFDISEASE IN VIETNAMEFFECT ON SISTER CHROMATID EXCHANGEIN ACHANG ETHNIC GROUP A MINORITYPOLYMORPHISM ON LIPOPROTEIN LIPIDPOLYMORPHISM TO THE GENETIC
EIA SUBUNITS ASSOCIATION WITH ANE3 LEIDEN IN AN EXTENDEDEAR ANOMALIES A NEW DOMINANTLY /MINOR
ANOMALIES VERTEBRAL DEFECTS ANDARE NOT ASSOCIATED WITH RENAL
EARLY AMNIOCENTESES /INAMNIOCENTESIS A RETROSPECTIVEAMNIOCENTESIS AND COMPARISON /OFAMNIOCENTESIS CLINICAL ANDAMNIOCENTESIS COMPLEMENTED WITHAMNIOCENTESIS COMPLICATIONS INAMNIOCENTESIS FOR PRENATALAMNIOCENTESIS PROSPECTIVEAND LATE CVS BY TRANSABDOMINALCHD DEATHS /RISK FAMILIES AVOIDCHILDHOOD /GONADOBLASTOMA INDIAGNOSIS OF GLUTARIC ACIDEMIADIAGNOSTIC DIFFICULTIES /ANDFINDINGS FROM THE STUDY OF AHUMANS /DNA AND THE DISPERSAL OFMANIFESTATIONS OF THEONSET ADDITIONAL EVIDENCE OFONSET ALZHEIMER DISEASE /GENE INONSET DEAFNESS /STUDIES OFONSET FAMILIAL BREAST CANCER /OFPRENATAL DIAGNOSIS OF FRASERSECOND PRENATAL DIAGNOSIS OFSECOND TRIMESTER OLIGOHYDRAMNIOSVERSUS MID TRIMESTER /UNDERGOING
EARS MENTAL RETARDATION REPORT OFEAST ASIA AND MULTIPLE MIGRATION /IN
MEDITERRANEAN /AND HB S IN THESCOTLAND PREDICTIVE TESTING AND
EASTERN INDIA OVER A 10 YEAR PERIODQUEBEC /WITHIN A FAMILY OF
EBRO DELTA /IN CATALONIANS FROM THEEBV BASED EXPRESSION VECTORS /INECBALLIUM ELATERIUM /SUPRESSION BYECLAMPSIA A PRELIMINARY EXCLUSION MAPECLAMPSIAIECLAMPSIA /STUDIES IN PREECOGENETICS OF CONGENITAL
OF MACHADO JOSEPH DISEASEECONOMIC BURDEN OF GENETIC DISEASES
COMMUNITY A QUESTIONNAIRECOMMUNITY STUDY ON THESTRATA IN SANTIAGO CHILE
ECORI OF THE APOLIPOPROTEIN B GENEECTODERMAL DYSPLASIA /HYPOHIDROTIC
DYSPLASIA LOCUSDYSPLASIA SWEAT PORE ANDDYSPLASIA SYNDROME
ECTODERNAL DYSPLASIA /HYDROTICECTOPIA AND PELVIC LIPOMATOSIS /RENALECTOPIC CERVICAL THYMUS WITH LIPECTRODACTYLY AN EXPANDED PHENOTYPEECUADOR /DIAGNOSIS EXPERIENCE INECUADOREAN PATIENTS WITH LARON /INEDEMA HYPSARRHYTHMIA AND OPTIC /WITHEDH DEHYDROGENASE DEFICIENCIES /ANDEDUCATING HEALTH PROFESSIONALS /WHILEEDUCATION AND PROMOTION /HEALTH
AND TRAINING IN THE UNITEDIN AUSTRALIA /GENETICIN GENETICS IN AFRICAIN GENETICS IN CHINAIN GENETICS IN THE UNITEDIN HUMAN GENETICS IN INDIAIN MEDICAL GENETICS IN JAPANIN MEDICAL GENETICS IN THEIN THE NATION'S SCHOOLSOF GENETIC COUNSELORS 22OF MEDICAL GENETICS IN THEOF NURSES IN EVERY SETTINGOF THE MEDICAL PUBLIC /FORSYSTEM (VACARES) 1987 BIRTH
EDUCATIONAL MATERIALS FOR USE IN HIGHEEG TO 20013.2 20013.3 AND LINKAGEEFFECTIVENESS AND ACCEPTANCE OFEFFICACY IN MULTICULTURAL PATIENTS
OF ENZYME REPLACEMENT THERAPYEFFICIENCY OF RAPID IN SITUEFFUSIONS /ANALYSES OF PLEURALEGYPTIAN SAMPLE OF FRAGILE X CASES /ANEHLERS DANLOS SYNDROME TYPE 1 /TO
DANLOS TYPE IV /KINDRED OFDANLOS VI FURTHER
EOF 4E /BY INITIATION FACTORELASTICUM AND NEUROOPHTHALMICELASTIN FIBERS ABNORMALITY AT 28 /WITHELATERIUM /SUPRESSION BY ECBALLIUMELDERLY AND YOUNG INDIVIDUALS /DISEASEELECTROMAGNETIC RADIATIONS /LOW LEVELELECTROMORPHS /GROUPS AND PROTEINELECTRON MICROSCOPIC STUDY OF THE
MICROSCOPY /HYBRIDIZATION INMICROSCOPY HIGH RESOLUTIONMICROSCOPY RESULTING IN /FORTRANSFER FLAVOPROTEIN AND
2148448793
1568185626892775241699682681772416131631
6112321212126212261252125316467248189319692614187791
229022
20246521142926
1241710
2876390860
27602002267424761301191911567752331789334180228812746110611269048126481508834819162596986626417771772333328327330329331332335394177917821773396
27301780202817561758555127913748222025697717
245068611451301158424222842420147620662085264
ELECTROPHORESIS /BY PULSED FIELD GEL/CLAMPED GRADIENT GEL/DENATURANT GEL/DENATURANT GEL/DENATURANT GEL/DENATURING GRADIENT/GRADIENT GEL/GRADIENT GEL/GRADIENT GEL/GRADIENT GEL/GRADIENT GEL/GRADIENT GEL/OF HBS KORLEBU ONAFTER NRUI DIGESTIONANALYSIS /STRAND GELAND DIRECT SEQUENCINGDETECTION OF /GELIN ITALIAN CYSTIC /GELOF PCR AMPLIFIED /GELOF PCR AMPLIFIED DNAPROSPECTIVE STUDY OFTECHNIQUE IN ITALIANTO DETECT POINT /GEL
ELECTRORETINOGRAM OF ALAND ISLAND EYEELEGANS /GENOME MAP OF CAENORHABDITIS
/GENOME OF CAENORHABDITIS/GERMLINE PROLIFERATION IN C
ELEVATED ALPHA FETOPROTEIN LEVELS ININ VIVO SOMATIC MUTATION ATINCIDENCE OF CYSTIC FIBROSISMATERNAL SERUM HCG AND FETALMSAFP CONCENTRATIONS /AFTERMSAFP DUE TO FETAL CARDIACMSAFP INDEPENDENT OF OPENRATES OF SPONTANEOUSSWEAT SODIUM LEVELS /WITHOUTTEMPERATURES AS A TEST FOR
ELUPTOCYTOSIS IN SOUTHERN ITALYELUCIDATION OF A BALANCED COMPLEX
OF A Y;15 TRANSLOCATIONOF PHENOTYPE ANDOF THE KARYOTYPE IN TWO
EMBRYO /OF THE PREIMPLANTATIONFETAL DEVELOPMENT /THE STUDY OF
EMBRYOLETHAUTY /ASPECTS OFEMBRYOLOGICAL PROBLEMS /TARGETING TOEMBRYONAL CARCINOMA CELLS /IN HUMAN
CARCINOMA CELLS /OFCELLS /OF THE RAT
EMBRYONIC CELLS /METHOTREXATE IN HUMANEXPRESSION OF THE MURINEGROWTH AND DEVELOPMENT /ANDSTEM CELLS /A 1 LOCUS INSTEM CELLS /B1 GENE INSTEM CELLS /IN MOUSESTEM CELLS DERIVATION ANDSTEM CELLS TO PRODUCE A /IN
EMBRYOPATHY /IN HUMAN RETINOIC ACID/RETINOIDELUCIDATION OF PHENOTYPEWITH A COINCIDENTAL
EMBRYOS /OOCYTES AND PREIMPLANTATIONCARRYING LETHAL MUTATIONS ATTHE TRIPOLAR SPINDLE /TRIPLOIDUSING NONRADIOACTIVE PROBES
EMERGENCE OF TWO OVERLAPPING /1 P36EMERY DREIFUSS MUSCULAR DYSTROPHY
DREIFUSS MUSCULAR DYSTROPHY /THEEMISSION COMPUTED TOMOGRAPHY IN RETT
TOMOGRAPHY FINDINGS INENAMEL PROTEIN AMELOGENIN IS /HUMANENCAPSULATED NONAUTOLOGOUS CELLS
RECOMBINANT FIBROBLASTSENCEPHALOCRANIOCUTANEOUS LIPOMATOSISENCEPHALOMYOIATHY BELONG TO THE SAME
LACTIC ACIDOSIS ANDENCEPHALOPATHIES /OF MITOCHONDRIALENCEPHALOPATHY LACTIC ACIDOSIS AND
LACTIC ACIDOSIS ANDWITH EDEMA /PROGRESSIVE
ENCODED BY CHROMOSOME 16 /GAMMA ISBY HUMAN CHROMOSOME 21 USINGBY LARGE GENOMIC REGIONSBY OPPOSITE DNA STRANDS OFGLYCOSYLTRANSFERASES IN HUMANREVERSE TRANSCRIPTASE ACTIVITY
ENCODES A BASIC/LEUCINE ZIPPER MOTIFA PROTEIN CONTAINING PROLINEA TUMOR SUPPRESSOR LOCUS AT /3
ENCODING A DYSTROPHIN CROSS REACTIVEA NEW MEMBER OF THE LEUCINEDRUG METABOLIZING ENZYMESGLUTARYL COA DEHYDROGENASEHUMAN CARBOXYPEPTIDASE TOHUMAN P58 A CELL CYCLE /GENEPHOSPHOGLYCERATE KINASE 1THE A SUBUNIT OF /IN THE GENETHE HUMAN RED AND GREENTHE MAJOR HUMAN APURINICTHE SECOND ENZYME OF THE
ENCYCLOPEDIA OF THE MOUSE GENOME /THEENDEMIC AREA IN TAIWAN /DISEASEENDOCIFUNE NEOPLASIA 1 REGION OF
NEOPLASIA 2A /TO MULTIPLENEOPLASIA TYPE 1 AND BCL 1
2119252021828032813279243746310081097205920731824621228310571039985251727932519265258881021262383248512535284018261201123511372548281425081063163216931295145512109081479
30245422431314155923251296246324352493
29250392426812951748362
2239159016841538781
2207683227
23672470248177133
9771010437101786621032281201
2298572188
24592288258823322380428232214622128506106723982270240918981363209019822184
NEOPLASIA TYPE 1 GENENEOPLASIA TYPE 1 GENETICNEOPLASIA TYPE 1 REGION OFNEOPLASIA TYPE 2 /MULTIPLENEOPLASIA TYPE 2A /MULTIPLENEOPLASIA TYPE 2A /MULTIPLENEOPLASIA TYPE 2A GENENEOPLASIA TYPE 2A REGIONNEOPLASIA TYPE 2B GENE TO
ENDOCRINOLOGICAL SYNDROMES /ANDENDOGENOUS RETROVIRAL LONG TERMINAL
RETROVIRAL SEQUENCES /HUMANRETROVIRUS IS ESSENTIAL /ANRETROVIRUSES /OF
ENDOMETRIAL CARCINOMA /OF CERVIX ONENDONUCLEASE A MEMBER OF A FAMILY OF
BANDING VARIANTS ONENDONUCLEASES UTILITY SHOWN BY TYPINGENDOREDUPUCATION TO TETRAPLOIDY /FROMENDS /THE PROPER FORMATION OF 3 MRNA
OF TERMINAL REARRANGED /BROKENENGINEERED FIBROBLASTS /BY GENEENGLAND AND WALES /REGISTER IN
FRANCO AMERICANS OF FRENCHENHANCER BINDING FACTOR 1 MAPPED TOENHANCES THE INDUCTION OF FRAGILE XENOLASE ACTIVITIES /OF NEURON SPECIFIC
CODING DNA SEQUENCES /OFENRICHED FOR FAMILIAL COMBINED /SAMPLE
IN HUMAN DERIVED /HIGHLYLIBRARIES /CHROMOSOME 22LIBRARY FOR CHROMOSOME 20MIDDLE ASIA FAMILIAL ISOLATE
ENVIRONMENT INTERACTION /GENOTYPEENVIRONMENTAL AND INDUSTRIAL FACTORS
ASSOCIATIONS AMONG MALECONTRIBUTION TO /ANDFACTORS IN THE ETIOLOGYFACTORS ON THE /ANDRISK /GENETIC DISEASE OR
ENVIRONMENTALLY INDUCED CANCER /OFENZYMATIC SYNTHESIS OF ALPHA /ANDENZYME ANALYSIS /BY DUAL RESTRICTION
AND AMNIOTIC FLUID GLYCINEAND SERUM PROTEIN /RED CELLDEFICIENCIES IN MAN /CHAINDEFICIENCY BIOCHEMICAL ANDDEFICIENT IN HEREDITARY /THEDIGESTION /BY RESTRICTIONMAPPING AROUND LOCUS Dl5S10 INOF THE HEME BIOSYNTHETICREPLACEMENT THERAPY /DISEASE BYREPLACEMENT THERAPY /OFREPLACEMENT THERAPY FOR /OFTHERAPY IN GAUCHER DISEASE /OF
ENZYMES /OF A FAMILY OF DNA REPAIRAND RESPONSES OF SICKLEDIN NONSPECIFIC MENTALIN THE CENTRAL REGION (VILLARELEVANCE TO INDIVIDUAL RISK
ENZYMOLOGY OF PRIMARY HYPEROXALURIAENZYMOPATHIES AND IN OTHER GENETICEPENDYMOMA /TUMOR SUPPRESSOR GENE INEPENDYMOMAS AND MEDULLOBLASTOMAS /INEPIDEMIOLOGIC APPROACH /RISK AN
INVESTIGATION OFSURVEY OF GENETICSURVEY OF GENETIC
EPIDEMIOLOGICAL AND GENETIC FACTORSAND MOLECULAR LINKAGEASPECTS OF NTDS INETIOLOGICAL ANDSTUDIES OF CLEFT LIPSTUDIES OF EARLY
EPIDEMIOLOGICALLY DIVERSE POPULATIONSEPIDEMIOLOGY /REGISTRIES TO GENETIC
AND EVALUATION OF GENEAND GENETICS OFAND MODELS FOR /GENETICAND PUBLIC HEALTH IMPACTAND SOME REGIONALOF ALCOHOLISM IN AOF CHROMOSOMAL DEFECTSOF CLEFT LIP WITH OROF COMPLEX PHENOTYPESOF DOWN SYNDROME IN TWOOF NARCOLEPSY /GENETICOF NTD IN TURKISH /INOF SINGLE GENE DEFECTSUSING MARKOV CHAINS IN
EPIDERMAL SURFACE ANTIGEN GENE MAPSEPIDERMOLYSIS BULLOSA /DYSTROPHIC
BULLOSA SIMPLEXBULLOSA SIMPLEX /WITHBULLOSA TO THE TYPE VII
EPILEPSIES /HYPERGLYCINEMIA OR WITHEPILEPSY /GENERALIZED AND PARTIAL
/IN PROGRESSIVE MYOCLONUSASSOCIATED WITH MENTALTO HLA /OF JUVENILE MYOCLONIC
EPILEPTIC PROBANDS /RELATIVES OFEPIMERASE DEFICIENCY IDENTIFIED BY /4EPIPHYSEAL DYSPLASIA (RIBBING TYPE)EPISKOPI BLINDNESS (NORRIE DISEASE)EPISOMAL COSMID IN A HUMAN CELL LINE
554
61210255951950195623402145217019821222242423372444414585
227016112528157624451655247435717881867159225762638272425212251237419472648548
276768161
2843666
27261635112056328665034874831007221924095535552483556
227021275202845428132484
1391136027082744276927786911989268058369226104026042646123149
26922725S752678265726972771836265927882372192720102257
7347347776756
20418771832762
20471646
Permuted Title Index
EPISTASIS /THAT INCLUDES VIABILITY ANDEPITHEIAL DIFFERENTIATION OF /DURING
TUMORS /18 IN OVARIANEPITHELOUMA (FERGUSON SMITH TYPE) TOEPITHEUUM /TO THE RESPIRATORYEQUIUBRIA AND APPLICATIONS /SELECTIONER 7 CHANGES AS A POSSIBLE GENETICERB B2 DIRECTLY CAUSES MALIGNANCY INERBBS ON MOUSE CHROMOSOME 11 /CLOSE TOERCC 1 /OF THE MURINE DNA REPAIR GENEERCC4 /MB OF THE EXCISION REPAIR GENEERROR FILTRATION OF HUMAN LINKAGE MAPS
IN FETAL DNA ANALYSIS DUE TOIN PRIMARY MYOPIA /REFRACTIVEINFLUENCE PHENOTYPE IN TRISOMYOF METABOLISM /INBORN
EBBORS /RESULTING FROM REPLICATION/WITH THREE CHROMOSOMEIN MITOCHONDRIAL DNA COPYOF COL2A1 METABOLISM /INBORNOF METABOLISM (CHANNEL II)OF METABOLISM /SPOTS AND INBORNOF METABOLISM IN HIGH RISKON RISK ESTIMATION FORON THE ESTIMATION OFPREVALENT AMIDST INBRED
ERYTHEMATOSUS /WITH SYSTEMIC LUPUSERYTHOROCYTES TO GRADED MOLAR /SICKLEDERYTHROCYTE AMP DEAMINASE /ON HUMAN
MEMBRANE PROTEINS IN /OFOF DUCHENNE MUSCULAR /AND
ERYTHROCYTES /ADHERENCE OF HUMAN/RECEPTOR ON HUMANFROM MATERNAL CIRCULATION
ERYTHROID DEVELOPMENT /AND GENETICS OFERYTHROLEUKEMIA /PREFERENTIALLY WITHERYTHROPOIETIC PORPHYRIA /CONGENITAL
PROTOPORPHYRIA /INERYTHROPOIETIN GENE /OF THE HUMANESCAPE INACTIVATION /AND GENES WHICH
X INACTIVATION /GENES THATESCAPES X INACTIVATION /A GENE WHICH
X INACTIVATION /DISTAL XP THATX INACTIVATION /GENE ON XP22.3
ESOPHAGEAL CANCER /HETEROZYGOSITY INCANCER /IN ARCHIVAL CHINESECANCER CELL LINE ENCODES ACANCER IN 221 HIGH RISK /OFCARCINOMAS /THE 90 CASES OF
ESSENTIAL DIFFERENCES IN ONCOGENEFATTY ACID AND CHOLESTEROLFOR DEVELOPMENT /PRODUCT CCFOR EXPRESSION OF THE HUMANHYPERTENSION /FEMALES WITHHYPERTENSION /TO PREDICTINGREGION OF THE FACTOR VilI
ESTERASE ABSENT IN WOLMAN DISEASEESTERIFICATION IN NIEMANN PICK MOUSEESTIMATION FOR PRESYMPTOMATIC TESTING
IN GENETIC EPIDEMIOLOGYOF AGE OF ONSET /TO THEOF ANEUPLOIDY LEVELS INOF CHROMOSOMAL LOADOF CHROMOSOME MAP LENGTHOF CYSTIC FIBROSIS CARRIEROF DUPLICATION OR DELETIONOF HEREDITARY DIFFERENCESOF PENETRANCE OF THE SOTOSOF PROPORTIONS DUE TO XOF THE EFFECTS OF FRAGILEOF THE FREQUENCY OF THE B
ESTRIOL /MSAFP HCG AND UNCONJUGATEDAND HCG SCREENING FOR TRISOMYIN MID PREGNANCY /UNCONJUGATEDLEVELS IN TWIN GESTATIONS
ESTROGEN AND GROWTH FACTORSETHICAL AND LEGAL ASPECTS
ASPECTS OF HUMAN GENETICSISSUES IN MEDICAL GENETICSISSUES WITH REGARD TO THIRD
ETHICS AND PUBLIC POLICY DEVELOPMENTCODE FOR GENETICISTS /A SPECIALFOR HUMAN GENETICISTS YES /OFIN HUMAN GENETICS AN OVERVIEWIN PRESYMPTOMATIC TESTING FORMAY NOW MANDATE INCREASING THETHE NATIONAL SOCIETY OF /OF
ETHNIC GROUP A MINORITY NATIONALITYGROUPS /EXCHANGES IN CERTAINGROUPS NNTR LOCI AMONG THREEGROUPS IN THE SAN LUIS VALLEYGROUPS INFLUENCE OF SELECTIONMINORITIES /FOR UNDERSERVED ANDORIGIN /HETEROZYGOTES OF MULTIPOPULATIONS OF TEXAS U.S.ASTATE /IN A LARGE MULTI
ETHNICITY VIA HUMAN MTDNA SEQUENCEETHNOCULTURAL DIVERSITY AND GENETICETHNOLOGICAL CLADOGENESIS OFETIOLOGICAL AND CYTOGENETIC PROFILESETIOLOGY /DISEASE HAVING COMPLEX
/DISEASES WITH COMPLEXOF 46,XX MALENESS /IN THEOF ATHEROSCLEROTIC DISEASEOF DEAFNESS IN AN /OF THE
205522432574598S9128081314257218642325170920171824895
1411439
234614343445
1843811
267517512076713
27332127491465829499
2858110S711368530
22142453S2922852440240223072609587
2288601604618913
24002444801273610022248523
175127882661
8316062076100616195487878022700274312331847125511972413181637
182140
17804241
Sil210182318141856284328372689S4
17901855
652701283417622842583
2738270
2225161
2761
OF ENVIRONMENTALLY INDUCEDOF MULTIFACTORIAL CONGENITAL
EUCHROMATIC LONG ARM OF THE HUMAN YY CHROMOSOME LONG ARM
EUGENICS /PAINLESSAND LYSENKOISM 1910 1990IN BRITAIN AND THE UNITED /TOON THE BASIS OF FAIRNESS /AND
EUKARYOTIC GENE REGULATION AND /OFEUROPE /DEHYDROGENASE DEFICIENCY IN
/NYHAN FAMILIES FROM NORTHERN/OF G551D AND DELTAF508 IN/PHENYLKETONURIA IN SOUTHERN
EUROPEAN AND OTHER POPULATIONS /INAND SOUTH ASIAN ORIGIN /OFCASE OF THE OHDO /FIRSTCOMMUNITY CONCERTED ACTIONCOUNTRIES IMPLICATIONS FORECONOMIC COMMUNITY A /IN THEECONOMIC COMMUNITY STUDY ONFAMILIES /ASCERTAINED
EUTHYROID HYPERTHYROXINEMIA /TRANSIENTEVANS CINNAMON RATS /ACTIVITY IN LONG
CINNAMON RATS /IN LONGEVENTRATION A NEW SYNDROMEEVOLUTION S3
AND ITS CONSEQUENCES FORAND NEW TECHNOLOGIESAND TISSUE EXPRESSION OFIN B CELL PROLYMPHOCYTICIN CHRONIC MYELOGENOUSNONRANDOM CHROMOSOME ER 7OF ALPHA SATELLITE DNAOF GLYCOPHORIN GENE LOCUSOF HOMINIDS /WITH THEOF HUMAN MITOCHONDRIAL DNAOF T CELL LEUKEMIA IN ANOF THALASSEMIA SCREENINGOF TISSUE SPECIFICITY ANOF V KAPPA IMMUNOGLOBULINOF WEST AFRICAN POPULATIONSRECONSTRUCTED BY MOLECULARTHROUGH RRNA GENES /AND APE
EVOLUTIONARY ANALYSIS OF MUTATIONSCONSERVATION OF AMINOCONSERVED SEQUENCES FROMIMPLICATIONS /ANDMECHANISMS /AND
EWING TRANSLOCATION ON CHROMOSOME 22EX VIVO GENE THERAPY IN LDL RECEPTOREXCHANGE AND CHROMOSOME ABNORMALITIES
DETERMINATION TECHNIQUEFREQUENCY IN ICTERIC NEWBORNSHIGH PERFORMANCE LIQUIDIN MALNUTRITION /CHROMATID
EXCHANGES /OF SISTER CHROMATIDAND HUMAN REPRODUCTIVEIN CERTAIN ETHNIC GROUPSIN HUMAN LYMPHOCYTE CULTURESIN MOUSE TUMOR AND ASCITIC
EXCISION REPAIR GENE ERCC4 /MB OF THEREPAIR PATHWAYS IN HUMAN /DNA
EXCLUSION AS THE CAUSATIVE GENE INDATA FOR THE LONG-QT(ROMANOMAP /ECLAMPSIA A PRELIMINARYMAP USING RFLPS AND /ANOF 5011 013,5034 OTEROF CANDIDATE LOCI /BLACKSOF CANDIDATE REGIONS ONOF LINKAGE TO TRANSFORMINGOF THE ARSACS GENE FROMOF THE DELETED INOF THE GENE FOR FAMILIALOF THE GENE FROM CHROMOSOME
EXCLUSIONS /BY APPARENT MATERNALEXCRETION APPLICABLE TO SMALLEXOGENOUS CHOLESTEROL ESTERIFICATION
DNA INTEGRATION LEADING TODNA PREFERENTIALLYSTEROID SULFATASE IN SV 40
EXON 17 OF THE AMYLOID PRECURSOR /THE8 AND CARRIERS IN HIS FAMILY /OFAMPLIFICATION /REGION BYDELETION IN GYRATE ATROPHY /IN ANDELETION IN THE DYSTROPHIN GENEMUTATION IN HUMAN B /NOVELSKIPPING DURING SPLICING OFSKIPPING IN THE CANINE
EXONIC (C2K19T) AND INTRONIC SEQUENCEEXONS AMPLIFIED IN MULTIPLEX /OF 14
IN A PATIENT WITH DUCHENNE /OF 3EXPANSILE OSTEOLYSIS EXCLUSION OF THE
OSTEOLYSIS FROM EXTENSIVEEXPERIMENTAL HYPERTENSION /MAPPING IN
MOSAICISM IN INTERPHASEEXPERIMENTS BASED ON BINARY SCORINGEXPRESSION /FREQUENCY AND PHENOTYPIC
/HUMAN LDH C4 GENE AND ITS/HYDROXYLASE GENE/OF LOW LEVEL FRAGILE X/ON FETAL G GLOBIN GENE/PREVALENCE AND PHENOTYPIC/TRAIT WITH VARIABLENARIABILITY IN CLINICAL/WITH SPERM SPECIFIC GENE
2726128821052176181532131918182619195
105327032280191666
763354174733418022043853512438640
ONS32578S34237913041327131426402625261326392604386
2444185726342641165186
26322260262326192083423130216041568565158625651196284325431341170924121996219719192021204320002030101320041991201619292810577523
25561705492
1071690
2383280223511112235196747110332549192920161866164821211078128624621550242327312237858
2416
ANALYSIS /MAPPING ANDANALYSIS OFAND ACATALASEMIA /GENEAND IN VITRO PROTEINAND INHERITANCE OF A 40KAND PROLONGED PROLIFERATIONAS AN APPROACH TO REVEALAS AN INDICATION OF /SITEASSOCIATED WITH AGE /GENEAT THE PEPD LOCUS /CLINICALCLONINGS /GENE MAMMALIANDURING THE RAT DEVELOPMENTIN AUTOIMMUNE DISEASE /ANDIN DIFFERENT NEUROBLASTOMAIN HEPATOCYTES /TRANSGENEIN HUMAN CANCERSIN HUMAN HEPATOMA CELLSIN HUMAN OVARIAN CANCERIN LYMPHOCYTES FROM /SITESIN NF1 A TWIN STUDY /ININ NORMAL AND TRIPLOID /GPDIN SMALL CELL LUNG CANCEROF A HUNTINGTON DISEASEOF A PARTIALLY DELETEDOF ACYLPEPTIDE HYDROLASEOF ALLOGENEIC SWINE CLASSOF B HEXOSAMINIDASE A GENEOF CALPAINS IN SKELETALOF CARTILAGE DEFECTS INOF COLLAGEN GENESOF COMMON FRAGILE SITES INOF FETAL HEPATIC ALPHAOF HEREDITARY GINGIVALOF HUMAN CYSTATHIONINE BOF HUMAN FACTOR IX CDNA INOF LYMPHOCYTE CELL SURFACEOF PLACENTAL PROTEINS INOF PRIMARY CONGENITALOF RECOMBINANT DYSTROPHINOF THE DMD LIKE LOCUS ONOF THE HUMAN /ANDOF THE HUMAN /INDUCIBLEOF THE HUMAN /TRANSFER ANDOF THE HUMAN SALIVARY /FOROF THE MURINE DNA REPAIROF THE MYOTONIC DYSTROPHYOF THE PROSAPOSINE GENEOF THE RETINOBLASTOMA GENEOF THE SRY GENE IN COS /THEPATTERNS OF MATRIX GENESREGULATION IN THE PROCESSVECTORS /IN EBV BASEDWITH CHROMOSOME SPECIFIC
EXPRESSIONS ALTERATION OF NEURON /GENEOF HEMOGLOBIN E /AN
EXTENDED COSMID WALK OF 460 KB IN AFAMILY CARRYING AN INVERTEDHAPLOTYPES IN A FAMILY WITHMULTIGENERATION PEDIGREE /AN
EXTENSION A NOVEL QUANTIFIABLE METHODEXTERNAL EAR ARE NOT ASSOCIATED WITHEXTRACELLULAR AMINOACID SUBSTITUTIONEXTRACTION NERSUS PHENOL:CHLOROFORM
FROM FORMALIN FIXED TISSUEEXTRACTS AND IS ASSOCIATED WITHEXTRAGONADAL GERM CELL TUMORS /OFEXTRAMICROCHROMOSOME /X SYNDROME WITHEXTRANODAL LARGE CELL LYMPHOMA /ANDEXUDATIVE VITREORETINOPATHY /FAMILIALEYE ABNORMALITIES /ANTERIOR CHAMBER
DISEASE /ANALYSIS OF ALAND ISLANDDISEASE /AND ALAND ISLANDDISEASE/INCOMPLETE CONGENITALDISEASES /GENES FOR THE X LINKEDLENS SPECIFIC PROTEIN AN ANIMAL
F
FS0B CYSTIC FIBROSIS MICRODELETIONF7R /AND NORMAL COAGULATION STUDIESFABRY DISEASE /STUDIES AND THERAPY OF
DISEASE /WITH THE X LINKEDFACIAL ABNORMALITIES MICROMELIA AND
AND SKELETAL ANOMALIES CAUSEDANOMALIES SYNDROME /INSTABILITYAPPEARANCE /AND DISTINCTAPPEARANCE SYNDROME (MIM-CLEFTING IN CHILE /ANALYSIS OFDIGITAL SYNDROME TYPE I AND 11DIGITAL SYNDROMES /ON THE ORALDIGITAL SYNDROMES TO LUMP ORDYSMORPHOLOGY /ANOMALIES ANDGESTALT IN SIBLINGS A NEWGROWTH RABBIT MODEL FOR /IN
FACIES IN TWO SIBLINGS /DISTINCTIVEMIXED DEAFNESS SYNDROMESYNDROME THE FIRST REPORT OF A
FACIO CUTANEOUS SKELETAL INVOLVEMENTCUTANEOUS SKELETAL SYNDROME /THE
PACIOSCAPULOHUMERAL DISEASE WITH /OFDYSTROPHY LOCUS
555
22594832448193
26849185761623409
232725922230425
242024852580242524131390
132451224
2391246125792490244648647
35313631205684
23232474625919764
24802379247124532492244423252222243925842393930
2233247616442576107223961453693996974724
24552508108124171311148661885714941905712810
25312268
1092150024751743888698644903667803831342633836773931792883728646646
20121966
Permuted Title Index
MUSCULAR /OFMUSCULAR /OF THEMUSCULAR /OF THEMUSCULAR /THEMUSCULAR DYSTROPHY
FACTOR 1 MAPPED TO HUMAN CHROMOSOME 4A AND B CHAIN PROMOTER REGIONSA MALE FERTILITY GENE ON THEALPHA GENE /TRANSFORMING GROWTHALPHA TO NONSYNDROMIC CLEFTALPHA WITH CLEFT LIP AND PALATEB1 GENE IN EMBRYONIC STEM CELLSCYTOKINE THERAPY /STIMULATINGElF 4E /BY INITIATIONEVIDENCE FROM THE EXPRESSIONFOR NONDISJUNCTIONGENE (SPI) AND THE 1,25GENE AS A CAUSE FOR TYPE IlBGENE CAUSING A DOMINANTGENE IN FAMILIAL ORTHOSTATICINJECTION EXTRACTED FROM FETUSINVOLVED IN INDUCTION OF CLASSIX CDNA IN ANIMALS BY GENEIX FROM GENETICALLY MODIFIEDIX FUNCTION AS SPACER ELEMENTSIX GENE A MODEL FOR STUDYINGIX GENE HAVE A G+ C CONTENT OFIX GENE IN TRANSGENIC MICEIX IN 64 HEMOPHILIA B PATIENTSIX MUTATION /MOSAICISM FOR AIX THROUGH MICRO ENCAPSULATEDLOCI MAY BE INVOLVED IN /CELLMAPPING ON Y CHROMOSOMEMUTANT CELL LINE OF THYMIDINEPCRFLPS BY HIGH RESOLUTIONRECEPTOR (C KIT) GENE COMPLEXRECEPTOR A MASTISTEM CELLRECEPTOR GENE ISOLATED FROMRECEPTOR GENE WITHIN THE X YRECEPTOR PROTO ONCOGENE INTO THE DISTAL EUCHROMATIC YVil GENE /CPG ISLAND 5 OF THEVil GENE /POINT MUTATIONS OFVil GENE BY A FAST PROCEDUREVil GENE IN HEMOPHILIA A /THE
FACTORS /ENVIRONMENTAL AND INDUSTRIAL/KARNATAKA INDIA EVIDENCE ANDAND REVERSE TRIKODOTHYRONINECREATES HOT SPOTS FORFROM FETAL BOVINE TISSUESIN ETIOLOGY OF MULTIFACTORIALIN IMMUNODIFFERENTIATIONIN NTDS /OF GENETICIN PRIMARY GLAUCOMA /GENETICIN THE ETIOLOGY OFIN THE GROWTH OF CHILDREN OFIN WOMEN'S ACCEPTANCE OFIN YOUNG MONOZYGOTIC TWINSINVOLVED IN CARCINOGENESISINVOLVED IN PARENTALON THE INCIDENCE OFREGULATION OF C MYC AND C FOSTHAT CONTROL DETERMINATION
FAINT POSITIVE ACETYLCHOLINESTERASEFAIRNESS /AND EUGENICS ON THE BASIS OFFALSE NEGATIVE RESULTS /ALSO LEAD TO
POSITIVE AFAFP AND ACHE TESTSFAMILES /OF 20 PRADER WILLI SYNDROMEFAILIAL (13;22) ROBERTSONIAN /OF
ADENOMATOUS POLYPOSIS BY /OFADENOMATOUS POLYPOSIS COLIADENOMATOUS POLYPOSIS GENEADENOMATOUS POLYPOSIS IN 16ADENOMATOUS POLYPOSIS LOCUSAGGREGATION AND TRANSMISSIONAGGREGATION OF AMYOTROPHICAGGREGATION OF ANDAGGREGATION OF BLOODAGGREGATION OF LEISHMANIAAGGREGATION OF STROKE /OFAGGREGATION OF SYMPTOMSALZHEIMER DISEASE /21 LOCI INALZHEIMER DISEASE /GENE INALZHEIMER DISEASE /JAPANESEALZHEIMER DISEASE IN JAPANAMINO ACID SUBSTITUTION INAMYCTROPHIC LATERAL SCLEROSISAMYLOID POLYNEUROPATHY I /INAMYLOIDOTIC POLYNEUROPATHYAMYOTROPHIC LATERAL /OFAMYOTROPHIC LATERAL SCLEROSISAND NONFAMILIAL ALZHEIMER /INAND SPORADIC OVARIAN BREASTASSOCIATION /AND TWINNING ABALANCED CHROMOSOME /OFBALANCED T(BP;130) /OF ABRAIN TUMOR REGISTRYBREAST CANCER /OF EARLY ONSETBREAST CANCER /SUFFERINGBREAST CANCER EVIDENCE FORCANCER /COUNSELING ANDCANCER /IMPORTANCE OFCANCER IN THE NETHERLANDS /OFCASE AND REVIEW OF THE /OF ACASE OF PARTIAL TRISOMY 2031
1904143
2217204220371867241522051015101322422435619
245023931591187010684441037253321032474248826322437282124876582599248125661665246620842296229623842360189
21762154994100222835481845144225409501288119
2235691161
28811744921S931760284324133261274181810601165103515691876591
21321051101
271327042739272026512744276319922381107173911901910275757880
1938281160391512471421615
2024596202626927327215361406
CASE WITH 17011.2 DNA /OF ACASES OF GASTROSCHISIS IN ACHANGES IN PLASMA AMMONIACHROMOSOMAL INSTABILITY /NEWCHROMOSOMAL TRANSLOCATIONCOMBINED HYPERLIPIDEMIA /FORCONGENITAL ATAXIA MENTALCREUTZFELDT JAKOB DISEASECREUTZFELDT JAKOB DISEASECREUTZFELDT JAKOB DISEASE /INCREUTZFELDT JAKOB DISEASE ISDEFECTIVE APOLIPOPROTEIN BDELETION OF 8P23.1 MINIMALDILATED CARDIOMYOPATHY /INDISEASES /IN ANALYSIS OFDISEASES A FORMULATION /FORDYSAUTONOMIA /ANALYSIS INDYSBETALIPOPROTEINEMIAEVALUATION DETERMINES AEXPANSILE OSTEOLYSISEXPANSILE OSTEOLYSIS FROMEXUDATIVE VITREORETINOPATHYFIBROMUSCULAR DYSPLASIA OFGENETICS ABNORMALITY INHYPERCHOLESTEROLEMIA /AMONGHYPERCHOLESTEROLEMIA AND /FORHYPERCHOLESTEROLEMIA INHYPERCHOLESTEROLEMIA LDLRHYPERTROPHIC CARDIOMYOPATHYHYPOTRANSFERRINEMIA /OFINCIDENCE OF TWINNING AMONGISOLATE /ENRICHED MIDDLE ASIAMEDITERRANEAN FEVER ANMEDITERRANEAN FEVER A /INMEDITERRANEAN FEVER PATIENTSMEDITERRANEAN FEVER PATIENTSMEDULLARY THYROID CARCINOMANARCOLEPSY /HETEROGENEITY INNEONATAL CONVULSIONS IN ANEONATAL SEIZURES AUTOSOMALOCCURRENCE OF IDIOPATHICOCCURRENCE OF PORENCEPHALYORTHOSTATIC INTOLERANCE /INOSTEOARTHROSIS AND MUTATIONSOVARIAN CANCER /AT ONSET FORPARACENTRIC INVERSIONPARACENTRIC INVERSION OF 9PPERICENTRIC INVERSION OFPOROCYSTIC OSTEODYSPLASIAPSEUDOHYPERALDOSTERONISMRISKS OF CONGENITAL /OFSACRAL DYSGENESISTRANSLOCATION /DUE TOTRANSMISSION OF SEGMENTALTRICHO RHINO PHALANGEAL TYPE
FAEUAUTY IN BREAST CANCER IN AFAIUES/1022 23 IN 45 BRITISH
/13 NORWEGIAN CYSTIC FIBROSIS/90H + VARIANT BAND IN TWO/ASCERTAINED EUROPEAN/BECKER MUSCULAR DYSTROPHY/CHICAGO AREA CYSTIC FIBROSIS/EXPERIENCES WITH 100/FIBROMATOSIS A REPORT OF TWO/IMMUNOGLOBULINS IN TWIN/IN 221 HIGH RISK CHINESE/IN ITALIAN HEMOPHILIA B/INHIBITOR IN DOWN SYNDROME/MALIGNANT LYMPHOMA AND THEIR/MARKERS IN FOURTEEN DANISH/NEVUS SYNDROME IN CHINESE/OF HUMAN SATELLITE DNA/OF SEVEN PREVIOUSLY REPORTED/ONTO CHROMOSOME 4QTER IN TWO/PORENCEPHALY IN TWO SWEDISH/RISK IN LEFT FLOW DEFECT[THYROID DISEASE IN/TO D5S39 IN FRENCH CANADIAN/WITHIN AMERICAN (U.S.A.)A COMMON UNDERREPORTED /FIVEAFFECTED BY CONGENITALAND 16 SPORADIC CASES AN 9AND REVIEW OF SEVEN /TWO NEWAVOID EARLY CHD DEATHS /RISKBY ASTHMA SUBTYPE /ASTHMATICBY SOUTHERN BLOT AND PCRFROM A GEOGRAPHICALLY /INFROM NORTHERN EUROPE /NYHANIN LATIN AMERICA /AMONGIN NORTH CHINA AND THEIRIS THERE AN AGE EFFECTON CHROMOSOME 10 AND 12 AREON HUMAN CHROMOSOME 21REVEALS NO LINKAGE /DYSTROPHYTOWARD GENETIC COUNSELINGUSING CA POLYMORPHISMS IN AUSING DATA FROM A TUMORUSING DYSTROPHIN PROTEIN ANDUSING SOUTHERN BLOTTING ANDWITH A LOW PENETRANCE FORMWITH BIPOLAR DISORDER /INWITH DYSKERATOSIS CONGENITAWITH FRAGILE X SYNDROME /INWITH GENERALIZED RECESSIVEWITH HEREDITARY /STUDIES IN
63588447714361153272464510002390229110031036150010622643278618809961417192920168577051159268210362329280419204692666194718728581245155418882019833761659719103746
5821748158914778738392650880150981810796071967110715132043104618291757684
264460126521595134919231359169619341132719
26502663201818937826546761934164789958
28401053269611141474223421202848176497860010961110221
209180285419271930
WITH HUNTINGTON DISEASE /INWITH LEBER HEREDITARY OPTICWITH MANIC DEPRESSIVE /OFWITH MARKERS FROM THE [TYPE 1WITH MULTIGENERATIONAL /ANDWITH ORNITHINE /PIGMENTOSAWITH PARACOCCIDIOIDOMYCOSISWITH POLYMORPHIC PROBES /16WITH PROXIMAL SPINAL /INWITH RECURRENT TRISOMY 21 /OFWITH THE SIMPSON GOLABI /NEWWITH THE X LINKED FABRY /IN
FAMILY /102150 REPORT OF A SECOND/AND BIOCHEMICAL SCREENING OF A/BELONGS TO AN ACID LIPASE GENE/DISEASE IN A THREE GENERATION/DXS52 IN A FRAGILE X NEGATIVE/GENE OF JUN/FOS ONCOGENE/HETEROZYGOSITY REPORT OF A/OF EXON 8 AND CARRIERS IN HIS/OF HAN AND ZHUANG MINORITIES/ON A LARGE FIVE GENERATION/RECURRENCE OF DELliP15 IN A/SAME MITOCHONDRIAL DNA GENE/SYNDROME TYPE I CORROBORATIVE[THE LEUCINE RICH GLYCOPROTEIN2 CYSTATINS MAP TO TWO /OTHERALLELES RESULTING FROM GENE /PAS A MODEL FOR ANALYSIS OFCARRYING AN INVERTED /EXTENDEDCASE REPORT /ANOMALIES ACHARACTERIZED BY MONOMERICDATA /ONSET DISTRIBUTIONS FROMDISPLAYING X LINKED RECESSIVEDOCTOR RELATIONSHIP ETHICAL /INEVIDENCE FOR MULTIPLE ORIGINEXHIBIT A COMPLEX METHYLATIONHEALTH EVALUATION INCREASINGHISTORIES OF BREAST CANCERHISTORY DATA ON SEIZURE /OFHISTORY OF CANCER /RELATION TOINFORMATIVE ABOUT PHENOTYPE /11INVOLVEMENT OF /AND EXTENSIVEMEMBERS IN THE CLINICAL /OFMEMBERS OF AUTISTIC PROBANDSOF DEFECTIVE HUMAN ENDOGENOUSOF DNA REPAIR ENZYMES /OF AOF EASTERN QUEBEC /WITHIN AOF MIRROR REFLECTED AND WIDEOF PUTATIVE ZINC FINGER GENESOF RECEPTOR MEDIATED TERATOGENSPEDIGREE /ANALYSIS OF APHENOTYPE AND LINKAGE TOPLANNING PROGRAM /THROUGH AREGISTER OPPORTUNITY FORSCREENING FOR AUTOSOMAL /OFSTUDIES /USEFUL INSTUDY AND GENETIC ANALYSES /ASTUDY OF OBSESSIVE COMPULSIVETESTING AND POPULATIONUNLINKED TO CHROMOSOME 10 /2 AWHERE CLOSE LINKAGE TO HLA ISWITH A SEVERE FORM OF /THE SAMEWITH AUTOSOMAL DOMINANTWITH BI VARIANT OF GM2 /IN AWITH CROUZON SYNDROME /IN AWITH DOMINANT INHERITANCE OFWITH EIGHT AFFECTED MEMBERSWITH EPIDERMOLYSIS BULLOSA /AWITH EPISKOPI BLINDNESS /IN THEWITH FAMILIAL MEDULLARY /IN AWITH FEATURES OF THE /NEWWITH HEREDITARY COLON CANCERWITH HEREDITARY NEPHRITIS /IN AWITH MEDIUM CHAIN ACYL COA /AWITH MITOCHONDRIAL MYOPATHY /AWITH PELIZAEUS MERZBACHER /IN AWITH THREE AFFECTED SIBLINGS /AWITH X LINKED ICHTHYOSIS AND /AWITH X LINKED SPINOCEREBELLAR
FAMMM SYNDROME /INSTABILITY IN THEFANCONI ANEMIA /A CANDIDATE GENE FOR
ANEMIA /GLYCOPHORIN A LOCUS INANEMIA /HETEROGENEITY INANEMIA AND ATAXIA /OFANEMIA AND ITS CORRECTION INANEMIA CELLS /REPAIR DEFECT OFANEMIA DEFECT BY GENE /OF THEANEMIA LIKE CHINESE HAMSTERANEMIA LINKAGE ANALYSIS WITHANEMIA LYMPHOBLASTS /LOCUS INANEMIA PATIENTS [TOANEMIA PATIENTS IN VIVO /ONANEMIA PATIENTS IN VIVO /ONANEMIA REGISTRY A NEED FORANEMIA WITH SIX MARKERS ON /OFNEPHROPATHY (GLYCOGEN STORAGE
FARLANE SYNDROME PROBABLY RECESSIVEFARMS IN HAINAN PROVINCE CHINA /STATEFASCICUN II FUNCTIONS AS A NEURONALFAST PROCEDURE DETECTS 3 NOVEL /BY AFASTING INSULIN LEVELS IN HISPANIC MENFATAL BRAIN DISORDER /POSSIBLE IN THIS
HYPERAMMONEMIA RESULTING FROM AFATHER AND TWO MOTHERS /FROM SAME
556
211101920381998517
19312673105110931713735174366710252248149019802308632690
2851737
157233
6852380218327972619145363916942661689181610702436177760827232695452732
1610625
23372270200224332272129163419611512082491039270527192511077205249699910591447808
147122572047188811045996934984371083840805198713161874253523761609296
227522742250196225591522140114186961965846769
2768325100226661935559747
Permuted Title Index
MOTHER AND SIB SIB DEPENDENCEWAS UNAVAILABLE FOR TESTING
FATTY ACID AND CHOLESTEROL IN NEUACID OXIDATION DEFECTSACID OXIDATION DISORDERSACID TRANSPORT DISORDERS /CHAINACIDS IN X ADRENOLEUKODYSTROPHYACYL COA OXIDASE A NOVEL /CHAIN
FEDERAL REPUBLIC OF GERMANY A REPORTFEIL ANOMALY /THORACIC FUSION KLIPPELFELINE MODEL FOR ACHONDROPLASIAFEMALE WITH 45,X/46,XR(X) AIN A
WITH INGUINAL HERNIA AIN AWITH MIXED GONADAL DYSGENESISWITH REPEATED FETAL LOSS /IN AWITH X;3 BALANCED TRANSLOCATION
FEMALES COUNSELING ISSUES AND LONG /XWITH CARCINOMA OF CERVIX ONWITH ESSENTIAL HYPERTENSIONWITH X/Y TRANSLOCATION
FEMORAL HYPOPLASIA UNUSUAL FACIESFEMUR FIBULA ULNA COMPLEX AN ANALYSISFERGUSON SMITH TYPE TO THE LONG ARMFERRIC REDUCTASE GENE OF THE YEASTFERROCHELATASE SEQUENCE CHROMOSOMALFERTIUTY AND MALARIAL POLYMORPHISMS
GENE ON THE HUMAN Y /A MALEFERTILIZATION PROCEDURE /THE IN VITROFERTILIZING ABILITY OF SPERM INFETAL ANEUPLOIDY RISK SPECIFICATION
BLOOD A PROBLEM FOR DETECTIONBLOOD BY CORDOCENTESIS /AND INBOVINE TISSUES IMPROVE LIFECARDIAC DISEASE /MSAFP DUE TOCARDIAC ULTRASOUND ANDCELL SAMPLING INFUSION OF THECELLS IN MATERNAL BLOODCELLS IN MATERNAL BLOODCELLS IN THE MATERNALCELLS IN THE MATERNAL /USINGCELLS NEW RESULTS FROM A LARGECHROMOSOMAL ANOMALIES /OFCHROMOSOMAL DISORDERS /FORCHROMOSOME ABERRATIONS /OFCHROMOSOME ABNORMALITIES /OFCONGENITAL MALFORMATIONS /ANDCYTOGENETIC ABNORMALITY /OFDEATH /OF MACERATED INTRAUTERINEDEMISE /FINDINGS AFTERDEVELOPMENT /THE STUDY OF EMBRYODEVELOPMENT AND PREGNANCY /CVSDIAGNOSIS TECHNIQUES AND OUTCOMEDNA ANALYSIS DUE TO /ERROR INDNA IN MATERNAL BLOOD BY PCR /OFDOWN SYNDROME /THE RISK OFDOWN SYNDROME IN WOMEN LESS /FORDYSMORPHOLOGY IN 250G GLOBIN GENE EXPRESSION /ONHEMOGLOBIN LEVELS IN ADULTS ISHEPATIC ALPHA FETOPROTEIN IN /OFHYDROPS /A CASE OF RESOLVEDINFECTION /PLACENTAL MARKER FORINTRA ABDOMINAL CALCIFICATIONSKARYOTYPING /COUNSELING ANDKARYOTYPING AT CHULALONGKORNLOSS /IN A FEMALE WITH REPEATEDMALFORMATIONS AND ANEUPLOIDYMICROSCOPIC ARCITECTURE /OFMOSAICISM /ALWAYS INDICATE TRUEMOSAICISM /RESULTING INMUSCLE BIOPSY /DYSTROPHY BYNUCHAL FLUID PHYSIOLOGIC ORNUCLEATED ERYTHROCYTES FROM /OFOR NEWBORN LIVER BY /THEOUTCOME CHANCE OR CLINICALLYPHENOTYPES AND PARENTAL ORIGINPREGNANCY REDUCTION /MULTIREPORT OF A CASE OF MOSAIC /ORRICKETS /THE HISTOPATHOLOGY OFSEX DETERMINATIONS PRENATALSEX SELECTION POLICIESSIZE MARKERS IN SCHIZOPHRENIA AT CELL RECEPTOR B JUNCTIONALTISSUE OF TWIN GESTATION /ANDUS ANOMALIES /PREGNANCIES WITHVENTRAL WALL DEFECTS /HCG ANDWASTAGE /A POSSIBLE CAUSE OFWASTAGE /MARRIAGES DUE TO
FETO PLACENTAL INTERACTIONS /INFETOPROTEIN IN DOWN SYNDROME AN /ALPHA
LEVELS IN NONLETHAL /ALPHAFETUS /HUMAN CHIMERISM IN A STILLBORN
/MOLAR PREGNANCY AND LIVEBRAIN /INJECTION EXTRACTED FROMDATA FROM THE GERMAN /AND THEWITH PRENATALLY DETECTED 5P/1OP
FETUSES /AGAINST TRISOMY 16 MOUSE/DETECTION OF ANEUPLOID/FEVER PATIENTS AND THEIR/LOSS OF HLA COMPATIBLE/NORMAL AND TRIPLOID OPOSSUMAND NEWBORNS IN BYELORUSSIAAT RISK AND PCR TESTING FORWITH DOWN SYNDROME /INWITH SKELETAL DYSPLASIAS /TWO
2643287791326225926151652718028328091452147713861230147211415858011458728235598
236322142645220512841552122591112859501235275128760
1131109115111
12681155161418231290112911491691908914S831824106011271844941
242375
12059221133118212731249123012741174142315691207946110
24691135104
12761231925
16911784909
2240164194118261158123611611205851937
115425331264142914322761245932
2451269911857581526
WITH TRISOMY 21 /IN 98FEVER /IN FAMILIAL MEDITERRANEAN
/REACTION AND RECURRENTA GENETIC DISORDER WITH MARKEDPATIENTS /FAMILIAL MEDITERRANEANPATIENTS AND THEIR FETUSES
FIBERS ABNORMALITY AT 28 WEEKSFIBRILLAR COLLAGENS /IN GENE FORFIBRILUN /AND GENETIC LINKAGE OF
CDNA A CANDIDATE GENE FORGENE FOR MARFAN SYNDROME
FIBROBLAST LINE /IN A WERNER SYNDROMESPECIFIC TRANSCRIPT THAT /A
FIBROBLASTS /AND FLAVIN METABOLISM IN/BY GENE ENGINEERED/ENCAPSULATED RECOMBINANT/IN RECONSTRUCTIONS OF/LEVELS IN CULTURED/OF SV40 TRANSFORMED HUMAN/SV 40 TRANSFORMED HUMAN/TYPE VIAND LEUKOCYTES OF /INAND LYMPHOBLASTS FROM /INBY RETROVIRAL MEDIATEDBY THE TRANSFER OF HUMANMALE PRONUCLEI AND /NUCLEIOF SIALIDOSIS PATIENTS /INSTABLY EXPRESSING NORMALVECTOR MEDIATED /HUMANWITH THE NORMAL AND /HUMAN
FIBROMATOSIS A REPORT OF TWO FAMILIESFIBROMUSCULAR DYSPLASIA OF THEFIBROSIS /A DIAGNOSIS OF CYSTIC
/ELEVATED INCIDENCE OF CYSTIC/GENETICS AND CYSTIC/NOT ASSOCIATED WITH CYSTIC/PRENATAL DIAGNOSIS OF CYSTIC/SCREENING FOR CYSTIC/SCREENING FOR CYSTIC/TO HEMOPHILIA A AND CYSTIC/WITH REFERENCE TO CYSTICALLELES /IN BRAZILIAN CYSTICAMONG PREGNANT WOMEN INAND A 1 ANTITRYPSIN /CYSTICCARRIER FREQUENCY IN /CYSTICCARRIER TESTING ASSESSINGCD508 MUTATION FROM SINGLECENTERS /SERVICES BY CYSTICCFTR AND CHLORIDE CHANNELEXPERIENCES FROM A /OF CYSTICFAMILIES /13 NORWEGIAN CYSTICFAMILIES /CHICAGO AREA CYSTICGENE /FUNCTION OF THE CYSTICGENE /WITHIN THE CYSTICGENE CARRIERS COMPARISON OFGENE FROM HUMAN MONKEYGENE IN BASHKIR POPULATIONGENE IN JEWISH AND ARABGENE MUTATIONS /OF CYSTICGENE MUTATIONS IN MALES WITHGENOTYPING BY DIRECT PCR OFIN A NEWBORN SCREENINGIN LENINGRAD /OF CYSTICIN NATIVE AMERICANS OF THEIN THE CLINICAL LABORATORYIN U.S.A COUPLES WITHOUT ALOCUS /GENE AND THE CYSTICMICRODELETION /F508 CYSTICMUTATION G542X IN JEWISHMUTATIONS /FOUR COMMON CYSTICMUTATIONS /THREE NOVEL CYSTICMUTATIONS AMONG GERMAN ANDMUTATIONS BY CHEMICAL /CYSTICMUTATIONS BY MEANS OF ASOMUTATIONS IN FAMILIES FROM AMUTATIONS IN HIGH AND LOWMUTATIONS IN ITALY FREQUENCYMUTATIONS IN SPAIN /OF CYSTICMUTATIONS IN TORONTO /CYSTICMUTATIONS USING /CYSTICMUTATIONS USING A MULTIPLEXMUTATIONS USING PCR MEDIATEDPATIENTS /IN ITALIAN CYSTICPATIENTS HAVE DIFFERENTPATIENTS IN FRANCE /OF CYSTIC
FIBULA APLASIA AND COMPLEXULNA COMPLEX AN ANALYSIS OFUNUSUAL FACIES MIXED DEAFNESS
FICTION /OF HUMAN SOLID TUMORS FACT ORFIELD DEFECT /AS A DEVELOPMENTAL
ELECTROPHORESIS AFTER NRUIGEL ELECTROPHORESIS /BY PULSEDVOLE MICROTUS AGRESTIS /IN THE
FILAMENT PROTEINS DURING EPITHELIALFIUPINOS /AMONG CHINESE LAOTIANS ANDFILTER PAPER /SAMPLES COLLECTED ON
PAPER BLOOD SPECIMENS /DRIEDFILTRATION AND RECIRCULATION OF THE
OF HUMAN LINKAGE MAPSFINE GENETIC MAPPING OF THE JUVENILE
MAPPING OF THE X LINKEDMAPPING OF X LINKED CLASPEDRESOLUTION PHYSICAL MAP OF THESTRUCTURE MAPPING BY IN SITU
FINGER GENES /ANALYSIS OF HUMAN ZINC
83518721321858155412451145
443459493
25482399497
247424812141501
25984924671000513
249126012153495
23642587144568470511822840
6887100425118422525273228631848S911006183612101769S511030110718292418100918302612231725512798106
1840110227412676111318412883109222451047231123442814184928409701078107422611105993997985
2798463847235883372889621
211917102243267911861102126620171972112619252177
542263
GENES MAPPING TO CHROMOSOME 22GENES ON HUMAN CHROMOSOME 19PROTEIN GENES USING /HUMAN ZINC
FINGERPRINTING HUMAN CHROMOSOMES BYIN PARENTAGE TESTINGIN VERIFICATION OF /DNA
FINGERPRINTS /OF SIMILARITY OF DNAFINLAND /LETHAL ARTHROGRYPOSIS IN
/SPINAL MUSCULAR ATROPHY INFINNISH ASPARTYLGLUCOSAMINURIA /FROM
DUCHENNE AND BECKER MUSCULARPATIENTS WITH /DISEASE INPOPULATION /DISORDERS AND THETYPE /SYNDROME POSSIBLE
FINNS AND OTHERS /GYRATE ATROPHY AMONGFISSION OF FAMILIAL (13;22)FISTULA /ATRESIA AND TRACHEOESOPHAGEALFISTULAE AND OESOPHAGEAL ATRESIAFIX GENE /FOR POINT MUTATIONS IN THEFIXED TISSUE /ANALYSIS IN POSTMORTEM
TISSUE AND ITS CLINICALFK506 BINDING PROTEIN GENE AND /HUMANFLANKED BY THE MARKERS D11S424 AND /IS
BY THREE HIGHLY CONSERVED /ISFLANKING MARKERS FOR PREDICTIVE
MICROSATELLITES /OF SEQUENCESREGION 5 TRANSCRIBED REGIONREGIONS OF HUMAN RDNA CLONED
FLASK/COLONY AMNIOTIC FLUID MOSAICISMFLAVIN METABOLISM IN FIBROBLASTS /ANDFLAVOPROTEIN AND EDH DEHYDROGENASEFLAVORS /MAP TO CHROMOSOME BANDFLOW CYTOMETRIC DIAGNOSIS OF
CYTOMETRY /BIVARIATE BRDU HOECHSTCYTOMETRY AND CONFIRMATION BY PCRCYTOMETRY AND FLUORESCENCE IN /OFDEFECT FAMILIES /RISK IN LEFTSELECTIVE AND NEUTRAL /GENESORTED CHROMOSOMES FOR X /OFSORTED HUMAN CHROMOSOMES /FROMSORTED HUMAN CHROMOSOMES USINGSORTING AND ALU ELEMENT MEDIATED
FLUCTUATIONS IN HUMAN POPULATIONS OFFLUID /PLASMA AND CEREBROSPINAL
AND FETAL BLOOD A PROBLEM FORCELL CULTURES /IN AMNIOTICCELLS IN ANENCEPHALY /AMNIOTICDURING SAMPLING /OF THE AMNIOTICGLYCINE /ENZYME AND AMNIOTICMOSAICISM DOES NOT ALWAYSPHYSIOLOGIC OR PATHOLOGICSAMPLES ACHIEVED BY FILTRATIONSPECIMENS PROCESSED WITH IN
FLUORESCENCE /BY TIME RESOLVEDIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION fOFIN SITU HYBRIDIZATION AIN SITU HYBRIDIZATION ININ SITU HYBRIDIZATION ININ SITU HYBRIDIZATION OFIN SITU HYBRIDIZATION OFIN SITU HYBRIDIZATION OFIN SITU HYBRIDIZATION TOIN SITU HYBRIDIZATION TOLABELING OF DNA PROBES
FLUORESCENT IN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /BYIN SITU HYBRIDIZATION /OFIN SITU HYBRIDIZATION AIN SITU HYBRIDIZATION ANDIN SITU HYBRIDIZATION BEIN SITU HYBRIDIZATION TOIN SITU HYBRIDIZATION TOIN SITU IDENTIFICATION OF
FLUORO URACIL ALTERS THE ASYNCHRONOUS
557
2251227221441627274057964
89626874661046714
51160S4
15692646816984111910812276196718651950209724322158142349726441114261609109183
2650285521222499177
16052795572911
12211173126656314239461266122810411184128113771607163616421648169017041728214821512171184217944
11711656172420872129215622011364216183
1719185200
2153182
1667199
133715461650118913221355151616341679169212821626216116681706170816051557
Permuted Title Index
FLUOROPHORE LABELED CHROMOSOME /DIRECTFLUORSCENT IN SITU HYBRIDIZATION /ANDFNRB LOCUS WITH YEAST ARTIFICIAL /THEFOLATE SENSITIVE FRAGILE SITE /OTHERFOLLICLE CENTER CELL LINEAGE /OF NONFOLUCULAR B NON HODGKIN LYMPHOMASFOLUCULARIS SPINULOSA DECALVANSFOOTPRINT ANALYSIS AND GENOMIC NIVOFORAMEN MAGNUM AND CORD INTEGRITYFOREBRAIN AND MEDULLA OBLONGATA CDNAFORENSIC INVESTIGATIONS /OF VNTRS FOR
PRACTICE /OF DNA TESTS INFORMAUN FIXED TISSUE AND ITS /FROMFORMULATION ASSUMING AN UNDERLYING /AFOB AND C RAS ONCOGENE HOMOLOGS IN /C
EXPRESSION IN HUMAN OVARIAN CANCERFOUNDER EFFECT /QUEBEC IS DUE TO A
EFFECT AND GENE MIGRATIONEFFECT AS A CAUSE FOR /AND
FOURTEEN CASES WITH SPECIAL EMPHASISDANISH FAMILIES /MARKERS INPROBANDS WITH AN ADDITIONAL
FOX TERRIER A NEW DOG MODEL WITH NOFRA(X)027.2) PRESENT IN ONLY 1 OFFRACTIONS (COMPATIBLE WITH GROWTH
OF HETEROCHROMATIN /IN OTHERFRAGILE SITE /STUDIES AROUND THE
SITE AT 3P14 AND INCREASESSITE EXPRESSION AS ANSITE FRA(X)(Q27.2) PRESENT INSITE FRAXA /CONTIG AROUND THESITE FRAXA /CONTIG AROUND THESITE OF 2013 /CLOSE TO THESITE USING LASER /NEAR THESITES /INTERCROSSINGS ANDSITES ARE DEPENDENT ON DNASITES ASSOCIATED WITHSITES BY APHIDICOLIN AND /OFSITES EXPRESSION INSITES IN UNTREATED NON /COMMONSITES IN YQ12 /INDUCED COMMONX (MARTIN BELL) SYNDROME INX AND A MARKER CHROMOSOME /OFX ASSOCIATED BREAKPOINT /THEX BREAKPOINT CLUSTER REGIONX CASES /AN EGYPTIAN SAMPLE OFX CHROMOSOME /INDUCTION OF THEX EXPRESSION /OF LOW LEVELX FEMALES COUNSELING ISSUESX FREQUENCY IN MENTALLYX GENOTYPE IS CHARACTERIZEDX IN A 4 YEAR OLD MALE /ANDX IN AN INSTITUTION FOR /FORX LOCUS /SEQUENCES AT THEX LOCUS IN THE CONTEXT OF /THEX MALES EVIDENCE FOR GENETICX NEGATIVE FAMILY /DXS52 IN AX ON DISTRIBUTIONS OF /OFX PATIENTS WITH ATYPICALX REGION /OF THEX REGION /SITES IN THEX SCREENING /BANDING INCLUDINGX SITE /CONTIG PROXIMAL TO THEX SITE MOLECULAR AND GENETICX SITE OF THE FRAGILE X /OFX STUDIES WHAT IS PRACTICALX SYNDROMEX SYNDROME /AFFECTED BYX SYNDROME /DIAGNOSIS OFX SYNDROME /IN FAMILIES WITHX SYNDROME /LINKAGE TO THEX SYNDROME /MARKERS FOR THEX SYNDROME /MEASUREMENTS INX SYNDROME /OF THEX SYNDROME /SCREENED FOR THEX SYNDROME /THE DIAGNOSIS OFX SYNDROME /X SITE OF THEX SYNDROME AND DIAGNOSTIC /THEX SYNDROME AND SMALL MARKERX SYNDROME AND THE /OFX SYNDROME DETERMINATION OFX SYNDROME IMPACT OF GENETICX SYNDROME IN MENTALLYX SYNDROME LOCUS /TO THEX SYNDROME WITHX TESTING OF FAMILY MEMBERSX USING TRIMETHOPRIM AND DNA
FRAGILITY /BRACHYSYNDACTYLY AND BONYAND AUTISM IN A CHILEAN
FRAGMENT IN A TURNER MOSAIC /OF AIN THE BETA GLOBIN GENE BYMELTING POLYMORPHISMS A
FRAGMENTATION AND GENOME MAPPINGFRAGMENTS /ARTIFICIAL CHROMOSOME END
FOR DETECTION OF VARIATIONFROM 5011.2 13.3 USING /DNAOF CHROMOSOME 5 HARBORINGOF FLOW SORTED CHROMOSOMESUSING TRANSPOSONS /CLONED
FRAME DELETION OF THE PHENYLALANINEFRAMESHIFT MISMATCH REPAIR IN HUMANFRANCE DETERMINATION BY DENATURING /INFRANCO AMERICANS OF FRENCH CANADIANFRASER SYNDROME /PRENATAL DIAGNOSIS OFFRAUMENI SYNDROME /Ll
16971867195016231387139219852428744
2333314110310812786256924132698S4
1746636192314044641612950
262637617051623161237823892147S7763113751405155913901363156414711688S7720058221623155011411285379141516172361373
2672198027001511374103816302159375159216031715001198854S771894709828161219081592377
1451103812591850149320051486161014877051492166925172449249820752793211021322122250544925444631788652271
SYNDROME A LINKAGE STUDY /LiFRAXA /CONTIG AROUND THE FRAGILE SITE
/CONTIG AROUND THE FRAGILE SITEFREE BETA /SCREENING THE USE OF
RADICALS /ACTIVITY TO OXYGENSIALIC ACID STORAGE DISORDER /A
FRENCH ACADIAN KINDREDS /1A IN FIVECANADIAN ANCESTRY PUBLIC /OFCANADIAN FAMILIES /TO D5S39 INCANADIAN MYOTONIC DYSTROPHY /ACANADIAN PHENYLKETONURIA /OF ACANADIAN POPULATION WHICH HASCANADIANS /DISEASE MUTATIONS INCANADIANS /DNA POLYMORPHISM INCANADIANS /LIPID METABOLISM INCANADIANS SEARCH FOR COMMON /INPOPULATION BETWEEN MYOTONICSURVEY /CHROMOSOMAL ANOMALIES A
FREQUENCIES AT THE PHENYLALANINEFOR THE ALPHA GLOBIN /GENEMEASURED BY THE PCR ANDOF DETRIMENTAL RECESSIVESOF HLA ANTIGENS All ANDOF N MYC AMPLIFICATIONOF THE MURINE RB (6.16)STRONGLY CORRELATED WITHWITHIN THE BLACK AND
FREQUENCY AND ECONOMIC BURDEN OFAND MOLECULAR TYPES OFAND PHENOTYPIC EXPRESSIONAND TIMING OF PREGNANCYCLINICAL SIGNIFICANCE ANDDISTRIBUTION AND /ALLELEDISTRIBUTION OF ADISTRIBUTIONS AMONG HUMANIN 10 YEARS AND 26,000 CASESIN EUROPEAN COUNTRIES /F 508IN ICTERIC NEWBORNSIN MENTALLY RETARDED /XIN MICE /AND HYPERHAPLOIDYIN WISCONSIN USING CDF508OF AMP DEAMINASE DEFICIENCYOF AN ALLELE RAISINGOF CHROMOSOME ABERRATIONSOF CYSTIC FIBROSISOF CYSTIC FIBROSISOF CYSTIC FIBROSIS INOF DF508 MUTATION IN 13OF PREGNANCY LOSS AND /AGEOF SISTER CHROMATIDOF SISTER CHROMATID /THEOF STRUCTURAL CHROMOSOMALOF THE AUTOSOMAL RECESSIVEOF THE B ZERO THALASSEMIAOF UDP GAL 4 EPIMERASERADIATION CAN ALTER GENEREPETITIVE DNA SEQUENCE /LOW
FRIEDREICH ATAXIA IN A SPANISH /OFATAXIA IS PROBABLY DUE TOATAXIA LOCUS BY ANALYSISATAXIA REGION AT 9013 021.1ATAXIA WITHIN AMERICAN /TO
FRONTONASAL DYSPLASIA CLINICALFRUCTOSE INTOLERANCE /OF HEREDITARY
INTOLERANCE /WITH HEREDITARYFRYN SYNDROME CONGENITAL /DIAGNOSIS OFFRYNS SYNDROME ASSOCIATED WITH A /OFFSHB /WAGR REGION GENE BETWEEN AN2 ANDFUMARASE DEFICIENCY /DIETOTHERAPY INFUMARYLACETOACETATE HYDROLASE THE /OFFUNDUS ALBIPUNCTATUS UTILIZING PCR /OFFUNGICIDE RIDOMILL ON HUMAN CELLS INFUR MOUSE /HEPATOCYTES OF THE SPARSEFUSION /A #3P CHROMOSOME VIA MICROCELL
GENE A PRODUCT OF UNEQUAL ANDKLIPPEL FEIL ANOMALY [THORACICOF OLD AND NEW /MANAGEMENT ASTRATEGY /KINASE GENE BY CELLTHAT MAPS CLOSE TO THE FRAGILE
FUTURE /HISTORICAL LESSONS AND THEDIRECTIONS /SOMEHOLDS /SUMMARY AND WHAT THEPROSPECTS FOR THALASSEMIA
FVIII GENE CAUSING HEMOPHILIA A /OF
1892378
2389310
2229201319581788201820362712284022892878515
2662284817991114267911312841592584
15832628284417892873107836184
2854280028281187174715681285159410064892724159923442840274111071218158611961218780
2743183225762199198982081
217818937079812264119215202241562483
25232561247213952253832180524662147322S272913922794
G
G 6 PD DEFICIENCY NEONATES /HAVINGBANDED METAPHASES /OF THE QUAUTY OFGLOBIN GENE EXPRESSION /ON FETALGROUP CHROMOSOMES /IN HUMAN DPHOSPHOGLUCONATE DEHYDROGENASE LOCUSPROTEINS IN HUMAN COCHLEA /OF
G+C CONTENT OF 39 PERCENT /GENE HAVE AG2 PHASE X IRRADIATION IN RELATION TOG542X IN JEWISH PATIENTS /MUTATIONG551D AND DELTAF508 IN EUROPE /OFGGPD CLUSTER OF BAND XQ28 /WITHIN THE
MOLECULE AND THEIR POPULATIONGABA SUBUNIT CLASS HIGHLY EXPRESSEDGABAA RECEPTOR B3 SUBUNIT GENE /OF THE
17781618242315371928233828212695224527031964253
22732392
GABRB3 TO THE ANGELMAN/PRADER WILLIGAIT AND ADDUCTED THUMBS SYNDROMEGAL 4 EPIMERASE DEFICIENCY IDENTIFIEDGALACTOSEMIA /AND POLYMORPHISMS IN
HETEROZYGOSITY REPORT OFGALACTOSIALIDOSUS /GENETICS OF
AND MULTIPLE /WITHGALACTOSIDASE CDNA SEQUENCE OF 2 /BETA
DEFICIENCY /IN BETADEFICIENCY /OF HUMAN B
GAMETES /OF ANEUPLOIDY IN HUMANGA AMINOBUTYRIC ACID RECEPTOR GENE
GLUTAMYL TRANSPEPTIDASE GENESIRRADIATION /SENSITIVITY TOIS ENCODED BY CHROMOSOME 16
GANGUOSIDOSIS /PATIENTS WITH GM1/WITH Bi VARIANT OF GM2AMONG JEWS AND NON JEWS
GAP PCR FOR RAPID DETECTION OF SINGLEGARHWAL HIMALAYAS INDIA /IN THE
HIMALAYAS INDIA /IN THEGASTRIC ADENOCARCINOMA /IN PRIMARY
CARCINOMA STUDIES INVOLVINGCATHEPSIN E /ANALYSIS OF
GASTROSCHISIS IN A LARGE POPULATIONIN METROPOLITAN ATLANTA
GAUCHER DISEASE /A MOUSE MODEL OFDISEASE AIN A PATIENT WITHDISEASE AIN JAPANESEDISEASE AIN TYPE 1DISEASE /MILD PRESENTATION OFDISEASE /OF ENZYME THERAPY INDISEASE /TO THE TREATMENT OFDISEASE BY ENZYME REPLACEMENTDISEASE CLINICAL ASPECTSDISEASE EFFICACY OF ENZYMEDISEASE IN THE ASHKENAZIDISEASE MOLECULAR ANALYSIS OFDISEASE TYPE MOLECULAR ANDDISEASE USING IA TREATMENT FORDISEASE USING RECOMBINANT IFORPATIENTS /GENE AMONGPATIENTS WITH OCULOMOTOR IOF
GC CLAMPED DENATURING GRADIENT GELCLAMPED DENATURING GRADIENT GELCLAMPED GRADIENT GEL /DETECTED WITHPHENOTYPE IN ADULT MALES /WITHRICH DNA USING THE HOT PCR METHOD
GCMS /(CONDITIONS NOT RECOGNIZABLE BYGEL BLOTS /USING DENATURING GRADIENT
ELECTROPHORESIS /BY PULSED FIELDELECTROPHORESIS /CLAMPED GRADIENTELECTROPHORESIS /DENATURANTELECTROPHORESIS /DENATURANTELECTROPHORESIS /DENATURANTELECTROPHORESIS /GRADIENTELECTROPHORESIS /GRADIENTELECTROPHORESIS /GRADIENTELECTROPHORESIS /GRADIENTELECTROPHORESIS /GRADIENTELECTROPHORESIS /GRADIENTELECTROPHORESIS ANALYSIS /STRANDELECTROPHORESIS AND DIRECTELECTROPHORESIS DETECTION OFELECTROPHORESIS IN ITALIAN CYSTICELECTROPHORESIS OF PCR AMPLIFIEDELECTROPHORESIS OF PCR AMPLIFIEDELECTROPHORESIS PROSPECTIVE STUDYELECTROPHORESIS TECHNIQUE INELECTROPHORESIS TO DETECT POINT
GELS /POLYMORPHISMS ON AGAROSEGENE (COLlAl) AIN A TYPE PROCOLLAGEN
(COL4A5) WHICH CONTAINS /OF ITS(GABRB3) TO THE ANGELMAN/PRADER(PRO23HIS) /THE HUMAN RHODOPSIN(SPl) AND THE 1,25 /FACTOR(VDR) ARE COLOCALIZED ON HUMAN/5 HYDROXYTRYPTAMINElA RECEPTOR/A CANDIDATE FOR THE MEN2/A CANDIDATE HUNTINGTON DISEASE/A HUNTINGTON DISEASE CANDIDATE/AND MORE PRECISE MAPPING OF THE/AND MUTATIONS OF THE RHODOPSIN/AT XP21 LINKED TO THE DYSTROPHIN/BY THE 3 END OF THE DYSTROPHIN/CLONING THE MYOTONIC DYSTROPHY/CLOSE TO THE HUNTINGTON DISEASE/CONTAINS THE MYOTONIC-DYSTROPHY/CPG ISLAND 5 OF THE FACTOR VilI/DISRUPTION OF SUPPRESSOR/DNA REPAIR METHYLTRANSFERASE/DYSPLASIA ANALYSIS OF THE COL2A1/ENDOCRINE NEOPLASIA TYPE 1/ENDOCRINE NEOPLASIA TYPE 2A/EXPRESSION OF THE PROSAPOSINE/EXPRESSION OF THE RETINOBLASTOMA/FAMILIAL ADENOMATOUS POLYPOSIS/FOR POINT MUTATIONS IN THE FIX/FOR THE HUNTINGTON DISEASE/FOR THE HUNTINGTON DISEASE/FUNCTION OF THE CYSTIC FIBROSIS/HETEROGENEITY OR A CONTIGUOUS/HUMAN PROSTATIC ACID PHOSPHATASE/IN THE ABSENCE OF A CANDIDATE/IN THE ALPHA 1 ANTICHYMOTRYPSIN
558
2392737
18321866322808484511075284158719072130238821034511059
3976282528321299259922548842702250356023155574365562486553279555
42545837552
2483101851410972059252026852530261
20692119252021828032813437463100810972059207322831057103998525172793251926525882789106524052392799187018701882234723352391
779
7532269404239923702154258724011121612
2145243925842132984
227123962418743
2331370680
Permuted Title Index
GENE /IN THE HUMAN DYSTROPHIN/IN THE INSULIN RECEPTOR/INTEGRATED SINGLE COPY HSV 1 TK/LOCI AT 17P13 INCLUDING THE P53/MAP OF THE HUMAN DYSTROPHIN/MAPPING OF THE A L IDURONIDASE/MUTATION AT CODON 200 OF THE PRP/MUTATIONS IN THE HUMAN APRT/MUTATIONS IN THE RETINOBLASTOMA/MUTATIONS OF TYPE II PROCOLLAGEN/NEW MUTATIONS OF LDL RECEPTOR/OF A HUMAN PEPSINOGEN A/OF LARGE DELETIONS IN THE CFTR/OF THE ALPHA1 ANTICHYMOTRYPSIN/OF THE HUMAN ERYTHROPOIETIN/OF THE HUMAN PROSAPOSIN/OF THE TYPE 1 NEUROFIBROMATOSIS/PENETRANCE OF THE SOTOS SYNDROME/POINT MUTATIONS OF FACTOR VilI/POLYMORPHISMS WITHIN THE CFTR/RECKLINGHAUSEN NEUROFIBROMATOSIS/STOMACH ALDEHYDE DEHYDROGENASE/STUDY OF HUNTER SYNDROME IDS/THE ADENOMATOUS POLYPOSIS COLI/THE DUCHENNE MUSCULAR DYSTROPHY/THE DUCHENNE MUSCULAR DYSTROPHY/THE HUMAN RETINOBLASTOMA/THE HUMAN SYNEXIN (ANNEXIN VII)/THE MOUSE MDM2 TRANSFORMING/THE NEUROFIBROMATOSIS TYPE 1/THE ORNITHINE TRANSCARBAMYLASE/THE RAT ACYL PEPTIDE HYDROLASE[THE UNKNOWN 5 HALF OF THE COL4A5/TRANSFORMING GROWTH FACTOR ALPHA/WITHIN THE CYSTIC FIBROSIS3HYPERVARIABLE REGION ALLELES /B5 REGION ON THE ACTIVE AND /HPRTA MODEL FOR STUDYING THE /IXA PRODUCT OF UNEQUAL AND /FUSIONACTIVATION IN NEUROBLASTOMA /RASADH5 AND RELATED PSEUDOGENESAFFECTING THE 3 SPLICE SITEAMONG AFRICAN AMERICANS BY PCRAMONG GAUCHER PATIENTSAMONG PATIENTS WITH AUTOSOMALAMPLIFICATION AND DEAMPLIFICATIONAMPLIFICATION AT CHROMOSOME /OFAMPLIFICATION IN CANCER /ANDAMY1C IN PAROTID GLAND OFANALYSES /PROTEIN AND PCR BASEDANALYSIS /TO POPULATIONANALYSIS IN PRENATAL DIAGNOSISANALYSIS OF FUNDUS ALBIPUNCTATUSAND 46,XY PURE GONADAL DYSGENESISAND ASSOCIATION WITH CLINICALAND ATHEROSCLEROSIS /LP(A)AND ITS EXPRESSION /HUMAN LDH C4AND LOCI ON CHROMOSOME 9Q34 INAND MAPPING OF THE GENE TO NEARAND MOUSE CHROMOSOME 17 /THE PKD1AND MUTATION SPECTRUM INAND PART OF 180 AS THE LOCUS FORAND RELATED LOCIAND RELATED PSEUDOGENES /PROTEINAND THE CENTROMERIC REGION OFAND THE CYSTIC FIBROSIS LOCUSAND THEIR USE IN LINKAGE STUDIESAS A CAUSE FOR TYPE IIB VONASSOCIATED WITH MITOCHONDRIALASSOCIATIONS IN ADMIXED /DISEASEAT 4Q35 4QTER /MUSCULAR DYSTROPHYBETWEEN AN2 AND FSHB /WAGR REGIONBY A FAST PROCEDURE DETECTS 3BY A NEW MAPPING TECHNIQUEBY CELL FUSION STRATEGY /KINASEBY DENATURING GRADIENT GELBY DENATURING GRADIENT GEL /CFTRBY FLUORESCENCE IN SITUBY HOMOLOGOUS YEAST ARTIFICIALCANDIDATE REGION AMONG NEWCANDIDATE REGION AND PROGRESSCARRIERS COMPARISON OF TWOCAUSES 17A HYDROXYLASE DEFICIENCYCAUSES APOLIPOPROTEIN A I /ACAUSES CLASSICAL /IN THE NF1CAUSES PELIZAEUS MERZBACHERCAUSING A DOMINANT VARIANT OFCAUSING CONGENITAL /III SYNTHASECAUSING HEMOPHILIA A /OF FVIIICDNA CLONING MAPPING AND /XISTCLN3 /(BATTEN DISEASE)CLUSTER PHENYLALANINE /5B GLOBINCODING FOR VENTRICULAR MYOSINCODING HUMAN GLYCOSYLASPARAGINASECODON 717 MISSENSE MUTATION ISCOLOR VISION DEFICIENCIES AMONGCOMPLEX /FACTOR RECEPTOR (C KIT)COMPLEX AND MULTIPLE PSEUDOGENESCONSTRUCTS IN EBV BASEDCONSTRUCTS TO MOTOR NEURONS BYCONTENT TO CHROMOSOME MORPHOLOGYCONVERSION /READILY CAPABLE OFCONVERSION EVENT /EVIDENCE FOR ACONVERSION EVENTS INVOLVING THEDEFECT IN FAMILIAL DILATED [THE
98348525361373225623451000253858846
98024081014241124532365
98787994988
21332304104260916S7
2575226613612372559
2297236210151009714
242824372253602
2284111227431018
82458604369
2444109628561004252322381001162
1286235319071869
1119912339227620572883192710681017275822172241100220882466251798521718
2348102
1830104511181084972444530
2794225919722883216423552811886
229619732476248916432611237522101062
DEFECT IN SALLA DISEASE A FREEDEFECT IN X LINKED SPINAL ANDDEFECTS CAUSINGDEFECTS IN CHILE /OF SINGLEDELETION HOT SPOT /THE DYSTROPHINDELETION MUTANTS /FROM GLOBINDELETION SYNDROME /CONTIGUOUSDELETIONS /OF SINGLE ALPHA GLOBINDELETIONS DETECTED BY CDNA /OFDETECTION AND VISUALIZATION BYDETECTION BY HYBRIDIZATION TODIAGNOSIS /STUDY OF HEMOPHILIA ADIAGNOSIS OF DUCHENNE MUSCULARDIFFERENTIATION AND ADMIXTUREDIRECT SEQUENCING OF THE PCRDISORDERS /PHENOTYPE OF SINGLEDISORDERS AND THE FINNISH /SINGLEDIVERSITY AND GENETIC DISTANCEDUPLICATION /FUNCTIONS PRECEDEENCODED GLYCOSYLTRANSFERASES INENCODES A BASIC/LEUCINE ZIPPERENCODING A DYSTROPHIN CROSS /OF AENCODING HUMAN CARBOXYPEPTIDASEENCODING HUMAN P58 A CELL CYCLEENCODING THE A SUBUNIT OF AIN THEENCODING THE SECOND ENZYME OFENGINEERED FIBROBLASTS /BYERCC 1 /OF THE MURINE DNA REPAIRERCC4 /MB OF THE EXCISION REPAIREXPRESSED IN SPERMATIDSEXPRESSION /HYDROXYLASEEXPRESSION /ON FETAL G GLOBINEXPRESSION /WITH SPERM SPECIFICEXPRESSION AND ACATALASEMIAEXPRESSION AS AN APPROACH TO /OFEXPRESSION ASSOCIATED WITH AGEEXPRESSION DURING THE RAT /OF ZFYEXPRESSION IN DIFFERENTEXPRESSION OF CALPAINS INEXPRESSION REGULATION IN THE /OFEXPRESSIONS ALTERATION OF NEURONFAMILY /BELONGS TO AN ACID LIPASEFAMILY /SAME MITOCHONDRIAL DNAFLOW SELECTIVE AND NEUTRALFOR ATAXIA TELANGIECTASIA ISFOR CONGENITAL STATIONARY NIGHTFOR FAMILIAL ADENOMATOUS /OF THEFOR FAMILIAL EXPANSILE /OF THEFOR FAMILIAL HYPERTROPHIC /OF THEFOR FANCONI ANEMIA /A CANDIDATEFOR FIBRILLAR COLLAGENS /INFOR KALLMANN SYNDROME ON XP22.3FOR LOWE SYNDROME /CANDIDATEFOR LYMPHOID ENHANCER BINDINGFOR MARFAN SYNDROME /A CANDIDATEFOR MARFAN SYNDROME /FIBRILLINFOR MULTIPLE ENDOCRINE NEOPLASIAFOR MULTIPLE SELF HEALING /OF THEFOR PERLECAN TO MOUSE CHROMOSOMEFOR PROTEIN T AND IDENTIFICATIONFOR SPINAL MUSCULAR ATROPHY /THEFOR THE DETECTION OF A FAMILY OFFOR THE HUMAN CHORIORETINALFOR THE HUMAN LOW VOLTAGE EEG TOFOR THE VITAMIN D BINDING /OF THEFOR WAARDENBURG SYNDROME TYPEFOR WERNER SYNDROME /OF THEFOR X LINKED CONGENITAL /OF THEFOR X LINKED LIVER GLYCOGENOSISFOR X LINKED VITREORETINOPATHY /AFREQUENCIES FOR THE ALPHA GLOBINFREQUENCIES STRONGLY CORRELATEDFROM 3P21 THE COMMON REGION OFFROM AN INDIVIDUAL WITH /BFROM CHROMOSOME 6 AT THE HLAFROM CHROMOSOME 6 THUS EXCLUDINGFROM HUMAN MONKEY BOVINE RATFROM LINKAGE TO HUMAN CHROMOSOMEGENE ORGANIZATION AND A SEARCHGEOGRAPHY OF SOUTH AMERICAGS1 FROM DISTAL XP THAT ESCAPESHAVE A G + C CONTENT OF 39 PERCENTHYPERMETHYLATION IN CHRONICHYPERVARIABILITY IN GREAT APESHYPOTHESES FOR PRIMARY /OF MAJORHYPOTHESIS FOR DNA REPAIR DEFECTIDENTIFIED BY DIRECT DNA /SUBUNITIMPLICATED IN ERYTHROPOIETIC /THEIMPLICATED IN HUMAN RETINALIN A 1 MB CONTEXT OF XQ28 DNAIN A FAMILY WITH PELIZAEUS /PLPIN A JAPANESE FAMILY WITHIN A PATIENT WITH PELIZAEUS /PLPIN AUTOSOMAL DOMINANT POLYCYSTICIN BASHKIR POPULATION /FIBROSISIN CHINESE /OF A GLOBININ COS CELLS /OF THE SRYIN DISTAL BAND 17P11.2/TYPE IAIN DROSOPHILA MELANOGASTER /H2AIN EARLY ONSET ALZHEIMER DISEASEIN EMBRYONIC STEM CELLS /B1IN EPENDYMOMA /TUMOR SUPPRESSORIN FAMILIAL ALZHEIMER DISEASEIN FAMILIAL CREUTZFELDT JAKOBIN FAMILIAL ORTHOSTATIC /FACTOR
201395
23562659235733714439761098104124961050112328752305434
52862166572
24592332146221281067240924742325170918622462242324162448576409
22302420486
223325762248
33285519671928591
20161920187444
2294235218679493
23405981890233418861291234220282262
27197518781921194226792628224
226421971929261220042267286524022821617
26242649231410592214
102041083999
2358237123171125239319522456229024351391238122911037
IN GYRATE ATROPHY USING PCRIN HEMOPHILIA A USING PCR SINGLEIN HUMAN HEPATOCELLULAR /THE P53IN HUMAN MULTIPLE MYELOMA /BCL2IN HUMAN PROSTATE ADENOCARCINOMAIN HUMAN TRANSITIONAL CELL /P53IN HUMANS /SECOND SEX DETERMININGIN INDIVIDUALS OF EUROPEAN AND /BIN JAPANESE FAMILIAL ALZHEIMERIN JEWISH AND ARAB PATIENTS ININ JEWISH PATIENTS WITH HUNTERIN KINDREDS OF CHILDHOOD ANDIN LIMB AND KIDNEY MORPHOGENESISIN MALIGNANT HYPERTHERMIAIN MONOZYGOTIC TWINS /DYSTROPHYIN MURINE HEMATOPOIETIC CELL ININ MUTANT HUMAN LYMPHOCYTES /HPRTIN NAIL PATELLA SYNDROMEIN NEUROPSYCHIATRIC DISORDERSIN NONMUSCLE CULTURED CELLS FROMIN PATIENTS WITH WILMS TUMOR ANDIN SEVERELY AFFECTED SUBJECTSIN SWEDISH PATIENTS WITH ACUTEIN THE BRAIN /OF THE DYSTROPHININ THE CONGENITAL LACTASEIN THREE SAUDI ARABIAN DUCHENNEIN TRANSGENIC MICE /FACTOR IXIN TRIBAL POPULATIONS OF /(IGHG1)IN TYPE II DIABETES MELLITUSIN TYROSINEMIA TYPE IIIN VARIOUS ETHNIC GROUPSINACTIVITY PROTECTS NORMAL HUMANIS CONTAINED WITHIN A 350 KBIS DEREGULATED IN LYMPHOIDIS JOINED WITH 5 BCR IN SOME /ABLIS LOCATED IN THE ADH GENE /ADHIS NOT ALLELIC TO THE /SYNDROMEIS TIGHTLY LINKED TO D6S89 ON 6PISOLATED FROM MYELOID ML 1 CELLISOLATED FROM THE HUNTINGTONISOLATION AND ANALYSIS OF THE 5LEADING TO CLINICALLY DIFFERENTLINKAGE MAPPING /SYNDROMELOCATED IN THE MHC CORRESPONDSLOCI IN TOURETTE SYNDROMELOCUS /EVOLUTION OF GLYCOPHORINLOCUS /LINDAU TUMOR SUPPRESSORLOCUS /OF THE PRION PROTEINMAMMALIAN EXPRESSION CLONINGSMAPPING DIAGNOSTICS AND /FORMAPPING IN EXPERIMENTALMAPPING OF CHARCOT MARIE TOOTHMAPPING THAT INCLUDES VIABILITYMAPS NEAR THE NEUROFIBROMATOSISMAPS TO HUMAN CHROMOSOME 16MICROHETEROGENEITIES DETECTED BYMIGRATION /FOUNDER EFFECT ANDMODEL AND POSSIBILITY OF /MAJORMODELS AND THEIR APPLICATION TOMUTATED IN COLORECTAL CANCER ANDMUTATION IN A JAPANESE FAMILYMUTATION IN ECUADOREAN PATIENTSMUTATIONS /OF CYSTIC FIBROSISMUTATIONS BY ANALYSIS OFMUTATIONS IN BOHEMIA AND MORAVIAMUTATIONS IN MALES WITH /FIBROSISMUTATIONS IN PATIENTS WITH BONEMUTATIONS IN PELIZAEUS /PROTEINMUTATIONS IN THE CARBONICMUTATIONS IN TYPE IA [TYROSINASEMUTATIONS INTRODUCED BY TARGETEDMUTATIONS ON DIFFERENT NORMALMUTATIONS TWO FAMILIES WITH AOF A DUCHENNE MUSCULAR DYSTROPHYOF DUCHENNE MUSCULAR DYSTROPHYOF HUMAN TYPE II PROCOLLAGENOF JUN/FOS ONCOGENE FAMILYOF PATIENTS WITH GYRATE ATROPHYOF THE YEAST SCHIZOSACCHAROMYCESOF THREE PATIENTS WITH ALPORTOF TYPE COLLAGEN AN THE COLlAlON 4035 LINKAGE ANALYSIS OF THEON CHROMOSOME 190 /TROPONIN TON CHROMOSOME 3 Nll COLLAGENON CHROMOSOME 9 IN BASAL CELLON CORRELATIONS BETWEEN /MAJORON HUMAN CHROMOSOME 21 /RECEPTORON HUMAN CHROM(OSOMES 8 /OF SECONDON MEANS VARIANCES AND /RECEPTORON THE HUMAN Y CHROMOSOME BYON THE X CHROMOSOME /IN PART BY AON XP BETWEEN DXS146 AND DXS7ON XP22.3 ESCAPES X INACTIVATIONORGANIZATION AND A SEARCH FORORGANIZATION POLYMORPHISM ANDPARENTAL IMPRINTING SUGGESTED BYPC1 MAPS TO 6021 022 AND ISPRIMARY STRUCTURE AND LINKAGEPRODUCT CC ESSENTIAL FORPRODUCT THROUGH MICRO /OF A NOVELPROMOTER /HUMAN 17 IA NEOANTIGENEPROMOTER REGION FOUND IN HP2REARRANGEMENT ANALYSIS INREFINED MAPPING AND EXCLUSION ASREGION /GLUCOCORTICOID RECEPTOR
559
1057228324291674260625772341
66107125512255
722664292222247125501996979102922047210442050509958
24872815722507S4
25392036225
25971973609
2052258923842432194
2045186220722625605
22982592
921866141
2055237222581033S4
20672781101
1070969
279810892703106
2605110110202318250327972211080235124612308251923631011347143
236873
2583278319682314515
220575
191223072267425621130722862400247024652425103119982123
Permuted Title Index
REGION /HUMAN MYOTONIC DYSTROPHYREGION /OF THE MYOTONIC DYSTROPHYREGION /RFLPS IN THE APOAI CIIIREGION AND SUSCEPTIBILITY TOREGION FOR SPINAL MUSCULAR /THEREGION IN JAPANESE /PIGMENTREGION OF HUMAN CHROMOSOME 4REGIONS 3P lIP 130 17P AND 170REGULATION AND EVOLUTIONARYRESPONSIBLE FOR A /OF THE LIRESPONSIBLE FOR HUNTINGTON /THERESPONSIBLE FOR POLYCYSTIC /THERESPONSIBLE FOR TRANSIENT /OF THERESULT IN TWO ENTIRELY DIFFERENTRESULTING FROM REPLICATION ERRORSRESULTS IN A KINETIC VARIANT OFRESULTS IN AN EXON DELETION INRETINOBLASTOMA'S MUTATIONSBY /SPY AND A NEW Y LINKEDSEGMENTS FUNCTIONAL AND /REGIONSEQUENCE ANALYSIS REVEALS A IXISTSEQUENCES /ISOLATION OF POTENTIALSEQUENCES AND SITE SPECIFIC /FROMSEQUENCES IN INTERPHASE NUCLEISTRUCTURE AND EMBRYONICSTRUCTURE AND MUTATIONS LEADINGSTRUCTURE IN TWO POPULATIONSTARGETING /GENERAL STRATEGIES OFTARGETING AND INACTIVATION OFTARGETING IN MOUSE EMBRYONIC /BYTHERAPY /OR SOMATICTHERAPY AN INTERVENTION MODELTHERAPY FOR ADA DEFICIENCY ANDTHERAPY FOR HEMOPHILIA B /ONTHERAPY FOR HEPATIC DEFICIENCIESTHERAPY FOR PHENYLKETONURIATHERAPY IN INHERITED MYOPATHIESTHERAPY IN LDL RECEPTOR /EX VIVOTHERAPY OF CYSTIC FIBROSIS AND ATHERAPY OF HEMOPHILIA B /SOMATICTO 10022.1 024.3 /OF HUMAN PAX2TO BAND 015 021 OF CHROMOSOME 5TO BAND 024 OF CHROMOSOME 16TO CHROMOSOME 10 MARKERS LINKEDTO IDENTIFY FUNCTIONAL MUTATIONSTO NEAR THE CENTROMERE OF /OF THETO THE REGION 11022.3 23.1 /AT DTO THE Y CHROMOSOME /MATURATIONTRANSFER /BY RETROVIRAL MEDIATEDTRANSFER AS AN APPROACH TO THETRANSFER GENTRANET /OFTRANSFER MOLECULAR CLONING OF /BYTRANSFER OF HUMAN ORNITHINETRANSFER OF RECOMBINANTTRANSFER TO THE RESPIRATORYUNLIKELY /THE HUNTINGTON DISEASEUSING CONSTANT DENATURANT GELVNTR SITE /THE APOLIPOPROTEIN BWHICH ESCAPES X INACTIVATION /AWITH CORONARY ARTERY DISEASE INWITH LARGE ALLELE EFFECTS /SINGLEWITH LARGE ALLELIC EFFECTS ONWITH SCHIZOPHRENIA /DEAMINASEWITH THE FOUR BASE INSERTION OFWITHIN THE X Y PSEUDOAUTOSOMALWOBBLER MAPS CLOSE TO ERBB ONXRCC5 BY SOMATIC CELL /REPAIR
GENE(S) FOR BECKWITH WIEDEMANN /THETO A CM INTERVAL ON
GENERALIZATION OF UNIFIED MAJOR GENEGENERALIZED AND PARTIAL EPILEPSY
HYPOTONIA DEVELOPMENTALPEROXISOMAL DEFECT IN /ARECESSIVE DYSTROPHIC /WITH
GENERATED BY INTER ALU PCR /PROBESHETERODUPLEXES /BY PCR
GENERATION AN IN VIVO ACTIVATION OFASSESSMENT /DISEASE ONEFAMILY /DISEASE IN A THREEFAMILY /ON A LARGE FIVEOF 11022 24 MARKERS FROMOF A DNA PROFILE ANDOF A PANEL OF RADIATIONOF CHIMERIC MICE WITHOF CHROMOSOME 21 SPECIFICOF HIGHLY SPECIFIC DNAOF HUMAN CHROMQOOME 22 /PCROF NEW DNA PROBES IN THEOF REGION SPECIFICOF URATE OXIDASE DEFICIENT
GENERATIONS /4 VARIANT THROUGH THREEAND AN UNBALANCED /IN FOUR
GENES /3 UNTRANSLATED REGION OF HUMAN/AN APPROACH TO REVEAL NEW HUMAN/ANALYSIS OF HUMAN ZINC FINGER/AND APE EVOLUTION THROUGH RRNA/AND TECHNIQUES FOR ISOLATING/CANCER AND OTHER CANDIDATE/CARRYING DUPLICATED C4A/CONJUNCTION WITH HLA CLASS II/EXPRESSION OF COLLAGEN/HISTOCOMPATIBILITY COMPLEX/HISTORY AND GEOGRAPHY OF HUMAN/IN CELLS CHROMOSOMES AND/IN GENETIC COUNSELING LINKED
S8640524042711214623202384256726192278299
1994134823592346449280262018592623
962374247181
232528567S9
2244249324691816S91247424782482424423S9124942282217121721982268219072301234924912486247922742472532S911884280366
2440274627292736201124462360186418912181294
20674777735331927224710498722071490737
210828772132250321891635164921012109249395414461936576
2263165S13101
2211100353
26212545502006
/IN T CELL RECEPTOR/MAPPING THE ZELLWEGER SYNDROME/MUTATIONS IN THE RB AND P53/NORMAL AND MUTANT HUMAN CFTR/PEMPHIGOID ANTIGENS 1 AND 2/PROBES OF SINGLE COPY/STRATEGIES FOR MAPPING MOUSE/THE DEVELOPMENTAL REGULATION OFAMPLIFIED BY PCR ELIMINATION OFAND ANONYMOUS DNA PROBES USINGAND HAPLOTYPES A MOLECULAR /AlAND HEREDITARY TUMOR SYNDROMESAPPLICATION IN THE DETECTION OFBY CLONING TRANSLOCATION /NEWBY LINKAGE ANALYSIS /OF CLONEDBY LOW LEVEL ELECTROMAGNETICBY POSITIONAL CLONING /DISEASECAUSING MENTAL RETARDATION /OFCHARACTERIZATION OF 122CODING FOR THE HUMAN ALPHA 3COLlAl COL1A2 AND COL3A1 AREDETERMINING TUBEROUS SCLEROSISDURING DEVELOPMENT OF THE HUMANENCODING DRUG METABOLIZINGENCODING PHOSPHOGLYCERATE /OFENCODING THE HUMAN RED AND /THEFOR AICARDI SYNDROME AND GOLTZFOR HERITABLE DISORDERS OFFOR MULTIFACTORIAL DISEASESFOR MYOTONIC DYSTROPHYFOR THE X LINKED EYE DISEASESFOR THIS ANOMALY /OF REGULATINGFOR USHER SYNDROME /OF THEFOR VON HIPPEL LINDAU DISEASEFROM PERSONALITY PHENOTYPES [THEGENETIC EDUCATION OF NURSES INGENETIC MARKERS AND GENOMICIDENTIFIED NEAR THE FRAGILEIN A CANDIDATE REGION FOR THEIN ASIANS /ORIGIN OF THALASSEMIAIN BONE MARROW CELLS USING /AlIN BONE MARROW CELLS USING A /AIN DROSOPHILA /OF PATTERNINGIN HUMAN AND PRIMATES ANALYZEDIN MAMMALIAN DEVELOPMENTIN MULTIPLE SCLEROSIS /RECEPTORIN THE MOUSE /SUSCEPTIBILITYIN TYPE I DIABETES /HLA LINKEDINVOLVED IN HEARING FROMINVOLVED IN PRIMARY SEXINVOLVED IN THE SELECTIONIS RARE COMPARED TO MUTATIONMAPPING TO CHROMOSOME 22 BYMARK ACTIVITY STATES AND MAYOF RHEUMATOID ARTHRITIS INON HUMAN CHROMOSOME 19 /FINGERON THE INACTIVE HUMAN X /OFON THE MOUSE AND HUMAN X /OFOR MARKERS ASSOCIATED WITHPRB1 AND PRB2 /RICH PROTEINRP1 AND RP2 LOCATED IMMEDIATELYTHAT ESCAPE X INACTIVATIONTO HUMAN CHROMOSOME 22 ANDTRANSCRIBED FROM A CPG ISLAND 5USING A RECOMBINATION BASED /OFUSING NONRADIOACTIVE IN SITUWHICH ESCAPE INACTIVATION /ANDWITHIN HUMAN CHROMOSOMAL BANDWITHIN HUMAN CHROMOSOMAL BAND
GENETIC ABERRATIONS IN HUMAN BREASTALTERATIONS OF THE TUMORALTERATIONS UNDERLYINGANALYSES /A FAMILY STUDY ANDANALYSES /OF GIBBS SAMPLING TOANALYSES OF 20 PRADER WILLIANALYSES USING PCR FOLLOWEDANALYSIS FROM A /BANKING FORANALYSIS OF 14 SMALL CELLANALYSIS OF 21 OH MUTATED HLAANALYSIS OF APOLIPOPROTEIN(A)ANALYSIS OF CLEFT LIP WITH ORANALYSIS OF COMMON DISEASESANALYSIS OF FAMILIALANALYSIS OF GROWTH CONEANALYSIS OF MITOCHONDRIALANALYSIS OF SAME AGED TWINSANALYSIS OF THE /MOLECULARANALYSIS OF THE ATRIALANALYSIS OF THE DUCHENNEANALYSIS OF THE RED GREENAND BIOCHEMICAL MARKERS /OFAND BIOCHEMICAL SCREENING OFAND BIOCHEMICAL STUDIES ONAND ENDOCRINOLOGICAL SYNDROMESAND ENVIRONMENTALAND ENVIRONMENTALAND ENVIRONMENTAL FACTORS INAND ENVIRONMENTAL FACTORS ONAND GENE MAPPING OF CHARCOTAND HISTORICAL ASPECTSAND KARYOTYPIC ALTERATIONS INAND PHENOTYPIC HETEROGENEITYAND PHYSICAL DEFINITION OFAND PHYSICAL MAP OFAND PHYSICAL MAPPING AROUND
278420892553236423872085240
243725132059257303
2547124
19482422217420152553218220252022930428506
23981448351S32228725311468S8303S2417732187S772271107024902492S6918574331917594S3226
432143226272251230387622722452242120802253240322852130215425072144S292138219525952567113
2705278103510412737138066556727064267393251913999861037690232076610254911222
682767161
2843141
28391340670405
22121974
AND PHYSICAL MAPPING OFAND PHYSICAL MAPPING OF THEAND PHYSICAL MAPPING OF THEAND PHYSICAL MAPPING STUDIESAND POSITRON EMISSIONAND PROTEIN ALTERATIONS INAPPROACHES FOR HEALTHAPPROACHES TO MULTIFACTORIALASPECTS OF THE APOLIPOPROTEINBASIS FOR THE MULTIPLECASE MANAGEMENT A FUSION OFCHARACTERISTICS IN TWO NEWCHARACTERIZATION /ANDCHARACTERIZATION OF THE ROLECOMPONENTS IN ETIOLOGY OF /OFCONSERVATION OF ENOLASECONTINUITY OF ANCIENT /REVEALSCONTROL OF NONDISJUNCTION ISCOUNSELING /APPROACH TOCOUNSELING /FOR TRISOMY 8 ANDCOUNSELING /IMPLICATIONS FORCOUNSELING /INFORMATION FORCOUNSELING /THAN REACTIVECOUNSELING AND FAMIUAL CANCERCOUNSELING AND FETAL /FORCOUNSELING AND INTERNATIONALCOUNSELING AND PRESYMPTOMATICCOUNSELING AND SOCIAL PROBLEMSCOUNSELING CASES /OF 1575COUNSELING CHALLENGE /PATIENTCOUNSELING CLINIC IN HONG KONGCOUNSELING DILEMMA /A TRUECOUNSELING DILEMMA /PATIENTCOUNSELING EFFECTIVENESS ANDCOUNSELING FOR ADULTS WITHCOUNSELING FOR DEAF ADULTSCOUNSELING IN A NORTH INDIANCOUNSELING IN ABNORMALCOUNSEUNG IN FAMILIES WITHCOUNSELING IN JAPANESE /ANDCOUNSELING IN KUWAIT /ANDCOUNSELING IN NEUROMUSCULARCOUNSELING IN NOONAN SYNDROMECOUNSELING IN RETINITISCOUNSELING IN SPONTANEOUSCOUNSELING IN SPORADIC CASESCOUNSELING ISSUES IN CASE OFCOUNSELING LINKED GENES /INCOUNSELING OF CARRIERS WITHCOUNSELING OF DISEASES WITHCOUNSELING ON PATIENT ANXIETYCOUNSELING ON REPRODUCTIVE IOFCOUNSELING TRAINING AN /ANDCOUNSELING WITH DNACOUNSELOR IN A SCREENING [THECOUNSELOR STRESS ANDCOUNSELORS 22 YEARS /OFCOUNSELORS EXPERIENCE /OFCOUNSELORS REGARDING ETHICALDEAFNESS /IMPLICATIONS OFDEFECT IN FANCONI ANEMIA ANDDEFECT IN HOMOCYSTINURIA DUEDEFECT ON THE X CHROMOSOMEDEFECTS IN KARNATAKA INDIADEFECTS IN XERODERMADEFICIENCY IN ALDEHYDE /THEDEMOGRAPHY OF THE MULTIETHNICDETERMINANTS OF PLASMA ANDDIAGNOSIS /AND PREIMPLANTATIONDIAGNOSIS A COMPARATIVEDIAGNOSIS IN THE FEDERALDIAGNOSIS OF 1303 /PRENATALDIAGNOSIS OF MITOCHONDRIALDIAGNOSIS OF THE /TOWARDDISEASE /DIAGNOSIS OFDISEASE /INCREASED RISK FORDISEASE ANALYSIS /IN HUMANDISEASE OR ENVIRONMENTAL RISKDISEASE WHERE WE ARE /OFDISEASES BASIS FOR PLANNINGDISEASES IN A PEDIATRIC /OFDISEASES IN A PEDIATRIC /OFDISEASES IN GENERAL /SURVEY OFDISEASES IN GENERAL /SURVEY OFDISORDER WITH MARKED /FEVER ADISORDERS /AND IN OTHERDISORDERS /OF CHILDREN FORDISORDERS IN SECONDARY /OFDISSECTION OF THE FOLDING ANDDISTANCE AMONG SOME TRIBES OFDISTANCE AT VNTR LOCI AMONGDISTANCE COMPARED /MEASURINGDISTANCES ON HUMAN CHROMOSOMEDIVERSITY /FOR ESTABLISHINGDRIFT IN A BRAZILIAN ISOLATEDEDUCATION IN AUSTRALIAEDUCATION OF NURSES IN EVERYEFFECTS OF AFRICANEPIDEMIOLOGICAL STUDIES OFEPIDEMIOLOGICAL STUDIES OF /INEPIDEMIOLOGY /REGISTRIES TOEPIDEMIOLOGY AND MODELS FOREPIDEMIOLOGY OF ALCOHOLISM INEPIDEMIOLOGY OF CLEFT LIPEPIDEMIOLOGY OF COMPLEX
560
1955217821961971227587153S9566864180519343752662726263826101573156112021747226208269127317391764177076012461785116210801756173728
140312441743101917361735176310163661111176120061757100517521850176267517491784177918141821
25296
230022931845293
271628472759107
1177180212201010121062
17882532666422149777178927692778858484951664S4628622837168021072630283532817732557
2269
402123
272526782657
Permuted Title Index
EPIDEMIOLOGY OF NARCOLEPSYEPIDEMIOLOGY OF SINGLE GENEEPIDEMIOLOGY USING MARKOV /INFACTORS IN NTDS /OFFACTORS IN PRIMARY GLAUCOMAFACTORS IN THE GROWTH OFFACTORS INVOLVED INFAMILY REGISTER OPPORTUNITYFITNESS OF HEMOPHILIA A INHAZARDS OF RADIATION ANDHEALTH EDUCATION AND PROMOTIONHEALTH SERVICES IN DEVELOPINGHETEROGENEITY /CLINICAL ANDHETEROGENEITY /EVIDENCE FORHETEROGENEITY AMONG THEHETEROGENEITY AND ASSORTATIVEHETEROGENEITY IN /NONALLELICHETEROGENEITY IN FAMILIALHETEROGENEITY IN FANCONIHETEROGENEITY IN JAPANESEHETEROGENEITY IN SEVERE /OFHETEROGENEITY OF CHARCOT /ANDHETEROGENEITY OF EARLY ONSETHETEROGENEITY OF SKELETONHETEROGENEITY OF ULCERATIVEHETEROGENEITY OF USHERHETEROGENEITY OUTSIDE REGIONHETEROGENEITY REVEALS AHOMOGENEITY OF THE PALEO /THEIMPRINTING /AN EXAMPLE OFIMPRINTING /MECHANISM OFINFORMATION HOW FAR DO OURINSTABILITY /AND INCREASES THEINTERFERENCE USING THE /OFINTERVAL AND IDENTIFYING THEINVESTIGATIONS ON TONGUEINVESTIGATIONS WITH PATIENTS10 AND CONSEQUENCES /ASSESSINGISOLATE /OF SKIN COLOR IN AUMITS OF THE HUNTINGTON /ANDLINKAGE ANALYSIS OF BIPOLARLINKAGE ANALYSIS OF PANICLINKAGE CALCULATIONS /INLINKAGE MAP OF EIGHTLINKAGE MAP OF MOUSELINKAGE MAPS /CONSTRUCTION OFLINKAGE MAPS OF HUMAN /ANDLINKAGE OF DOMINANTLINKAGE OF FIBRILLIN /ANDLINKAGE STUDIES IN /ANDLINKAGE STUDIES IN AUTOSOMALLINKAGE TO SEVERE PRE /FORLINKAGE TO THE FRAGILE X /WITHLOCI IN SCHIZOPHRENIALOCUS /SUGGESTS A COMPLEXMAP /LOCUS AGAINST A COMPLETEMAP /THE SEARCH THEMAPPING /HYBRIDIZATION ANDMAPPING AND A REDUCED /FURTHERMAPPING OF A DINUCLEOTIDEMAPPING OF HLA F ON 6P21.3MAPPING OF THE JUVENILE ONSETMAPS FOR CHROMOSOMES 5 AND 10MAPS FROM NONDISJUNCTIONALMARKERS AND GENOMIC /GENESMARKERS FOR STUDYING DISEASESMARKERS ONTO THE COSMID /OFMECHANISM OF IMMORTALIZATIONMONITORING AMONG KIEV /LIMITEDMORBIDITY /YOUNG MOTHERS ANDORIGIN OF HYDATIDIFORM MOLARPOLYMORPHISMS /OF JEWS OF TWOPOLYMORPHISMS OF SERUM ANDPREDISPOSITION IN FEMALESPREDISPOSITION TO BREAST /ARELATIONSHIP BETWEEN DNASCREENING AND COUNSELING /FORSERVICE AND RESEARCH IN TAIWANSERVICES /AND ORGANIZATION OFSERVICES /PROBLEMS CONFRONTINGSERVICES /SOCIAL ASPECTS OFSERVICES BY CYSTIC FIBROSISSERVICES DEVELOPED NATIONS /TOSERVICES DEVELOPING NATIONSSERVICES IN A SOUTH AFRICANSERVICES IN SOUTH AFRICASERVICES INTO PRIMARY HEALTHSERVICES PROGRAMS IN THE U.S.ASERVICES TO NEW IMMIGRANTSSTRUCTURE USING SURNAMES INSTUDIES IN AO NAGAS NAGALANDSTUDIES OF AMERICAN HISPANICSTUDIES OF FRIEDREICH ATAXIASTUDIES OF HUMAN X CHROMOSOMESTUDIES OF JUVENILESTUDIES OF JUVENILESTUDIES OF PRIMARYSTUDIES ON CANCERATION OFSTUDY OF A VILLAGE POPULATIONSTUDY OF CONGENITAL CATARACTSTUDY OF PREDISPOSITION TOSTUDY OF THE SPINAL MUSCULARSTUDY ON SIX PRIMARY SQUAMOUSSTUDY ON THE TOE LENGTH OFSUPPORT GROUPS AS A MEANS TO
2771265927882235691
2881S93208
2812256217721803202326721885189920092019237623154561922202486127731077111618812637266726601820170520952371283159618362764102
2029194420861954186320602124
73345613
71919S7720642312063S6221612014203521371972216385
2187270
220313142782952928
26282845801
175466
2091810149
1806152
17693738
18081792151
179817402864286828241989145715
2681226513592827700
10952218131528511759
SURVEY IN THE ISOLATEDSUSCEPTIBILITY /INDICATOR OFSUSCEPTIBILITY TO BLEOMYCIN ASUSCEPTIBILITY TO CHRONICSUSCEPTIBILITY TO RETINOPATHYSYNDROMES WAS REACHED IN 8%TECHNIQUES /AND MOLECULARTESTING /CONFIDENTIALITY INTESTING LEGAL AND ETHICAL /INVARIABILITY OF COMPLEMENTVARIANCE OF NINE LIPID ANDVARIATION AND DISTANCEVARIATION AT THE /OFVARIATION IN HUMAN NVARIATION OF RED CELL ACIDVARIATION OF THE TRANSFORMING
GENETICAL AND TOMOGRAPHIC STUDY ON 26STUDY ON 26 BRAZILIAN /AND
GENETICALLY DETERMINED INDICES OFMODIFIED MYOBLASTS /FROMPREDISPOSED TO BREAST
GENETICIST INVOLVEMENT /AND THERAPYGENETICISTS /A SPECIAL ETHICS CODE FOR
YES /OF ETHICS FOR HUMANGENETICS /DISEASE AND THE ABUSE OF
/ETHICAL ISSUES IN MEDICAL/INDICATIONS AT INTEGRATED/PUBLIC NEED TO UNDERSTAND/SYSTEM FOR MEDICAL/SYSTEM IN CLINICAL/TRAINING ADOPTION WORKERS INABNORMALITY IN PRENATALACCESS TO GENETIC SERVICESAN OVERVIEW OF THE ISSUEAND CYSTIC FIBROSISAND ENZYMOLOGY OF PRIMARYAND EUGENICS ON THE BASIS OFAND FUNCTIONS SYSTEMS CONCEPTAND ITS RELATIONSHIP TOAND MUSEUMS /CURIOSITY ABOUTAND PATHOGENICITY OFAND THE PEOPLING OF THEAND TREATMENT /ON MOLECULARBEHAVIOR AND BRAIN IMAGINGCOUNSELING VERSUS MEDICALDEPARTMENT AT ROBERT REIDEDUCATION AND TRAINING INEUGENICS AND LYSENKOISM 1910HETEROGENEITY WITH EVIDENCEHISTORICAL LESSONS AND THEIN AFRICA /EDUCATION ININ CHINA /EDUCATION ININ GERMANY 1890 1950 /HUMANIN HONG KONG PROBLEMS ANDIN INDIA /EDUCATION IN HUMANIN JAPAN /IN MEDICALIN THE DIVISION OF /MEDICALIN THE EUROPEAN ECONOMICIN THE UNITED KINGDOM /ININ THE USSR MEDICAL SCHOOLINFORMATION AND SERVICES /TOK 12 LEAD TEACHER TRAININGNEEDS ASSESSMENT FOROF ALPORT SYNDROME /MOLECULAROF ASPARTYLGLUCOSAMINURIAOF ATHEROSCLEROSIS /THEOF CARDIOVASCULAROF CHILDHOOD ONSET SPINALOF DEVELOPMENTAL DYSLEXIAOF DIZYGOTIC TWINNING /ANDOF ERYTHROID DEVELOPMENT /ANDOF GALACTOSIALIDOSISOF HEREDITARY FRUCTOSEOF HUMAN BREAST CANCEROF HURLER AND HUNTEROF HYPERVARIABLE LOCIOF INTELLIGENCEOF LEUKEMIA /MOLECULAROF MONOAMINE OXIDASE INOF MOOD DISORDERS /INTO THEOF OBSTRUCTIVE SLEEP APNEAOF OESOPHAGEAL ATRESIA ANDOF POLYCYSTIC KIDNEY DISEASESOF THE ALTAIANS /POPULATIONOF THE CHROMOSOME 11P13OF THE CYP2D6 POLYMORPHISMOF THE D1S7 D2S44 AND D14S13OF THE D4S139 D16S85 D17S79OF THE HUMAN MUCI LOCUS INOF TUMOR FORMATION IN VONOF UIGURS /ON POPULATIONOF X LINKED DEAFNESSPROGRAMS /ORIENTED NATIONALRESEARCH LABORATORY /FOR ASCHOOL YARD EXPERIENCESSERVICE /NEW SOUTH WALESSERVICES /COMPREHENSIVESERVICES /NATIONALSERVICES /REFERRALS FORSERVICES FROM DISEASE /OFSTUDIES IN FAMILIES WITHTO NEW JERSEY PRENATAL CARE
GENITAUA NEWBORNS BY PCR /AMBIGUOUSGENITOURINARY ANOMALIES /MANAGEMENT OF
ANOMALIES /TUMOR AND
285727101339772
267023
16713940
2858277528832011549
2754224270783112132488173318134241
181718211786395
1811750
1776115937
Sli6
1321818121319397469255SS
195717817333333211423223273303201795331332178233432933517772061790382458163
266826871997400S71280981127282252
1734S76493122
27632646384
2850126S9328522836286726022860
24S30207939318001809S301783S30267317971175274220
GENODERMATOSIS /POIKILODERMA A NEWGENOME /ARE DISPERSED THROUGHOUT THE
/FOR MAPPING OF THE HUMAN/MAPPING OF THE YEAST NUCLEAR/PHYSICAL MAP OF THE DROSOPHILA/REGIONS AND OVER 60% OF THE/SITE CLEAVAGE OF THE MOUSE/THE ENCYCLOPEDIA OF THE MOUSE/THE HUMAN/WIDE SPREAD REPEATS IN HUMANALU CLUSTERS LOCALIZATION INANALYSIS /TECHNIQUE FORANALYSIS OF THE HUMAN X /INAND SEPARATE CHROMOSOMES FORBY HYBRIDIZATION IN SITU /HUMANCONTAINS HYPERVARIABLE /HUMANFOR MARKERS LINKED TO BIPOLARIMPRINTING DEVELOPMENTALIN A SYNDROME OF PROXIMALMAP OF CAENORHABDITIS ELEGANSMAPPING /FRAGMENTATION ANDMAPPING /STRATEGIES FORMAPPING PROJECT /KINGDOM HUMANOF CAENORHABDITIS ELEGANSSCAN FOR LINKAGE IN ANSCIENCE ETHICS AND PUBLICSEARCH METHOD EFFICIENT /TOTALSTRATEGY TO ISOLATE DISEASE /A
GENOME'S UNSTABIUTY AMONG /OFGENOMES /TO THE ANALYSIS OF LARGEGENOMIC CHANGES IN HUMAN GLIOMAS /OF
CLONE PROBES /CDNA ANDDATA THE ENCYCLOPEDIA OF THEDNA /OF DNA METHYLATION INDNA BY PCR /OF HUMANDNA SAMPLES DELIBERATE /POOLEDDNA USING DENATURING GRADIENTERRORS PREVALENT AMIDSTIMPRINTING /ANDIMPRINTING /EVIDENCE OFIMPRINTING /OF EVIDENCE FORIMPRINTING /SUPPORT FORIMPRINTING AND INSULINIMPRINTING IN THE BECKWITH /OFLIBRARIES USING THE BIOMEK /OFLIBRARY OF 150 200 KB INSERTSORGANIZATION /MARKERS ANDREARRANGEMENT IN MAMMALIANREARRANGEMENTS COMMON TOREGION OF INTEREST /AREGIONS /ENCODED BY LARGESEQUENCE OF 180 KB COMPRISINGSEQUENCING OF THE HPRT GENE 5STRUCTURE OF HUMAN STOMACH
GENOTOXIC AGENTS /EXPOSED TOEFFECT OF THE FUNGICIDEEFFECTS IN MEN /OFEFFECTS OF CHEMICALS /OFEFFECTS OF SULPHASALAZINE
GENOTOXICITY EVALUATION AND ITS /FOROF A PERMANENT BLACK
GENOTYPE DATA VALIDATE THE USE OF DNAENVIRONMENT INTERACTIONIS CHARACTERIZED BY AN /XPHENOTYPE RELATIONSHIPS INSPECIFIC VARIANCES AND /OFTO PHENOTYPE /RELATIONSHIP OFWITH PHENOTYPE IN TAY SACHS
GENOTYPES /THALASSEMIA AND 306 NORMALAND THE CONCEPT OF SOMATICASSOCIATED WITH DEFICIENTOF LACTASE PERSISTENCE
GENOTYPING /PHENOTYPE ASSIGNMENT BYASSORTMENT AND RELIABILITYBY DIRECT PCR OF GUTHRIEERRORS ON THE ESTIMATIONOF CATARACT ENRICHED /DNAOF HIGHLY POLYMORPHICPREIMPLANTATION MOUSE
GENTRANET /OF GENE TRANSFERGENU VALGUM /HEREDITARY PUBERTALGEOGRAPHIC CLUSTERS OF BIRTH DEFECTS
DIFFERENCES IN BRAZILIANORIGIN OF A FRENCH
GEOGRAPHICAL DISTRIBUTION IN ITALYGEOGRAPHICALLY DEFINED FRENCH /FROM AGEOGRAPHY OF HUMAN GENES /HISTORY AND
OF SOUTH AMERICA TESTINGGERM CELL TUMORS /ALLELOTYPING OF MALE
CELL TUMORS /OF EXTRAGONADALCELL TUMORS OF THE TESTIS /ALLLINE AND SOMATIC P53 GENE /OFLINE MOSAICISM FOR CHROMOSOME 5LINE MOSAICISM IN THE VON /ANDLINE MUTATIONS IN HUMAN BREAST
GERMAN AND ARGENTINIAN PATIENTS /AMONGCOLLABORATIVE STUDY ONCOLLOBORATIVE STUDY /FROM THE
GERMANY 1890 1950 /HUMAN GENETICS INA REPORT FROM THE EUROPEAN /OF
GERMINAL MOSAICISM IN CROUZONMOSAICISM IN X LINKED ANDMUTATIONS IN THE RB AND P53MUTATIONS IN THE REFLECTION
GERMUNE AND IN VIVO SOMATIC /OF
561
66119732098237239
200020741898
1243321311637179
2194207121871940241502
212624982511205423818771780S3221741838175
1382112318982449251627922069713
2653791
276515962708767
2125252921872556473
2321201
257524282304255825611213254728091608256025062648379
24192738
31283
1831292551
2647541110318402076194720622239247965127222863271228822840254
2865611
1311614
260511761068218
234412341264320180284028082553360
2538
Permuted Title Index
AND SOMATIC MOSAICISMDETERMINATION/FORMATION ANDMOSAICISM AS DEMONSTRATED INMOSAICISM IN PROGRESSIVEMOSAICISM IN X LINKED /ANDPROLIFERATION IN C ELEGANS
GERSTMANN STRAUSSLER SCHEINKER /OFGESTALT IN SIBLINGS A NEW SYNDROMEGESTATION/ABNORMALITY AT 28 WEEKS
/AND FETAL TISSUE OF TWIN/FROM 35 TO 42 WEEKS/MALFORMATIONS DURING HUMAN/OF MSAFP IN TRIPLET/PREGNANCY LOSSES THROUGHOUT
TATIONS /ESTRIOL LEVELS IN TWINSUPPORTS PRENATAL /IN TWIN
GG TRANSITION AT A SPLICE ACCEPTOR OFGH SECRETION /NORMAL GROWTH HORMONEGIANT CELL OSTEOGENIC SARCOMA /CASE OF
MARKER CHROMOSOME /WlITH A SINGLERING CHROMOSOME INCLUDING
GIBBS SAMPLING TO GENETIC ANALYSES /OFGIEDION SYNDROME ASSOCIATION WITH 80
SYNDROME CHROMOSOME REGIONGIENSA AND REVERSE BANDS /OF
OF CHROMOSOME 19/BY ALUIGILLES DE LA TOURETTE SYNDROME
DE LA TOURETTE SYNDROME /OFGINGIVAL FIBROMATOSIS A REPORT OF TWOGIRL /IN A PHENOTYPICALLY NORMAL
/SYNDROME IN A 15 YEAR OLDWITH CONSTITUTIONAL RING /IN AWITH DEL(X) (P22.2) /IN AWITH INCONTINENTIA PIGMENTI /N AWITH PLEXUSPAPILLOMA AND /IN AWITH SHORT STATURE AND DELAYED /AWITH XO/XX CHROMOSOMAL PATTERN /A
GLAND OF TRANSGENIC MICE AN PAROTIDGLAUCOMA/GENETIC FACTORS IN PRIMARY
/OF PRIMARY CONGENITALFROM TURKEY /CONGENITAL
GLIOMA BY MICROCELL MEDIATED TRANSFERGUOMAS /CYTOGENETICS OF LOW GRADE
/OF GENOMIC CHANGES IN HUMANGLOSIN DOMAIN /THE BETA
GENE BY DENATURING GRADIENTGENE CLUSTER PHENYLALANINE /58GENE DELETION MUTANTS /FROMGENE DELETIONS /OF SINGLE ALPHAGENE EXPRESSION /ON FETAL GGENE IN CHINESE /OF AGENE MUTATION IN A JAPANESE /BSWITCHING DURING DEVELOPMENT /BVARIANTS AMONG CHINESE /ALPHA
GLOBOID CELL LEUKODYSTROPHY /INFANCYGLOMERULAR BASEMENT MEMBRANE ALPORT
ERULOCYSTIC KIDNEY DISEASE ANDGLUCOCEREBROSIDASE A PH SENSITIVE
AND ARYLSULFATASEGENE AMONG GAUCHERGENE IN MURINEGENE MUTATIONSIN A PATIENT WITHIN HEPATOCYTESTARGETED TO /USING
GLUCOCORTICOID RECEPTOR GENE REGIONGLUCOSE 6 PHOSPHATE DEHYDROGENASE /AGLUCOSIDASE /OF HUMAN LYSOSOMAL A
/ROUTING OF LYSOSOMAL AACTIVITY /NORMAL ACID AFUNCTION /OF ACID B
GLUCOSYLCERAIDASE INTO ACIDIC /OFGLUCURONINSE DEFICIENCY AM (BETAGLUTAMATE FOR GLYCINE 853 OF THE /OFGLUTAMATERGIC AND CHOLINERGIC ENZYMESGLUTAMIC ACID IN PRIMARY GENERALIZEDGLUTAMYL TRANSPEPTIDASE GENES TOGLUTARIC ACIDEMIA TYPE 1 /DIAGNOSIS OFGLUTARYL COA DEHYDROGENASE /ENCODINGGLUTATHIONE REDUCTASE IN /THE ROLE OF
REDUCTASE PROBES FOR THEGLY 922 /SERINE SUBSTITUTION FOR A2(1)GLYCEROL KINASE AND ADRENAL /THE
KINASE DEFICIENCY /OF COMPLEXGLYCINE /ENZYME AND AMNIOTIC FLUID
853 OF THE TRIPLE HELICAL /FORAl 901 SUBSTITUTION IN A TYPECLEAVAGE ENZYME AND AMNIOTICIN THE All COLLAGEN CHAIN /FORSUBSTITUTION AT CODON 574 OFSUBSTITUTION AT POSITION 175
GLYCOGEN PHOSPHORYLASE ON CHROMOSOMESTORAGE DISEASE IN /(TYPE 11STORAGE DISEASE Xi GSD XiSTORAGE DISORDER (PSEUDO
GLYCOGENOSIS IN XP22 /X LINKED LIVERWITH FANCONI NEPHROPATHY
GLYCOPHORIN A LOCUS IN FANCONI ANEMIAGENE LOCUS /EVOLUTION OF
GLYCOPROTEIN FAMILY /THE LEUCINE RICHGENE PC1 MAPS TO 6021SYNDROME /DEFICIENT
GLYCOPROTEINS /DYSTROPHIN ASSOCIATEDGLYCOSAMINOGLYCAN EXCRETION /URINARY
TURNOVER IN THE /OF
2913232876261191324189677311451641912103
126136111971146280214071365137713692781507197
16571598276619246841532752132477464313761653825
2444691764628
256812981382336
25172883337976242311251070118A267986238314444362492101824712503560248355221232324568581529
2545526
2473522520477
2130481
23224534531054222068756352210655634464745341979574846529
1921846253526252380130718720577467
GLYCOSYLASE CDNA WHOSE GENE MAPS TOGLYCOSYLASPMRAGNAE /CODING HUMANGLYCOSYLATION SITES OF HUMANGLYCOSYLTRANSFERASES IN HUMAN SEMINALGM AND KM IN CHINESE AND MALAY
HAPLOTYPE DISTRIBUTION INGS1 GANGLIOSIDOSIS /PATIENTS WITHGM2 GANGLIOSIDOSIS /WITH B1 VARIANT OF
GANGLIOSIDOSIS AMONG JEWS AND NONGOITER /WITH A VERY HIGH PREVALENCE OF
WITH HYPOTHYROIDISM /HEREDITARYGOLABI BEHMEL SYNDROME /THE SIMPSONGOLDEN RETRIEVER MUSCULAR DYSTROPHYGOLDENMAR SYNDROME A NEUROCRISTOPATHYGOLTZ SYNDROME CONTIGUOUS A CASE OFGONADAL DYSGENESIS /AND 46,XY PURE
DYSGENESIS /FEMALE WITH MIXEDDYSGENESIS /IN X LINKEDDYSGENESIS AND HERMAPHRODITESDYSGENESIS AND PALATALDYSGENESIS IN 46,XXTUMOR WITH A 48,XY, + 7,+1(12P)
GOMADOSLASTOMA IN EARLY CHILDHOODGONADOTROPIN DEFICIENCY AND WHITEGONOSOMAL ABNORMALmES /SCREENING OFGM ASSAY IMPLICATIONS FOR AN VIVOGPD EXPRESSION IN NORMAL AND TRIPLOIDGRADE GLIOMAS /CYTOGENETICS OF LOWGRADED MOLAR SOLUTIONS OF TRACE ANDGRADIENT ELECTROPHORESIS /DENATURING
GEL BLOTS /USING DENATURINGGEL ELECTROPHORESISGEL ELECTROPHORESISGEL ELECTROPHORESISGEL ELECTROPHORESISGEL ELECTROPHORESISGEL ELECTROPHORESISGEL ELECTROPHORESISGEL ELECTROPHORESIS /CLAMPEDGEL ELECTROPHORESIS ANDGEL ELECTROPHORESIS INGEL ELECTROPHORESIS OF PCRGEL ELECTROPHORESIS OF PCRGEL ELECTROPHORESIS TOSEPARATED AMNIOCYTES IN
GRAFTED INTO MOUSE SKELETAL MUSCLEGRANULOCYTE COLONY STIMULATING FACTOR
MACROPHAGE COLONY /HUMANGRAPHIC DISPLAYS OF GENOMIC DATA THEGREEK DUCHENNE AND BECKER MUSCULARGREEN COLOR VISION DEFICIENCY /FOR RED
MONKEY (C AETHIOPS) /THE AFRICANPIGMENT PROTEINS /HUMAN RED ANDVISUAL PIGMENT GENE REGION IN
GRIDDING OF GENOMIC LIBRARIES USINGGROLL HIRSCHOWITZ SYNDROME /WOMAN WITHGROUP (X/Y) POLYMORPHISM /B ANTIGEN
/4 YIELD A SINGLE UNKAGE/CHROMOSOME 6 AT THE HLA LINKAGEA AND B GENE ENCODED /BLOODA MINORITY NATIONALITY IN CHINAAND SURVEY OF PARTICIPANTSCHROMOSOMES /IN HUMAN D GD CELLS BY MICRO CELLMEDIATEDFOR COUPLES WHO HAVE TERMINATEDIN MALFORMED NEWBORNS AND THEIRSPECIFIC COMPONENT /PROTEIN
GROUPS /CAUCASIAN AND HISPANIC RACIAL/CAUCASIAN AND HISPANIC RACIAL/DERMATOGLYPHICS AND ABO BLOOD/EXCHANGES IN CERTAIN ETHNIC/IN 40 PATIENTS IN 5 HIGH RISKNNTR LOCI AMONG THREE ETHNICAND PROTEIN ELECTROMORPHSAS A MEANS TO INCREASE /SUPPORTAT RISK FOR CHROMOSOMECOME OF AGE! /PARENT SUPPORTIN RELATION TO ASTHMA ANDIN THE SAN LUIS VALLEY COLORADOINFLUENCE OF SELECTION FOUNDEROF HUMAN BLOOD LYMPHOCYTES /AGEOF JEWS OF TWO GENETIC
GROWTH AND DEVELOPMENT /AND EMBRYONICAND DEVELOPMENT OF HUMAN TWINSCONE GUIDANCE IN DROSOPHILA/OFDISTURBANCES (OLIVER AND MACFACTOR A AND B CHAIN PROMOTERFACTOR ALPHA GENE /TRANSFORMINGFACTOR ALPHA TO NONSYNDROMICFACTOR ALPHA WITH CLEFT LIPFACTOR B1 GENE IN EMBRYONICFACTOR INJECTION EXTRACTEDFACTOR RECEPTOR (C KIT) GENEFACTOR RECEPTOR A MAST/STEMFACTOR RECEPTOR GENE ISOLATEDFACTOR RECEPTOR PROTO /CELLFACTORS AND REVERSE /LIKEFACTORS FROM FETAL BOVINEFACTORS REGULATION OF C MYCHORMONE (GH) SECRETION /NORMALHORMONE BINDING AND CAUSESHORMONE RECEPTOR GENE MUTATIONHORMONE RECEPTOR IMPAIRS /HUMANHORMONE RELEASING FACTORIN A HUMAN RENAL CARCINOMA
22582355568572
27332564511059
328276627359678151448223813B6197612291466780138667264514802546245112982127279220694374631008109720592073265225201057985
25172793588445
24886192360189622922231678
23982320212595098619712197572
18561731153723011766265522622836285218512843806
2837284217591167175527522689S4
2542262812962721325769
2415101510132242243525332296229623841891442950241314072455969245520641395
IN CARTILAGE HAIR HYPOPLASIAOF CHILDREN OF HIGH AND LOWRABBIT MODEL FOR /IN FACIALRETARDATION /AND SEVERERETARDATION /NTRAUTERINERETARDATION CONFIRMATION OFRETARDATION IN DOWN SYNDROMERETARDATION IS NOT EXPLAINED
GSI FROM DISTAL XP THAT ESCAPES XGS Xi AN AUTOSOMAL RECESSIVE /XIGT REPEAT POLYMORPHISMS USINGGTMSE ACTIVATING PROTEINS /BYGUADALAJARA CAMPTODACTYLY SYNDROMEGUARAN AMERINDIANS FROM BRAZIL /ANDGUIDANCE IN DROSOPHILA FASCICUN II
IN THE COMMON CHROMOSOMALGUN PCR /HUMAN CHROMOSOMES USING SHOTGUSTATORY HABITS /AGE DEPENDENCE OFGUTHRIE BLOOD SPOTS /BY DIRECT PCR OFGYRATE ATROPHY /N AN EXON DELETION IN
ATROPHY AMONG FINNS AND OTHERSATROPHY OF THE CHOROID ANDATROPHY UPDATE ON MOLECULARATROPHY USING PCR DENATURING
H
H Y SEROLOGICAL ANTIGEN AND MULLERIANH162 (D22S68) IN LINKAGE STUDIES /WITHH2A GENE IN DROSOPHILA MELANOGASTERH4 IS CORRECTED AFTER TRANSFECTION OFHAD1T /AGE DEPENDENCE OF GUSTATORYHAI[TUS AND LAMININ DEFICIENCY
MICROCEPHALY MENTAL /MARFANOIDHAENSZEL PETO AND DERSIMIONIAN LAIRDHAIKOU /UNDER THE AGE OF SIX IN
CITY PEOPLE /HELD AMONG 87,521HAINAN PROVINCE CHINA/STATE FARMS INHAIR DYE /OF A PERMANENT BLACK
HYPOPLASIA /GROWTH IN CARTILAGESHAFTS /DNA ISOLATED FROM HUMAN
HAIRED FOX TERRIER A NEW DOG MODELHALF OF THE COL4A5 GENE (THE UNKNOWN 5HALL SYNDROME /SURVIVAL IN PALLISTER
SYNDROME ASSOCIATED WITH ANHALLEVORDEN SPATZ DISEASE ANTEMORTEMHALLUX VIRUS WITH SUPERNUMERARY TOESHAMSTER CELL MUTANT V H4 IS CORRECTEDHAN AND ZHUANG MINORITIES FAMILY /OFHAND AND TEMPORAL BONE CT FINDINGS
MALFORMATIONS (SPLIT HAND) ONON THREE OF THEM /(SPLIT
HANDICAPPED IN BRAZIL /FOR MENTALLYHAPLOID SET /ORIGIN OF THE EXTRAHAPLOTYPE 1 AND 4 ALLELES IN /OF
ANALYSIS OF A FRENCHDISTRIBUTION IN AMERINDIANS
HAPLOTYPES, /P49A DETECTS COMPLEX PVUIIA MOLECULAR ANALYSIS OFAT THE INSULIN RECEPTORCARRYING DUPLICATED C4AEXTENDING OVER A 350 KB /OFIDENTIFIED BY DNA RFLPS ININ A FAMILY WITH /EXTENDEDIN DISORDERS OF PUBERTYIN EAST ASIA AND MULTIPLEIN THE sB GLOBIN GENE /ANDIN THE PROVINCE OF COSENZA
HAPTOGLOBIN AND TYPE III COLLAGENGENE PROMOTER REGIONPOLYMORPHISM IN PREGNANCY
HARBORING SCIDXI /OF X013 REGIONTHE FAMILIAL ADENOMATOUS /5THE MOUSE MDM2 TRANSFORMING
HARM POTENTIAL BENEFIT THE ONE YEARHARNESSING NEW TECHNOLOGIESHARVESTING /SITU CULTURE AND ROBOTICHASHARON SYNDROME OF MENTAL /RAMBAMHAUSER SYNDROME /ROKITANSKY KUSTERHAVANA /MENTALLY RETARDED PATIENTS INHAVEN AND ROCHESTER COLLABORATION /NEWHAZARDOUS FOR DISJUNCTION IN MEIOSISHAZARDS OF PCR BASED MOLECULAR /OF THE
OF RADIATION AND CHEMICALSHB S IN THE EAST MEDITERRANEAN /ANDHBE AND MALARIA AMONG THE AO NAGASHISS KORLEBU ON ELECTROPHORESIS /OFHCG (TRISOMY 18 USING MSAFP UE3 AND
AFP AND UE3 /THAN 35 YEARS OF AGEAND FETAL VENTRAL WALL DEFECTSAND UE3 /PROGRAM USING MSAFPAND UE3 EFFECTS OF MATERNAL /MSAFPAND UE3 LEVELS IN THE MID /ONAND UNCONJUGATED ESTRIOL /MSAFPAND UNCONJUGATED ESTRIOL IN MID /BAND UNCONJUGATED ESTRIOL LEVELSIN PRENATAL DIAGNOSIS OF TRIPLOIDYIN SECOND TRIMESTER TRISOMY 18IN TWIN PREGNANCIES /MSAFP ANDPROSPECTIVE STUDY /MATERNAL SERUMSCREENING FOR TRISOMY 21 FIRST
562
7652881931736
11529441442117424028461981
126852859325174177
287418402802S4
2519S5
1057
10519012456225028741061882129327792777276825607652500464
2362706701899747
225028517966366361617104
10272036256
2872257
28012211
8124046936652876288327278672425657
2221213213611771S2712286881420754
1941113610432562390
27491824123818441826124211401144123312551197923113918331081847
Permuted Title Index
HDL C IN BABOONS /ON SERUM LEVELS OFCHOLESTEROL /OF SAME AGED TWINSCOMPOSITION STUDIES WITH /AND
HEAD AND NECK /CELL CARCINOMAS OF THEAND NECK /CELL CARCINOMAS OF THEAND NECK A POSSIBLE PRIMARY /THEAND NECK ARE CYTOGENETICALLY /THEAND NECK CANCERS /ORAL CAVITY AND
HEADACHE IN VIRGINIAN AND NORWEGIANHEALING SQUAMOUS EPITHELIOMA /SELFHEALTH BEHAVIOR IN WOMEN GENETICALLY
CARE TECHNOLOGIES IN PRACTICECARE THROUGH A FAMILY PLANNINGEDUCATION AND PROMOTIONEVALUATION INCREASING PUBLICIMPACT OF GENETIC DISEASESISSUES IN APPROACHING /PUBLICMAINTENANCE AND ANTICIPATORYPROFESSIONALS /WHILE EDUCATINGPROMOTION /APPROACHES FORSERVICE /ORIENTED NATIONALSERVICES IN DEVELOPING /GENETIC
HEARING FROM AUDITORY TISSUES /INLOSS /12% HAD NONSYNDROMIC
HEART AND BRAIN DISEASE /IN CHRONICANOMALIES EAR ANOMALIESBLOCK IN DOWN SYNDROMEDEFECTS IN TRISOMY 8 MOSAICISMDISEASE /AND CONGENITALDISEASE /THE PREMATURE CORONARYDISEASE /THE RISK FOR CORONARYDISEASE AND TURNER SYNDROMEDISEASE IN A PATIENT WITHMALFORMATIONS /FOR ISOLATEDMUSCLE /OF ANALYSIS OF HUMANNEPHROMEGALY AND DISTINCTIVE
HEATLABILE HEXOSAMINIDASE B POPULATIONHEAVY CHAIN GENE ORGANIZATIONHELICAL DOMAIN OF TYPE II COLLAGENHELSINKI AREA /YEAR EXPERIENCE IN THEHEMANGIOBLASTOMAS /ANDHEMATOLOGIC DISORDER SHOWING LOSS OF
DISORDERS AT INCREASEDMALIGNANCIES /WITHMALIGNANCIES BY IN SITU
HEMATOLOGICAL PARAMETERS FOR 586PROBLEMS /TARGETING TO
HEMATOPOIETIC CELL IN VIVO /IN MURINEPROGENITORS /IN HUMANSTEM CELLS USING /MURINE
HEME BIOSYNTHETIC PATHWAY /OF THEHEINFACIAL MICROSOMIA /ANOMALIES INHEMOCHROMATOSIS DISEASE LOCUS
IN PORTUGAL A STUDYHEMOGLOBIN E /AN EXPRESSIONS OF
E IN ACHANG ETHNIC GROUP AIN BLOOD DONORS OF THE /ANDLEVELS IN ADULTS IS /FETALSWITCHING /CONTROL OFVARIANTS IN A LARGE MULTIVARIANTS USING ANION /OF
HEMOGLOBINOPATHIES AND HEMOGLOBIN /OFHEMOGLOBINOPATHY SCREENING PROGRAMHEMOGLOBINS IN THE TRIBAL POPULATIONHEMOPHILIA A /OF FVIII GENE CAUSING
A AND CYSTIC FIBROSIS [TOA GENE DIAGNOSIS /STUDY OFA IN A GIRL WITH XO/XXA IN SOUTH AUSTRALIA /OFA PATIENTS /IN TWOA USING PCR SINGLE STRANDB /MUTATIONS AND MILDB /SOMATIC GENE THERAPY OFB EXPRESSION OF HUMAN /FORB FAMILIES /IN ITALIANB MUTATIONS IN A COMPLETEB PATIENTS /FACTOR IX IN 64
HEMORRHAGE WITH AMYLOIDOSIS (DUTCH)HEPATIC ALPHA FETOPROTEIN IN DOWN
BILIARY ATRESIA AND /EXTRADEFICIENCIES IN A LARGE /FORTRANSPLANTATION IN TYPE 1
HEPATMS B VIRUS INFECTION /CHRONICHEPATOCELLULAR CARCINOMA /OF PRIMARY
CARCINOMA /WITH PRIMARYCARCINOMA CELLS /HUMANCARCINOMA RENAL CELLTRANSPLANTATION OR /BY
HEPATOCYTES /GLUCOCEREBROSIDASE INOF THE SPARSE FUR MOUSETRANSPLANTED INTO RAT /IN
HEPATOMA CELLS /ACTIVITY IN MURINECELLS /EXPRESSION IN HUMAN
HEFATORENAL GLYCOGENOSIS WITH FANCONITYROSINEMIA UNUSUAL
HEPG2 NUCLEAR EXTRACTS AND IS /TOHERBAL MEDICINES /AFRICAN TRADITIONALHEREDITARY CEREBRAL HEMORRHAGE WITH
COLON CANCER AND A /WITHCYSTATIN C AMYLOID /DUE TODEAFNESS /IN THE STUDY OFDIFFERENCES DISPLAY /OFDISEASES CONTROL PROGRAMDISEASES IN B.S.S.R /SYSTEMDISEASES IN POPULATIONS OF
2690399
27591319138513941393583
265859817331802151
17721777149
1788174
1777153150
18032623
67181714631499711
111842714141413901
2233792461425522184713251356232130913061831S9
247124842468240984221172731107218562754
75S712701565
270118462717279425251050825
281210022283
7024942474265210056589641205653
2478557772
226513972429302248924832472248524772425846893241725579645991026S8548
179127282715
DISEASES IN UZBEKISTANELLIPTOCYTOSIS IN SOUTHERNFRUCTOSE INTOLERANCE /OFFRUCTOSE INTOLERANCE /WITHGINGIVAL FIBROMATOSIS A /OFGOITER WITH HYPOTHYROIDISMHEMATOLOGIC DISORDERS ATHEMOCHROMATOSIS INHYDRONEPHROSIS TO THE MHCHYPERPARATHYROIDISM JAWINCONTINENTIA PIGMENTIINHABITANTS /OF TURKMEN SSRKIDNEY DISEASEMACULAR TYPE OF BULLOUSMENTAL DEFICIENCY AND ITSMICROSPHEROCYTOSIS /WITHMOTOR AND SENSORY /DOMINANTNEPHRITIS /IN A FAMILY WITHNONPOLYPOSIS COLON CANCERNONPOLYPOSIS COLORECTAL [TOOPTIC NEUROPATHY /LEBEROPTIC NEUROPATHY /LEBEROPTIC NEUROPATHY AND /LEBEROPTIC NEUROPATHY MUTATIONOPTIC NEUROPATHY PARTLYOPTIC NEURORETINOPATHYPATHOLOGY TO HUMANGENETIKPUBERTAL GENU VALGUMRENAL ADYSPLASIA WITHRETINOBLASTOMA CARRY THESPASTIC PARAPLEGIA /LINKEDTUMOR SYNDROMES IN THE /ANDTYROSINEMIA /DEFICIENT INTYROSINEMIA II FAMILY
HEREDITY TYROSINEMIA II EFFECTS ANDHERITABILITY ESTIMATES /AND ASSOCIATED
OF ANKYLOSING APONDYLITISOF RECALLED AGE ATOF RESTRICTION /ANDOF THE SUDDEN INFANT
HERITABLE CONNECTIVE TISSUE DISORDERSCONNECTIVE TISSUE DISORDERSDISORDERS OF CONNECTIVE /FORVARIATION IN PLASMA
HERMAPHRODITE AND A 45,XO TURNER /TRUEHERMAPHRODITES /GONADAL DYSGENESIS AND
/IN XX MALES AND TRUEHERMAPHRODITISM A SEX LIMITED /XX TRUEHERNDON SYNDROME CONFIRMATION OF THEHERNIA /ASSOCIATION FOR DIAPHRAGMATIC
/IN A FEMALE WITH INGUINALNOT AMENABLE TO PRENATAL REPAIR
HERPES SIMPLEX VIRUS TYPE 1 /MUTANT OFVIRUS WHICH INFECTS T /TO A
HETEROCHROMATIN /DIFFERENT VIEW OF/IN OTHER FRACTIONS OFAND CARDIOVASCULAR /0BY ALUI GIEMSA OFPREDISPOSES FORREGIONS /CHROMOSOMAL 0
HETEROCHROMATION DURING MEIOSISHETERODUPLEX ARTIFACTS /ELIMINATION OF
FORMATION AND DENATURINGHETERODUPLEXES /BY PCR GENERATEDHETEROGENEITY /20013.3 AND LINKAGE
/CLINICAL AND GENETIC/EVIDENCE FOR GENETIC/SHOW LITTLE INTRATUMOR/WITH HIGH MUTATIONALAMONG THE CHILDHOODAND ASSORTATIVE MATINGAND GEOGRAPHICAND NATURAL HISTORYAND PRENATAL DIAGNOSISAND VARIABLE CLINICALCOMPARISON OF THE TWOIN A FAMILY WITH MEDIUMIN A FAMILY WITH XIN BETA GALACTOSIDASEIN DIFFERENT /FORIN FAMILIAL NARCOLEPSYIN FANCONI ANEMIAIN ISOLATED /CAUSALIN JAPANESE GAUCHERIN NEUROFIBROMATOSISIN ROMANO WARD SYNDROMEIN SEVERE /OF GENETICIN T(11;19) ACUTEIN TUBEROUS SCLEROSISMULTIGENICOF ADULT POLYCYSTICOF CARCINOMA IN SITU OFOF CHARCOT MARIE TOOTHOF EARLY ONSET FAMILIALOF HAPLOTYPE 1 AND 4OF P FAMILY ALLELESOF RESPIRATORY CHAINOF SKELETON DYSPLASIAOF TAY SACHS DISEASEOF ULCERATIVE COLITISOF USHER SYNDROME TYPEOR A CONTIGUOUS GENEOUTSIDE REGION 15011 13REVEALS A SECOND LOCUSWITH EVIDENCE FOR LOCI
26921063981
2264684662232
2731193219341930287938019902735465191469360019915131019973107320321022320651639221708303483452452
2783273427551611274835235435149923951229982223764215201477119216812590316
2626173015982228157917102513279210492028202326721393100518851899286367644223271906498805107577
2019237623023152009670456132319132603104813181922202410272797S10861
32773107774311161881142
HETEROGENEOUS FORM OF OSTEOGENESISMUTATIONS IN THE /BYNUCLEAR RNA /DERIVEDPOPULATION THE U.S.A /A
HETEROLOGOUS TRANSCRIPTSHETEROMORPHISM CYTOGENETIC ANALYSIS
DETECTION AND /FOROF 9Q13;Q21 IN A
HETEROMORPHISMS IN TWO SAMPLES OF THEHETEROPLASMY IN A FAMILY WITH /OF
IN DISORDERS ASSOCIATEDHETEROZYGOSITY /DEFICIENCY
AND CONSTRUCTION OF /OFAND INTERMARKER /OFAT LOCI ON CHROMOSOMESFOR TAY SACHS DISEASEFOR THE DN ALLELE OFIN CANCER /BY LOSS OFIN ESOPHAGEAL CANCERIN HUMAN POPULATIONSOF B GLOBIN GENEON 17P AND P53 /LOSS OFON CHROMOSOME 18 IN /OFPROBABILITIES FORREPORT OF A FAMILY
HETEROZYGOTE ANALYZED BY FLUORESCENCEDIAGNOSIS OF SICKLE CELL
HETEROZYGOTES OF MULTI ETHNIC ORIGINHETEROZYGOTIC INDIVIDUAL FOR TWO /ANHETEROZYGOUS DELETION OF VON /IN A
FOR STRUCTURAL /OF MENHEXA 7.6KB DELETION IN FRENCHHEXABRACHION GENE REFINED MAPPING ANDHEXOKINASE 1 ON CHROMOSOME 10 /HUMAN
TARGETING TO MITOCHONDRIAHEXOKINASES /ANALYSIS OF MAMMALIANHEXOSAMINIDASE A EXPRESSED IN COS
A GENE WITH THE FOUR /BA IN 35 TAY SACHS /OFA IN A LATE INFANTILEA SUBUNIT GENE /THE BACTIVE SITE HOMOLOGYB POPULATIONB SUBUNIT GENE /HUMAN B
HGPRT BRDURD ASSAY IN THE MONITORINGHHAI RFLPS BY DENATURING GRADIENT GELHIERARCHIES OF MITOCHONDRIAL DNAHIGH AND LOW RISK POPULATIONS /IN
AND LOW SOCIO ECONOMIC STRATA INBLOOD PRESSURE IN THE AFRICAN /OFCONCENTRATION OF GENES CAUSING /ADEGREE OF POLYMORPHISM OF THEDEGREE OF SEQUENCE SIMILARITY TODENSITY GRIDDING OF GENOMICFREQUENCY OF AMP DEAMINASE /THEMUTATIONAL HETEROGENEITY /WITHMYOPIA AND RETINAL DETACHMENTSPERFORMANCE LIQUID CHROMATOGRAPHYPERFORMANCE LIQUID CHROMATOGRAPHYPREVALENCE OF GOITER /WITH A VERYPREVALENCE OF THE B THALASSEMIAPREVALENCE OF VITAMIN DRATE OF LOSS OF HETEROZYGOSITYRESOLUTION BANDING INCLUDING /BYRESOLUTION CHROMOSOME ANALYSISRESOLUTION CHROMOSOME ANALYSISRESOLUTION CHROMOSOME ANALYSISRESOLUTION CHROMOSOME BANDING /ARESOLUTION GENETIC AND PHYSICALRESOLUTION LINKAGE AND PHYSICALRESOLUTION LINKAGE MAP OF /ARESOLUTION LOCALIZATION OFRESOLUTION LOCALIZATION OF 69RESOLUTION MAPPING OF CHROMOSOMERESOLUTION PHYSICAL MAPPING OFRESOLUTION RADIATION HYBRIDRESOLUTION RADIATION HYBRID MAPRESOLUTION RESTRICTION MAPPINGRISK CHINESE FAMILIES /IN 221RISK FAMILIES AVOID EARLY CHDRISK FOR MEIOTIC NONDISJUNCTIONRISK GROUPS /IN 40 PATIENTS IN 5RISK MEDITERRANEAN POPULATION /ARISK PATIENTS IN BRAZIL NINE /INRISK PEDIATRIC POPULATION /IN ARISK REGISTRY FOR WOMEN WITHSCHOOL BIOLOGY CLASSES /USE INYIELD OF DNA ISOLATED FROM HUMAN
HILLS BIHAR INDIA /TRIBES OF RAJMAHALHIMACHAL PRADESH INDIA /OF CHAMBAHIMALAYAS INDIA /IN THE GARHWAL
INDIA /IN THE GARHWALHIP DISLOCATION AND ACETABULARHIRSCHOWITZ SYNDROME /WOMAN WITH GROLLHIRSCHSPRUNG DISEASE AND CHROMOSOME
DISEASE LINKAGE ANALYSISHISPAIC AND NATIVE AMERICANS (U.S.A.)
ETHNIC GROUPS IN THE SAN /ANDMEN /INSULIN LEVELS INPATIENTS AT THE LOS ANGELESPOPULATIONS USING /AMERICANRACIAL GROUPS /CAUCASIAN ANDRACIAL GROUPS /CAUCASIAN ANDWHITES IN THE SAN LUIS /NON
HISPANICS AND NON HISPANIC WHITES IN
563
53448525211852242415811619137928234371064123720562063606178810592442609278710702571257427916321171250418552747444407
26621996213524062616283
2446106749410595284611112255826522447970
2881678
201523602297212548910051443565570
2827267426982574163015051541163216201971160
2048206621442201237
2170S892084601164
1577806250
26751410608178025002833287028252832881950647
2020286726892656114328242836285226692669
Permuted Title Index.
HISTOCOMMTIMBUTY COMPLEX /THE MAJORCOMPLEX AND T CELLCOMPLEX GENESCOMPLEX PROBES IN
HISTOLOGIC FINDINGS IN MALE /ANDHISTOLOGICAL SUDES /FROM STAINEDHISTOLOGY IN TRISOMY 21 /CARDIACHISTONE ARRAY OF DROSOPHILA /THE
DEPLETED CHROMOSOMES /ONH2A GENE IN DROSOPHILA /OF THE
HISTOIATHOLOGY OF FETAL RICKETS /THEHISTORICAL ASPECTS /GENETIC AND
LESSONS AND THE FUTURESIGNIFICANCE IN THE /ANDSPREAD OF G551D AND /ON THE
HISTORIES OF BREAST CANCER /FAMILYHISTORY /OF THE PHENOTYPE AND NATURAL
AND GEOGRAPHY OF HUMAN GENESBASED ON 39 INDIVIDUALS IN 9DATA ON SEIZURE DISORDERSFROM ANCIENT AND MODERN DNAOF ANGELMAN SYNDROME /NATURALOF CANCER /RELATION TO FAMILYOF HUMAN GENETICS AND ITSOF LEFT HYDRONEPHROSIS /THEOF PRADER WILLI SYNDROMEOF RECURRENT NON SYNDROMALOF THE NONLETHAL SKELETALOF TRISOMY 14 MOSAICISM
HIT 1 IN SEARCH OF THE SECONDHIV 1 VARIATION IN AIDS PATHOGENESIS
I RETROVIRAL GENES GENETIC /OFHLA /MENINGOCELE TESTING LINKAGE TO
/OF JUVENILE MYOCLONIC EPILEPSY TOANTIGENS All AND 827 /OFANTIGENS TYPING IN PATIENTS WITHASSOCIATIONS IN PATIENTS AND INCLASS II ASSOCIATIONS WITH THECLASS II GENES /CONJUNCTION WITHCLASS II GENES AND HAPLOTYPES ACOMPATIBLE FETUSES /LOSS OFCOMPLEX /BY DNA RFLP ANALYSIS OFCOMPLEX /CHROMOSOMES FROM THEDP /BETWEEN HODGKIN DISEASE ANDDOAl AND D4S175 IN ANCIENT /OFF ON 6P21.3 /GENETIC MAPPING OFGENES AMPLIFIED BY PCRHAPLOTYPES IN DISORDERS OF PUBERTYIS EXCLUDED /CLOSE LINKAGE TOLINKAGE GROUP /CHROMOSOME 6 AT THELINKED GENES IN TYPE I DIABETESPOLYMORPHISM IN THE KAINGANG AND
HNCDNA LIBRARY HIGHLY ENRICHED INHODGKIN DISEASE AND HLA DP /BETWEEN
DISEASE AND MALIGNANT /WITHLYMPHOMA /IN FOUR CASES OF NONLYMPHOMA /IN NONLYMPHOMA /IN UNTREATED NONLYMPHOMAS /FOLLICULAR B NONSYNDROME USING MULTIPLE /RAPP
HOECHST FLOW CYTOMETRY /BIVARIATE BRDUHOLOPROSENCEPHALY ASSOCIATED WITH
DUE TO FAMILIALHOMAGE COMPUTER PROGRAM TO PERFORM AHOME DELIVERIES TO INFORMED CONSENTHOMEOSOX GENE IS DEREGULATED IN /A NEWHOMEOSTASIS DEVELOPMENT AND DISEASEHOMINIDS /WITH THE EVOLUTION OFHOMINOO CHROMOSOME EVOLUTION
PHYLOGENY EVALUATING /ANDHOMOCYSTINURIA /OF PLATELETS IN
AND VASCULAR DISEASEDUE TO CYSTATHIONINE B
HOMOGENEITY OF THE PALEO INDIANS ANDTEST USING AGE AT ONSET /A
HOMOLOGIES AND GENES WHICH ESCAPEWITH HUMAN CHROMOSOME 50
HOMOLOGOUS /MINIGENES AND DYSTROPHINCROSSING OVER BETWEEN /ANDRECOMBINATION /LOCUS BYRECOMBINATION IN EMBRYONICTO THE AVIAN V MAF /MOTIFYEAST ARTIFICIAL /GENE BY
HOMOLOGS IN DIFFERENT SPECIES OFOF SYNTENIC HUMAN AND MURINE
HOMOLOGUE GENE EXPRESSED IN SPERMATIDSGENE LOCATED IN THE MHC
HOMOLOGY AT THE NUCLEOTIDE SEQUENCEBETWEEN CHROMOSOME 16P ANDMODELING OF PROTEINS FROMTO BCL 2 /1 HAS SIGNIFICANTWITH LYSOZYME /ACTIVE SITE
HOMOZYGOSITY MAPPING OF THE GENE FORHONG KONG /AND PRENATAL DIAGNOSIS IN
KONG /COUNSELING CLINIC INKONG PROBLEMS AND POTENTIALS /IN
HORMONE (GH) SECRETION /NORMAL GROWTHBINDING AND CAUSES LARONDEFICIENCY IN A TURKISH BOYRECEPTOR GENE MUTATION INRECEPTOR IMPAIRS GROWTHRELEASING FACTOR PCRFLPS BYSECRETION /ANTIDIURETICSENSITIVE LIPASE /INSTUDY /THE CANCER AND STEROID
24031917262121171506622934
264216332456925
2839322470
27036087172546762723315170
269531995316970417321522222952187195320415921349590277010025793211082114589
261721372513665
20522197S32285925215891349133313301363139216661609148315091970174022545326132641167872
2323230026371970S291863
172253224425032459
18256918611862186222341556247258952819753881785179514072455891969245520846591983277
HORMONES /AMONG SEX STEROID/AND HUMAN REPRODUCTIVEAND DIETARY INTAKE /STEROID
HOSPITAL (ALIGARH) /IN A NORTH INDIAN/REID CABRAL CHILDREN'S/THAN WOMEN AT A NONSECTARIANBANGKOK THAILANDIN BRAZIL /IN A PEDIATRICIN OSAKA CITY 1948 1990MORE LIKELY TO REJECTOF A DEVELOPING COUNTRY
HOST AND HIV 1 VARIATION IN AIDSCELLS IN SEX MISMATCHED BONE
HOT PCR METHOD /GC RICH DNA USING THESPOT /THE DYSTROPHIN GENE DELETIONSPOTS FOR CYCLOBUTANE PYRIMIDINE
HOUSESTAFF /TEACHING DYSMORPHOLOGY TOHOX 1.2 PROTEIN /OF THE MURINEHOX11 A NEW HOMEOBOX GENE ISHP*l IN HUMAN SOMATIC AND SPERM CELLSHP'2 TO HP'l IN HUMAN SOMATIC ANDHP2 1MOD INDIVIDUALS AFFECTS /FOUND INHPAI SITE 20 BASE PAIRS FROM AHPLC OF URINARY OLIGOSACCHARIDESHPRT CDNA USING THE PCR IN /IN
DEFICIENT MICE /IN THE BRAINS OFGENE 5 REGION ON THE ACTIVE ANDGENE IN MUTANT HUMAN LYMPHOCYTESLOCUS IN FANCONI ANEMIA /AT THELOCUS IN LESCH NYHAN FAMILIES
HSP70 HOMOLOGUE GENE EXPRESSED INHOMOLOGUE GENE LOCATED IN THE
HSV 1 TK GENE /INTEGRATED SINGLE COPYHTF ISLANDS AND THE LOCUS DNF15S2 /TWO
SPECIFIC CLONES /PROBES ANDHUI AUTONOMOUS REGION /IN NINGXIAHUMAN (MARKER ) CHROMOSOMES USING /OF
17 IA NEOANTIGENE GENE PROMOTER21 HYDROXYLASE DEFICIENCY3 METHYLADENINE DNA GLYCOSYLASE70 KD PEROXISOMAL MEMBRANE /THEA LCR IS FLANKED BY THREEA SATELLITE DNA INTO SIMIAN /OFADENOSINE DEAMINASE IN HUMAN /OFALBINO MUTATIONS DEFINEALCOHOL DEHYDROGENASE GENE ADH5ALPHA 1 ANTITRYPSIN VARIANTS BYALPHA 3 BETA 4 AND ALPHA 5 /THEAND APE EVOLUTION THROUGH RRNAAND CHIMPANZEE 'AMONGAND MURINE CHROMOSOMAL MARKERSAND PRIMATES ANALYZED BY /INAND XERODERMA PIGMENTOSUM CELLSAPOLIPOPROTEIN A 1 PREVENTSAPRT GENE /MUTATIONS IN THEAPURINIC ENDONUCLEASE A MEMBERAUTOSOMES /22 AND OTHERB GALACTOSIDASE DEFICIENCY /OFB GLOBIN SWITCHING DURING /OFB HEXOSAMINIDASE B SUBUNIT GENEB1 GAMMA AMINOBUTYRIC ACID /THEBLOOD /INDIVIDUALITY OFBLOOD LYMPHOCYTES /AGE GROUPS OFBONE MARROW CELLS BY /CLASSIFIEDBRAIN /CDNA CLONES EXPRESSED INBREAKAGE SYNDROMES /MODELS FORBREAST CANCER /ABERRATIONS INBREAST CANCER /GENETICS OFBREAST CANCER INVESTIGATION OFBREAST CANCER USING LOCUS /INBREAST CARCINOMAS /AND 170 INBREAST CARCINOMAS USING /INBUT DIFFER IN OTHER FRACTIONSCA3 AND MOUSE STRAIN CAR 2 /THECALPASTATIN GENE TO BAND 015CANCER /A COMMON STEP INCANCER AND TOXICITY /RISK OFCANCERS /EXPRESSION INCARBONIC ANHYDRASE A POSSIBLECARBOXYPEPTIDASE TO THE DISTALCD1 PYRROLINE 5 CARBOXYLATECDNA CLONE THAT CAN PARTIALLY /ACDNA PROBES ENCODING GLUTARYLCELL LINE /EPISOMAL COSMID IN ACELLS /MISMATCH REPAIR INCELLS /REPAIR PATHWAYS INCELLS IN VITRO /RIDOMILL ONCELLS WITHOUT MTDNA A SYSTEMCENTROMERE ANTIGEN CENP B AND /ACENTROMERIC REGIONS /DNA FROMCEREBELLAR CDNA CLONES TO HUMANCFTR GENES /NORMAL AND MUTANTCHIMERISM IN A STILLBORN FETUSCHOLANGIOCARCINOMA CELL LINECHONDRODYSPLASIAS /IN THECHORIORETINAL DYSTROPHY /FOR THECHROMOSOMAL ANOMALIES IN CHINACHROMOSOMAL BAND 3P21.1 /WITHINCHROMOSOMAL BAND 3P21.1 /WITHINCHROMOSOMAL 0 HETEROCHROMATINCHROMOSOMAL REGION 8024 LINKEDCHROMOSOMALLY INTEGRATED SINGLECHROMOSOME 1 MAPPING ADDITIONALCHROMOSOME 11 CONTAINING THE /OFCHROMOSOME 11013 /ONCOGENE FROM
273911962767140373317421249777
26881742178922951668253023572540137
22262254404402425959569
281347824282550255910531862186225362297S7727801605246523752258190
186516632484525
228420732182165
2615186118572539192
253822702130284
118A1112190728532542167625272972595127
1373217
2567218
262625282171S634282580275114622279227523221646254424122561191412168218972364937137847
2342154321382195157925912536220221842608
CHROMOSOME 13 MAPPING REAGENTSCHROMOSOME 15 /WILU REGION OFCHROMOSOME 16 /GENE MAPS TOCHROMOSOME 16 /LINKAGE MAPS OFCHROMOSOME 16P CONTAINING THECHROMOSOME 17 USING RADIATIONCHROMOSOME 17021 /CLONING OFCHROMOSOME 18 /BY TRANSFER OFCHROMOSOME 19 /CONTIG MAP OFCHROMOSOME 19 /FINGER GENES ONCHROMOSOME 19 STRATEGIES AND /OFCHROMOSOME 190 /DISTANCES ONCHROMOSOME 19013.3 WHICH /OFCHROMOSOME 10 /LOCUS ONCHROMOSOME 2 AN ANCESTRAL /OFCHROMOSOME 21 /FAMILIES ONCHROMOSOME 21 /HYBRID MAP OFCHROMOSOME 21 /NEW COSMIDS FORCHROMOSOME 21 /RECEPTOR GENE ONCHROMOSOME 21 /REGION OFCHROMOSOME 21 IN MEIOTIC /OFCHROMOSOME 21 USING VARIOUS /BYCHROMOSOME 22/TO MAPPING OFCHROMOSOME 22 AND OTHER HUMANCHROMOSOME 22 PROBE SPECIFIC /OFCHROMOSOME 22 USING YEAST /OFCHROMOSOME 20 /DNA MARKERS ONCHROMOSOME 3 ENCODES A TUMORCHROMOSOME 3 SEQUENCES PRESENTCHROMOSOME 3PTER 3P25.1 /AF8T TOCHROMOSOME 4 (023 025) AND /TOCHROMOSOME 4/A PHYSICAL MAP OFCHROMOSOME 4 /GENE REGION OFCHROMOSOME 4 ALU BANDING BY /OFCHROMOSOME 4 YIELD A SINGLE /ONCHROMOSOME 50 /HOMOLOGIES WITHCHROMOSOME 6 /BY THE TRANSFER OFCHROMOSOME 7022 32 REGION /THECHROMOSOME 9 /FROM A MARKEDCHROMOSOME 9 /FROM LINKAGE TOCHROMOSOME AND LOCALIZATION OFCHROMOSOME ARM 120 AND RAT /ONCHROMOSOME BAND 11P15.5 /MAP OFCHROMOSOME HYBRIDS /FROM SINGLECHROMOSOME REGION SPECIFIC /OFCHROMOSOME X BY FLUORESCENCE INCHROMOSOMES /DNA ADDUCTS ONCHROMOSOMES /FROM FLOW SORTEDCHROMOSOMES /IN THE STUDY OFCHROMOSOMES 2 13 AND 21 /ONCHROMOSOMES 21 AND 18 BY /ONCHROMOSOMES 5 AND 16 /CLONES TOCHROMOSOMES 8 /OF SECOND GENE ONCHROMOSOMES 8 10 AND 12 /FORCHROMOSOMES AT INTERPHASE AS /OFCHROMOSOMES BY CHROMOSOME /OFCHROMOSOMES BY IN SITU NICK /THECHROMOSOMES BY PCR MEDIATED DNACHROMOSOMES ISOLATED IN /INCHROMOSOMES REVEALED BY TAQI /OFCHROMOSOMES USING RADIATION /OFCHROMOSOMES USING RADIATION /OFCHROMOSOMES. USING SHOT GUN PCRCLEAVAGE SIGNAL 1 PROTEINCLONES USING COT 1 DNA NEW /OFCOCHLEA /OF G PROTEINS INCOFACTOR DEFICIENCY /MODEL FOR ACOLORECTAL TUMORS /13 AND 17 INCOMPLEMENT C4 PROMOTER /OF THECOMPLEMENT COMPONENT C4A AND /OFCOSMID CA476 CONTAINS TWO HTFCOSMID CLONES FROM SOMATIC CELLCYSTATHIONINE B SYNTHASE RAPIDD G GROUP CHROMOSOMES /INDERIVED HETEROGENEOUS NUCLEARDISEASES /AS DEMONSTRATED INDISEASES /OF IMPRINTING FORDISORDERS /AS OBSERVED INDNA /POLYMORPHIC LOCI INDNA /TRANSFECTION OF NORMALDNA MARKERS PROGRESS INDNA SEQUENCES RELATED TO CFTRDNA SURROUNDING THE ARGININO /OFDOPAMINE D2 RECEPTOR DNA /OFDOPAMINE D2 RECEPTOR LOCUS /THEDYSTROPHIN GENE /IN THEDYSTROPHIN GENE /MAP OF THEEMBRYONAL CARCINOMA CELLS /INEMBRYONIC CELLS /METHOTREXATE INEMBRYOS USING NONRADIOACTIVE /INENAMEL PROTEIN AMELOGENIN ISENDOGENOUS RETROVIRAL SEQUENCESERYTHROCYTE AMP DEAMINASE /ONERYTHROCYTES /ADHERENCE OFERYTHROCYTES /RECEPTOR ONERYTHROPOIETIN GENE /OF THEESOPHAGEAL CANCER CELL LINE /AFACTOR IX CDNA IN ANIMALS BY /OFFACTOR IX GENE HAVE A G +C /THEFACTOR IX GENE IN TRANSGENICFACTOR IX THROUGH MICRO /OFFERROCHELATASE SEQUENCEFETAL T CELL RECEPTOR B /OFFIBROBLASTS /OF SV40 TRANSFORMEDFIBROBLASTS /SV 40 TRANSFORMED
564
2209239222582124186921502306875
22032272176
21072370213421472120S89208219682057420
2281199
2130164921622031258821982104186721852384165619711863260121922149200423011870214220812070212913432499214320202156189723141635164017211652162720961563158
2040177
230920822338231225932467240322972321232315372521287245289
20992250206223662140109410769832256245415591684236723374914992858245322882474282124872481221422402598492
Permuted Title Index
FIBROBLASTS BY THE TRANSFER OFFIBROBLASTS VECTOR MEDIATEDFIBROBLASTS WITH THE NORMAL ANDFK506 BINDING PROTEIN GENE ANDFOREBRAIN AND MEDULLA OBLONGATAGAMETES /OF ANEUPLOIDY INGENES /3 UNTRANSLATED REGION OFGENES IAN APPROACH TO REVEAL NEWGENES /HISTORY AND GEOGRAPHY OFGENES THAT ESCAPE X INACTIVATIONGENETIC DISEASE ANALYSIS /INGENETICISTS YES /OF ETHICS FORGENETICS ACCESS TO GENETIC /OFGENETICS AN OVERVIEW OF THE /INGENETICS AND ITS RELATIONSHIPGENETICS HISTORICAL LESSONS ANDGENETICS IN GERMANY 18901950GENETICS IN INDIA /EDUCATION INGENETICS IN THE EUROPEANGENETICS K 12 LEAD TEACHER IOFGENETICS SCHOOL YARD EXPERIENCESGENOME /FOR MAPPING OF THEGENOME /THEGENOME /WIDE SPREAD REPEATS INGENOME ALU CLUSTERS /MAPPING OFGENOME BY HYBRIDIZATION IN SITUGENOME CONTAINS HYPERVARIABLEGENOME MAPPING PROJECT /KINGDOMGENOME SCIENCE ETHICS AND /THEGENOMIC DNA BY PCR /OFGENOMIC DNA USING DENATURING /INGESTATION /MALFORMATIONS DURINGGLIOMAS /OF GENOMIC CHANGES INGLUCOCEREBROSIDASE A PH /370 OFGLUCOCEREBROSIDASE AND /OF THEGLUCOCEREBROSIDASE GENE IN /THEGLUCOCEREBROSIDASE INGLUCOCORTICOID RECEPTOR GENEGLYCOSYLASPARAGINASE /CODINGGRANULOCYTE MACROPHAGE COLONYGROWTH HORMONE RECEPTOR IMPAIRSHAIR SHAFTS /DNA ISOLATED FROMHAPTOGLOBIN GENE PROMOTER /THEHEART MUSCLE /OF ANALYSIS OFHEMATOPOIETIC PROGENITORS /INHEPATOCELLULAR CARCINOMA CELLSHEPATOMA CELLS /EXPRESSION INHEREDITARY GOITER WITH /FOR AHEXOKINASE 1 ON CHROMOSOME 10HISTORY FROM ANCIENT AND MODERNHSP70 HOMOLOGUE GENE LOCATED INIDS GENE IN A 1 MB CONTEXT OFIMMUNOGLOBULIN HEAVY CHAIN GENEINTERFERON ALPHA RECEPTOR GENEINTERSPERSED LOW FREQUENCY /OFIRON METABOLISM /FORKERATINOCYTES WITH FUNCTIONALLDH C4 GENE AND ITS EXPRESSIONLINE 1 ELEMENT IDENTIFICATIONLINE ENCODED REVERSE /OF ALINKAGE MAPS /FILTRATION OFLONG CHAIN ACYL COA /BASIS OFLOW VOLTAGE EEG TO 20Q13.2/THELUNG CARCINOMA /OF ONCOGENES INLYMPHOCYTE CULTURES /INLYMPHOCYTE CULTURES IN VITRO IINLYMPHOCYTES /HPRT GENE IN MUTANTLYSOSOMAL A GLUCOSIDASE /OFMALIGNANT GLIOMA BY MICROCELLMETAPHASE CHROMOSOMES /ONMINISATELLITES /AND MUTATION INMITOCHONDRIAL DNA IN AFRICAN /OFMONKEY BOVINE RAT MOUSE ANDMTDNA SEQUENCE SPECIFIC NIAMUC1 LOCUS IN ASIAN BLACK /THEMULTIPLE MYELOMA /BCL2 GENE INMYC ONCOGENE /THE DOMAIN OF THEMYOBLASTS /OF TRANSPLANTEDMYOTONIC DYSTROPHY GENE REGIONN ACETYLATION POLYMORPHISM ANDN ACETYLTRANSFERASE AT THE NAT1NERVOUS SYSTEM ISOLATING THENEURAL RETINA SPECIFIC GENENEURAL RETINA SPECIFIC GENE OFNORMAL AND TUMOR CELLS /LEVEL INOBESITY /TWIN STUDIES OFONCOGENES BY CHROMOSOMAL INOOCYTE MATURATION /STUDIES OFOOCYTES /POLYSPERMICORAL CAVITY AND HEAD AND NECKORNITHINE TRANSCARBAMYLASE CDNAOVARIAN CANCER /13Q AND XP INOVARIAN CANCER /EXPRESSION INOVARIAN CANCER /RAS ONCOGENE INOVARIAN TERATOMAS USING DNA /INOVARIAN TUMORS /REACTIVATION INP58 A CELL CYCLE REGULATEDPARVOVIRUS INFECTION INPAX2 GENE TO 10022.1 Q24.3 /OFPEPSINOGEN A GENE /OF APERICENTROMERIC HETEROCHROMATINPHENYLALANINE HYDROXYLASE GENEPHENYLALANINE HYDROXYLASE GENEPIEBALDISM /PROTO ONCOGENE INPLACENTA /TERMINAL REPEATS IN
2601258714452276233315871936576254
22852532
4137
S1l319322320331334206393
20981
24332131207121872054178025162069103
1382436
2492247124832123235523602455250024252233248424292425662
21353151862204425196821992363247612862460188
2017231620281313254328092550568
25681611313
263926122834286716742570
21S86545549303
245923081354401
216012401258583
2472606
241359341013892128922
22822408159824322462189
2424
PLACENTA BY HIGH PERFORMANCE /INPLACENTAS OF CIGARETTE SMOKERSPLATELET DERIVED GROWTH FACTORPOLYDACTYLY /STUDY OFPOPULATIONS /HETEROZYGOSITY INPOPULATIONS /RECESSIVES INPOPULATIONS OF THE U.S.S.R /INPROSAPOSIN GENE /OF THEPROSTATE ADENOCARCINOMA /GENE INPROSTATIC ACID PHOSPHATASE GENEPROTAMINE 1 AND 2 CDNAS /OFPROTEIN CDNA BANK /OFRACES (DIFFERENTIATION OFRACIAL POPULATIONS /AMONGRADIATION REPAIR GENE XRCC5 BYRDNA CLONED IN YEAST ARTIFICIALRED AND GREEN PIGMENT PROTEINSRED/GREEN COLOR VISION DEFECTSRENAL CARCINOMA CELL LINE BY /ARENAL DIPEPTIDASE GENE TO BANDREPRODUCTIVE HORMONES /ANDRETINA /HIGHLY EXPRESSED IN THERETINAL STRUCTURE AND /INRETINOBLASTOMA GENE [THERETINOIC ACiD EMBRYOPATHY /INRHODOPSIN GENE (PRO23HIS) [THERIBOSOMAL RNA MULTIGENE FAMILYRODENT SOMATIC CELL HYBRIDS /INSALIVARY AMYLASE GENE AMY1C INSATELLITE DNA FAMILIES /OFSCAVENGER RECEPTOR GENE PRIMARYSEMINAL PLASMA AND /INSERUM BUTYRYLCHOLINESTERASE /OFSKELETON /DEVELOPMENT OF THESLOW TROPONIN T GENE ON /OF ASOLID TUMORS FACT OR FICTION /OFSOMATIC AND SPERM CELLS USINGSOMATIC CELLS /OF MUTAGENIZEDSPECIES /OF DNA VARIATION IN THESPECIFIC INTER ALU PCR PROBESSPERM /OF CHROMOSOME LESIONS INSPERM CHROMOSOME ABNORMALITIESSPERM OOCYTES AND /FINDINGS INSPERM USING FLUORESCENCE IN /INSPERM USING FLUORESCENCE IN /INSPERMATOZOA USING CHROMOSOME /INSPONTANEOUS ABORTIONS /OFSPONTANEOUS ABORTUSES WITHSRY GENE AND 46,XY PURE GONADALSTOMACH ALDEHYDE DEHYDROGENASESTRUCTURAL CHROMOSOME /INSYNEXIN (ANNEXIN VII) GENE /THET(14Q21Q) ROBERTSONIAN /OFTELOMERES FUNCTION ONTERATOGEN /MELLITUS AS ATESTIS DETERMINING FACTORTISSUE NONSPECIFIC ALKALINE /THETISSUES BY THE PCR /TRACETRANSCRIBED SEOUENCES PRODUCEDTRANSITIONAL CELL CARCINOMA /INTRIPLOID CELLS WITH CONFLUENCEDTRISOMY /RELEVANCE TOTUMORS IS TRANSCRIPTIONALLYTWINS /GROWTH AND DEVELOPMENT OFTYPE II PROCOLLAGEN (COL2A1) INTYPE VII COLLAGEN AND BULLOUSUROTHELIAL CELL LINES ARISINGVIRAL BASED GENOMIC LIBRARY OFVITAMIN D RESISTANT RICKETS /OFX AND Y CHROMOSOMES SPECIALX CHROMOSOME /ANALYSIS OF THEX CHROMOSOME /LONG ARM OF THEX CHROMOSOME /ON THE INACTIVEX CHROMOSOME A GENOME STRATEGYX CHROMOSOME INACTIVATION /OFX CHROMOSOME SPECIFIC /A NOVELX CHROMOSOMES /ON THE MOUSE ANDX INACTIVATION CENTER REGIONX LINKED INHERITED /ANALYSIS INX024 OTER HNCDNA LIBRARY HIGHLYY CHROMOSOME /LONG ARM OF THEY CHROMOSOME /REGION OF THEY CHROMOSOME BY COMPARATIVE /THEY CHROMOSOME PCR AND /OFZINC FINGER GENES /ANALYSIS OFZINC FINGER PROTEIN GENES USING
HUMANGENETIK HUMAN GENETICS IN /TOHUMANS /CALCIUM CHANNEL SUBUNITS IN
/DNA AND THE DISPERSAL OF EARLY/IN CONTEMPORARY AND ANCIENT/LYMPHOBLASTOID CELL LINES FROM/ORIGIN OF NONDISJUNCTION IN/SECOND SEX DETERMINING GENE INAND NONHUMAN PRIMATES NNTR IN
HUMERAL LENGTH SHORTENING IN FETUSESHUNAN CHINA BY PCR /MUTATIONS INHUNGARIAN SURVEILLANCE OF GERMINALHUNTER SYNDROME /JEWISH PATIENTS WITH
SYNDROME /OF PATIENTS WITHSYNDROME IDS GENE /STUDY OFSYNDROMES /OF HURLER AND
HUNTINGTON DISEASE /AT RISK FORDISEASE /IMPLICATION FORDISEASE /IN FAMILIES WITHDISEASE /OF THE DNA TEST OF
57012942296786
278728412795236526062331245725122636282818912158239824191395217211962273
102575924799
24362501244416962286572546930
2368372440
2807312
2321156616293621184128183
91614792238230415882266164724986741665472
2509250125771575409
244127212461238713832529891
2515179
211824522174145
16582421
97971
25212105198
2205206122632144320
2180261426221438408
23412631758
2820360
225522001042282227
24422111100
DISEASE /RESPONSIBLE FORDISEASE /TESTING FORDISEASE /TESTING FORDISEASE /TESTING FORDISEASE /TESTING FORDISEASE /TESTING FORDISEASE /TESTING INDISEASE /TESTING INDISEASE [THE EXPERIENCE OFDISEASE A WORLD WIDE /FORDISEASE AND IN THEIR SIBSDISEASE AND PATERNAL AGEDISEASE AND THE ABUSE OFDISEASE CANDIDATE GENEDISEASE CANDIDATE GENE /ADISEASE CANDIDATE REGIONDISEASE GENE /A CANDIDATEDISEASE GENE /CLOSE TO THEDISEASE GENE /FOR THEDISEASE GENE /FOR THEDISEASE GENE BY A NEW [THEDISEASE GENE CANDIDATE [THEDISEASE GENE CANDIDATE [THEDISEASE GENE REGION OF /THEDISEASE GENE UNLIKELY [THEDISEASE IN NORTH EASTDISEASE IN THE NETHERLANDSDISEASE OUTCOME OF 136 ATDISEASE REGION (4P16.3)DISEASE REGION /IN THEDISEASE REGION /THEDISEASE REGION WITH YEASTDISEASE THE CASE FOR /FORDISEASE THE PHYSICAL MAPDISEASE THE VALUE OF /FORDISEASE THROUGH A /OFDISEASE WITH RIGIDITY AND
HURLER AND HUNTER SYNDROMES /OFHUTCH /HYPOGLAUCUM (LEVEL)HUTTERITE KINDRED WITH X LINKED /IN AHYA AND SPY FROM THE SXR REGION OFHYBRID ANALYSIS [TRANSFER AND X RAY
CELL LINE EXPRESSINGCONTAINING 20 CM OF HUMAN DNADNAS /FROM SOMATIC CELLIN THE REGION AROUND X LINKEDMAP OF 24 LOCI ON THE LONG ARMMAP OF HUMAN CHROMOSOME 21MAP OF THE PROXIMAL LONG ARMMAPPING AND TECHNIOUES FORMAPPING IN PROXIMAL 100 ANDMAPPING PANEL FOR THE PROXIMALPANEL /REDUCED SOMATIC CELL
HYBRIDIZATION /ANALYSIS AND IN SITU/ANALYSIS AND IN SITU/AND FLUORSCENT IN SITU/AND NONISOTOPIC IN SITU/BY FLUORESCENCE IN SITU/BY FLUORESCENCE IN SITU/BY FLUORESCENCE IN SITU/BY FLUORESCENCE IN SITU/BY FLUORESCENCE IN SITU/BY FLUORESCENCE IN SITU/BY FLUORESCENCE IN SITU/BY FLUORESCENCE IN SITU/BY FLUORESCENT IN SITU/BY FLUORESCENT IN SITU/BY FLUORESCENT IN SITU/BY FLUORESCENT IN SITU/BY FLUORESCENT IN SITU/BY IN SITU/BY SUBTRACTIVE/BY THE PCR AND IN SITU/CHROMOSOME BY IN SITU/FLUORESCENCE IN SITU/FLUORESCENCE IN SITU/FLUORESCENCE IN SITU/FLUORESCENCE IN SITU/FLUORESCENCE IN SITU/FLUORESCENCE IN SITU/FLUORESCENCE IN SITU/FLUORESCENT IN SITU/FLUORESCENT IN SITU/IN A CHILD BY IN SITU/IN SITU SUPPRESSION/INTERPHASE IN SITU/MALIGNANCIES BY IN SITU/MAPPING BY IN SITU/NONISOTOPIC IN SITU/NONRADIOACTIVE IN SITU/NONRADIOACTIVE IN SITU/OF REVERSE DOT BLOT[TECHNIQUES AND IN SITUA NEW APPLICATION INA SENSITIVE METHOD FORANALYSIS OF /IN SITUANALYSIS OF A WELL /SITUANALYSIS OF AN EXTRAAND CYTOGENETICS OFAND DIGITAL IMAGE /SITUAND GENETIC MAPPINGAND PCR TECHNIQUES /SITUBE USED TO DETECT /SITUHAS ALLOWED ELUCIDATIONIN DETERMINING THE /SITU
565
2992109661732177118071751176824830017652660181722672391238323352399227123962088102
234823841884860176730182
2336221022041822298173817457912821853441
2343189125472140205
20142208S892184S132170213921361581163218671640184217944
1171172421292156220111891322135516791692368225211311700118416361642164816902148217115461650171721601209130654180
214422301113169516262161085137717032458215121611364166814551669
Permuted Title Index
IN ELECTRON MICROSCOPYIN MAPPING AND AN SITUIN MILLER DIEKER /SITUIN PRENATAL DIAGNOSISIN SITU /HUMAN GENOME BYINHERITED LOW SIGNALINTERPHASE CYTOGENETICSMETHOD /IN SITUMETHODS FOR PRENATALMICROCELL MEDIATED /CELLOF DNA SEQUENCES TOOF RETROVIRALLY /IN SITUOF THREE CHROMOSOME 150OF YEAST ARTIFICIALOF YEAST ARTIFICIALSTUDIES IN DIFFERENTSTUDIES OF /IN SITUTECHNIQUES /BY IN SITUTO CHROMOSOME SPECIFICTO CHROMOSOME SPECIFICTO CONSTRUCT AN ORDEREDTO IDENTIFY /IN SITUTO INTERPHASE AND /SITUTO OLIGONUCLEOTIDES /BYUSING A SPECIFIC X /SITUUSING DNAS FROM AN SITUWITH A CHROMOSOME /SITUWITH A COSMID PROBEWITH APPLICATION TOWITH BIOTINYLATED PCRWITH DIGITAL IMAGINGWITH DNA PROBES /IN SITUWITH PCR LABELED PROBESWITH SATELLITE DNA /SITU
HYBRIDIZATIONS OF DIRECT FLUOROPHOREHYIBRIIZED IN SITU /SPECIFIC DNA PROBE
PROBES OF SINGLE COPY GENESPROBES WITHIN CHROMOSOME
HYBRIDS /17 USING RADIATION REDUCED/CHROMOSOMES USING RADIATION/CHROMOSOMES USING RADIATION/FROM SINGLE HUMAN CHROMOSOME/IN HUMAN RODENT SOMATIC CELL/ISOLATED IN MONOCHROMOSOMALAND COSMIDS FOR ANALYSIS OFAND SIMPLE SEQUENCE REPEATAND YEAST ARTIFICIALCARRYING FRAGMENTS OF /CELLCONTAINING A GENOMIC REGIONCONTAINING PORTIONS OF THEFROM A MARKED HUMAN /RADIATIONFROM CHROMOSOME 14 IRS PCRTO ISOLATE REGION SPECIFICUSEFUL FOR X027 28 MAPPINGUSING ALU PCR AMPLIFICATION
HYATIDIFORM MOLAR PREGNANCY AND DNAHYDRATASE ACTIVITY ICOAHYDROCARBON HYDROXYLASE IN /ARYLHYDROCEPHALUS AS A POSSIBLE
ASSOCIATED WITH /OFASSOCIATION WITH DNALOCUS WITH SEVEN /LINKEDTO X028 /OF X LINKED
HYDROLASE GENE /THE RAT ACYL PEPTIDEIS FREQUENTLY DECREASED INTHE ENZYME DEFICIENT IN
HYDROLETHALIS SYNDROME WITHHYDRONEPHROS1S /THE HISTORY OF LEFT
TO THE MHC ONHYDROPEROXYCYCL I PURGED /4HYDROPS /A CASE OF RESOLVED FETALHYDROTIC ECTODERNAL DYSPLASIAHYDROXYACYL COA DEHYDROGENASE /CHAIN 3HYDROXYLASE (P450C21) IN RELATION TO
DEFICIENCY /CAUSES 17ADEFICIENCY EVIDENCE FOR AGENE AND THE CYSTICGENE EXPRESSIONGENE ISOLATION ANDGENE RESULTS IN A KINETICIN TROPHOBLAST CELLSLOCUS OF PHENYLKETONURIAMRNA THE MOST COMMON
HYDROXYLATION (CYP2D6) PHENOTYPEHYDROXYMETHYLOLUTARYL COA LYASEHYDROXYTRYPTAMINEA RECEPTOR GENE /5HYGROMA /POSTERIOR NUCHAL CYSTIC
23 CASES /DIAGNOSIS OF CYSTICBY PRENATAL STUDIES TRUEWITH A DE NOVO /AND CYSTIC
HYPER HYPOPIGMENTATION MICROCEPHALYHYPERACTIVITY DISORDER /DEFICITHYPER A RESULTING FROM A C TOHYPERCHOLESTEROLEMA /IMPROVEMENT OF
AND FAMILIALIN ASHKENAZI JEWSLDLR MUTATIONPATIENTS WITH A
HYPERCOAGULABILITY A NEW AUTOSOMALHYPERGLYCINEMIA BY ASSAY OF CVS
OR WITH EPILEPSIESHYPERHAPLOIDY FREQUENCY IN MICE /ANDHYPERNIDROSIS [TEETH AND SEVEREHYPERHYDROXYPROLNURIA ASSOCIATED /ANDHYPERUPIDEMIA /FOR FAMILIAL COMBINED
1476183
167317192071128216071337127918912153209617181852001683242713031667170821991706182
24961698172816341516199165620871281
91170416971676206520662150158
20402081250120961722211020652132232121182149216521662058210892812171294531939816195920462297257948385695319321367922648263
24141045237528832462243244912941114228054148818827041142116893866867355942310362329280426828825634731594841521
2724
HYPERUPIDEMCS FOR FAMILIAL /AFRICANHYPERMELANOSS AN ADDITIONAL FOURHYPERMETHYLATION IN CHRONIC MYELOIDHYPEROSMOLAUTY /INDUCED BY PLASMAHYPEROXALURIA TYPE I /OF PRIMARYHYPEROXIA A CYTOGENETIC STUDY /IN VIVO
ENHANCES THE INDUCTION OFHYPERPARATHYRONDISM /11 IN UREMIC
JAW TUMORHYPERPLASIA /BY CONGENITAL ADRENAL
BY DNA RFLP ANALYSIS OFHYPERPROUNURIA ANDKYPERPYREXIA IN PRADER WILLI SYNDROMEHYPERTENSION /FEMALES WITH ESSENTIAL
/IN PREGNANCY INDUCED/MAPPING IN EXPERIMENTAL[TO PREDICTING ESSENTIAL
HYPERTHERMA /GENE IN MALIGNANT/RISK FOR MALIGNANTSUSCEPTIBILITY USINGSUSCEPTIBLE KINDREDS
HYPERTHYROXINEMA /TRANSIENT EUTHYROIDHYPERTONIA ARTHROGRYPOSIS AND MENTALHYPERTRIGLYCERIDEMIC SUBJECTS /INHYPERTROPIC CARDIOMYOPATHY TOHYPERTROPHY WITH AND WITHOUT /LIMBHYPERVARIABILITY IN GREAT APES /GENEHYPERVARIABLE DNA LOCI /USING
DNA REGIONS /FORELEMENTS SIMILAR TOLOCI /GENETICS OFMICROSATELLITES /ANDMULTILOCUS DNA PROBES
HYPOCHODROGENESIS /TYPE 11 COLLAGEN INHYPOCHONDROPLASIA /DIAGNOSIS OFHYPOIPLO LYMPHOCYTES IN LONG TERMHYPODONTIA SHORT ROOTEDNESS AND OTHERHYPOGLAUCUM (LEVEL) HUTCHHYPOHIDROTIC ECTODERMAL DYSPLASIA
ECTODERMAL DYSPLASIAHYPOMELANOSIS OF ITO IN A GIRL WITHHYPOPARATHYRONDISM WITH DYSMORPHICHYPOPERISTALSIS SYNDROME EVIDENCE FORHYPOPHOSPiATASIA fIN SEVERE
POINT MUTATIONS INHYPOPHOSPHATEMIC RICKETS /EXHIBITINGHYPOPIGIENTATION DEAFNESS IN A FEMALE
MICROCEPHALY MENTALHYPOPLASIA /GROWTH IN CARTILAGE HAIR
CONGENITA LOCI /AND ADRENALPOLYDACTYLY AND OTHERUNUSUAL FACIES SYNDROME
HYPOPLASWAPLASIA SYNDROME (MIMHYPOPLASUADYSPLASIA /DUE TO RENALHYPOPLASTIC CARPAL BONES AND ABSENCE
LEFT HEART NEPHROMEGALYHYPOTELORISM SMALL CUPID BOW MOUTHHYPOTHALAIC GONADOTROPIN DEFICIENCY
HYPERPYREXIA IN PRADERHYPOTHESES FOR PRIMARY COMPONENTS OFHYPOTHYROIDISM /HEREDITARY GOITER WITHHYPOTONIA AND SEVERE MENTAL /DEFORMITY
DEVELOPMENTAL RETARDATIONHYPOTONIC TREATMENT /UNDER PROLONGEDHYPOTRANSERRINENA /OF FAMILIALHYPOTROPHY MADELUNG'S DEFORMATIONHYPOXIA INDUCIBLE EXPRESSION OF THEHYPOXYGENATION A CYTOGENETIC STUDYHYPSARRHYTHMA AND OPTIC ATROPHY
IA OCULOCUTANEOUS ALBINISM /IN TYPEISD APPROACH TO MULTIPOINT LINKAGEICELAND /POLYCYSTIC KIDNEY DISEASE INICHTHYOSIS AND KALLMANN SYNDROMEICTERIC NEWBORNS /FREQUENCY INIDENTICAL TWIN PREGNANCY /IN ANIDENTIFICATION /REPEATS FOR PERSONAL
/TO RAPID POLYMORPHISMAND ANALYSIS OFAND ANALYSIS OF ITSAND CHARACTERIZATIONAND CHARACTERIZATIONAND HERITABILITY OFOF 8 NOVEL DELETERIOUSOF A CPG ISLAND /T ANDOF A DE NOVO COMPLEXOF A DE NOVO MINUTEOF A FAMILY OF /ANDOF A KERATIN 14OF A MARKER CHROMOSOMEOF A MARKER CHROMOSOMEOF A MARKER CHROMOSOMEOF A MOLECULAR GENETICOF A NEURON SPECIFICOF A NEW MUTATION INOF A SPLICE SITEOF A SPLICING MUTATIONOF A UNIQUE MUTATIONOF A3 AND AS CHAINS OF
1036874617955132
14181592595193465411085216498016571866273642969610121911853143047119206412624282421942187252
20212871474897162481418531106112613767367534564728241452668765
2220720728681718738792710645649
26496628707731576469770
24531401866
231820681902805156814852506203582
24602340248616111067233415471700227222571546165317192300226722772264662441383
OF ADDITIONALOF CANDIDATE GENES FOROF CHROMOSOME MARKERSOF CIS REGULATORYOF DIAGNOSTIC DNAOF FRAGILE X AND AOF GENES WITHIN HUMANOF GENETIC FACTORS INOF HUMAN (MARKER)OF HUMAN CHROMOSOMESOF INTRAGENIC GROWTHOF LARGE DELETIONS INOF MANIFOLD TRACE /SEXOF MARKER CHROMOSOMEOF MULTIPLE CPGOF NATURAL MUTATIONSOF NEW HIGHLY /ANDOF NEW POSSIBLY /THEOF NOVEL CAOF NOVEL RHODOPSINOF PARTIAL TRISOMY 70OF PCR BASED DNAOF POINT MUTATIONS INOF SECOND GENE ON /XP AOF SEQUENCES ANDOF SIX NOVEL ZINCOF SMALL MOSAICOF THE 9:22 /AND RAPIDOF THE BCL 1 ONCOGENEOF THE MOLECULAROF THE ORIGIN OFOF THREE CYSTICOF TWO DISTINCT BRDUOF TWO MEMBERS OF AOF YEAST ARTIFICIAL
IDENTITY /IN UTEROIDOATHIC CARDIOMYOPATHY AND WITH
HEMOCHROMATOSIS DISEASEINAPPROPRIATE ANTIDIURETICINFERTILITY /OF MEN WITHJUVENILE OSTEOPOROSIS /OF
IDS GENE /STUDY OF HUNTER SYNDROMEGENE IN A 1 MB CONTEXT OF XQ28 DNA
IDURONATE SULFATASE ACTIVITY ONSULFATASE GENE IN JEWISH
IDURONIDASE GENE /MAPPING OF THE A LIGFIMANNOSE 6 PHOSPHATE RECEPTOR /OFIGI GENE IN TRIBAL POPULATIONS OFIGK VARIABLE REGION GENE SEGMENTSNS VON WILLEBRAND DISEASE /FOR TYPEILE IN THE EXON 17 OF THE AMYLOIDILLEGITIMATE TRANSCRIPTIONILLNESS /ANALYSIS OF BIPOLAR AFFECTIVE
/LINKAGE STUDIES OF BIPOLARAND WOLFRAM SYNDROME OBSERVEDWITH MARKERS FROM CHROMOSOME
IMAGE ANALYSIS /AND DIGITALANALYSIS OF BRAIN MORPHOMETRYPROCESSING /PROBES BY DIGITAL
IMAGING /BY MAGNETIC RESONANCE/GENETICS BEHAVIOR AND BRAIN/LABELED PROBES AND DIGITALABNORMALITIES OF THE BRAIN INAPPLICATION TO THE STUDY OFEXPOSURE /MAGNETIC RESONANCEMICROSCOPY/WITH DIGITAL
IMBALANCE MODE A PREDICTIVE STUDY /ANDIMMIGRANTS FROM THIRD WORLD COUNTRIESIMMORTALIZATION IN HUMAN FIBROBLASTS
OF SV40 TRANSFORMEDOF THE RAT EMBRYONAL
IMMUNE DEFICIENT POIKILODERMA A NEWIMMUNOCYIOGENETIC IN VITRO MODEL FORIM N F CENTROMETRICIMM IF TION /FACTORS INIMMUNOFLUORESCENCE METHOD OF /INDIRECTIMMUNOGENETIC AND RED CELL /AFRICANIMMUNOGLOBULIN (IGHG1) GENE IN TRIBAL
ALLOTYPES GM AND KM INGENES IN HUMAN ANDHEAVY CHAIN GENE /HUMANLEVELS /EFFECT ON
IMMNOGU IN TWIN FAMILIESIMMu M ANALYSES OFIMMUNONISTOPATHOLOGY AND GENETICIMMUNOLOGIC ANALYSIS /DNA REPAIR ANDIMMUNOLOGICAL ANALYSIS OF IN VITRO
ANALYSIS OF THE CELLSAND MIGRATORYPROBLEMS /TARGETING TO
IMMU IY CLASSIFIED HUMAN BONE_MMUN1P1ENTYPI NORMAL BONE MARROWimu Msall C _l /WITHIMMUNOSU RENAL TRANSPLANTIMPAIRED EXOGENOUS CHOLESTEROLIMPAIRS GROWTH HORMONE BINDING ANDIMPERFECTA /DEFORMING OSTEOGENESIS
/FORM OF OSTEOGENESIS/LETHAL OSTEOGENESISAND OSTEOPOROSISBIOCHEMICAL STUDY OFTYPE I COMMONLY DUE TOTYPE III /OF OSTEOGENESISTYPE IV ASSOCIATED WITHWITH INTRAFAMIUAL
566
2551253111892438189416882138223516051721208410142509172423961931950103821661097168620596802314203
225117141649260847017252814156422732220181933
211765922059571042204500
22552345150228152623106810711029202918797902038215165016978991957
91143390825552087156217402601259813146611343644119
16162618281527331857425284926444603451838230974121S9
167613451608592523
2455626534446
2497450246449610541065
I
Permuted Title Index
IMPLEMENTATION OF HEREDITARY DISEASESPROCESS OF PRENATAL
IMPLICATED IN ERYTHROPOIETIC /THE GENEIN HUMAN RETINAL STRUCTURE
IMPRINTIG /AN EXAMPLE OF GENETIC/AND GENOMIC/EVIDENCE OF GENOMIC/MECHANISM OF GENETIC/OF EVIDENCE FOR GENOMIC/SUPPORT FOR GENOMICAND INSULIN DEPENDENTDEVELOPMENTAL SIGNIFICANCEFOR HUMAN DISEASES /OFIN MAN FROM STUDIES IN MICEIN THE BECKWITH WIEDEMANNREFLECTED IN CYTOGENETICREVEALED BY LOSS OFSUGGESTED BY PULSE FIELDTO THE PHENOTYPE IN TURNER
IMPROVEMENT /DETERMINATION TECHNIQUEOF HYPERCHOLESTEROLEMIAOF POLYMORPHIC
IMPROVEMENTS IN TECHNOLOGY FOR THEINACTIVATION /A GENE WHICH ESCAPES X
/AND GENES WHICH ESCAPE/DISTAL XP THAT ESCAPES X/GENE ON XP22.3 ESCAPES X/GENES THAT ESCAPE X/METHYLATION AND X/MULTIPLE MECHANISMS OF X/OF HUMAN X CHROMOSOME/REPEAT CORRELATES WITH XITO THE PROBLEM OF XAND METHYLATION OF XCENTER REGION /HUMAN XCONFIRMATION BY A /OF XIN MZ TWINS DISCORDANT /XOF THE MOUSEOF THE MOUSE AMYLOID /ANDPROCESS IN THE MOUSE /XSTATUS OF GENES ON THE
INACTIVATION/REACTIVATION A MODELINACTIVE /TUMORS IS TRANSCRIPTIONALLY
DERIVATIVE CHROMOSOME /OF ANHUMAN X CHROMOSOME /ON THEX CHROMOSOME /OF THEX CHROMOSOMES /THE ACTIVE ANDX SPECIFIC TRANSCRIPTS FROM
INACTIVITY PROTECTS NORMAL HUMAN ANDINAPPROPRIATE ANTIDIURETIC HORMONEINBORN ERROR OF METABOLISM
ERRORS OF COL2A1 METABOLISMERRORS OF METABOLISM (CHANNELERRORS OF METABOLISM /SPOTS ANDERRORS OF METABOLISM IN HIGH
INBRED POPULATIONS /PREVALENT AMIDSTINBREEDING AND CONGENITAL CATARACTS
AND SELECTION INTENSITY INEFFECT ON IMMUNOGLOBULINON THE FREQUENCIES OF /TERM
INCEST WITH POLYMORPHIC MARKERS /OFINCESTOUS MATINGS IN FAMILIES WITHINCONTINENTIA PIGMENTI /HEREDITARY
PIGMENTI AIN A GIRL WITHINCORPORATING GENETICS TO NEW JERSEY
GENOTYPE ENVIRONMENTINCORPORATION OF GENETIC SERVICESINDENTATIONS A DOMINANTLY INHERITEDINDEPENDENT AMPLIFICATION OF /SEQUENCE
DELETIONS IN THE /TWODNA EXCISION REPAIR /ANDOF OPEN NEURAL TUBE ORSEGREGATION BETWEEN A
INDEX /OF BLOOD PRESSURE AND BODY MASSCASES AN INDICATOR OF GENETICCASES THROUGH MSAFP PROGRAM /OF
INDIA /A MUSLIM COMMUNITY FROM BIHAR/AMONG SOME TRIBES OF SOUTH WEST/AMONG THE AO NAGAS NAGALAND/AND CONGENITAL CATARACTS IN/CLEFT PALATE IN NORTHERN/EDUCATION IN HUMAN GENETICS INAIN THE GARHWAL HIMALAYAS/IN THE GARHWAL HIMALAYAS/OF BETA THALASSEMIA IN NORTH/OF CHAMBA HIMACHAL PRADESH/PARDHIS OF ANDHRA PRADESH SOUTH/POPULATION FROM ANDHRA PRADESH/POPULATION OF ANDHRA PRADESH/REPORT OF TWO CASES FROM/RETARDED POPULATION OF WESTERN/STUDIES IN AO NAGAS NAGALAND/TRIBES OF RAJMAHAL HILLS BIHAREVIDENCE AND FACTORS /KARNATAKAOVER A 10 YEAR PERIOD /EASTERNPRELIMINARY RESULTS /REGISTRY IN
INDIAN EXPERIENCES (1984 90) NYEARS OFHOSPITAL (ALIGARH) AIN A NORTHPOPULATION /OF ADIPOSITY IN ANPOPULATION /PRESSURE IN AN
INDIANA KINDRED /DISEASE IN THEINDIANS AND SUGGESTS A PRE CLOVIS
IN SINGAPORE /IN THE DRAVIDIANINDICATOR OF FETAL CYTOGENETIC
OF GENETIC SUSCEPTIBILITY
179118022214
1026672653791
266027651596270824124524276724324462189
1604423
209353
2440S29240223072285147148145959144
166097
1542223124632244146
2421157124411659245215572428
97253965943945
1843811
2675713
26642822284928412790854193064317972648151663
205310802412113720022707271011832822286227492664267833128252832102428702866734
271785614932868283318452760776114714032713272018962637287311292710
INDICATORS OF DEVELOPMENTAL OUTCOMEINDICES OF REPRODUCTIVE FUNCTION ININDIVIDUAL FOR TWO TRANSTHYRETIN
RISK OF HUMAN CANCER ANDWITH FAMILIAL CREUTZFELDTWITH HEREDITARY FRUCTOSEWITH MATERNAL DISOMY OFWITH THREE CHROMOSOME /AN
INDIVIDUALITY OF HUMAN BLOODINDIVIDUALS /AND UNRELATED CONTROL
/DISEASE ELDERLY AND YOUNG/IN 4000 JAPANESEAFFECTED WITH MALIGNANTAFFECTS EXPRESSION INAS DETERMINED USING THEEXPOSED TO GENOTOXIC /OFFREQUENCY OF THE /IN 46,XXFROM NORMAL POPULATION AININ 9 FAMILIES AND 16 /39IN DIFFERENT /AMONGOF EUROPEAN AND SOUTH /INPRESUMED TO CARRY AWITH THE USE MICRONUCLEAR
INDONESIAN RED CROSS YOGYAKARTA BRANCHINDUCIBLE ARYL HYDROCARBON
CHLORIDE CONDUCTANCE INEXPRESSION OF THE HUMANRECOMBINANT REPORTER GENE
INDUCTION IN MOUSE BONE MARROW BYOF CHROMOSOMAL VARIANTSOF CHROMOSOME ALTERATIONSOF CLASS II MHC ANTIGENS BYOF FRAGILE SITES BYOF FRAGILE X SITE OF THEOF SISTER CHROMATID /ONOF THE FRAGILE X CHROMOSOME
INDUSTRIAL FACTORS /ENVIRONMENTAL ANDINDUSTRY /BY NEWER METALS USED ININFANCY GLOBOID CELL LEUKODYSTROPHYINFANT /SYNDROME IN A TURKISH MALE
ASSOCIATED WITH PATERNALCOLIC /A COMMON CAUSE OFDEATH SYNDROME AN ANALYSIS OFDEATH SYNDROME AND ITS /SUDDENDEATH SYNDROME PATIENTS /SUDDENREFERRALS FOR GENETICS SERVICESUTILIZING FLUORESCENT IN SITUWITH AN INTERSTITIAL 210 /IN ANWITH DEL (4) (P14P16) /IN ANWITH GALACTOSIALIDOSIS ANDWITH RING CHROMOSOME 11 /IN AN
INFANTILE FORM OF NEURONAL CEROID /THELYSOSOMAL GLYCOGEN STORAGEMARFAN SYNDROME /CASES WITHSLEEP APNEA /RELATIONSHIP TOSPASMS AND DYSMORPHICTAY SACHS Bi VARIANT /A LATETAY SACHS DISEASE /OF JEWISHTAY SACHS DISEASE MUTATIONS
INFANTS IN NINGXIA HUI AUTONOMOUSWITH MYELOMENINGOCELE /IN
INFARCTION /TO MYOCARDIALINFECTION /CHRONIC HEPATITIS B VIRUS
/PLACENTAL MARKER FOR FETAL/WITH PARACOCCIDIOIDOMYCOSISAND THE INTERACTION WITHIN PREGNANCY A CASE OF
INFECTS T LYMPHOCYTES NIRUS WHICHINFERENCES /ON MTDNA PHYLOGENETICINFERRING STRATEGIES OF THE GENESINFERTILE COUPLES /POLYMORPHISMS IN
MALES /ON MEIOTIC PROCESS ININFERTILITY/OF 115 MALE PATIENTS WITH
/OF MEN WITH IDIOPATHICINFLAMMATORY BOWEL DISEASE /FORMS OFINFORMATION AND SERVICES WHILE
CONTENT OF DNA MARKERS BYFOR GENETIC COUNSELINGHOW FAR DO OUR PERSONALON THE 1P34 1P36.1 REGIONSERVICE UPDATE /TERATOGENSYSTEM FOR MEDICAL /OF AN
INFORMATIVE ABOUT PHENOTYPE /Al FAMILYASSAY FOR LINKAGE /ANDDNA POLYMORPHISMS WITHINFAMILIES IS THERE AN AGEFLANKING MARKERS FORPCR MARKER LINKED TOPERICENTRIC MARKERS
INFORMATIVENESS OF BILINEAL PEDIGREESOF TRINUCLEOTIDE AND
INFORMATIVITY OF THE DNA TEST OF /THEINFORMED CONSENT REPRODUCTIVE GENETICINFUSION OF THE UTERUS WITH SALINEINFUSIONS OF GLUCOCEREBROSIDASE IN AINGUINAL HERNIA /IN A FEMALE WITHINHABITANTS /OF TURKMEN SSR HEREDITARYINHALATION AND EMBRYONIC GROWTH ANDINHERENT IN THE METHOD OF LIKELIHOODINHERITANCE /AND AUTOSOMAL DOMINANT
/EVIDENCE FOR MENDELIAN/TO X LINKED AND AUTOSOMAL/UNDER COMPLEX MODES OF/WITH AUTOSOMAL RECESSIVE/WITH AUTOSOMAL RECESSIVE
76812132747428
23902264158214342853493158415451352242525462558780
2831676
287166
106718382754129423642453129118532555271621031559159225651623548
2563862797
1565457975
27482377178315461465804848
13981935529727
2748852494
2446228927807681095772113326732651922
25902869S24156011931525220527701777209322618202202179318114529781968147419501043191426832049110017401287560147728791296121689271
8022714839849
/X LINKED RECESSIVEOF A 175 KB REGION OF THEOF A 40K TYPE 1 ACIDICOF ACRODYSOSTOSISOF AN UNUSUAL CHROMOSOMEOF CAUDAL DYSGENESISOF EXTENSIVE CERVICAL ANDOF LONG OT SYNDROMES /THEPATTERN REVISITED /AND
INHERITED AND APPARENTLY BALANCED /ANBALANCED TRANSLOCATIONS ANDBONE DISORDER /DOMINANTLYCANINE COPPER TOXICOSIS /ONCATARACTS /ANIMAL MODEL FORDEFECT OF THE KREBS CYCLEDELETION OF IMMUNOGLOBULINDISEASES BY DNA ANALYSIS INDISORDERS /MALFORMATIONS ANDDUPLICATION OF THEDYSMYELINATING DISEASEFORM OF CHILDHOOD EPILEPSYFROM A NORMAL PARENTFROM AN ASYMPTOMATIC MOSAICLOW SIGNAL POLYMORPHISMMETABOLIC DISORDERS AMYOPATHIES /GENE THERAPY INMYOPATHY AND CARDIOPATHY ASYNDROME /A NEW DOMINANTLYTRAIT /A DOMINANTLYX Y TRANSLOCATION AND A /AN
INIuBmNG SUBSTANCE THE SAMEINHIBITOR 1 LEVELS /ACTIVATOR
1 PROMOTER SHOWS ALLELEIN DOWN SYNDROME FAMILIES
INITIAL 150 CASES COMPARED TO /IN150 CASES OF TRANSABDOMINALDELETION SCREENING METHOD FORMAPPING STUDIES /ANDMOLECULAR CHARACTERIZATION INSCREENING FOR POINT MUTATIONSSTUDIES IN ZELLWEGER SYNDROME
INITIATION COMPLEX MECHANISMS OFFACTOR EIF 4E /BY
INJECTION EXTRACTED FROM FETUS BRAININSENSITIVITY SYNDROME /ANDROGENINSERT USING A COMBINED PCR WALKINGINSERTED DOMINANT SELECTABLE MARKERS
INTO A MOUSE CHROMOSOMEINSERTION OF JEWISH INFANTILE TAY
OF Y SEQUENCES INTO X IN ANINSERTION(S) /CARRYING AN INVERTEDINSERTIOAL TRANSLOCATION /IN ANINSERTIONS IN THE HUNTINGTON DISEASEINSERTS /GENOMIC LIBRARY OF 150 200 KBINSIGNIFICANT /SIGNIFICANT CLINICALLYINSTABILITY /AND INCREASES THE GENETIC
DISORDER /CHROMOSOMALFACIAL ANOMALIES SYNDROMEIN CHILDREN WITH DOWNIN CLASSICAL AND LOWIN FIRST DEGREE RELATIVESIN THE FAMMM SYNDROMEIN THE SCHWARTZ JAMPELSYNDROMES INCREASEDSYNDROMES OF MAN
INSTITUTION FOR MENTALLY HANDICAPPEDINSTITUTIOAL FETAL SEX SELECTION /ANDINSULIN DEPENDENT DIABETES MELLITUS
DEPENDENT DIABETES MELLITUSDEPENDENT DIABETES MELLITUSDEPENDENT DIABETICS /INGENE IN TYPE II DIABETES /THEGENE REGION AND /BETWEEN THELEVELS IN HISPANIC MENLIKE GROWTH FACTORS AND /TORECEPTOR GENE /IN THERECEPTOR LOCUS IN MEXICAN /THERESISTANCE CAUSED BY /SEVERE
INTACT MEMBERS OF A LARGE FAMILY OFINTAKE COMPONENTS IN TWINS /DIETARYINTEGRATED APPROACH TO THE ANALYSIS
GENETICS /INDICATIONS ATSINGLE COPY HSV 1 TK GENE
INTEGRATES INTO THE COMMON FRAGILEINTEGRATION LEADING TO COMPLEX /DNA
OF HUMAN A SATELLITE DNAOF THE COSMID CONTIG MAPSITE PREFERENCES OF
INTEGRITY WITH REVIEW OF THE /AND CORDINTELLECTUAL MEASURES USING A MAXIMUMINTELLIGENCE /GENETICS OF
QUOTIENT AMONG FRAGILE XINTENSITY IN A MUSLIM COMMUNITY FROMINTER ALU PCR /PROBES GENERATED BY
ALU PCR GENERATION OF HUMANALU PCR PROBES FOR ISOLATION OF
INTERACTION /GENOTYPE ENVIRONMENTOF A HUMAN CENTROMEREWITH THE AB0 BLOOD SYSTEM
INTERACTIONS /IN FETO PLACENTALBETWEEN MUTATIONS
INTERCALARY SATELLITES ANINTERCROSSINGS AND FRAGILE SITESINTEREST /A GENOMIC REGION OFINTERFERE WITH THE EVOLUTION OF
567
689100
268486995480683284390714571409738
18712268447
28152504726502971756
16011498128278442435
826663902105
24172417159512621262969
2165488984190118
24502533441
27852096413244616921453117123482529758170514366446996771397131689425541574161717842663270827112670722
271126561442485
2801485
23372767175
178625361705255616632124414744
27001734267228222247164923212648412
265111619731602631
23212613
Permuted Title Index
INTERFERENCE USING THE LINKAGEINTERFERON ALPHA RECEPTOR GENE ON
GAMMA IS ENCODED BY /BYINTERGENIC CONVERSION BETWEEN MURINEINTERMARKER DISTANCE ON MAPPING A NEWINTERMEIATE FILAMENT PROTEINS DURINGINTERMITENT PORPHYRIA /WITH ACUTE
PROPHYRIA MUTATIONSINTERNAL MAPPING OF VARIANT REPEAT
PROMOTER /AND ANALYSIS OF ITSINTERNATIONAL CODE OF ETHICS FOR
COLLABORATION /OF ANCOLLABORATION /OF ANCONSENSUS SURVEY /ANDCONSORTIUM /OF THEFANCONI ANEMIA REGISTRYREGISTRY OF ABNORMALX LINKED
INTERPHASE AND METAPHASE NUCLEI /TOAS REVEALED BY ISOTOPIC /ATCELL NUCLEI FIBROBLASTS /TOCELLS FROM PATIENTS WITHCELLS ISOLATION AND /OFCYTOGENETICS A STRATEGYCYTOGENETICS DEMONSTRATESCYTOGENETICS FORCYTOGENETICS IMPROVEDCYTOGENETICS IN CHILDHOODCYTOGENETICS IN HUMANDETECTION OF TRISOMY 12 INFLUORESCENCE IN SITU /BYIN SITU HYBRIDIZATIONNUCLEI /GENE SEQUENCES INNUCLEI /REGIONS WITHINNUCLEI USING FLUORESCENCE
INTERSPECIES DIFFERENCES IN LIGHT OFINTERSPERSED LOW FREQUENCY REPETITIVE
REPETITIVE SEQUENCE PCRINTERSTITIAL 180 DELETION SYNDROME
210 DELETION /WITH ANDELETION ASSOCIATED WITHDELETION OF THE LONG ARMDELETIONS 10 THE ROLE OFINSERTION OF Y SEQUENCESTELOMERE SEQUENCES IN A
INTERVAL 6 AND 7 PROBES TO PREDICT /OFAND IDENTIFYING THE MUTATEDON CHROMOSOME 11023 /TO A CMPARENTAL ORIGIN AND NEW
INTERVALS DURING THE CYTOSTATICINTERVENTION MODEL WITH EMPHASIS ININTESTINAL HYPOPERISTALSIS SYNDROMEINTOLERANCE /IN FAMILIAL ORTHOSTATIC
/OF HEREDITARY FRUCTOSE/WITH HEREDITARY FRUCTOSE
INTRA ABDOMINAL CALCIFICATIONS THEEXON DELETION IN THE DYSTROPHIN
INTRACELLULAR ANTIPROLIFERATIVE /NOVELROUTING OF LYSOSOMAL ATRANSPORT OF /IN THE
INTRACHROMOSOMAL ALU ALU RECOMBINATIONMITOTIC RECOMBINATIONRECOMBINATION IN A
INTRACRANIAL TERATOMA /PROGRESSIVEINTRAFAMIUAL VARIABILITY IS CAUSEDINTRAGENIC GROWTH HORMONE RELEASING
RFLPS BY PCR AMPLIFICATIONINTRATUMOR HETEROGENEITY /SHOW LITTLEINTRAUTERINE FETAL DEATH /OF MACERATED
GROWTH RETARDATIONGROWTH RETARDATION /INGROWTH RETARDATION IS
INTRAVENOUS INFUSIONS OF /WITHINTRONIC SEQUENCE VARIATION /ANDINV (Y) MOSAICISM /WITH 45,X/46,X
DEL (6) /PRENATAL DIAGNOSIS OFDUP (15) KARYOTYPE /AND 47 XX +
INV(2) (PL2Q14) A REVISED APPROACH TOINV(3XP25021) /CEN 021 SEGMENT OF ANINV(7)(P21032) /WITH PATERNALINV(9) CHROMOSOMES IN 4000 JAPANESEINVASIVE PROCEDURES FOR FETAL
PROCEDURES IN UTERO FORINVERSE RELATIONSHIP BETWEEN AGE ATINVERSION (X)(P1 1.4022) ASSOCIATED
/FAMILIAL PARACENTRIC/LEAD TO CONDITIONAL XY SEX/WITH A CHROMOSOMEFROM POLY(ADP RIBOSYL)ATIONIN ACUTE MYELOMONOCYTIC /16OF 9P /FAMILIAL PARACENTRICOF CHROMOSOME 13
INVERSIONS /PERICENTRIC AUTOSOMALAND TRANSLOCATIONSOF THE X CHROMOSOME REPORT
INVERTED INSERTION(5) /CARRYING ANTANDEM DUPLICATION OF THE /AN
IONIC STRENGTH /ARE THE FUNCTIONS OF10 AND CONSEQUENCES /ASSESSING GENETICIRANIAN FAMILY WITH EIGHT AFFECTED /AN
HEREDITARY PUBERTAL GENUIRIS COLOBOMAS AND CONNECTIVE TISSUEIRON METABOLISM /FOR HUMAN
SULFUR PROTEINS /OF MITOCHONDRIALIRRADIATION /SENSITIVITY TO GAMMA
2095196821032627206322431044100827892460
411883201217391436963581082182
1640215313061635208913181607111
1320217135516361209181
17161648167
219920581425146515851512150516921701910
2371294170213441816753103798122641182235124005814662549255425481277106520841040139311491152944117456047115061503152115611687156515451249114
266014901748119012432573170915891477151515561536145315852564183614716518792363482
2388
HYBRIDS USING ALU PCRIN RELATION TO FAMILY /XREDUCED HYBRIDS TO /FROMREDUCED SOMATIC CELL /11
IRREGULARITIES IN ALPHA SATELLITE DNAIN TURKEY /CHROMOSOME
IRS PCR AMPLIFIED YEAST ARTIFICIAL /OFPCR CHARACTERIZATION AND INITIALPCR PRODUCTS FROM IRRADIATION
ISLAND /T AND IDENTIFICATION OF A CPG5 OF THE FACTOR VIII GENE /CPGAND PHYSICAL MAP OF THE HUMANENRICHED LIBRARY FOR /CPGEYE DISEASE /ANALYSIS OF ALANDEYE DISEASE /AND ALANDEYE DISEASE/INCOMPLETE /ALANDFROM A REGION OF HUMAN /RICH
ISLANDS AND ASSOCIATED TRANSCRIPTS INAND THE LOCUS DNF1SS2 WITH AAT XQ24 XQ28 LOCUS /CPG
ISO (4P),ISO 4(Q) /OF CHROMOSOME 4 ANDISOCHROMOSOME 18P ASSOCIATED WITH /AN
IN A CHILD WITH MILDIN CVS AND FETAL TISSUEY IDENTIFIED BY IN SITU
ISODICENTRIC 18 /ON A NEWBORN WITHISODISOMY/14 SUGGESTED BY UNIPARENTAL
RESULTING FROM SOMATICISOELECTRIC FOCUSING AN INVESTIGATION
FOCUSING OF HUMANISOFORM PHENOTYPES /APOLIPOPROTEIN(A)ISOFORMS AND NONDELETION/DUPLICATIONISOLATE /ENRICHED MIDDLE ASIA FAMILIAL
/OF SKIN COLOR IN A GENETICDISEASE GENES BY POSITIONALREGION SPECIFIC COSMID YEASTYEAST ARTIFICIAL CHROMOSOMES
ISOLATED ABNORMALITIES OF THECASES AFFECTED BY /OFCOMMNUNITY MIYAMA /IN THECOMMUNITY /IN A BRAZILIANFROM A Y LIBRARY DETECTS THEFROM FIRST TRIMESTER HUMANFROM HUMAN HAIR SHAFTS /DNAFROM MYELOID ML 1 CELL /GENEFROM THE HUNTINGTON DISEASEHEART MALFORMATIONS /FORIN MONOCHROMOSOMAL HYBRIDSLISSENCEPHALY /INLISSENCEPHALY SEQUENCE /AND
ISOLATING GENES /AND TECHNIQUES FORTHE GENES FOR VON HIPPEL
ISOLATION AND ANALYSIS OF LARGEAND ANALYSIS OF THE 5 /GENEAND CHARACTERIZATION OFAND CHARACTERIZATION OFAND CHARACTERIZATION OFAND CHARACTERIZATION OFAND CHARACTERIZATION OFAND ENZYMATIC SYNTHESIS OFAND LOCALIZATION OF A HUMANAND MAPPING OF NOT1 LINKINGAND PHYSICAL MAPPING OF AAND REGIONAL LOCALIZATIONAS A YEAST ARTIFICIAL /ITSBY MULTIPARAMETER FLOWCHARACTERIZATION ANDOF A 450KB YEAST ARTIFICIALOF A CANDIDATE GENE FOR THEOF A CDNA FROM THEOF A CDNA IN THAT REGIONOF A HUMAN CDNA CLONE THATOF A NEW GENE GS1 FROMOF A SIGNIFICANT PROPORTIONOF AN X CHROMOSOME SPECIFICOF CDNAS ENCODED BY HUMANOF CDNAS ENCODED BY LARGEOF COSMID AND BACTERIOPHAGEOF COSMID CLONES CONTAININGOF DNA PROBES WITHIN /RAPIDOF FETAL NUCLEATED /FOR THEOF GENES USING AOF HUMAN COSMID CLONES FROMOF LARGE NUMBERS OF YEASTOF POTENTIAL GENE SEQUENCESOF PROBES IN THE REGION OFOF REGION SPECIFIC CDNASOF SEQUENCES INVOLVED INOF SOMATIC CELL HYBRIDS ANDOF THE Li GENE RESPONSIBLEOF TRANSCRIBED SEQUENCESOF VARIANT TRANSTHYRETIN /BYOF X CHROMOSOME SPECIFIC
ISOMERASE IN TROPHOBLAST CELLSISOTOPIC AND NONISOTOPIC IN SITU /BYISOVALERIC ACIDEMIA /RESPONSIBLE FORISOVALERYL COA DEHYDROGENASE /OFISOZYME DETERMINE THE ALCOHOL /2ISRAEL /IN JEWISH AND ARAB PATIENTS IN
/PREGNANCY SCREENING INIS CAUSED BY POLYCYSTIC KIDNEY
ISRAEL ARAB COMMUNITY /INPATIENTS WITH DUCHENNE AND /INPOPULATIONS USING RFLPS AND
ISSUE /GENETICS AN OVERVIEW OF THE
210826952168213616392677216021652168233421542123237419057128102370239622972152158216501456164114761675207715882838275156715
19472764217421682145724
2791285728359911294250025892384901
209623058
S1330349
24322114211822602285238816352368219121862216102109
2082237323422383208822752402219822472281201
200821522058110
250723212075237422172022252172222782113578
252712691640490490271625511208998174610982883511
IT'S BEEN AND WHERE IT'S GOING /WHEREGOING /WHERE IT'S BEEN AND WHERE
ITALIAN CYSTIC FIBROSIS PATIENTS /INFAMILIES AFFECTED BY /ON 72FAMILIES USING SOUTHERN /INHEMOPHILIA B FAMILIES /IN
ITALY /CLINICAL ANOPHTHALMIA IN/ELLIPTOCYTOSIS IN SOUTHERN/GEOGRAPHICAL DISTRIBUTION IN/IN THE PROVINCE OF COSENZA/SCA1 AND D6S89 AND D6S109 INAND SPAIN /MYOTONIC DYSTROPHY INDATA BANK AND CELL REPOSITORYFREQUENCY AND PHENOTYPIC /IN
ITO IN A GIRL WITH PLEXUSPAPILLOMA /OF
IJACOBSON SYNDROME /WITH SIGNS OFJAMPEL SYNDROME /IN THE SCHWARTZJAPAN /DUCHENNE MUSCULAR DYSTROPHY IN
/FAMILIAL ALZHEIMER DISEASE IN/IN MEDICAL GENETICS IN
JAPANESE /OF RHEUMATOID ARTHRITIS INADRENOLEUKODYSTROPHY PATIENTSBRAZILIANS /BAND 3 INFAMILIAL ALZHEIMER DISEASEFAMILIES WITH LEBER /INFAMILY EVIDENCE FOR MULTIPLEFAMILY WITH AUTOSOMAL /IN AGAUCHER DISEASE /INHAPLOTYPES CARRYING /OF THEINDIVIDUALS /IN 4000PATIENTS /A STUDY OF 13 NONPOPULATION /AMPLIFICATION INPOPULATION /IN
JAW TUMOR SYNDROME CLINICAL ANDJEFFERSON COUNTY ALABAMA U.S.A AND /INJERSEY PRENATAL CARE /GENETICS TO NEWJEWISH AND A MOSLEM ARAB KINDRED FROM
AND ARAB PATIENTS IN ISRAEL /INAND OTHER POPULATIONSINDIVIDUALS PRESUMED TO CARRYINFANTILE TAY SACHS DISEASE /OFPATIENTS /MUTATION G542X INPATIENTS WITH HUNTER SYNDROME
JEWS /AMONG JEWS AND NON/IN ASHKENAZI/ON CHROMOSOME 9034 IN ASHKENAZICAND NON JEWS /AMONGOF TWO GENETIC POLYMORPHISMS /OF
JOHANSON BLIZZARD SYNDROME /STUDY OFJUMP SIZE /LIBRARY SECTIONED BYJUMPING CLONING STRATEGY /WALKING AND
LIBRARY SECTIONED BY JUMP SIZETRANSLOCATION /SYNDROME AND A
JUNFOS ONCOGENE FAMILY /GENE OFJUNCTION WITH THE CHROMOSOME ARM /AJUNCTIONAL DIVERSITY /CELL RECEPTOR BJUVENILE MYOCLONIC EPILEPSY TO HLA /OF
ONSET CEROID LIPOFUSCINOSISOSTEOPOROSIS /OF IDIOPATHICPERIODONTITIS /STUDIES OFPERIODONTITIS /STUDIES OF
JUXTA CENTROMERIC CHROMOSOME 14 /OF AJUXTAPOSED VNTR TYPES AND HAPLOTYPES
K
K 12 LEAD TEACHER TRAINING /GENETICSRAS MUTATIONAL SPECTRA IN /P53 ANDREVI PROTEINS BY GTPASE ACTIVATING
KABUKI MAKE UP (NIIKAWA KUROKI)MAKE UP SYNDROME A STUDY OF 13
KAINGANG AND GUARANI AMERINDIANS FROMKALLMANN SYNDROME /ICHTHYOSIS AND
SYNDROME ON XP22.3 /GENE FORKAPPA IMMUNOGLOBULIN GENES IN HUMAN /VKARNATAKA INDIA EVIDENCE AND FACTORSKARYOTYPE /ADULT WITH 49 XYYYY
/AND 47 XX + INV DUP (15)/LIVEBORN WITH THE/THE 4P SYNDROME BUT NORMAL/THE NORMAL AND ABNORMALBIOCHEMICAL ASPECTS OFIN A PATIENT WITH R(18)IN HER ABNORMAL CHILD WITHIN TWO YOUNG BOYS WITH /THEOF THE ZYGOTE AND THE FETUSPATTERN IN MALIGNANT /OFPHENOTYPE CORRELATIONS /9
KARYOTYPES /REGISTRY OF ABNORMALKARYOTYPIC ABNORMALITIES IN TWO
ALTERATIONS IN PROSTATEASSOCIATION FOR /1LQ22 32 AEVOLUTION IN B CELL
KARYOTYPING /COUNSELING AND FETALAT CHULALONGKORN HOSPITAL
568
42142198565411102652276210632882272719371984265410781376
1720894179473933287623202629107110191070999
2315221115452342313551193426711797998
25514
1067244622452255
323292353
32628723217527852175170123082213224020411972957715
268116662801
20661012
692234
2859805
229418571845151015211501171114451479151716321455126413321529358152613401520130412731249
Permuted Title Index
KAUFMAN OCULOCEREBROFACIAL SYNDROMEKB COMPRISING THE HUMAN /OF 180
DNA PROBES USED AS RFLP MARKERS /20IN A CANDIDATE REGION FOR THE /460INSERTS /GENOMIC LIBRARY OF 150 200MAJOR BREAKPOINT CLUSTER REGION INREGION CONTAINING THE VON /A 600REGION IN 9013 021 /OVER A 350REGION OF CHROMOSOME 19013.3 /A 350REGION OF THE TCR B CHAIN LOCUS INYEAST ARTIFICIAL CHROMOSOME CONTIG
KD PEROXISOMAL MEMBRANE PROTEIN CDNAKDA AND 63 KDA PROTEOLYTIC PEPTIDES
PROTEOLYTIC PEPTIDES OF THE REDKEARNS SAYRE SYNDROME /DNA IN
SAYRE SYNDROME /LEADING TO THESAYRE SYNDROME /OF A WOMAN WITH
KERATIN /OF A 40K TYPE 1 ACIDIC14 MUTATION IN A FAMILY WITH
KERATINOCYTES WITH FUNCTIONAL GENEKERATOSIS FOLLICULARIS SPINULOSA /OFKETOGLUTARATE DEHYDROGENASE /2KETOTIC HYPERGLYCINEMIA BY ASSAY OFKI 1 POSITIVE ANAPLASTIC LARGE CELLKIDNEY DISEASE /DOMINANT POLYCYSTIC
DISEASE /DOMINANT POLYCYSTICDISEASE /FOR ADULT POLYCYSTICDISEASE /HEREDITARYDISEASE /OF ADULT POLYCYSTICDISEASE 1 /CAUSED BY POLYCYSTICDISEASE AND DOWN SYNDROMEDISEASE AND ITS CLINICALDISEASE IN AN UZBEKI JEWISHDISEASE IN ICELAND /POLYCYSTICDISEASE IN ITALIAN FAMILIESDISEASE NEW INFORMATION FORDISEASES /OF POLYCYSTICDISEASES /TO ASTHMA ANDMORPHOGENESIS /GENE IN LIMB ANDTUMORIGENESIS BY SUBTRACTIVE
KIEV NEWBORNS IN THE CONNECTION WITHKILLIAN SYNDROME /REGION FOR PALLISTERKILLING FUNCTIONS /AII IN MACROPHAGEKINASE /A CELL CYCLE REGULATED PROTEIN
1 VARIANTS IN CHILDREN OFAND ADRENAL HYPOPLASIADEFICIENCY /OF COMPLEX GLYCEROLDEFICIENCY /TO PHOSPHORYLASE BGENE BY CELL FUSION STRATEGY
KINDRED /DISEASE IN THE INDIANA/IN A BRITISH COLUMBIA NATIVEFROM ISRAEL IS CAUSED BY /ARABLINKED TO CHROMOSOME 20OF EHLERS DANLOS TYPE IVWITH FIRST COUSINS AFFECTED /AWITH X LINKED ANDROGEN
KINDREDS /1A IN FIVE FRENCH ACADIAN/COLORECTAL CARCINOMA IN FIVE/HYPERTHERMIA SUSCEPTIBLEOF CHILDHOOD AND ADOLESCENTSUGGESTS A COMPLEX GENETIC
KINETIC VARIANT OF PHENYLKETONURIA /AKINETICS AND X RAY INDUCED CHROMOSOME
OF LEUKEMIC VERSUS NORMALKING RICHARD III /ASSOCIATION OF
SYNDROME CLINICAL FINDINGS /THEKIT (MAST/STEM CELL GROWTH FACTOR /C
AND STEM CELL FACTOR LOCI MAY BEGENE COMPLEX /FACTOR RECEPTOR (C
KLIPPEL FEIL ANOMALY /THORACIC FUSIONTRENAUNAY SYNDROME AND ITS
KM IN CHINESE AND MALAY PATIENTS WITHKOBE /OF DUCHENNE MUSCULAR DYSTROPHYKONG /AND PRENATAL DIAGNOSIS IN HONG
/COUNSELING CLINIC IN HONGPROBLEMS AND POTENTIALS /IN HONG
KOREA /DNA POLYMORPHISM INKOREAN TWINS /CHOLESTEROL LEVELS OFKORLEBU ON ELECTROPHORESIS /OF HBSKOSTIANN AGRANULOCYTOSIS TREATED WITHKREBS CYCLE /INHERITED DEFECT OF THEKUROKI SYNDROME IN FIVE SPANISHKUSTER HAUSER SYNDROME /ROKITANSKYKUWAIT /AND GENETIC COUNSELING IN
752257526302396252913702133
812036100
2159190
262926299951115228
2684225724761985447563
1331249
2371176438010489981444199499819021110226384
2752266
22522782143724312128506
2220687846
2466189619099988336971459441
195819911911
72231449
153113371267698189
25662296832641
273323513881785179528462691182461944769214201736
L
L CYSTEINE AND PRIMARY BILIARYIDURONIDASE GENE /MAPPING OF THE A
LI GENE RESPONSIBLE FOR A /OF THEL2 /ACUTE LYMPHOCYTIC LEUKEMIA (ALLLABELED CHROMOSOME SPECIFIC PROBES BY
PROBES AND DIGITAL IMAGINGLABELING AND SYNTHESIS /FOR PROBE
FLUORESCENT IN SITU /A DOUBLEIN LYMPHOCYTE CULTURES AS AOF DNA PROBES FOR IN SITUOF NUCLEIC ACIDS FOR GENE
LABORATORY /FOR A GENETICS RESEARCH/FROM A COMMERCIAL/FROM A COMMERCIAL
5422345227813691697
9125141337160819992
207910302740
BY COLOR PCR AND ANERRORS ON RISK ESTIMATIONGUIDELINES FOR PREDICTIVEPERIMETERS AND PITFALLS
LACTASE DEFICIENCY /IN THE CONGENITALGENE IN THE CONGENITAL /OF THEPERSISTENCE PHENOTYPE /OF
LACTIC ACIDOSIS AND STROKE LIKEACIDOSIS AND STROKE LIKEACIDOSIS AND STROKE LIKE
LAFORA DISEASE IN A SMALL TOWN INLAIRD COCHRAN METHODS OF METALAMBDA CONTIG MAP OVER A 600 KB /OF ALAMININ DEFICIENCY /HABITUS ANDLAMY SYNDROME (MPS VI) BY BONE MARROWLANDMARK RFV MARKER LOCI ON /TEN NEWLANGE SYNDROME /CASE OF BRACHMANN DELANGER GIEDION SYNDROME ASSOCIATION
GIEDION SYNDROME CHROMOSOMELANGUAGE FOR PENETRANCE SPECIFICATIONLANKA /THE SINHALESE AND TAMILS OF SRILAOTIANS AND FILIPINOS /AMONG CHINESE
AND ITS EFFECTS AN /INLARON DWARFISM /BINDING AND CAUSES
DWARFISM /PATIENTS WITHLASER MICRODISSECTION PROBES AND HTFLATE CVS BY TRANSABDOMINAL ROUTE 1700
INFANCY GLOBOID CELLINFANTILE TAY SACHS B1 VARIANT /AONSET ALZHEIMER DISEASE AN /ANDONSET DISORDERS THE EXPERIENCEONSET FORM OF FRIEDREICH ATAXIAONSET MOSAIC FORM OF DOWN /AONSET PSYCHOSIS IN THEX REPLICATION STUDIES /POSTNATAL
LATERAL SCLEROSIS /AMYCTROPHICSCLEROSIS /AMYOTROPHICSCLEROSIS DEMENTIA ANDSCLEROSIS TO CHROMOSOME 21
LATIN AMERICA /AMONG FAMILIES INAMERICA /OF BIRTH DEFECTS IN
LATITUDE /STRONGLY CORRELATED WITHLATICE CORNEAL DYSTROPHY TYPE /INLAXA WITH MARPHANOID HABITUS ANDLAXOVA SYNDROME /CHOLESTEROL IN NEULCR IS FLANKED BY THREE HIGHLY /ALDH C4 GENE AND ITS EXPRESSION /HUMANLDL RECEPTOR DEFICIENT RABBITS LEADS
RECEPTOR GENE /NEW MUTATIONS OFRECEPTOR GENE ON MEANS VARIANCESRECEPTOR GENE TO IDENTIFY /TO THE
LDLR MUTATION DETECTION WITH THELEBER HEREDITARY OPTIC /WITH
HEREDITARY OPTIC NEUROPATHYHEREDITARY OPTIC NEUROPATHYHEREDITARY OPTIC NEUROPATHY /INHEREDITARY OPTIC NEUROPATHY /OFHEREDITARY OPTIC NEUROPATHY AND
LEC1THIN/CtlOLESTEROL ACYLTRANSFERASELEFT FLOW DEFECT FAMILIES /RISK IN
HEART NEPHROMEGALY ANDHYDRONEPHROSIS /THE HISTORY OF
LEGAL AND ETHICAL ISSUES WITH REGARDASPECTS /ETHICAL ANDSTANDARD SETTING FOR GENETIC
LEIDEN IN AN EXTENDED MULTIGENERATIONLEIOMYOMA APPLICATION OF FLUORESCENCELEIOMYOSARCOMA OF THE SINONASAL TRACTLEISHMANIA DONOVANI INFECTION AND THELEMU OPITZ SYNDROME /OF THE SMITH
OPITZ SYNDROME(S) A NUMERICALLENGTH /ESTIMATION OF CHROMOSOME MAP
OF HAN AND ZHUANG MINORITIESSHORTENING IN FETUSES WITH
LENINGRAD /OF CYSTIC FIBROSIS INLENS CRYSTALLINS NEW FUNCTIONS /OF
FINDINGS IN 40 PATIENTS IN 5/2SPECIFIC PROTEIN AN ANIMAL MODELTO ESTIMATE GENETIC HAZARDS OF
LEPRECHAUNISM A SYNDROME OF SEVERELESCH NYHAN FAMILIES FROM NORTHERN /INLESIONS IN HUMAN SPERM /OF CHROMOSOME
MICROPHTHALMIA AND ANTERIORPATHOGENIC DIAGNOSTIC AND
LESSONS AND THE FUTURE /HISTORICALLETHAL ARTHROGRYPOSIS ABSENT PATELLAE
ARTHROGRYPOSIS IN FINLANDDISORDERS /IN THE DIAGNOSIS OFMUTATIONS AT THE AGOUTI LOCUSNEONATAL SHORT LIMB DWARFISMOSTEOGENESIS IMPERFECTAPOPLITEAL PTERYGIUM SYNDROMESPONDYLOEPIPHYSEAL DYSPLASIA
LEU(UUR) GENE ASSOCIATED WITH /TRNALEUCINE RICH GLYCOPROTEIN FAMILY /THELEUKEMIA (ALL L2) /ACUTE LYMPHOCYTIC
/ACUTE LYMPHOBLASTIC/IN ACUTE NONLYMPHOCYTIC/IN AN ACUTE MYELOGENOUS/IN B CELL PROLYMPHOCYTIC/IN CHRONIC MYELOGENOUS/IN CHRONIC MYELOGENOUS/IN CHRONIC MYELOID/IN PATIENTS WITH ACUTE/MARROW IN ACUTE LYMPHOCYTIC
1113175118071610509509
26474379771017865129321331061561
216114961507197
20862875267910722455969S771253862494
266724882015041741145719101938270480
2696272226281055106191318651286423980515
268228041022513101920321073973
2690265079295340
1816209996136413622651751679
20762851758
2741166806
226825624851053156614941305322640896139
2239650446637522101723801369132025821370130413271649135113281345
/MOLECULAR GENETICS OF/NEW TRANSLOCATION IN T CELL/OF T(8;21) IN ACUTE MYELOID/WITH ACUTE LYMPHOBLASTIC/WITH ACUTE MYELOGENOUS/WITH CHRONIC MYELOGENOUS/WITH PHILADELPHIA POSITIVEAND IN MYELODYSPLASTICAND LYMPHOMA USING PCR /INASSOCIATED BREAKPOINTS ON /OFBEFORE AND AT DIFFERENTBY FLUORESCENT IN SITUDIAGNOSED BY IN SITU /ININ A GIRL WITH /LYMPHOBLASTICIN AN ATAXIA TELANGIECTASIAMCL 1 HAS SIGNIFICANT /1 CELLPATIENTS /ACUTE MYELOBLASTICPATIENTS BY DENSITOMETRY OFSUB TYPE M4 /NONLYMPHOCYTICTERMINATING IN RICHTERTO WITHIN 1 MB OF THEVIRUS TRANSFORMED CELLS
LEUKEMIAS /IN T(11;19) ACUTELEUKEMIC CLONE IN CHRONIC MYELOGENOUS
INVERSIONS AND TRANSLOCATIONSVERSUS NORMAL CELLS BY A /OF
LEUKEMOID REACTION AND RECURRENT FEVERLEUKOCYTES OF PATIENTS WITH FAMILIALLEUKODYSTROPHY /INFANCY GLOBOID CELLLEVEL /AT THE NUCLEOTIDE SEOUENCE
ELECTROMAGNETIC RADIATIONS /LOWFRAGILE X EXPRESSION /OF LOWGENERAL HOSPITAL OF A /A SECONDHUTCH /TRIPTERYGIUM HYPOGLAUCUMIN HUMAN NORMAL AND TUMOR CELLSMAP OF THE MYOTONIC DYSTROPHYOF HETEROZYGOSITY IN HUMANPROGRAM /WITH A MASTERS
LEVELS /1 AT THE DNA RNA AND PROTEIN/ACTIVATOR INHIBITOR 1/EFFECT ON IMMUNOGLOBULIN/WITHOUT ELEVATED SWEAT SODIUMAMONG HISPANICS AND NON /LIPIDAND THE RISK FOR CORONARYIN A SAMPLE ENRICHED FOR /BIN ADULTS IS DETERMINED ININ CULTURED FIBROBLASTSIN EARLY SECOND TRIMESTERIN HISPANIC MEN /INSULININ HUMAN SPERMATOZOA USINGIN NONLETHAL CONGENITALIN SERUM AND ERYTHROCYTE OFIN THE ANGLO AND HISPANICIN THE MID TRIMESTER /AND UE3IN TRIPLET PREGNANCY /MSAFPIN TWIN GESTATIONS /ESTRIOLOF AN ESSENTIAL FATTY ACID ANDOF B HCG AND UNCONJUGATED /ANDOF GLUTAMATERGIC AND /CSFOF HDL C IN BABOONS /ON SERUMOF KOREAN TWINS /CHOLESTEROLOF MOSAICISM IN TISSUES OF AWITH REFRACTIVE ERROR IN
LEYDIG CELL MATURATION GENE TO THE YU FRAUMENI SYNDROMEFRAUMENI SYNDROME A LINKAGE STUDY
UABILITY MODEL /AN UNDERLYINGUBRARIES /AND MEDULLA OBLONGATA CDNA
/CHROMOSOME 22 ENRICHED/CHROMOSOME SPECIFIC DNA/CHROMOSOME SPECIFIC DNA/USING ARRAYED CDNAAND FLUORESCENT IN SITU /DNAFROM FLOW SORTED HUMANFROM FLOW SORTED HUMANUSING CHROMOSOME /SPECIFICUSING THE BIOMEK 1000
UBRARY /BY A CHROMOSOME SPECIFIC DNA/WITH CHROMOSOME SPECIFIC/YEAST ARTIFICIAL CHROMOSOMEDETECTS THE YQ11 REGION /A YFOR CHROMOSOME 20 CLONING ANDFROM SORTED CHROMOSOMESHIGHLY ENRICHED IN HUMANOF 150 200 KB INSERTS /GENOMICSECTIONED BY JUMP SIZEUSING FLUORESCENCE IN SITU
UBYA /DOWN SYNDROME INUCHEN AMYLOIDOSIS AS A /SYNDROME WITHUDDLE SYNDROME WITH AUTOSOMALUFESFAN OF DROSOPHILA MELANOGASTERUFESTYLES SUBJECTIVE SOMATIC /AMONGUGASE DEFECT IN BLOOM SYNDROME /DNA
MEDIATED GENE DETECTION AND /BYUGHT CHAIN IS LOCATED ON CHROMOSOME
OF WITHIN SPECIES VARIATION /INPHOTOTHERAPY AND VITAMIN E /BLUE
UM AND KIDNEY MORPHOGENESIS /GENE INDEFECTS WITH HYDROCEPHALUSDEFORMITY GENE IN UMB AND /MOUSEDWARFISM WITH DYSMORPHIC FACEGIRDLE MUSCULAR DYSTROPHY TO /OFHYPERTROPHY WITH AND WITHOUTREGENERATION IN THE PRESENCE AND
UMB/PELVIS HYPOPLASIAUAPLASIA
569
S76135713421326139613792597617
1031185
134413551303132426042589135858613461366170913411323586
1556133713211000862223424221550178918531354231027871779281824172849?8142669427
272475
501926265683
851829
26891144115711979131255520
269026911412895
234927118922786233322511677171523301706177
2499207021251542164421029912374216725212529217521511750743839
28192772295
10412164167
156826681626665078
6411289681
Permuted Title Index
UMBED DWARFISM AND DISTINCT FACIALDWARFISM DEFECTIVE NEUTROPHILTYPE A PREVIOUSLY UNREPORTED
UMITED AUTOSOMAL DOMINANT TRAIT WITHGENETIC MONITORING AMONG KIEV
UNE /EPISOMAL COSMID IN A HUMAN CELL/HUMAN CHOLANGIOCARCINOMA CELL/IN A CHOLANGIOCARCINOMA CELL/IN A MALIGNANT SCHWANNOMA CELL/IN A WERNER SYNDROME FIBROBLAST/PATIENT MOSAIC FOR A NORMAL CELL1 ELEMENT IDENTIFICATION AND1 RETROTRANSPOSON EXPRESSION IN1 SEQUENCES ARE READILY CAPABLEAND NO VIRILIZATION /OF 46,XYAND SOMATIC P53 GENE MUTATIONSARE SIMILAR TO THOSE IN CELLSBY INTRODUCTION OF A #3P /CELLBY PCR IN A PATIENT WITH /CELLDERIVED FROM A MALIGNANT /A CELLENCODED REVERSE TRANSCRIPTASEENCODES A PROTEIN CONTAININGEXPRESSING CYTOCHROME P450 GENESMOSAICISM FOR CHROMOSOME 5 CRIMOSAICISM IN THE VON WILLEBRANDMUTATIONS IN HUMAN BREAST /GERMOF THYMIDINE KINASE GENE BY CELLOF TRANSMISSION IN HUNTINGTONRESOURCE FOR THE UNITED KINGDOMWITH TRISOMY 10 IN A CONFINED
UNEAGE /OF NON FOLLICLE CENTER CELL/OF THE MYOGENIC
UNEAR AND WHORLED NEVOIDSKIN LESIONS MICROPHTHALMIA /OF
UNES /ORIGIN OF SV40 TRANSFORMED CELL/STUDIES OF ZELLWEGER CELLAND DURING NEURONAL /CELLARISING FROM BLACKFOOT DISEASEFROM HUMANS /LYMPHOBLASTOID CELLFROM SUBJECTS AFFECTED BY /CELLOF EVIDENCE FOR GENOMIC /TWO
UNK4%GE /CANCER EVIDENCE FOR 170/STUDIES OF ASSOCIATION ANDANALYSES /PEDIGREES FORANALYSES /TRIMETHOPRIM AND DNAANALYSIS /AND MOLECULARANALYSIS /BY MEANS OF RFLPANALYSIS /OF CLONED GENES BYANALYSIS /OLIGOGENIC TRAITS BYANALYSIS /POLYPOSIS BYANALYSIS /SWEAT PORE ANDANALYSIS A SIMULATION STUDYANALYSIS AND PRENATAL /FORANALYSIS AND RFLP BASED /TOANALYSIS FOR MAPPING OFANALYSIS FOR X LINKEDANALYSIS IN A FAMILY WITH XANALYSIS IN AUTOSOMALANALYSIS IN CANDIDATE GENESANALYSIS IN FAMILIALANALYSIS IN FAMILIAL /INANALYSIS IN FAMILIES WITHANALYSIS IN HUMAN X LINKEDANALYSIS IN LATTICE CORNEALANALYSIS IN SCHIZOPHRENIAANALYSIS IN THE FAMILY WITHANALYSIS OF /MULTIPOINTANALYSIS OF A BIVARIATE /ANDANALYSIS OF ALAND ISLAND EYEANALYSIS OF AN X LINKED /BYANALYSIS OF BIPOLAR AFFECTIVEANALYSIS OF CANDIDATE REGIONSANALYSIS OF CHARCOT MARIEANALYSIS OF CHROMOSOMES 19ANALYSIS OF COMPLEX DISORDERSANALYSIS OF FAMILIES WITHANALYSIS OF FANCONI ANEMIAANALYSIS OF GERSTMANNANALYSIS OF MARFAN SYNDROMEANALYSIS OF PANIC DISORDERANALYSIS OF PROXIMAL DNAANALYSIS OF THE INTERNATIONALANALYSIS OF USHER SYNDROME INANALYSIS OF X LINKEDANALYSIS OF X LINKED OCULARANALYSIS REVEALS MOLECULARANALYSIS WITH ADA AND /ANEMIAANALYSIS WITH MICROSATELLITEANALYSIS WITH MULTIPLE /PAIRAND LINKAGE DISEQUILIBRIUM /OFAND PHYSICAL MAPPING OF THEAND PHYSICAL MAPS /RESOLUTIONAPPROACHES TO MAPPING NON HLABETWEEN THE INSULIN GENECALCULATIONS /IN GENETICDATA AT THE X LINKED /FURTHERDATA FOR ANGIOGENIN AND LIVERDISEQUILIBRIA AMONG CADISEQUILIBRIUM /OF LINKAGE ANDDISEQUILIBRIUM BETWEEN SCAlDISEQUILIBRIUM BETWEEN THE /OFDISEOUILIBRIUM IN THE /OFDISEQUILIBRIUM IN THE FRENCHDISEQUILIBRIUM MAKE A /ANDDISEQUILIBRIUM WITH MYOTONIC
903688823
2237278216461378166226002548143924602580261115342605798139510322232188
2288254711761068218
2466791
20541209138732687414945791435242013831438500
2765202610762683148719891021194863
18769041899978
275320681887198718732059187218801093971105520432047201227141905703
20292020195819921963203819651896188319441908143
20231931205120191962200320271949612160S3227112086195919799831949193719162336284818841875
DISEQUILIBRIUM WITHIN THEFOR TWO LOCUS MODELS OFGENOTYPE WITH PHENOTYPE INGROUP /4 YIELD A SINGLEGROUP /CHROMOSOME 6 AT THE HLAHETEROGENEITY /20Q13.3 ANDIN FAMILIES WITH BIPOLARIN SCHIZOPHRENIA /SCAN FORLOCALIZATION /STRUCTURE ANDMAP OF CHROMOSOME 8MAP OF EIGHT CHROMOSOME 22011MAP OF MOUSE CHROMOSOME 18MAP SPANNING THE DIASTROPHICMAPPING /SYNDROME GENEMAPPING OF CHROMOSOME 21MAPPING OF DNA FRAGMENTS FROMMAPPING OF FAMILIALMAPPING OF HIGHLY INFORMATIVEMAPS /CONSTRUCTION OF GENETICMAPS /FILTRATION OF HUMANMAPS /METHODS FOR UPDATINGMAPS IN THE MOUSE /OF MITOTICMAPS OF HUMAN CHROMOSOME 16MARKERS FOR CHROMOSOME 21 /ASOF AN AUTOSOMAL DOMINANT FORMOF DOMINANT DYSTROPHICOF FACIOSCAPULOHUMERAL /OFOF FAMILIAL AMYOTROPHICOF FIBRILLIN /AND GENETICOF HEREDITARY HYDRONEPHROSISOF JUVENILE MYOCLONIC /OF THEOF MATURITY ONSET DIABETES OFOF THE MULTIPLE ENDOCRINEOF TWO CHROMOSOME 9 MARKERSOF X LINKED HYDROCEPHALUS TOOF ZFY 2,ZFY 1,SRYHYA SPYPROGRAMS /USING THERELATIONSHIPS /JOSEPH DISEASERELATIONSHIPS OF THE LOCI FORSCREENING USING AFFECTEDS ONLYSEARCH FOR AN AUTOSOMAL LOCUSSEARCH UPDATE NEW HAVEN ANDSTUDIES AND MOLECULARSTUDIES IN AUTOSOMAL DOMINANTSTUDIES IN FAMILIES WITHSTUDIES IN MACHADO JOSEPHSTUDIES IN NINE FAMILIES WITHSTUDIES IN PRESTUDIES IN PROGRESSIVESTUDIES IN RETINOBLASTOMASTUDIES IN SENSORIMOTORSTUDIES IN TUBEROUS SCLEROSISSTUDIES IN TUBEROUS SCLEROSISSTUDIES IN X LINKED GONADALSTUDIES OF ALPORT SYNDROMESTUDIES OF BIPOLAR ILLNESSSTUDIES OF FAMILIAL BREASTSTUDIES OF SCHIZOPHRENIASTUDIES OF SCHIZOPHRENIA WITHSTUDIES OF X LINKED CLEFTSTUDIES ON INHERITED CANINESTUDIES USING CEPH PEDIGREESSTUDIES WITH THE TRANSFORMINGSTUDY /Li FRAUMENI SYNDROME ASTUDY AND PRESYMPTOMATICSTUDY FOR PRELINGUAL DEAFNESSSTUDY OF AUTOSOMAL DOMINANTSTUDY OF CHRONIC SPINALSTUDY OF GILLES DE LASTUDY OF THE PSEUDOAUTOSOMALSTUDY OF X LINKED DOMINANTTO 110 AND 140 MARKERS /OFTO CHROMOSOME 17 LOCI /ANDTO D5S39 IN FRENCH CANADIANTO DXS52 IN A FRAGILE XTO HLA /MENINGOCELE TESTINGTO HLA IS EXCLUDED /CLOSETO HUMAN CHROMOSOME 9 /FROMTO NINE X CHROMOSOMAL RFLPTO SEVERE PRE ECLAMPSIA ATO THE BOUNDARY OF THE /MIMICTO THE FRAGILE X SYNDROMETO TRANSFORMING GROWTH FACTORTO XQ21 /SYNDROME ANDUNDER HETEROGENEITY /OF
UNKED ADRENOLEUKODYSTROPHY /OF XADRENOLEUKODYSTROPHY AND ITS /XAND AUTOSOMAL DISORDERS NEW /XAND AUTOSOMAL INHERITANCE /TO XANDROGEN INSENSITIVITY SYNDROMECHARCOT MARIE TOOTH DISEASE ONCLASPED THUMB AND MENTAL /OF XCLEFT PALATE IN A BRITISH /OF XCOMPLICATED FORM OF SPASTIC /XCONGENITAL STATIONARY NIGHT /XDEAFNESS /GENETICS OF XDEAFNESS AND CHOROIDEREMIA /XDILATED CARDIOMYOPATHY /XDISEASES /MOSAICISM IN XDISEASES /SPORADIC CASES OF XDISEASES IN DIFFERENT /XDISORDER AND WITH SPERMDOMINANT /RARE VARIANT OF XDOMINANT HEREDITARY MOTOR ANDDYSTONIA PARKINSONISM /(X
19642718283
19712197202820911877228620481954186319182045193821101910196820602017159
205621242094
7873
19048034519322041
741982189320461859209519952031S32198819412255
71930188919271156
766131900191519811976381
1879202620301986190918711901101518929901999190220181924189519141913196120181980195320522004192319192034S77101311041906864130
2808802441
2007192519096751878
241086238511911111965
241682419142044
DYSTONIA PARKINSONISM SYNDROMEECTODERMAL DYSPLASIA SWEAT /XEYE DISEASES /GENES FOR THE XFABRY DISEASE /WITH THE XFAMILIAL EXUDATIVE /CHROMOSOMEGENE COLOR VISION DEFICIENCIESGENE SBY /SPY AND A NEW YGENES /IN GENETIC COUNSELINGGENES IN TYPE I DIABETES /HLAGONADAL DYSGENESIS /IN XGPD EXPRESSION IN NORMAL AND /XHEREDITARY SPASTIC PARAPLEGIAHPAII SITE 20 BASE PAIRS FROMHYDROCEPHALUS LOCUS WITH SEVENHYDROCEPHALUS TO XQ28 /OF XHYPOHIDROTIC ECTODERMAL /IN XHYPOHIDROTIC ECTODERMAL /THE XICHTHYOSIS AND KALLMANN /WITH XINHERITED DYSMYELINATING /XLIVER GLYCOGENOSIS IN XP22 /XLOCI /II EFFECTS ANDLOCUS /DETERMINED BY AN XLOCUS AT XP21 LINKED TO THE /XLYMPHOPROLIFERATIVE DISEASE /XLYMPHOPROLIFERATIVE DISEASE /XLYMPHOPROLIFERATIVE DISEASE /XMARKERS /DYSTROPHY AND CLOSELYMENTAL RETARDATION LINKED TO /XMENTAL RETARDATION SYNDROME /XMENTAL RETARDATION SYNDROME /XMENTAL RETARDATION WITH ATAXIAMYOPATHY WITH EXCESSIVE /FOR XOCULAR ALBINISM /ANALYSIS OF XOCULAR ALBINISM /AROUND XPROGRESSIVE CONE DEGENERATIONRECESSIVE CHONDRODYSPLASIA /XRECESSIVE INHERITANCE /XRETINITIS PIGMENTOSA /OF XRETINITIS PIGMENTOSA FAMILIESRFLPS /USING CLOSELYSPINAL AND BULBAR MUSCULAR /XSPINOCEREBELLAR ATAXIA AND /XTO ALPP ON CHROMOSOME 2 FIRSTTO BIPOLAR AFFECTIVE DISORDERTO CHROMOSOME 10 /IS NOTTO CHROMOSOME 20 /KINDREDTO D6S89 ON 6P IN A FAMILYTO DXS369 AT XQ27 /RETARDATIONTO EHLERS DANLOS SYNDROME TYPETO MULTIPLE ENDOCRINE /MARKERSTO MULTIPLE ENDOCRINE /TIGHTLYTO MYB /MAPS TO 6021 022 AND ISTO MYOTONIC DYSTROPHY /MARKERTO MYOTONIC DYSTROPHY IN ITALYTO ONCOGENESIS /REGION 8024TO THE DYSTROPHIN GENE /AT XP21TO THE FRAGILE X SYNDROME LOCUSTO THE WILSON DISEASE LOCUSTRANSGENES /METHYLATION OF XVITREORETINOPATHY /A GENE FOR XWITH G PHOSPHOGLUCONATE /MAY BEWITH THE CYSTIC FIBROSIS GENE
UNKING CLONES ON CHROMOSOME 22 /NOT1UP AND PALATE /ALPHA WITH CLEFT
AND PALATE /ANALYSIS OF CLEFTAND PALATE /MALFORMATIONS CLEFTAND PALATE /PATIENTS WITH CLEFTAND PALATE /STUDIES OF CLEFTAND PALATE /TO NONSYNDROMIC CLEFTAND PALATE ASSOCIATION AND /CLEFTPRINT AND GENETIC STUDY OFPSEUDOCLEFTS FURTHER CONFIRMATIONWITH OR WITHOUT CLEFT PALATE INWITH OR WITHOUT CLEFT PALATE IN
LUIFASE /IN HORMONE SENSITIVEGENE FAMILY /BELONGS TO AN ACIDLOCUS WITH FASTING INSULIN
UPID AND APO TRAITS NARIANCE OF NINEAND LIPOPROTEIN VARIATION AMONGLEVELS AMONG HISPANICS AND NONLEVELS IN THE ANGLO ANDMETABOLISM IN FRENCH CANADIANS
UPODYSTROPHY (BERARDINELLI SEIPNASU /(MEMBRANOUS
UPOFUSCINOSIS (BATTEN DISEASE) GENETO THE SHORT ARM OF
UPOMATOSIS /RENAL ECTOPIA AND PELVICAND THE PROTEUS SYNDROME
LIPOPROTEIN LIPASE LOCUS WITH FASTINGLIPID LEVELS AMONG /IV ANDLIPID LEVELS IN THE ANGLOVARIATION AMONG FAMILIAL
UPOPROTEIN(A) /OF PLASMALEVELS AND THE RISKPARTICLE DENSITY AND
UPOSARCOMA WITH A SINGLE GIANTUPOSOMES /PHOSPHOLIPID CONTAININGUQUID CHROMATOGRAPHY /PERFORMANCE
CHROMATOGRAPHY /PERFORMANCEUSSENCEPHALY /IN ISOLATED
SEQUENCE /AND ISOLATEDUSU NATIONALITIES OF SICHUAN CHINAUTHIUM COUNTERTRANSPORT TO /ON SODIUMUTHUANIAN MUTATION CAUSING FAMILIALUVE FETUS /MOLAR PREGNANCY AND
570
1949904
2531174385788618592006S32197624517089591959204611061126805971
19214522032753968108212632848194671685296318872051201470390268919391931101295
198779
19401888833205219462025198219561307104319842591753200523731660194219282317219122422774775
236969
10131015700834
267827061983224826562775268226692689515891873197219351508771
2656266926892682
674272434137752656557023058
2769273623291154
Permuted Title Index
UVEBIRTHS IN EASTERN INDIA OVER A 10UVEBORN /PRENATALLY WITH AN AFFECTED
INFANT ASSOCIATED WITH /IN AMALE WITH A RECOMBINANTWITH THE KARYOTYPE
UVER /TRANSPLANTED INTO RATBY HEPATOCELLULAR /OR NEWBORNDAMAGE IN CHRONIC ALCOHOLICSGLYCOGEN PHOSPHORYLASE ON /ANDGLYCOGENOSIS IN XP22 /X LINKEDSAMPLES FOR THE PRESENCE OF THESPECIFIC TRANSCRIPTION /OFTRANSPLANTATION FOR METABOLIC
LLQ;22Q TRANSLOCATION IN FOURLOAD /ESTIMATION OF CHROMOSOMALLOCAL IMPACT /DIAGNOSTIC SERVICESLOCALIZATION /STRUCTURE AND LINKAGE
AND ANALYSIS OF THE GENEAND CONSERVATION OF NRSAND FUNCTIONAL ANALYSISAND HIGH DEGREE OFAND LARGE SCALE ANALYSISBY LINKAGE ANALYSIS OFBY SILVER AMPLIFIED ININ UNSTABLE CHROMOSOMEOF 60 BRAIN CDNASOF 69 POTENTIAL HUMANOF 75 CHROMOSOME 5OF A GENE FOROF A GENE FOR THE HUMANOF A GENE FOR X LINKEDOF A HUMAN SLOW TROPONINOF AZOOSPERMIA FACTOR AOF CHROMOSOME 13 CLONESOF COSMID CLONES ONOF HUMAN PAX2 GENE TOOF HYBRIDIZED PROBESOF LUBAG (X LINKEDOF REGULATING GENES FOROF SIMPLE SEQUENCEOF THE AT D GENE TO THEOF THE ATAXIAOF THE CHARCOT MARIEOF THE CRITICAL REGIONOF THE GABM RECEPTOR B3OF THE GENE DEFECT INOF THE GENE FOR FAMILIALOF THE GENE FOR MULTIPLEOF THE GENE FOR X LINKEDOF THE GENES CODING FOROF THE GENES FOR USHEROF THE HEREDITARYOF THE HUMAN SYNEXIN /ANDOF THE P ARM BREAKPOINTOF THE SPINOCEREBELLAROF THE WISKOTT ALDRICHOF TUBEROUS SCLEROSIS 1OF X LINKED CHARCOTTO 7P21 P22 /OF PDGFA
LOCATIONS OF ONCOGENES IN HUMAN LUNGLOCI /AND ADRENAL HYPOPLASIA CONGENITA
/AND LINKAGE TO CHROMOSOME 17/AT THE NAT1 AND NAT2/GENE AND RELATED/GENETICS OF HYPERVARIABLE/II EFFECTS AND LINKED/NEOPLASIA TYPE 1 AND BCL 1/USING HYPERVARIABLE DNAAMONG ASIAN BLACK CAUCASIAN ANDAMONG ASIAN BLACK CAUCASIAN ANDAMONG THREE ETHNIC GROUPS NNTRAND ASSORTATIVE MATING /DISEASEAROUND THE VON HIPPEL LINDAUAT 17P13 INCLUDING THE P53 GENEBY THE PCR /AMPLIFICATION OF VNTRCHROMOSOMAL REGIONS AND OVER 60%DELETED IN ANGELMAN AND PRADERFOR OLIGOGENIC TRAITS BY LINKAGEFOR TYPE III COLLAGEN AND /OF THEIN FAMILIAL ALZHEIMER DISEASE /21IN HUMAN DNA /POLYMORPHICIN SCHIZOPHRENIA /GENETICIN THE HUMAN CHROMOSOMAL REGIONIN THREE CANADIAN ABORIGINALIN TOURETTE SYNDROME /GENELONG RANGE RESTRICTION MAPS /XPMAY BE INVOLVED IN OVARIANON CHROMOSOME 13 AND 17 IN HUMANON CHROMOSOME 20 /TO POLYMORPHICON CHROMOSOME 20 /TWO DIFFERENTON CHROMOSOME 3P ORDERED BYON CHROMOSOME 9034 IN ASHKENAZICON CHROMOSOMES 130 AND XP IN /ATON CHROMOSOMES 9 AND 11 /FORON THE LONG ARM OF CHROMOSOME 5ONE OF WHICH IS TIGHTLY LINKEDRELEVANT TO HERITABLE CONNECTIVEWITHIN AND BETWEEN FOUR ETHNICWITHIN THE PRADER WILLI /TO
LOCUS (5021 022) CONTAINS THE GENE(CYP2DP8) ON CHROMOSOME 22 WITH(DlS80) DETECTED BY THE PCR/A PUTATIVE PAGET DISEASE/CLINICAL EXPRESSION AT THE PEPD/CPG ISLANDS AT X024 X028
276012571565158915012485246950419791921975
2430157
144616061801228622142308S5123602221703
20962131217921442216
272028194223682205211621292282206620441468169623012942039169523922013192059818782182S8
19902266170920011912191320072111131322201961549
2339252452
218428242836285228372027605137325222000186863
2031199220992064259128292072217325662593
74218321612353606142
220879
35265
2299101
20352313192923272152
/DETERMINED BY AN X LINKED/DREIFUSS MUSCULAR DYSTROPHY/ECTODERMAL DYSPLASIA/EVOLUTION OF GLYCOPHORIN GENE/GENE AND THE CYSTIC FIBROSIS/HEMOCHROMATOSIS DISEASE/LETHAL MUTATIONS AT THE AGOUTI/LINDAU TUMOR SUPPRESSOR GENE/LINKED TO THE WILSON DISEASE/MAP OF THE MYOTONIC DYSTROPHY/NEAR THE ATAXIA TELANGIECTASIA/OF MUTATIONS AT THE NF1/OF THE PRION PROTEIN GENE/OF THE SPINAL MUSCULAR ATROPHY/OF THE SPINAL MUSCULAR ATROPHY/PHOSPHOGLUCONATE DEHYDROGENASE/SEQUENCES AT THE FRAGILE X/SUGGESTS A COMPLEX GENETIC/THE DIASTROPHIC DYSPLASIA/TO THE FRAGILE X SYNDROME/TO THE SPINAL MUSCULAR ATROPHY1 AND PHOSPHOGLYCOLATEAGAINST A COMPLETE GENETIC MAPAND FOUR DNA POLYMORPHISMS INAND THE CLOSE MARKER D13S31AS THE CLASSICAL FORM ON 90AT 3P21 /A TUMOR SUPPRESSORAT XP21 LINKED TO THE /X LINKEDBY ANALYSIS OF HAPLOTYPESBY ANALYSIS OF LINKAGE ANDBY HOMOLOGOUS RECOMBINATIONCOMBINATION STRATEGIES /OPTIMALCONTROL REGION /ANALYSIS OF THED15S10 IN PRADER WILLI SYNDROMEDNF15S2 WITH A HIGH DEGREE OFFOR MARFAN SYNDROME /A SECONDFOR SCHIZOPHRENIA AT XP21 OR ANFOR SUSCEPTIBILITY TO /AS THEFOR THE SPINAL MUSCULAR /DISEASEIN ASIAN BLACK CAUCASIAN /MUC1IN CONJUNCTION WITH HLA CLASSIN EMBRYONIC STEM CELLS /A 1IN FANCONI ANEMIA /GLYCOPHORIN AIN FANCONI ANEMIA LYMPHOBLASTSIN LESCH NYHAN FAMILIES FROMIN LI FRAUMENI SYNDROME A /RB1IN MEXICAN AMERICANS /RECEPTORIN NOONAN NEUROFIBROMATOSIS 1 /1IN THE CONTEXT OF YEAST /XIN XP11.23 /AROUND THE RP2MITOCHONDRIAL NUCLEAR GENE /TWOMODELS OF DISEASE /FOR TWOOF PHENYLKETONURIA FAMILIES INOF THE HUMAN X INACTIVATIONON 1501.5 02.1 /MARFAN SYNDROMEON 4035 /DYSTROPHYON 90 32 34 /SYNTHETASEON CHROMOSOME 15 /1 RELATEDON CHROMOSOME 17 /OVARIAN CANCERON CHROMOSOME 22 /TYPE 2ON CHROMOSOME 22 RESPONSIBLEON CHROMOSOME 6 /OF THE DMD LIKEON HUMAN CHROMOSOME 10ON SERUM LEVELS OF HDL C INON THE SUBTELOMERIC REGION OF 40ON XP11.3 /OF THE NORRIE DISEASEPROBES AS EVIDENCED BY APPARENTPROBES WITHIN AND AMONG /SINGLESPECIFIC PROBES DETECTION OFSTUDIES OF ASSOCIATION ANDTHE USE OF INTERVAL 6 AND 7 /AZFTO 13033.1 /OF ONE DISEASETO 5031.3 5033.3 /SYNDROMETO A 6 CM SUBREGION OF /ATAXIAUNDERLYING BIPOLAR AFFECTIVEVERSUS ADMIXTURE MODELS /THE TWOWITH 10 DNA MARKERS ON 150WITH FASTING INSULIN LEVELS INWITH SEVEN POLYMORPHIC DNAWITH YEAST ARTIFICIAL /THE FNRBWITHIN 17P11.2 /TYPE 1 (CMT 1A)WT1 /11P13 WILMS TUMOR
LOGIC PROGRAMMING APPROACH TOLOGISTIC MODELS FOR FAMILIAL DISEASES
MODELS IN LINKAGE ANALYSISLONDON DYSMORPHOLOGY DATABASE /THELONG ARM /EUCHROMATIC Y CHROMOSOME
ARM OF CHROMOSOME 11 AND /OF THEARM OF CHROMOSOME 20 /OF THEARM OF CHROMOSOME 22 /OF THEARM OF CHROMOSOME 4 ANALYZED /THEARM OF CHROMOSOME 5 /LOCI ON THEARM OF CHROMOSOME 9 /OF THEARM OF CHROMOSOME 9 /TYPE TO THEARM OF CHROMOSOME 9 KARYOTYPEARM OF HUMAN CHROMOSOME 11ARM OF THE HUMAN X CHROMOSOMEARM OF THE HUMAN Y CHROMOSOMEARM OF THE X CHROMOSOME CONTAINSCHAIN 3 HYDROXYACYL COACHAIN ACYL COA DEHYDROGENASECHAIN FATTY ACID TRANSPORTEVANS CINNAMON RATS /ACTIVITY INEVANS CINNAMON RATS /INLIMBED TYPE A PREVIOUSLY /OF THE
2032220711262625288321172239605
237323101955
14229821012112192823612311918200523322628206319161926820
258875381
194922442062338
2219229718812050199119432867100
246325352559105318922801
993731974278127181114
97110919662140232819772169901
23792134269020422196281028542171076910647193320011988190618832656195919502039126
203327861963134
2176201614621481167022081512598
15292184211821052015263
2316261512438823
OT SYNDROMES /THE INHERITANCE OFQT(ROMANO WARD) SYNDROME GENERANGE MAPPING OF THE X CHROMOSOMERANGE ORGANIZATION OF ALPHOIDRANGE RESTRICTION ENZYME MAPPINGRANGE RESTRICTION MAP OF HUMAN /ARANGE RESTRICTION MAP OF THERANGE RESTRICTION MAPS /XP LOCITERM CULTURE /LYMPHOCYTES INTERM EVALUATION OF THE LEUKEMICTERM FOLLOW UPS /ISSUES ANDTERM INBREEDING ON THE /OFTERM METABOLIC CONTROL /ANDTERM SURVIVOR WITH TRISOMY 18TERMINAL REPEATS IN HUMAN
LONGITUDINAL GENETIC ANALYSIS OF SAMELONGTERM SURVIVAL IN PALLISTER HALLLOS ANGELES COUNTY UNIVERSITY OF /THELOSS /12% HAD NONSYNDROMIC HEARING
/IN A FEMALE WITH REPEATED FETAL/WITH RECURRENT PREGNANCYAND FREQUENCY OF STRUCTURALAND SUBSEQUENT CLONAL EVOLUTIONDETECTION IN TUMOR SAMPLESDURING CARCINOGENESIS IN MICEFROM CHROMOSOMES 5 AND 7 ININ FAMILIAL AND SPORADIC OVARIANIN LEBER HEREDITARY OPTIC NISUALIN THE MULTIPLE ENDOCRINEOF CHROMOSOMAL HETEROZYGOSITY INOF CHROMOSOME 7 DERIVED MARKEROF HETEROZYGOSITY ANDOF HETEROZYGOSITY AT LOCI ONOF HETEROZYGOSITY IN CANCER /BYOF HETEROZYGOSITY ON 17P AND P53OF HETEROZYGOSITY ON CHROMOSOMEOF HLA COMPATIBLE FETUSESOF TUMOR SUPPRESSOR GENE BY /ANDOF Y CHROMOSOME /DISORDER SHOWING
LOSSES /FIRST TRIMESTER PREGNANCYON 3P IN SPORADIC RENAL CELLREVEALS THE PRESENCE OF TUMORTHROUGHOUT GESTATION /PREGNANCY
LOUISIANA ACADIAN POPULATION CLINICALLOW ACCEPTANCE RATE IN FAMILIES WITH
DOSE OF XRAYS IN DIFFERENT AGE /TODOSE RATE MODULATED MICROWAVE ANDFREQUENCIES OF N MYCFREQUENCY REPETITIVE DNA SEQUENCEGRADE GLIOMAS /CYTOGENETICS OFIN ISRAELI PATIENTS WITH DUCHENNELEVEL ELECTROMAGNETIC RADIATIONSLEVEL FRAGILE X EXPRESSION /OFMATERNAL SERUM HCG IN PRENATALMATERNAL SERUM HCG IN SECONDMSAFP IN SUCCESSIVE PREGNANCIESPENETRANCE FORM OF HEREDITARY /ARADIOSENSITIVITY ATAXIA /ANDRISK POPULATIONS /IN HIGH ANDSIGNAL POLYMORPHISM /INHERITEDSOCIO ECONOMIC STRATA IN SANTIAGOVOLTAGE EEG TO 20013.2 20013.3
LOWE SYNDROME /CANDIDATE GENE FORLP DELETIONS IN NEUROBLASTOMA TUMORSLP(A) GENE AND ATHEROSCLEROSISLP36 IN OVARIAN SEROUS ADENOCARCINOMASLPL DEFICIENCY /SEPARATE PROBANDS WITHLO DELETION AND 200 TRISOMY /OFL022 32 A KARYOTYPIC ASSOCIATION FORLUBAG (X LINKED DYSTONIA PARKINSONISM)LUMP OR TO SPLIT /DIGITAL SYNDROMES TOLUNG /SQUAMOUS CELL CARCINOMAS OF THE
ADENOCARCINOMAS /IN EIGHT PRIMARYCANCER /EXPRESSION IN SMALL CELLCANCER VICTIMS INCLUDING RADONCANCER WITH A CONSISTENT /INCARCINOMA /OF ONCOGENES IN HUMANCARCINOMAS /OF 14 SMALL CELL
LUPUS ERYTHEMATOSUS /WITH SYSTEMICLYMPHOCYTES DEMONSTRATE
LYASE INITIAL MOLECULAR /COALYMPHOBLASTIC LEUKEMIA /ACUTE
LEUKEMIA /WITH ACUTELEUKEMIA IN A GIRL WITH
LYMPHOBLASTOID CELL LINES FROM /ONCELL LINES FROM HUMANS
LYMPHOBLASTS /ATAXIA TELANGIECTASIA/IN ZELLWEGER SYNDROME/LOCUS IN FANCONI ANEMIAFROM PATIENTS WITH LEBER
LYMPHOCYTE ADENOSINE A2 RECEPTORS INCELL SURFACE MARKERS IN /OFCULTURES /IN HUMANCULTURES AS A METHODOLOGYCULTURES IN VITRO /IN HUMAN
LYMPHOCYTES /AGE GROUPS OF HUMAN BLOOD/ALTERATIONS IN PERIPHERAL/HPRT GENE IN MUTANT HUMAN/MRNA IN PERIPHERAL BLOODNIRUS WHICH INFECTS TACQUIRE MMC SENSITIVITYDEMONSTRATE INCREASEDFROM NORMAL PERSONS ANDFROM PATIENTS WITH /INFROM PATIENTS WITH DOWN
571
84321972109212022192142136121731624586
11412841524
146924243997061143
2312301540121813271317305
2581603
2032595
260913962056606244
2571257493221713561195260713733612023211
25422576584
21991298109824221550923113911352216779701282288120282352584162
13384707491520204463313151336224610224
1313138027334434881320132613245001438677505
2559513517625
254316082809254227162550108925901522443147313901531
Permuted Title Index
IN LONG TERM CULTUREIN PARENTS ARE HAZARDOUSINDUCED BY APHIDICOLIN INOF COLCHICINE TREATED /INOF NEUROBLASTOMA PATIENTSTO G2 PHASE X IRRADIATION
LYMPHOCYTIC LEUKEMIA (ALL L2) /ACUTELEUKEMIA /MARROW IN ACUTELEUKEMIA BY FLUORESCENT
LYMPHOID ENHANCER BINDING FACTOR 1NEOPLASIAS WITH THE /IN
LYM EOIA /ANAPLASTIC LARGE CELL/AND EXTRANODAL LARGE CELL/IN FOUR CASES OF NON HODGKIN/IN NON HODGKIN/IN UNTREATED NON HODGKINAND THEIR FAMILIES /MALIGNANTUSING PCR /IN LEUKEMIA AND
LYMPHOMAS /(11;18) TRANSLOCATION IN/FOLLICULAR B NON HODGKIN/P53 MUTATIONS IN BURKITT
LYMIIPHOPROLUFERATIVE DISEASE /X LINKEDDISEASE /X LINKEDDISEASE REGISTRY
LYNCH SYNDROME FAMILIES USING DATALYSENKOISM 1910 1990 /EUGENICS ANDLYSOSOMAL A GLUCOSIDASE /OF HUMAN
A GLUCOSIDASE /ROUTING OFCHOLESTEROL ESTERASE ABSENTDISEASE /AND ROLE INDISORDERS /DIFFERENTGLYCOGEN STORAGE DISORDERMEMBRANE TRANSPORT /OFSTORAGE DISEASES IN NORTHTRANSPORT AND RECYCUNG OFTRANSPORT OF VITAMIN B12
LYSOSOME CORRECTION OF STORAGE IN /THELYSOZYME /ACTIVE SITE HOMOLOGY WITH
1624113613521554138826951369134513551867225
1331618133313301363134910316231392259496812631082600321568581
2248286
2359529281558479476467528
M
M4 /NONLYMPHOCYTIC LEUKEMIA SUB TYPEM5 AND M6 ALPHA ANTITRYPSIN ALLELES
M5 AND M6 ALPHA ANTITRYPSIN ALLELESW ALPHA ANTITRYPSIN ALLELES /M5 ANDMAC FARLANE SYNDROME PROBABLY /ANDMACERATED INTRAUTERINE FETAL DEATH /OFMACHADO JOSEPH DISEASE /OF ONSET IN
JOSEPH DISEASE /STUDIES INJOSEPH DISEASE LINKAGEJOSEPH DISEASE THE /OF
MACROCEPHALY ASSOCIATED WITHMACROPHAGE COLONY STIMULATING FACTOR
KILLING FUNCTIONS /AII INMACROPHAGES /TARGETED TOMACULAR DYSTROPHY AN EXCLUSION MAP
TYPE OF BULLOUS DYSTROPHY TOMADELUNG'S DEFORMATION PATELLAMAF ONCOGENE PRODUCT /TO THE AVIAN VMAGENIS CONTIGUOUS GENE DELETION
SYNDROME (DEL(17)(P11.2))MAGNETIC RESONANCE IMAGING
RESONANCE IMAGINGRESONANCE IMAGING /BYRESONANCE IMAGING EXPOSURE
MAGNUM AND CORD INTEGRITY WITH REVIEWMAIN CYSTIC FIBROSIS MUTATIONS BYMAINE 1980 TO 1989 /DOWN SYNDROME INMAINTENANCE AND ANTICIPATORY GUIDANCEMAJORS OUTCOME OF 39 FETUSES AT RISKMALABSORPTION SYNDROME A COMMON CAUSEMALARIA /WITH PROTECTION FROM SEVERE
AMONG THE AO NAGAS NAGALANDMALARIAL POLYMORPHISMS IN SARDINIAMALAY PATIENTS WITH SYSTEMIC LUPUSMALDEVELOPMENT IN MAN /MALE SEXUALMALE /AND FRAGILE X IN A 4 YEAR OLD
CARRIERS /(6.16) TRANSLOCATION INFERTILITY GENE ON THE HUMAN Y /AGERM CELL TUMORS /ALLELOTYPING OFINFANT /SYNDROME IN A TURKISHMICE /CAN CAUSE MEIOTIC DAMAGE INPATIENTS WITH INFERTILITY /OF 115PHENOTYPE AFTER PRENATAL /NORMALPOPULATION OF BUDAPEST /IN THEPRONUCLEI AND METAPHASEPSEUDOHERMAPHRODITISM WITH /INSEX STEROID HORMONES AND DIETARYSEXUAL MALDEVELOPMENT IN MANSHOWN BY FLUORESCENT IN SITU /XXSIBLINGS /RETARDATION IN TWOSIBS A NEW SYNDROME /IN TWOSIBS WITH AUTOSOMAL RECESSIVETWIN /IN ONE MILDLY AFFECTEDWITH A RECOMBINANT CHROMOSOMEWITH MYELODYSPLASTIC SYNDROME /AWITH UNUSUAL MOSAICISM
MALENESS /IN THE ETIOLOGY OF 46,XXAND XX TRUE HERMAPHRODITISM
MALES /ABNORMALITIES IN TRANSSEXUAL/ON MEIOTIC PROCESS IN INFERTILE
1346239723972397769114954418891995233630
23602431552
20211990770
24591443170290814338992555744
18491134174
1185457
2618274926452733267141515632205611797
1371152514501166215315062767267169287082184914841589134714312225223712061193
/WITH GC PHENOTYPE IN ADULTAND TRUE HERMAPHRODITES AN XXEVIDENCE FOR GENETIC /FRAGILE XWITH CONGENITAL BILATERAL /IN
MALFORMATION /I AND A CEREBRAL A V/A CHILD WITH CONGENITALHIGHER RISK IN LEFT FLOWIN A FAMILY DISPLAYING XIN CHILDREN /CONGENITALOF DERIVATIVES OF THETRACHEOMALACIA PECTUS
MALFORMATIONS (SPLIT HAND) ON THREE/AND ASSOCIATED SYSTEMIC/AND CONGENITAL/AND FETAL CONGENITAL/AND MULTIPLE/ASSOCIATED WITH RENAL/CARDIOVASCULAR/CENTRAL NERVOUS SYSTEM/FOR ISOLATED HEART/WITH CONGENITAL/WITH MULTIPLEAND ANEUPLOIDY /FETALAND INHERITED DISORDERSAND SEVERE SWALLOWINGAND TWINNING A FAMILIALAS A DEVELOPMENTALAT A MATERNITY HOSPITALCLEFT LIP AND PALATEDURING HUMAN GESTATIONIN A FEMALE WITH X;3IN CHILDREN WITH CLEFTIN ISRAELI ARAB /MAJORNEW IDEAS FROM AREGISTER BEYOND
MALFORMED NEWBORNS AND THEIR MOTHERSMAU AFRICA WITH A VERY HIGH /INMAUGNANCIES /WITH HEMATOLOGIC
BY IN SITU HYBRIDIZATIONEVIDENCE FOR MENDELIAN
MALIGNANCY IN ONCOGENESIS OF PRIMARYMALIGNANT ASTROCYTOMAS /PATTERN IN
CELLS DERIVED FROM CHILDRENDISEASES /RELATED TO VARIOUSGLIOMA BY MICROCELL /HUMANHUMAN UROTHELIAL CELL LINESHYPERTHERMIA /GENE INHYPERTHERMIA /RISK FORHYPERTHERMIA SUSCEPTIBILITYHYPERTHERMIA SUSCEPTIBLE /INLYMPHOMA AND THEIR FAMILIESMELANOMA(DYSPLASTIC NEVUSMYELOID DISORDERS /AND 7 INPEDIATRIC BRAIN TUMORS /OFSCHWANNOMA CELL LINE /IN ASCHWANNOMA IN A PATIENT /ATUMOR /AFFECTED WITHTUMORS IN NEUROFIBROMATOSIS
MALNOURISHED CHILDREN /IN SECONDARYMALNUTRITION /CHROMATID EXCHANGE INMALTOSE AS A SUBSTRATE /BIOPSY USINGMAMMALIAN ALLELES INTERGENIC /NORMAL
CELLS /INDUCED MUTATIONS INCELLS /REARRANGEMENT INCHROMOSOME ORGANIZATIONCHROMOSOMES /OFCHROMOSOMES A NEW TOOL FORCHROMOSOMES IN YEAST /OFDEVELOPMENT /GENES INDNA CLONED AS YEAST /OFEQUIVALENT OF THE D /AS THEEXPRESSION CLONINGS /GENEHEXOKINASES /ANALYSIS OFSEX DETERMINATION /TO
MAMMARY PATHOLOGIES CYTOGENETICMANAGEMENT /DATABASE OF CALL
A FUSION OF OLD AND NEWOF GENITOURINARY ANOMALIESOF WILSON DISEASE /AND
MANDATE INCREASING THE RISK CUTOFFMANDIBULOACRAL DYSPLASIA VARIEDMANDIBULOFACIAL DYSOSTOSIS ANDMANIC DEPRESSIVE ILLNESS WITH MARKERSMANIFESTATION OF ADAMS OLIVER SYNDROME
OF TRISOMY SYNDROMEMANIFESTATIONS IN COWDEN DISEASE A
OF GAUCHER DISEASE BYOF THE CARBOHYDRATEOF VON HIPPEL LINDAU
MANIFOLD TRACE HUMAN TISSUES BY THEMANIPULATION OF MAMMALIAN DNA CLONEDMANTEL HAENSZEL PETO AND DERSIMIONIANMAP /ECLAMPSIA A PRELIMINARY EXCLUSION
/HUNTINGTON DISEASE THE PHYSICAL/LOCUS AGAINST A COMPLETE GENETIC/THE SEARCH THE GENETICAND AZF LOCUS THE USE OF INTERVALAROUND THE FACIOSCAPULOHUMERALAT THE CENTROMERE OF CHROMOSOME 1LENGTH /ESTIMATION OF CHROMOSOMEOF 24 LOCI ON THE LONG ARM OFOF CAENORHABDITIS ELEGANS /GENOMEOF CHROMOSOMAL REGION 4035OF CHROMOSOME 11P12 P14 /PHYSICALOF CHROMOSOME 18 /RECOMBINATION
2685982
26721067321760265068912889248706368855371290848724232868901696933127472680091588926887751031472956174626689492655282713091306
7125721332131213502568138342969810121911134913532581219
2600223213522226641586574
2627253425561643S132498
4943350
2400259226164301308179318052749471823878819203877911486165531872312509
5012931919298
2063S62910204221992076220821262212196
2188
OF CHROMOSOME 21 BY PULSED FIELDOF CHROMOSOME 8 /LINKAGEOF EIGHT CHROMOSOME 22011 012OF HUMAN CHROMOSOME 17 USINGOF HUMAN CHROMOSOME 19 /CONTIGOF HUMAN CHROMOSOME 19 STRATEGIESOF HUMAN CHROMOSOME 21 /HYBRIDOF HUMAN CHROMOSOME 4 /A PHYSICALOF HUMAN CHROMOSOME BAND 11P15.5OF MOUSE CHROMOSOME 18 HOMOLOGIESOF THE DOUBLE MINUTES HARBORINGOF THE DROSOPHILA GENOME /PHYSICALOF THE HUMAN DYSTROPHIN GENEOF THE HUMAN GLUCOCORTICOIDOF THE MOUSE X CHROMOSOMEOF THE MYOTONIC DYSTROPHY LOCUSOF THE PROXIMAL LONG ARM OF HUMANOF THE SHORT ARM OF CHROMOSOME 5OVER A 600 KB REGION CONTAININGSPANNING THE DIASTROPHIC /UNKAGETO CHROMOSOME BAND FLAVORSTO TWO DIFFERENT LOCI ONUSING CLONE POOLING SCHEMESUSING RFLPS AND HYPERVARIABLEWITH THE CYTOGENETIC AND GENETIC
MAPLE SYRUP URINE DISEASE /TYPE OFSYRUP URINE DISEASE CORRELATION
MAPPING /CHARACTERIZATION AND/CHROMOSOMES FOR X CHROMOSOME/FRAGMENTATION AND GENOME/HIGH RESOLUTION RESTRICTION/HYBRIDIZATION AND GENETIC/STRATEGIES FOR GENOME/SYNDROME GENE LINKAGEA NEW LOCUS AGAINST A /ONA STRATEGY FOR PHYSICALADDITIONAL INFORMATION ON THEAND A REDUCED RADIATIONAND DIAGNOSTIC CYTOGENETICSAND EXCLUSION AS THE /REFINEDAND EXPRESSION ANALYSISAND ISOLATION OF A CDNA INAND ITS USE IN RAPID /X027 28AND SEQUENCING OF YEASTAND SEQUENCING THE HUMANAND TECHNIQUES FOR ISOLATINGAROUND LOCUS DliS10 IN PRADERAROUND THE RP2 LOCUS INBY FLUORESCENCE IN SITU /PROBEBY IN SITU HYBRIDIZATIONDIAGNOSTICS AND FUNCTIONALFUNCTIONAL SEQUENCES /FORGENES FOR MULTIFACTORIAL /FORIN EXPERIMENTAL HYPERTENSIONIN PROXIMAL 100 AND /HYBRIDIN THE GENE REGION FOR SPINALMOUSE GENES /STRATEGIES FORNON HLA LINKED GENES IN TYPEOF A DINUCLEOTIDE REPEAT ATOF A GENE ENCODING AOF A GENE ENCODING HUMAN P58OF A HUMAN RADIATION REPAIROF A NOVEL MYC RELATEDOF A REGION OF CHROMOSOMEOF CANCER SUSCEPTIBIlUTYOF CHARCOT MARIE TOOTH DISEASEOF CHROMOSOME 110 MARKERSOF CHROMOSOME 19 BY /PHYSICALOF CHROMOSOME 21 MARKERS ANDOF CHROMOSOME 40 MARKERS INOF CHROMOSOME 9 BY /RESOLUTIONOF CLONED GENES BY LINKAGEOF DIHYDROPYRIDINE SENSITIVEOF DNA FRAGMENTS FROM 5011.2OF FAMILIAL AMYCTROPHICOF GENES DETERMINING TUBEROUSOF HIGHLY INFORMATIVE DNAOF HLA F ON 6P21.3 /GENETICOF HUMAN CHROMOSOME 22 /TOOF HUMAN CHROMOSOME 22 USINGOF HUMAN CHROMOSOMES USINGOF HUMAN CHROMOSOMES USINGOF HUMAN CLONES USING COT 1OF HUMAN GENOME ALU CLUSTERSOF IGFI/MANNOSE 6 PHOSPHATEOF IRS PCR AMPLIFIED YEASTOF LOCI DELETED IN ANGELMANOF MICRODELETIONS IN THE YOF MOUSE CHROMOSOME 7 AND THEOF MULTIPLE GAMMA GLUTAMYLOF NOTI LINKING CLONES ON /ANDOF ONE DISEASE LOCUS TOOF ORNITHINE DOF QUANTITATIVE TRAITS /FOROF SCAI ON CHROMOSOME 6POF SENESCENCE LOCUS ON HUMANOF THE A L IDURONIDASE GENEOF THE APC REGION /PHYSICALOF THE AZOOSPERMIA FACTOR TOOF THE DISTAL EUCHROMATICOF THE EMERY DREIFUSSOF THE FACIOSCAPULOHUMERALOF THE FRIEDREICH ATAXIAOF THE GENE /AND MORE PRECISEOF THE GENE FOR SPINAL
572
21192048195421502203176S892185214218631361239
225621231951231021842177213319184112183
52202121241058524
21672122249820842161251120452063207122022014183
199622592088205827851780S13221919742087
5492202S32186621702146240S32203523322128189121862215594141
1955182
1938203722011948218021101910202219682137199
2162158
2040208221311502216018682205S8621302191647
215320681993213423452206217621052207143
217877
1886
Permuted Title Index
OF THE GENE FOR WERNEROF THE GENE FOR X LINKEDOF THE GENE RESPONSIBLE FOROF THE GENE TO NEAR THE /ANDOF THE HUMAN CHROMOSOME 7022OF THE HUMAN GENOME /FOROF THE JUVENILE ONSET CEROIDOF THE LANGER GIEDIONOF THE MULTIPLE ENDOCRINEOF THE NEUROFIBROMATOSIS TYPEOF THE NORRIE DISEASE LOCUSOF THE REGION ASSOCIATED WITHOF THE REGION SURROUNDING THEOF THE X CHROMOSOME /RANGEOF THE X LINKED DYSTONIAOF THE X LINKED HYPOHIDROTICOF THE YEAST NUCLEAR GENOMEOF TWO HUMAN CEREBELLAR CDNAOF USHER TYPE II REGION ONOF VARIANT REPEAT UNITS ANDOF X LINKED CLASPED THUMB ANDOF XQ24 28 /CHROMOSOME BASEDOF YEAST ARTIFICIAL /PHYSICALON CHROMOSOMES X 4 5 AND 16ON Y CHROMOSOME /FACTORPANEL FOR THE PROXIMAL SHORTPROJECT /KINGDOM HUMAN GENOMEREAGENTS /HUMAN CHROMOSOME 13SITES OF DNA METHYLATION INSTRATEGIES IN THE MOUSESTUDIES /AND INITIALSTUDIES AROUND THE FRAGILESTUDIES ON HUMAN CHROMOSOME 4TECHNIQUE ASSOCIATION MAPPINGTHAT INCLUDES VIABILITY ANDTHE CRITICAL REGION INTHE DISEASE LOCUS FOR THETHE FRIEDREICH ATAXIA LOCUSTHE MOUSE SXR REGION IN YEASTTHE MULTIPLE ENDOCRINETHE ZELLWEGER SYNDROME GENESTO CHROMOSOME 22 BY SCREENINGTREACHER COLLINS SYNDROMEUNDER DIFFERENT MODELS OFUSING YEAST ARTIFICIAL
MAPS /CONSTRUCTION OF GENETIC LINKAGE/FILTRATION OF HUMAN LINKAGE/METHODS FOR UPDATING LINKAGE/RESOLUTION LINKAGE AND PHYSICAL/XP LOCI LONG RANGE RESTRICTIONCLOSE TO ERBB ON MOUSE /WOBBLERCLOSE TO THE FRAGILE SITE OF 2013CLOSE TO THE HUNTINGTON DISEASEFOR CHROMOSOMES 5 AND 10 /GENETICFROM NONDISJUNCTIONAL AND NORMALIN THE MOUSE /OF MITOTIC LINKAGENEAR THE NEUROFIBROMATOSIS TYPEOF HUMAN CHROMOSOME 16 /LINKAGETO 6021 022 AND IS LINKED TO MYBTO CHROMOSOME 12 /MUTATIONTO DISTAL IIP /DOPAMINE RECEPTORTO HUMAN CHROMOSOME 16 /GENE
MARCO POLO ALLELE /NEW MUTATIONS AND AMARFAN SYNDROME /A CANDIDATE GENE FOR
SYNDROME /A SECOND LOCUS FORSYNDROME /CASES WITH INFANTILESYNDROME /CLINIC FORSYNDROME /FIBRILLIN GENE FORSYNDROME IMMUNOHISTOPATHOLOGYSYNDROME LOCUS ON 1501.5 02.1SYNDROME LOCUS WITH 10 DNA /OFSYNDROME NO EVIDENCE FOR
MARFANOID HABITUS MICROCEPHALY MENTALMARKER (D10S97) TIGHTLY LINKED TO
ANTINEUTROPHIL CYTOPLASMICCHROMOSOME /OF FRAGILE X AND ACHROMOSOME /THE CASE WITH 14P+CHROMOSOME /WITH A SINGLE GIANTCHROMOSOME /WITH AN ADDITIONALCHROMOSOME 15 /WITH ACHROMOSOME BY CYTOGENETIC /ACHROMOSOME BY FLUORESCENCE INCHROMOSOME BY IN SITU /MINUTECHROMOSOME IN A /A PERSISTENTCHROMOSOME IN AN INFANT /OF ACHROMOSOME IN PRENATAL /OFCHROMOSOME WITH Y CHROMOSOME /ACHROMOSOMES AND OUTCOME OFCHROMOSOMES IDENTIFIED ATCHROMOSOMES IN AUTISM /SMALLCHROMOSOMES IN PRENATALCHROMOSOMES PRESENTATION OFCHROMOSOMES RESULTS IN THECHROMOSOMES USING FLOWD13S31 /LOCUS AND THE CLOSED19S63 SHOWS LINKAGE /ANONYMOUSDXS548 FOR PRENATAL DIAGNOSISFOR ALZHEIMER DISEASEFOR FETAL INFECTION /PLACENTALFOR NORRIE DISEASE /DIAGNOSTICLINKED TO MYOTONIC DYSTROPHYLOCI AROUND THE VON HIPPEL /RFVLOCI ON CHROMOSOME 3P ORDEREDSTUDIES OF POSSIBLE GENE /DNA
MARKER/RING CHROMOSOMES IN PATIENTS
1975 MARKERS /AGE AND THREE BIOCHEMICAL192113481907219220981972197612
21692196216811092109194911262371897215527891925373
2156185
16652139205422092449S36216537619712088205586
194381
185920902089225119332095218920602017159160
2173186421472399216385
20562372212413072010190322582246
941881727178793
34511091883
7788219562773168815441377140415351667171917001662154617241653149184
14511162146713961605192618751038745
113319451043605
216122101725
/CHROMOSOME 10 PERICENTROMERIC/DYSTROPHY AND CLOSELY LINKED/HUMAN AND MURINE CHROMOSOMAL/INFORMATIVE PERICENTRIC/OF 75 CHROMOSOME 5/OF EIGHT CHROMOSOME 22011 012/OF GENETIC AND BIOCHEMICAL/OF INCEST WITH POLYMORPHIC/OF LINKAGE TO 110 AND 140/OVARIAN TERATOMAS USING DNA/PARENTAL ORIGIN AND NEW/RELATED AND OTHER X SHORT ARM/THE REGION WITH FURTHER/UNLINKED TO CHROMOSOME 10
/WEIGHT DETERMINATIONS OF VNTRANALYSIS /WITH 17011.2 DNAAND CFTR GENE ANALYSIS INAND GENOMIC ORGANIZATIONAND OTHER MARKERS IN FAMILIALANEUPLOIDY BUT NOT FORASSOCIATED WITH QUANTITATIVEBY EXPLORING MICROSATELLITEBY FLUORESCENT IN SITUD11S424 AND /IS FLANKED BY THEDERIVED FROM SEX CHROMOSOMESFOR CHROMOSOME 21 /AS LINKAGEFOR CHROMOSOME 3 /PCR BASEDFOR ESTABLISHING GENETIC /RFLPFOR PREDICTIVE TESTING INFOR STUDYING DISEASES WITHFOR THE FRAGILE X SYNDROMEFROM CHROMOSOME X AND 11 /WITHFROM IRRADIATION HYBRIDS /24FROM THE MULTIPLE ENDOCRINEFROM THE PROXIMAL SHORT ARMIN AUTOSOMAL DOMINANT ANIRIDIAIN FAMILIAL AMYOTROPHIC /OTHERIN FIRST DEGREE FAMILYIN FOURTEEN DANISH FAMILIESIN HUMAN CHROMOSOMES ISOLATEDIN MID TRIMESTER PREGNANCYIN PRENATAL SCREENING FORIN RELATION TO /CHROMOSOME 40IN SCHIZOPHRENIA A DISCORDANTIN SCREENING FOR FETAL /SERUMIN THE DETECTION OF THELINKED TO BIPOLAR AFFECTIVELINKED TO MULTIPLE ENDOCRINELINKED TO MYOTONIC DYSTROPHYNEAR THE ATAXIA/I1QOF CHROMOSOME 110 /WITHOF DIFFERENT CHROMOSOMALOF XQ28 /SEVEN POLYMORPHIC DNAON 150 RESULTS OF AN /10 DNAON 4Q RESULTS OF AN /WITHON CHROMOSOME 200 /ADDITIONALON CHROMOSOME 20Q /WITH SIXON HUMAN CHROMOSOME 20 /DNAONTO THE COSMID CONTIG MAP OFPROGRESS IN MULTIPLEXING ANDRN1 AND VK23 USED IN THE /DNATO FRIEDREICH ATAXIA WITHIN /9TO STUDY THE ALZHEIMER
MARKOV CHAINS IN THE COMPUTER PROGRAMMAROTEAUX LAMY SYNDROME (MPS VI) BYMARPHANOID HABITUS AND LAMININ /WITHMARRIAGES DUE TO FETAL WASTAGE
IN ALIGARH /FIRST COUSINMARROW BY TRIPTERYGIUM HYPOGLAUCUM
CELLS BY BIOTINYLATED Y /BONECELLS IN VIVO AND THEIR /BONECELLS USING A REPLICATION /BONECELLS USING RECOMBINANT /BONECULTURES FOR CHROMOSOMAL /BONEFINDINGS IN 15 PATIENTS WITHIN ACUTE LYMPHOCYTIC LEUKEMIATRANSPLANT FOR /BONETRANSPLANT STUDIES /BONETRANSPLANTATION /BONETRANSPLANTATION /BONETRANSPLANTATION /IN UTERO BONETRANSPLANTATION NI BY BONETRANSPLANTATION FOR STORAGETRANSPLANTATION IN CANINE /BONETRANSPLANTATION TO FANCONI
MARROWS WITH NORMAL OR UNCERTAIN /BONEMARSHALL SYNDROME (MIM NUMBER 154780)MARTIN BELL SYNDROME IN AN IRANIANMASA (MENTAL RETARDATION APHASIA
SYNDROME IN X028 /RETARDATIONMASKED BY PREMATURITY AND CONGENITALMASS INDEX /OF BLOOD PRESSURE AND BODYMAST/STEM CELL GROWTH FACTOR /C KIT
CELL GROWTH FACTOR RECEPTORMASTERS LEVEL PROGRAM /WITH AMAT/1, + DER (1) T(1;12) (Q42.3;P12.2)
TRANSLOCATION /T(5;10)(P13;Q1 1.2)MATERIALS FOR USE IN HIGH SCHOOLMATERNAL AGE /ASSOCIATED WITH YOUNG
AGE /RATE IN ADVANCINGAGE /WITH RESPECT TOAGE AND NONTRISOMIC /BETWEENAGE AND THREE BIOCHEMICALAGE DEPENDENCE OF FETAL /ON
1215188828481861191422161954766
279019134101702193122181077252463510042187193816222080209311891967169920941978263019502701894203821082170199819601938625192320961208942
20379091155415194019821984195519861714195918832012196219652031220320621908189320572788561
10611236116418531676130124922490163813091345564166813671607154561156
247315222168551471737
1925711
2707189
2296177914401429178093612041523124812151268
AGE FREQUENCY OF PREGNANCYBLOOD BY PCR MAY ALSO LEADBLOOD FREQUENCIES MEASUREDBLOOD PROSPECTS FOR /CELLS INCELL CONTAMINATION INCELL CONTAMINATION IN /ANDCIRCULATION /CELLS IN THECIRCULATION /FROMCIRCULATION ISOLATION BY /THECONTROL OF PATTERN FORMATIONDISOMY FOR CHROMOSOME 7 /WITHDISOMY IN PRADER WILLI /OFDISOMY OF CHROMOSOME 4 ANDEXCLUSIONS /BY APPARENTGENES INVOLVED IN THE /OF THEHEREDITY TYROSINEMIA IIPHENYLKETONURIA /AMERICANPHENYLKETONURIA PREGNANCYPROTEIN S DEFICIENCY ARACE AND WEIGHT ON HCG ANDRACE ON MSAFP AND AFAFP /OFSERUM BIOCHEMICAL SCREENINGSERUM DOWN SYNDROME /ENHANCEDSERUM HCG AND FETAL VENTRALSERUM HCG IN PRENATAL /LOWSERUM HCG IN SECOND /LOWSERUM HCG PROSPECTIVE STUDYSERUM MARKERS IN SCREENINGSERUM SCREENING FOR FETALTOBACCO SMOKE INHALATION ANDTRACE ELEMENTS AND FETALTRANSLOCATION WITH /DUE TOTRANSMISSION OF DELETED /NOWEIGHT ADJUSTMENT ON /OFWEIGHT ADJUSTMENT ON MSAFPWEIGHT AND LEVELS OF B HCGWEIGHT AND RACE /EFFECTS OF
MATERNALLY INHERITED DUPLICATION OFINHERITED MYOPATHY ANDRELATED RELATIVES /THEIR
MATERNITY HOSPITAL IN OSAKA CITY 1948MATHEMATICAL PATHOLOGIES INHERENT INMATING /DISEASE LOCI AND ASSORTATIVE
ON LINKAGE ANALYSIS AMATINGS IN FAMILIES WITH FRAGILE XMATRIX /SPECIMENS COLLECTED ON A PAPER
GENES DURING DEVELOPMENT OF /OFMATURATION /STUDIES OF HUMAN OOCYTE
GENE TO THE Y CHROMOSOMEOF PROSAPOSIN SIALIDASE INOF SEGREGANTS /DIFFERENTIAL
MATURITY ONSET DIABETES OF THE YOUNGMAXIMUM LIKELIHOOD SCORING TECHNIQUEMB CONTEXT OF XQ28 DNA /GENE IN A 1
DUCHENNE MUSCULAR DYSTROPHY GENEOF THE EXCISION REPAIR GENE ERCC4
MB1 FAMILY OF MIRROR REFLECTED ANDMCL 1 HAS SIGNIFICANT HOMOLOGY TO BCLMDM2 TRANSFORMING GENE /THE MOUSEMDX TRANSGENIC MICE /DYSTROPHIN INMEANS OF ANALYSIS OF HUMAN HEART /BY
OF ASO REVERSE DOT BLOT /BYOF RFLP LINKAGE ANALYSIS /BYTO INCREASE PATERNAL /AS AVARIANCES AND CORRELATIONS OF
MEASURE OF SIMILARITY OF DNA /NEWMEASURES OF LIPID METABOLISM IN /OF
USING A MAXIMUM LIKELIHOODMECONIUM PERITONITIS NOT ASSOCIATEDMEDIATED CHROMOSOME TRANSFER AND
CHROMOSOME TRANSFER AND XDIRECT GENE TRANSFER TO THEDISRUPTION OF SUPPRESSOR GENEDNA AMPLIFICATION /BY PCRGENE DETECTION AND /BY LIGASEGENE TRANSFER /BY RETROVIRALPCR /SORTING AND ALU ELEMENTSITE DIRECTED MUTAGENESISTERATOGENS /OF RECEPTORTRANSDUCTION OF ORNITHINETRANSFER OF CHROMOSOME 9
MEDICAL AND CULTURAL IMPLICATIONSCENTER /OF SOUTHERN CALIFORNIAETHICS MAY NOW MANDATEGENETIC COUNSELING AND SOCIALGENETICS /ETHICAL ISSUES INGENETICS /SYSTEM FORGENETICS COUNSELING NERSUSGENETICS DEPARTMENT AT ROBERTGENETICS IN JAPAN /INGENETICS IN THE DIVISION OFGENETICS IN THE USSR MEDICALPUBLIC /FOR EDUCATION OF THESCHOOL /GENETICS IN THE USSR
MEDICINE FOR LATE ONSET DISORDERS THEMEDICINES /AFRICAN TRADITIONAL HERBALMEDITERRANEAN /AND HB S IN THE EAST
FEVER /IN FAMILIALFEVER A GENETICFEVER PATIENTS /FAMILIALFEVER PATIENTS ANDPOPULATION /A HIGH RISKPOPULATIONS /ON THREE
MEDIUM CHAIN ACYL COA DEHYDROGENASECHAIN ACYL COA DEHYDROGENASE
573
12181060113160
118712281151101093231712159315822810143245221283611581144122430831018269231139108
11551844129612901329228120311691255114050235
9772688121620271899854577930124023494951552
74270020418
17092433258913612480223318491021175951564
515270088720891891S9125871627104124911605997
129124772568
281143182317701821181117817333321782335396335248
2557390187285815541245250
2838195265
Permuted Title Index
CHAIN ACYL COA DEHYDROGENASECHAIN ACYL COA DEHYDROGENASECHAIN ACYL COA DEHYDROGENASECHAIN ACYL COA DEHYDROGENASECHAIN ACYL COA DEHYDROGENASECHAIN ACYL COA DEHYDROGENASE
MEDULLA OBLONGATA CDNA LIBRARIES /ANDMEDULLARY THYROID CARCINOMA IS NOTMEDULLOBLASTOMAS /IN EPENDYMOMAS ANDMEGACYSTIS MICROCOLON INTESTINALMEGALOCORNEA MENTAL RETARDATION
MENTAL RETARDATION 2MEIOSIS /HAZARDOUS FOR DISJUNCTION IN
/NONDISJUNCTIONAL AND NORMAL11 NONDISJUNCTION ON HIS /TOINVESTIGATIONS IN THE FIELD
MElOTIC AND SOMATIC NONDISJUNCTION INDAMAGE IN MALE MICE /CAN CAUSENONDISJUNCTION /HIGH RISK FORPROCESS IN INFERTILE MALES /ONPROPHASE /CHROMOSOME 21 INRECOMBINATION MAP OF THERECOMBINATION OF A COMPLEX /TOSEGREGATION IN AN INSERTIONALSTAGE OF NONDISJUNCTION EVENTS
MELANOGASTER /H2A GENE IN DROSOPHILA/LIFESPAN OF DROSOPHILAGENE PRODUCT CC /OF THE D
MELANOMA /CHROMOSOME 9P INVOLVEMENT INMELANOMA/DYSPLASTIC NEVUS SYNDROMEMELLITUS /GENE IN TYPE II DIABETES
/INSULIN DEPENDENT DIABETESAND CEREBELLAR ATAXIAAS A HUMAN TERATOGENRHEUMATOID ARTHRITIS ANDRISK AN EPIDEMIOLOGIC
MELPHALAN INDUCED MUTATIONS IN /OFMELTING POLYMORPHISMS A POTENTIALLYMEMBRANE ALPORT ALLOANTIBODIES
BAND 3 IN JAPANESE BRAZILIANSGLYCOPROTEIN GENE PCI MAPSPROTEIN CDNA AND INITIALPROTEINS /OF PEROXISOMALPROTEINS IN PATIENTS WITHTRANSPORT /OF LYSOSOMAL
MEMBRANOUS LIPODYSTROPHY NASUMEMORY TEST APPLIED TO TWINSMEN2 GENE /A CANDIDATE FOR THEMENDEUAN DISORDERS IN THE PREGNANT
INHERITANCE /EVIDENCE FORMENINGIOMAS /AND BEHAVIOR IN 32MENINGOCELE TESTING LINKAGE TO HLAMENKES DISEASE /IN THE STUDY OFMENOPAUSE A TWIN STUDY /AGE ATMENTAL DEFICIENCY AND ITS /HEREDITARY
DEFICIENCY PARTIAL /ATAXIARETARDATION (MASA SYNDROME) INRETARDATION /ASSOCIATED WITHRETARDATION /ASSOCIATED WITHRETARDATION /IN NONSPECIFICRETARDATION /OF GENES CAUSINGRETARDATION /TRANSLOCATIONS ANDRETARDATION 2 /(MEGALOCORNEARETARDATION A NEW SYNDROMERETARDATION AND /MICROCEPHALYRETARDATION AND CEREBELLARRETARDATION AND CHROMOSOMERETARDATION AND NORMAL /SLIGHTRETARDATION APHASIA SHUFFLINGRETARDATION ASSOCIATED WITH ARETARDATION CYTOGENETIC ANDRETARDATION GENETIC COUNSELINGRETARDATION IN CARRIERS OFRETARDATION IN THREE SIBS ARETARDATION IN TWO MALE /SEVERERETARDATION LINKED TO DXS369RETARDATION REPORT OF SECONDRETARDATION SHORT LIMBED /OFRETARDATION SYNDROMERETARDATION SYNDROME THE DEEPRETARDATION SYNDROME WITHRETARDATION WITH ATAXIA ANDSTATES SEEN IN TWINS /AND
MENTALLY HANDICAPPED IN BRAZIL /FORRETARDED CHILDREN AINRETARDED CHILDREN /INRETARDED CHILDREN AND IN IINRETARDED PATIENTS EXAMINEDRETARDED PATIENTS IN HAVANARETARDED POPULATION OF /INRETARDED SCHOOL CHILDREN IN
MERZBACHER DISEASE /(PELIZAEUSDISEASE /CAUSES PELIZAEUSDISEASE /IN PELIZAEUSDISEASE /WITH PELIZAEUSDISEASE /WITH PELIZAEUS
MESENCHYMAL ORIGIN (IN TUMORS OFMESODERMAL DYSPLASIA SPECTRUM CONCEPTMESOMEUC DYSPLASIA WITHMETA ANALYSIS IN CLINICAL TERATOLOGYMETABOUC CONTROL /AND LONG TERM
CORRECTION OF NIEMANN PICKDISEASE /TRANSPLANTATION FORDISORDERS A RESEARCH ANDSCREENING ON MENTALLY /AND
4754989751119227723772333188813607536246241136
8514191710124513711577119342019511422117116542456281924002231353722
2711502674
266327082534249383
26291307190945465281873S8523471246
7113101953571
27552735645192552175652020151409624888882668
27681500737
1430107967568789087019467106886247168529632772161748051912851630754149318549719721101108323582586859738
1293524
24911577841854
METABOUSM (CHANNEL II) /ERRORS OF/FOR HUMAN IRON(INBORN ERROR OF/INBORN ERRORS OF COL2A1/SPOTS AND INBORN ERRORS OF/STUDY OF COUMARINAND THE AGE OF ONSETIN CARRIERS OFIN FIBROBLASTS /AND FLAVININ FRENCH CANADIANS /LIPIDIN HIGH RISK PATIENTS ININ LONG EVANS CINNAMON RATSIN THE 3T3 CELL LINE AREOF DEBRISOQUINE/SPARTEINEOF S CARBOXYMETHYL L /POOROF THE CBLC FORM
METABOUTE PROFILE OF /URINARYMETABOLIZING ENZYMES RELEVANCE TOMETAL DEPENDENT ENZYMES AND RESPONSESMETALS USED IN INDUSTRY /BY NEWERMETAPHASE CHROMOSOMES /ON HUMAN
CHROMOSOMES /PRONUCLEI ANDNUCLEI /TO INTERPHASE ANDRING/PLATE /IN THE
METAPHASES /OF THE QUALITY OF G BANDEDMETAPHYSEAL DYSPLASIA ANALYSIS OF AMETHIONINE MALABSORPTION SYNDROME A
SYNTHASE ACTIVITY ANDMETHODOLOGY FOR GENOTOXICITY /AS AMETHOTREXATE IN HUMAN EMBRYONIC CELLSMETHYL BRANCHED CHAIN FATTY ACYL COAMETHYLADENINE DNA GLYCOSYLASE CDNA (3METHYLATION /MOLAR PREGNANCY AND DNA
AND X INACTIVATIONIN GENOMIC DNA /OF DNAIN THE ANGELMAN AND /DNAOF AN INACTIVE DERIVATIVEOF CPG SEQUENCES ON THEOF X LINKED TRANSGENESPATTERN /EXHIBIT A COMPLEXSTATUS OF AN X LINKED
METHYLCOBALAMIN LEVELS IN CULTUREDMETHYLCYTOSINE IS PREVENTED BY A /AT 5METHYLENETETRAHYDROFOLATE REDUCTASEMETHYLGLUTACONIC ACIDURIA WITH NORMALMETHYLGLUTACONYL COA HYDRATASE /3METHYLGUANINE/04 METHYLTHYMINE DNA /06METHYLMALONIC ACIDEMIA (CBL F) AND
ACIDEMIA/HOMOCYSTINURIAACIDURIA /CBIC TYPE OFACIDURIA /THERAPY OF MUT
METHYLMALONYL COA MUTASE ACTIVITY INCOA MUTASE DEFICIENCYCOA MUTASE FOR
METHYLTHYMINE DNA REPAIRMETHYLTRANSFERASE GENE /DNA REPAIRMEXICAN AMERICANS /RECEPTOR LOCUS IN
POPULATION /DISORDER IN AMHC ANTIGENS BY INTERFERON GAMMA IS
CORRESPONDS TO A MOUSE HSP70 /THEHAPLOTYPES IN EAST ASIA AND /OFON CHROMOSOME 6P /TO THESUSCEPTIBILITY GENES OF
MIAO AND LISU NATIONALITIES OF /YIMICE /AND HYPERHAPLOIDY FREQUENCY IN
/ATHEROSCLEROSIS IN TRANSGENIC/CAN CAUSE MEIOTIC DAMAGE IN MALE/DYSTROPHIN IN MDX TRANSGENIC/FACTOR IX GENE IN TRANSGENIC(IN MAN FROM STUDIES IN/IN PAROTID GLAND OF TRANSGENIC/IN PRIMARY SEX DETERMINATION IN(IN THE BRAINS OF HPRT DEFICIENT/LOSS DURING CARCINOGENESIS IN/ON PHENOTYPE OF SEX REVERSEDAND POSSIBLE ANIMAL MODELS (INBY GENE TARGETING IN MOUSEDISPLAY CLINICAL FEATURES OFPRODUCES A PHENOTYPE OF ATHAT CARRY A MUTANT COPY OF THETHAT OVEREXPRESS S1OOB PROTEINWITH GLUCOCEREBROSIDASE GENE
MICRO CELLMEDIATED CHROMOSOME /BYENCAPSULATED NONAUTOLOGOUS CELLSENCAPSULATED RECOMBINANT
MICROCELL FUSION /A #3P CHROMOSOME VIAMEDIATED CHROMOSOMEMEDIATED CHROMOSOMEMEDIATED TRANSFER OF /BY
MICROCEPHALY AND SHORT STATURE INFACIAL ABNORMALITIESINFANTILE SPASMS ANDMENTAL RETARDATION ANDMENTAL RETARDATION AND
MCROCHROMOSOME ASSOCIATED WITH AMICROCLONING IN HUMAN GENETIC DISEASE
TECHNIQUE /PCR ANDMICROCOLON INTESTINAL HYPOPERISTALSISMICRODELETION /F508 CYSTIC FIBROSIS
DEL (13)(032.3033.2) /AMICRODELETIONS IN THE Y CHROMOSOME OF
OF CHROMOSOME 17P13 INMICRODIFFERENTIATION /OF POPULATIONMI1CRODISSECTED CHROMOSOMAL DNA /FOR
CHROMOSOMAL MATERIAL
1843236343945
811540233
2426497515
26754387985515425085384282127256316112153182
1580161863445750116081559527
2258928147
244922241659165216602436959501
2552501121712172401476508531532570511532
2401240128012719210318622876193287627691594192
1371248024872422444432478305222718682493418
2461799419
250323012470248113951891208925687828888526688821703253220617531092647
220558
286525102053
MI1CRODISSECTION AND MOLECULARAND MOLECULARAND PCR MICROCLONINGOF HUMAN Y CHROMOSOMEOF MAMMALIANPCR /USING CHROMOSOMEPROBES AND HTF /LASER
MICROFIBRILS /ANALYSES OFMICROGNATHIA AND OTHER ANOMALIES /WITH
ASSOCIATED WITH MINORIN TWO UNRELATED PATIENTS
MICROHETEROGENEITES DETECTED BY /GENEMICROINJECTED POLYSPERMIC HUMAN /OFIWCROMELIA AND MILD MENTALMICRONUCLEAR CHROMOSOME DNA REPAIRMICRONUCLEUS LEVEL IN HUMAN NORMAL /OF
TEST APPLIED IN PATIENTSMICROPHTHALMA AND ANTERIOR CHAMBERMICROSATELLITE DNA POLYMORPHISMS IN
POLYMORPHISMS WITHINREFLECTS THESEQUENCES /BY EXPLORING
IWCROSATELLITES /AND HYPERVARIABLE/OF SEQUENCES FLANKING
MICROSCOPIC ARCITECTURE /OF FETALSTUDY OF THE BANDING AND
MICROSCOPY /HYBRIDIZATION IN ELECTRON/WITH DIGITAL IMAGINGHIGH RESOLUTION /ELECTRONRESULTING IN CLEARER
MICROSOMIA /ANOMALIES IN HEMIFACIALMICROSPHEROCYTOSIS/WITH HEREDITARYMICROTUS AGRESTIS /IN THE FIELD VOLEMCROWAVE AND RADIO FREQUENCYMD PREGNANCY /UNCONJUGATED ESTRIOL IN
TRIMESTER /AND UE3 LEVELS IN THETRIMESTER AMNIOCENTESIS /BYTRIMESTER AMNIOCENTESIS (VERSUSTRIMESTER HCG AND UNCONJUGATEDTRIMESTER PREGNANCY SCREENING IN
MIDDLE ASIA FAMILIAL ISOLATE /ENRICHEDMIDUNE MALFORMATIONS AS A /OFMIDTRIMESTER AMNIOCENTESES WHAT ARE
OLIGOHYDRAMNIOS /CVS ANDULTRASONOGRAPHY /ABNORMAL
MGRAINE HEADACHE IN VIRGINIAN ANDMIGRATION /FOUNDER EFFECT AND GENE
OF HUMAN FIBROBLASTS WITHROUTES OF THE ANCESTRAL
MIGRATIONS (OF ANCIENT MONGOLOIDMGRATORY PROPERTIES OF TRANSPLANTEDMILLER (POSTAXIAL ACROFACIAL /CASE OF
DIEKER SYNDROME /INDIEKER SYNDROME AND ISOLATED
MIM 27268 /HYPOPLASIA/APLASIA SYNDROMENUMBER 154780 /MARSHALL SYNDROME
MIM` 102150 REPORT OF A SECONDMIMIC LINKAGE TO THE BOUNDARY OF THEMINIGENES AND DYSTROPHIN HOMOLOGOUSMNIMAL DYSMORPHIC FEATURES SLIGHT
PHENOTYPIC ANOMALIES IN THREEREGIONS FOR 23 FEATURES OF /OF
MINISATELLITE ALLELE DISCRIMINATIONMINISATELLITES /AND MUTATION IN HUMANMIISTRY OF SCIENCE AND TECHNOLOGYMINNESOTA EXPERIENCE /THEMINOR EAR ANOMALIES A NEW DOMINANTLY
ELEMENTS IN SICKLE CELL DISEASEMINORMES /FOR UNDERSERVED AND ETHNIC
FAMILY /OF HAN AND ZHUANGMINORITY NATIONALITY IN CHINA /GROUP AMINUTE CHROMOSOMES IN /DOUBLE
MARKER CHROMOSOME BY IN SITUIANUTES HARBORING THE MOUSE MDM2MIRROR REFLECTED AND WIDE SPREAD /OFMISCARRIAGE RATE IN ADVANCINGMISDIAGNOSIS OF HBS KORLEBU ON /DUE TOMISMATCH CLEAVAGE INCLUDING A
CLEAVAGE OF 14 EXONSREPAIR IN HUMAN CELLSREPAIR SYSTEM /SHORT PATCH
MISMATCHED BONE MARROW TRANSPLANT /SEXMISSENSE MUTATION (VAL ILE) IN THE /A
MUTATION IN TWO MILDLY /AMUTATION IS RARE IN FAMILIALMUTATION SER106 PRO IN THEMUTATIONS /CARRY THE SAMEMUTATIONS AND EVOLUTIONARYMUTATIONS AND MILD
MISSING PERSONS (INVOLVINGTEETH AND SEVERE HYPERHIDROSIS
MITOCHONDRIA STUDIED BY DNA /TOMITOCHONDRIAL AND PEROXISOMAL B
DISEASES /ANALYSIS OFDISEASES /MODELS OFDISORDERS /TO TWODNA ANALYSIS CONFIRMSDNA ANALYSIS REVEALSDNA AND GENETIC /OFDNA AND OUANTITATION OFDNA AND RNA IN /OFDNA AND THE DISPERSALDNA AND THE SPREAD OFDNA CAN BE AN EFFICIENTDNA CONTROL REGION
574
5662225322061S132070S7746011282676210331258888183813541344149420039882800209320212097117442014762087206620858424651710257612551144920
12411197120819478891180115011292658S4
144528762610
21797167358
681855667
203417
15001555152827893131234564826
2127179028511856137217001361243312041824281410332544255216681071281428111045221
263270
2861841
240626019136
2781263726101019437
24272614168
21002635
Permuted Title Index
DNA COPY NUMBER AINDNA CYTOCHROME BDNA DAMAGE IN CHRONICDNA DISEASEDNA DISEASESDNA GENE FAMILY /SAMEDNA IN AFRICAN /OF HUMANDNA IN KEARNS SAYREDNA LEADING TO THE /INDNA POLYMORPHISM INDNA POLYMORPHISM INDNA POLYMORPHISMSDNA POLYMORPHISMS INDNA REARRANGEMENTS INDNA SEQUENCEDNA TO A CHILD OF AENCEPHALOMYOPATHY /INENCEPHALOMYOPATHY /WITHENCEPHALOPATHIES /OFGENOME IN A SYNDROME OFIRON SULFUR PROTEINS /OFLONG CHAIN FATTY ACIDMUTATIONS ASSOCIATED /OFMYOPATHIES /AND RNA INMYOPATHY ENCEPHALOPATHYMYOPATHY IMPLICATIONSMYOPATHY WITH /WITHNUCLEAR GENE MODELS ANDPOINT MUTATIONS /WITHPROCESSING (TYPE 11) /ATRNA LEU(UUR) GENE /THE
MrTOTIC LINKAGE MAPS IN THE MOUSE /OFNONDISJUNCTION IS INDUCED BYRECOMBINATIONSEGREGATION /AND PROPER
MIXED DEAFNESS SYNDROME /FACIESGONADAL DYSGENESIS /FEMALE WITH
MIXOPLOID DOWN SYNDROME /ORIGIN OFMIYAMA AN THE ISOLATED COMMNUNITYML 1 CELL LEUKEMIA MCL 1 HAS /MYELOIDMLC ALK PRE MRNA OF DROSOPHILA /OF THEMMC SENSITIVITY AFTER BONE MARROWMN1i HHAI RFLPS BY DENATURING /OFOBTY POLYMORPHISMS ON AGAROSE GELS
SHIFTING NUCLEOTIDE ANALOGSMODE A PREDICTIVE STUDY /AND IMBALANCEMODEL /AN UNDERLYING LIABILITY
/DEFICIENCIES IN A LARGE ANIMAL/INACTIVATIOW/REACTIVATION A/ORIGIN OF MAN A CYTOGENETICAND POSSIBILITY OF LIKELIHOODFOR A HUMAN COFACTOR DEFICIENCYFOR ACHONDROPLASIA /FELINEFOR ANALYSIS OF EUKARYOTIC GENEFOR CRANIOSYNOSTOSIS /RABBITFOR INHERITED CATARACTS /ANIMALFOR RETINITIS PIGMENTOSA /ANIMALFOR STUDYING THE DEVELOPMENTALFOR THE DETECTION OF CHRYSENEFOR TRAINING ADOPTION WORKERSOF GAUCHER DISEASE /A MOUSEOF NIEMANN PICK DISEASE /MOUSEOF NIEMANN PICK DISEASE /MOUSEOF NIEMANN PICK DISEASE /MOUSEOF WILSON DISEASE I COPPER ANDOF WILSON DISEASE 11 SERUMSYSTEM /USING CHICKENS AS ATO ACCOUNT FOR SYMMETRICALTO EXPLAIN UNUSUAL PEDIGREES INWITH EMPHASIS IN FAMILY DOCTORWITH NO SOMATIC REVERSION /DOG
MODELING GERMINAL MOSAICISM IN XOF PROTEINS FROM GENE
MODELS /CRANIOFACIAL ANOMALIES MOUSE/DEVELOPMENTS IN REGRESSIVE/IN MICE AND POSSIBLE ANIMAL/THE TWO LOCUS VERSUS ADMIXTUREAND THEIR APPLICATION TO TWOFOR EVALUATING THE RISK OFFOR FAMILIAL DISEASES AFOR HUMAN BREAKAGE SYNDROMESFOR SCHIZOPHRENIA /ANDIN LINKAGE ANALYSIS OF COMPLEXIN THE STUDY OF HEREDITARYOF DISEASE /FOR TWO LOCUSOF GENETIC INTERFERENCE USINGOF MITOCHONDRIAL DISEASESOF POPULATION /AMERICA TESTING
MODERN DNA SEQUENCES /FROM ANCIENT ANDPEOPLE /DNA AND THE SPREAD OF
MODES OF INHERITANCE /UNDER COMPLEXMODIFICATON AND INTRACELLULAR
AND MANIPULATION OFMODIFED MYOBLASTS GRAFTED INTO MOUSEMODULATED MICROWAVE AND RADIO /RATEMODULATION BY INITIATION FACTOR EIF 4EMOLAR PREGNANCIES /REPEAT
PREGNANCY AND DNA METHYLATIONPREGNANCY AND LIVE FETUSSOLUTIONS OF TRACE AND MINOR
MOLECULAR ABNORMALmES OF COLLAGENANALYSES OF FAMILIES WITHANALYSIS /OF PCR BASEDANALYSIS /PRENATALLY BYANALYSIS /PROSPECTS FOR
34973671313233
2639995111528462878252026332447262222897733
10105024822611022242710172447437278110644901017205615772554166388313861428285725892438152226522789207815622786247815712620206723128092619931
2268799
2437134317762503627798875438512
2080264327761816464
2808247341S5818681906278111272786297123
1963S8
2718209536
2865315168
271458150
248825762450940928115421273501713104316612541
ANALYSIS AND CLINICALANALYSIS IN ANGELMAN /ANDANALYSIS OF A XQ /ANDANALYSIS OF ACID B /DISEASEANALYSIS OF APE CDNAANALYSIS OF B THALASSEMIAANALYSIS OF CARNITINEANALYSIS OF CHROMOSOME /ANDANALYSIS OF CHROMOSOME 11ANALYSIS OF DISTAL 15011013ANALYSIS OF DNA FROM DRIEDANALYSIS OF DOMINANTANALYSIS OF GASTRICANALYSIS OF GENOMIC CHANGESANALYSIS OF MALIGNANTANALYSIS OF MEDIUM CHAINANALYSIS OF MUTATIONSANALYSIS OF PATIENTS WITHANALYSIS OF PRION ALLELESANALYSIS OF QUANTITATIVEANALYSIS OF SEGMENTALANALYSIS OF SMITH MAGENISANALYSIS OF SOME WIDESPREADANALYSIS OF THE /AANALYSIS OF THE DELETIONANALYSIS OF THE GENE FORANALYSIS OF THE IDURONATEANALYSIS OF THE JAPANESEANALYSIS OF THE LACTASEANALYSIS OF THE LOCUSANALYSIS OF THE X028 REGIONANALYSIS OF TUMOR SECTIONSANALYSIS OF VAN DER WOUDEAND BIOCHEMICAL EVIDENCEAND BIOCHEMICAL STUDIES INAND CYTOGENETICAND CYTOGENETIC EVALUATIONAND EVOLUTIONARY ANALYSISAND GENETICAND GENETIC CHARACTERIZATIONAND PHENOTYPICAND PHENOTYPIC CORRELATIONSAND PHENOTYPIC CORRELATIONSAPPROACHES /NEWAPPROACHES IN PRENATAL /ANDAPPROACHES TO SCREENING FORASPECTS OF MEDIUM CHAINBASIS OF A CLASSICAL TYPEBASIS OF BETA THALASSEMIABASIS OF CANINE MUSCLEBASIS OF HUMAN LONG CHAINBASIS OF PHENYLKETONURIABASIS OF PHENYLKETONURIABASIS OF PHENYLKETONURIA INBASIS OF PROLIDASEBASIS OF THE FRAGILE XBIOLOGY AND PATHOGENESISBIOLOGY AND TREATMENTCHARACTERIZATIONCHARACTERIZATION IN MANCHARACTERIZATION OFCHARACTERIZATION OFCHARACTERIZATION OFCHARACTERIZATION OF ACHARACTERIZATION OF ACHARACTERIZATION OF ACHARACTERIZATION OF ALPHACHARACTERIZATION OF ANCHARACTERIZATION OF ANCHARACTERIZATION OF BCHARACTERIZATION OF BETACHARACTERIZATION OF GIEMSACHARACTERIZATION OF HUMANCHARACTERIZATION OF HUMANCHARACTERIZATION OF MARKERSCHARACTERIZATION OF THECHARACTERIZATION OF THECHARACTERIZATION OF THECHARACTERIZATION OF THECHARACTERIZATION OF THECHARACTERIZATION OF THECHARACTERIZATION OF THECHARACTERIZATION OF THE /ANDCHARACTERIZATION OF TWO NEWCLONES FOR GLUTATHIONECLONING ANDCLONING OF A PAIR OFCLONING OF CORRECTING DNACLONING OF HUMAN LDH C4CLONING OF THE LYSOSOMALCLONING TRANSCRIPTION ANDCYTOGENETICCYTOGENETICCYTOGENETICCYTOGENETIC ANALYSIS OFCYTOGENETIC ANALYSIS OFCYTOGENETIC IDENTIFICATIONCYTOGENETIC STUDIES OFCYTOGENETIC STUDIES OFCYTOGENETIC STUDY OF A 21 P+CYTOGENETIC STUDY OF SHORTCYTOGENETIC STUDY ON THECYTOGENETICS /ANALYZED BYCYTOGENETICS /BYDEFECTS /OF THE SEARCH FOR
7781549164125452270992
238256
172387
1102239422541382222195
255922002390546166417029652571066226222552211509338178622
2350158583716861459186266375
2636348349S831615280726510582354518
2316455
23022
987377264279
2385488416172625362324233426001034148817172799102416571647233116992012537444416722582S77623980453
238624032274128622482309136413781662170417291721219105214471537154418572641
48
DEFECTS OF FACTOR IX IN 64DEFECTS UNDERLYING /OF THEDEFINITION OF A SMALLDEFINITION OF MINIMALDEFINITION OF THEDELETION ANALYSISDELETION ANALYSIS IN XDELETION IN A PATIENT WITHDELETION PATTERNS IN FORTYDELETIONS IN CHINESE /OFDELINEATION OF A PROXIMALDELINEATION OF MEDIUM CHAINDETECTION OF 4P DELETIONSDETECTION OF ADIAGNOSIS OF /PROGNOSTICDIAGNOSIS OF CYSTICDIAGNOSIS OF FAMILIALDIAGNOSIS OF PRADER WILLIDIAGNOSIS OF SEX CHROMOSOMEDIAGNOSIS OF STROKE DUE TODIAGNOSTICS FOR MYELINDIAGNOSTICS OF CYSTICEVALUATION OF TWO UNRELATEDEVIDENCE OF TELOMEREEVOLUTION AND NEWEVOLUTION OF ALPHA /AN ENDGENETIC ANALYSES OF 20GENETIC ANALYSIS OF /FOR THEGENETIC ANALYSIS OF 14 /ANDGENETIC ANALYSIS OF 21 OHGENETIC ANALYSIS OF THEGENETIC ANALYSIS OF THE REDGENETIC AND KARYOTYPICGENETIC AND POSITRONGENETIC DEFECT IN /OF AGENETIC DEFECT ON THE X /THEGENETIC DIAGNOSIS OFGENETIC HETEROGENEITY INGENETIC STUDIES OF HUMAN XGENETIC STUDY OF THE SPINALGENETIC TECHNIQUES /ANDGENETICS AND ENZYMOLOGY OFGENETICS AND TREATMENT /ONGENETICS OFGENETICS OFGENETICS OF ALPORT SYNDROMEGENETICS OF DEVELOPMENTALGENETICS OF HEREDITARYGENETICS OF HURLER ANDGENETICS OF LEUKEMIAGENETICS OF MONOAMINE /ANDGENETICS OF POLYCYSTICGENETICS OF THE CYP2D6 /ANDGENETICS OF TUMOR FORMATIONGENETICS OF X LINKEDHETEROGENEITY ANDHETEROGENEITY AND VARIABLEHETEROGENEITY IN A FAMILYHETEROGENEITY IN BETAHETEROGENEITY OF TAY SACHSHLA CLASS II ASSOCIATIONSIN SITU HYBRIDIZATION /ANDLINKAGE ANALYSIS /ANDLOCALIZATION OF AZOOSPERMIAMARKERS AND CFTR GENEMECHANISM /SIGNIFICANCE ANDMECHANISMS OF AXISMECHANISMS OF CHROMOSOME /OFNOSOLOGY /TOWARD A COMPLETENOSOLOGY OPENING COMMENTSPATHOLOGY AND THE CLINICALPATHOLOGY OF HUMAN BPROCESSES /FOR ONCOGENESISREARRANGEMENT WITHIN THESCREENING OF HEMOGLOBIN ESTRUCTURE CHROMOSOMALSTUDIES AND THERAPY OFSTUDIES AROUND THE EWINGSTUDIES IN A NEW SYNDROMESTUDIES IN A NEWBORN WITHSTUDIES IN AN INFANT WITHSTUDIES IN GONADAL /ANDSTUDIES IN XX MALES ANDSTUDIES OF DIGEORGE SYNDROMESTUDIES OF HUMAN /ANDSTUDIES OF MONOSOMY 22011STUDIES OF TOPOISOMERASE 1STUDIES ON A NEWBORN WITHSTUDIES ON GENOTYPESTUDIES ON THE CLINICALSTUDIES ON THE REGULATIONSTUDY OF DUCHENNE MUSCULARSTUDY OF HUNTER SYNDROMESTUDY ON 72 ITALIANTECHNIQUES AND IN SITUTYPES OF DELETIONAL ALPHATYPING OF HUMAN NWEIGHT DETERMINATIONS OF /OF
MOLECULARLY /CYTOGENETICALLY ANDDEFINED CHROMOSOME
MOLECULE /AS A NEURONAL RECOGNITIONAND THEIR POPULATION /G6PD
MOLYBDENUM COFACTOR DEFECT ANMONGOLIA /AND ITS DISTRIBUTION IN
/DOWN SYNDROME IN
575
65847021061528417108611061711229210871470237796117201096103018761056106910261101111314581655S3426401035191
1380665986
23201340227
2300229310102019145
22181671132S52804583821997981282S76493384S93260224
286323274981075
3277017031989220510042413111574351344434284
257813701856230824752083736
14191465122998257
9161518187416752419805
2448102110426541695287354525241670200325253439
27351497
Permuted Title Index
MONGOLIAN SPOTS AND INBORN ERRORS OFMONGOLOD MIGRATIONS /OF ANCIENTMONGOLOIDS /POPULATION BLACKS ANDMONITORING AMONG KIEV NEWBORNS IN THE
INVESTIGATION ON BIRTHOF AMPLIFICATION OF PROTOOF INDIVIDUALS EXPOSED TOPATIENTS FOLLOWING /FOR
MONKEY (C AETHIOPS) /THE AFRICAN GREENBOVINE RAT MOUSE AND CHICKEN
MONOAMINE OXIDASE GENES MARK ACTIVITYOXIDASE IN ALCOHOLICS THEIR
MONOCHROMACY TO CHROMOSOME 14 /OF RODMONOCHROMOSOMAL HYBRIDS /ISOLATED INMONOCYTE SUPEROXIDE ANION GENERATIONMONOGENIC AND POLYGENIC DISEASES /INMONOMERIC ORGANIZATION /BYMONOSOMY 22011 AND ITS CLINICAL /OF
20 DUE TO A PATERNAL /80 AND7 IN PATIENTS WITH ACUTEFOR THE DIGEORGE LOCUS ON /ISSYNDROME /BRAIN IN THE 1802
MONOZYGOTIC TWINS /DYSTROPHY GENE INTWINS /FACTORS IN YOUNGTWINS /STUDIES WITH
MOOD DISORDERS /INTO THE GENETICS OFDISORDERS /MORBIDITY RISKS IN
MORAVIA HYPOTHESIS ON THE HISTORICALMORBIDITY /YOUNG MOTHERS AND GENETIC
RISKS IN MOOD DISORDERSMORPHOGENESIS /GENE IN LIMB AND KIDNEYMORPHOLOGY /GENE CONTENT TO CHROMOSOME
AND CYTOCHEMISTRY OFIN TRISOMY 15 PLACENTAS
MORPHOMETRY IN USHER SYNDROME /BRAINMORTEM LIVER SAMPLES FOR THE PRESENCEM0S46,XX,DEL(l8XP11.2Y46,XX,MOSAIC /OF A FRAGMENT IN A TURNER
/OF A RINGCHROMOSOME (20)/YQ REARRANGEMENTS WITHOUT 45,XCELL LINE WITH TRISOMY 10 IN AFOR A BALANCED RECIPROCAL [TRUEFOR A NORMAL CELL LINE /PATIENTFORM OF DOWN SYNDROME /ONSETKARYOTYPE IN A PATIENT WITHMARKERS OF DIFFERENT /OF SMALLMOTHER /FROM AN ASYMPTOMATICTRISOMY 13 PHENOTYPICTRISOMY 15 A CASE REPORTTRISOMY 16 DETECTED BY MIDTRISOMY 21 /AND PHENOTYPE OFTRISOMY 21 IN CYTOGENETICALLYTRISOMY 5 /REPORT OF A CASE OFXY/XYY AND FRAGILE X IN A 4
MOSAICISM /ALWAYS INDICATE TRUE FETAL/ANEUPLOIDY BUT NOT FOR/CASES OF CONFINED PLACENTAL/HEART DEFECTS IN TRISOMY 8/HISTORY OF TRISOMY 14/MECHANISMS LEADING TO/RESULTING IN FETAL/WITH 45,X/46,X INV (Y)45,X/47,XY, + 14 /WITH UNUSUAL46,XX,47,XX, + MAR ANDAN OVERVIEW /PLACENTALAND CYSTIC HYGROMA WITH AAND MATERNAL CELL /TRUEAS DEMONSTRATED IN HUMANAS OBSERVED IN HUMANCHORION CONFINED OR FETALDETECTED PRENATALLY WITH ANDOES NOT ALWAYS INDICATEFOR A FACTOR IX MUTATIONFOR CHROMOSOMAL ABERRATIONFOR CHROMOSOME 5 CRI DUFOR TRISOMY 8 AND GENETICIN 45,X TURNER SYNDROMEIN AN IDENTICAL TWIN /8IN CROUZON SYNDROME AIN CVS AN ANALYSIS OFIN CVS FETAL DEVELOPMENTIN DOWN SYNDROME BEIN INTERPHASE NUCLEI USINGIN INTRAUTERINE GROWTHIN PROGRESSIVE DEFORMINGIN RETT SYNDROME /CHROMOSOMEIN SPONTANEOUS ABORTIONIN THE VON WILLEBRAND /LINEIN TISSUES OF A PRENATALLYIN X LINKED AND AUTOSOMALIN X LINKED DISEASESSUMMARY AND WHAT THE FUTUREWITH PREPONDERANCE OF 46,XY
MOSAICISMS ON AMNIOTIC FLUID ANDMOSAICS IN CHORIONIC VILLUS /OFMOSLEM ARAB KINDRED FROM ISRAEL IS /AMOTHER /CHROMOSOME 21 DERIVED FROM HER
/FROM AN ASYMPTOMATIC MOSAIC/11 NONDISJUNCTION ON HISAND SIB SIB DEPENDENCE INAND THE UNBALANCED KARYOTYPE /A
MOTHERS /FROM SAME FATHER AND TWO/MALFORMED NEWBORNS AND THEIRAND BODY MEASUREMENTS ON /THEAND GENETIC MORBIDITY /YOUNG
8112610282327822780259625581607678
2612230349320772096872
2665169415181402139690114332222921
2759122
2745270395227452661643129918850975150116691519910120911701439150415171714149814241482920160012191231141514231622935149921529015691506143115322889381228287289
12311257142325991570117612021671148584012759141835164894462678336410681412280811912911534911126499813241498141926431632747
26551164952
OF TRISOMY 21 A PREDISPOSINGMOTIF HOMOLOGOUS TO THE AVIAN V MAFMOTOR AND SENSORY NEUROPATHY WITH
NEURONS BY RETROGRADE AXONAL /TOMOUSE /ESTERIFICATION IN NIEMANN PICK
/HEPATOCYTES OF THE SPARSE FUR/MAPPING STRATEGIES IN THE/OF MITOTIC LINKAGE MAPS IN THE/POLYPEPTIDE IN THE BALB/CBYJ/SUSCEPTIBILITY GENES IN THE/X INACTIVATION PROCESS IN THEAMYLOID PRECURSOR PROTEIN LOCUSAND CHICKEN REVEALS HIGHLY /RATAND HUMAN X CHROMOSOMES /ON THEAND RAT /REPEATS SHARED INAPOLIPOPROTEIN A 1 LOCUS IN /THEBONE MARROW BY TRIPTERYGIUM /INCHROMOSOME /GENE FOR PERLECAN TOCHROMOSOME /INSERTED INTO ACHROMOSOME 11 /CLOSE TO ERBB ONCHROMOSOME 17 /THE PKD1 GENE ANDCHROMOSOME 18 HOMOLOGIES WITHCHROMOSOME 3 BY SOUTHERN BLOTCHROMOSOME 7 /PROXIMAL REGION OFCHROMOSOME 7 AND THE HUMAN /OFEMBRYONIC STEM CELLS /INEMBRYOS CARRYING LETHALFETUSES /AGAINST TRISOMY 16GENES /STRATEGIES FOR MAPPINGGENOME /SITE CLEAVAGE OF THEGENOME /THE ENCYCLOPEDIA OF THEHSP70 HOMOLOGUE GENE EXPRESSEDLIMB DEFORMITY GENE IN LIMB ANDLOCI RELEVANT TO HERITABLEMDM2 TRANSFORMING GENE /THEMODEL OF GAUCHER DISEASE /AMODEL OF NIEMANN PICK DISEASEMODEL OF NIEMANN PICK DISEASEMODEL OF NIEMANN PICK DISEASEMODELS /CRANIOFACIAL ANOMALIESMODELS IN THE STUDY OF /USINGSKELETAL MUSCLE /GRAFTED INTOSKELETON AND LENS TO ESTIMATESTRAIN CAR 2 POLYMORPHISMS /ANDSXR REGION IN YEAST ARTIFICIALTUMOR AND ASCITIC RAUCHER /INX CHROMOSOME /MAP OF THEY CHROMOSOME /SXR REGION OF THE
MOUTH PROGNATHISM ABNORMAL EARS /BOWMPS VI BY BONE MARROW /LAMY SYNDROMEMRNA ENDS /THE PROPER FORMATION OF 3
IN GOLDEN RETRIEVER MUSCULARIN PERIPHERAL BLOOD LYMPHOCYTESOF DROSOPHILA /OF THE MLC ALK PREPRECURSOR DUE TO AN INTRA EXONSEQUENCE WHICH PARTICIPATES INSPLICE DONOR SITE /MUTATION IN ATHE MOST COMMON CAUSE FOR
MSAFP AND AFAFP MEASUREMENTS /RACE ONAND AGE /FOR DOWN SYNDROME USINGAND HCG IN TWIN PREGNANCIESCONCENTRATIONS CYTOGENETICDUE TO FETAL CARDIAC DISEASEHCG AND UE3 /PROGRAM USINGHCG AND UE3 EFFECTS OF MATERNALHCG AND UNCONJUGATED ESTRIOLIN SUCCESSIVE PREGNANCIES WITHIN TRIPLET GESTATION /OFINDEPENDENT OF OPEN NEURAL TUBELEVELS IN EARLY SECOND /ANDLEVELS IN TRIPLET PREGNANCYPROGRAM /OF INDEX CASES THROUGHSCREENING FOR DOWN SYNDROME INSCREENING FOR DOWN SYNDROME INSCREENING FOR DOWN SYNDROME THESCREENING FOR OPEN NTDS IN TWINSCREENING WITH DRIED BLOOD SPOTUE3 AND HCG /TRISOMY 18 USING
MSPI SITE OF THE ORNITHINE /AT AMSPL SITE IN A HUTTERITE KINDRED WITHMTDNA /DUE TO A POINT MUTATION OF THE
A SYSTEM FOR THE MOLECULARPHYLOGENETIC INFERENCES /ONSEQUENCE SPECIFIC NIA HUMANTRNALEU(UUR) MUTATION IN [THE
MUCI LOCUS IN ASIAN BLACK CAUCASIANMUCOLIPIDOSES II AND III /DIAGNOSIS OFMUCOPOLYSACCHARIDOSIS AUTOMATION OF A
THE MINNESOTATYPE VI /INVIl (BETA
MULLERIAN ANOMALIES A FAMILY CASEDUCT ABNORMALITIES ANDINHIBITING SUBSTANCE THE
MULTI ETHNIC ORIGIN /HETEROZYGOTES OFETHNIC STATE /IN A LARGEFETAL PREGNANCY REDUCTIONLEVEL MAP OF THE MYOTONIC
MULTIAXAL DIAGNOSTIC SYSTEM IN /OF AMULTICHANNEL ANALYZER FOR NEWBORNMULTICOLOR CHROMOSOMAL BAR CODES BY
FLUORESCENCE IN SITUIN SITU HYBRIDIZATION WITH
MULTICULTURAL PATIENTS /EFFICACY INMULTIDISCPLINARY CLINIC FOR MARFAN /A
1591245919142489523
2472S362056459594146
224426122421164524631853189041318641869186318671860S86249322391432240
20741898186226635213612503627798875341S8
2488256225281859134119512343710561
2445967108924382351244523262280122412031833120112351242114012331135126111379261157118311691250182812141186123855944135
19128692834977
28674425775644672473639632105
1855270112762310750184318418591
17581787
MULTIETHNIC POPULATION OF THE U.S.S.RMULTIFACTORIAL CONGENITAL /ETIOLOGY OF
DISEASES /GENES FORTRAITS AND DISEASES /TO
MULTIGENE FAMILY AS A MODEL FORFAMILY EXHIBIT A COMPLEX
MULTIGENERATION PEDIGREE /AN EXTENDEDMULTIGENERATIONAL ALCOHOLISM /WITH
MOLECULAR ANALYSISMULTIGENIC /HETEROGENEITYMULTILOCUS DNA PROBES /HYPERVARIABLE
GENOTYPE DATA VALIDATE THEMULTIARAMETER FLOW CYTOMETRY AND /BYMULTIPLE ABNORMALITIES DUE TO /AND
ABNORMALITIES OF /WITHACYL COA DEHYDROGENATIONANOMALIES AND NORMAL GROWTHCAFE AU LAIT SPOTS /WITHCELL MULTIPLE FLASK/COLONYCENTROMERIC SATELLITE DNACHROMOSOME ABNORMALITIES INCONGENITAL /RECESSIVECONGENITAL ANOMALIES/MENTALCONGENITAL DEFECTS /OFCONGENITAL MALFORMATIONS INCPG ISLANDS AND ASSOCIATEDDISEASE INDICATIONS AT /FORDISEASE LOCI AND ASSORTATIVEENDOCRINE NEOPLASIA 1 REGIONENDOCRINE NEOPLASIA 2A /TOENDOCRINE NEOPLASIA TYPE 1ENDOCRINE NEOPLASIA TYPE 1ENDOCRINE NEOPLASIA TYPE 1ENDOCRINE NEOPLASIA TYPE 1ENDOCRINE NEOPLASIA TYPE 2ENDOCRINE NEOPLASIA TYPE 2AENDOCRINE NEOPLASIA TYPE 2AENDOCRINE NEOPLASIA TYPE 2AENDOCRINE NEOPLASIA TYPE 2AENDOCRINE NEOPLASIA TYPE 2BEPIPHYSEAL DYSPLASIA /OFFLASK/COLONY AMNIOTIC FLUIDGAMMA GLUTAMYL /MAPPING OFIGK VARIABLE REGION GENE /OFLOCI ONE OF WHICH IS TIGHTLYMALFORMATIONS /ANDMALFORMATIONS /WITHMARKER CHROMOSOMES INMECHANISMS OF X INACTIVATIONMIGRATION ROUTES OF THE /ANDMYELOMA /BCL2 GENE IN HUMANORIGIN OF THALASSEMIA GENESPHENOTYPES OF X LINKED /THEPOINT MUTATIONS WITHIN THEPOLYMORPHIC LOCI IN HUMAN DNAPSEUDOGENES ARE DISPERSEDSCLEROSIS /CONCORDANT FORSCLEROSIS A FOLLOW UP STUDYSCLEROSIS IS DETERMINED BYSCLEROSIS SUSCEPTIBILITY /INSELF HEALING SQUAMOUS /FORSPONTANEOUS ABORTIONS INY CHROMOSOME SPECIFIC PROBES
MULTIPLEX (PCR) REACTIONS AS AN /TWO/OF 14 EXONS AMPLIFIED INAMPLIFICATION REFRACTORY /AAMPLIFICATION REFRACTORY /OFCONGENITA /IN ARTHROGRYPOSISDNA AMPLIFICATION OF TWOPCR /BY QUANTITATIVEPCR /MUSCULAR DYSTROPHY BY
MULTIPLEXING AND OPTIMAL LOCUS /INMULTIPOINT IBD APPROACH TO MULTIPOINT
LINKAGE ANALYSIS FOR /TOLINKAGE ANALYSIS OFLINKAGE ANALYSIS OF MARFANLINKAGE ANALYSIS REVEALSMAP AROUND THEMAPPING OF HUMANMAPPING OF HUMAN /FORMAPPING UNDER DIFFERENT
MULTIPURPOSE REGISTER OF CONGENITALMULTIVARIATE ASSOCIATIONS AMONG SEX
GENETIC ANDSEGREGATION ANALYSIS OF
MUMMIES /AND PROTEINS FROM PERUVIAN/D4S175 IN ANCIENT PERUVIAN
MURINE C4 RELATED GENES IS RARECATALASE GENE EXPRESSION ANDCHROMOSOMAL MARKERS /HUMAN ANDDNA REPAIR GENE ERCC 1 /OF THEHEMATOPOIETIC CELL IN VIVO /INHEMATOPOIETIC STEM CELLS USINGHEPATOMA CELLS /ACTIVITY INHOX 1.2 PROTEIN /OF THERB (6.16) TRANSLOCATION IN /THERB(6.16) TRANSLOCATION /OF THEXIST GENE CDNA CLONING MAPPINGXIST GENE SEQUENCE ANALYSIS
MUSCLE /GRAFTED INTO MOUSE SKELETAL/OF ANALYSIS OF HUMAN HEARTAN IN VITRO STUDY /ANDBIOPSY /DYSTROPHY BY FETALBIOPSY CONTRACTURE TESTING /ANDDYSTROPHIN /OF SMOOTH
576
28471288S32S9526192436996517778260328712506109884824971407742
142316661508879646183714722396178620272090198259561210252184195019K62145217023401982762142321302623
798489331162148
2876167410708641009209919732742759100
191759814001693989103399310471524988102311242062206820682012188320192042158
20402095726273927672764566
26172627244818612325247124682477222615831552225996
248822331292120719112443
Permuted Title Index
OF PATIENTS WITH DUCHENNEPHOSPHOFRUCTOKINASE DEFICIENCYSUCCINATE DEHYDROGENASE
MUSCULAR ATROPHIES /FOR THE SPINALATROPHIES /OF THE SPINALATROPHIES /ONSET SPINALATROPHY /PEDIGREES IN SPINALATROPHY /REGION FOR SPINALATROPHY /SPINAL AND BULBARATROPHY /THE GENE FOR SPINALATROPHY CONFIRMATION OFATROPHY FROM THE NETHERLANDSATROPHY GENE WOBBLER MAPSATROPHY IN FINLAND /SPINALATROPHY LOCUS /OF THE SPINALATROPHY LOCUS /OF THE SPINALATROPHY LOCUS /TO THE SPINALATROPHY REGION ENRICHING THEATROPHY USING POLYMORPHICDYSTROPHIES /AND BECKERDYSTROPHIES /IN PROGRESSINGDYSTROPHYDYSTROPHY /GOLDEN RETRIEVERDYSTROPHY /IN DUCHENNEDYSTROPHY /IN DUCHENNEDYSTROPHY /IN DUCHENNEDYSTROPHY /OF DUCHENNE TYPEDYSTROPHY /WITH DUCHENNEDYSTROPHY A SUSCEPTIBILITYDYSTROPHY AND BECKERDYSTROPHY AND BECKERDYSTROPHY BY FETAL MUSCLEDYSTROPHY BY MULTIPLEX PCRDYSTROPHY BY QUANTITATIVEDYSTROPHY CAUSED BY /DUCHENNEDYSTROPHY DELETIONS INDYSTROPHY FAMILIES /BECKERDYSTROPHY FAMILIES BYDYSTROPHY FAMILIES USING CADYSTROPHY GENE ITHE DUCHENNEDYSTROPHY GENE /THE DUCHENNEDYSTROPHY GENE AT 4035 4QTERDYSTROPHY GENE BY HOMOLOGOUSDYSTROPHY GENE ON 4Q35DYSTROPHY IN A WIRE HAIREDDYSTROPHY IN JAPAN /DUCHENNEDYSTROPHY IN NORTH CHINADYSTROPHY IN TWO MALE SIBS ADYSTROPHY KOBE /OF DUCHENNEDYSTROPHY LOCUS /DREIFUSSDYSTROPHY LOCUS ON THEDYSTROPHY PATIENT GENETICDYSTROPHY PATIENT WITH ADYSTROPHY PATIENTS /BECKERDYSTROPHY PATIENTS /BECKERDYSTROPHY PATIENTS /DUCHENNEDYSTROPHY PATIENTS /DUCHENNEDYSTROPHY PATIENTS AND THEIRDYSTROPHY PATIENTS IN /BECKERDYSTROPHY PATIENTS USING TWODYSTROPHY TO CHROMOSOME 40DYSTROPHY TO CHROMOSOME 5QDYSTROPHY WITH ATRIALDYSTROPHY WITH DYSTROPHINDYSTROPHY/MDX MUTATIONSTRANSCRIPTS PRODUCED BY THE
MUSEUMS /CURIOSITY ABOUT GENETICS ANDMUSUMI COMMUNITY FROM BIHAR INDIA /AMUT AND MUT PATIENTS WITH /AMONG
METHYLMALONIC ACIDURIA /THERAPY OFPATIENTS WITH METHYLMALONYL COA
MUTABILITY /CHANGES OF CHROMOSOMALFLUCTUATIONS IN HUMAN /OF
MUTAGENESIS /AND SITE SPECIFIC/MEDIATED SITE DIRECTEDSEQUENCE ANALYSIS OF THE
MUTAGENICITY TEST AND CLINICALMUTAGENIED HUMAN SOMATIC CELLS /OFMUTANT ALLELE /ACYL COA DEHYDROGENASE
ALLELE ACCOUNTS FOR THE HIGHALLELES WITH REFERENCE TO /OFCELL LINE OF THYMIDINE KINASECELLS ARE THE FUNCTIONS OFCOPY OF THE HUMAN RHODOPSIN /AHEXOSAMINIDASE A EXPRESSED INHUMAN CFTR GENES /NORMAL ANDHUMAN LYMPHOCYTES /HPRT GENE INOF HERPES SIMPLEX VIRUS TYPE 1P53 FROM HUMAN TUMORS ISPROTEINS /AND STABILITY OFV H4 IS CORRECTED AFTER /CELL
MUTANTS /CANDIDATE REGION AMONG NEW/FROM GLOBIN GENE DELETIONAS MODELS FOR HUMAN BREAKAGE
MUTASE ACTIVITY IN HUMAN PLACENTA BYDEFICIENCY /METHYLMALONYL COAFOR CHARACTERIZATION DIAGNOSIS
MUTATED GENE IN AUTOSOMAL DOMINANTHLA HAPLOTYPES IN DISORDERSIN COLORECTAL CANCER AND /GENEMITOCHONDRIAL DNA AND /OF
MUTATION (VAL ILE) IN THE EXON 17 OF/DEFICIENCY IS A POINT/GENE RETINOBLASTOMA'S/GENES IS RARE COMPARED TO
48651848219431239188527762146
9518862018109318642687210121122332221812231098813
2037967108110882319795486
205098911231207112410232549810104695897816S7
221718
14346417941021821
2351220720421080690989
2292731829109610401087190478
7811123
192269397
2822511532511
28052795247997
255025332807975489
273224662564799283
2364255016812441246
22502348337297570511532
2371665101437
1071518620
2627
/MOSAICISM FOR A FACTOR IXA COMMON STEP IN HUMAN CANCERANALYSIS AND GENETIC LINKAGEANALYSIS INANALYSIS IN POSTMORTEM FIXEDANALYSIS OF GAUCHER PATIENTSAND GENETIC FITNESS OFAND SEGREGATION IN NORMALASSOCIATED WITH MILDAT 5 METHYLCYTOSINE ISAT A MSPI SITE OF THE /C TO TAT CODON 200 OF THE PRP GENEAT THE GLYCOPHORIN A LOCUSAT THE SAME LOCUS AS THE /ACAUSING FAMILIAL /LITHUANIANCAUSING HUMAN 21 HYDROXYLASECREATING A NEW MSPL SITE INDETECTION IN THE ORNITHINE DDETECTION WITH THE SINGLEFROM HP-2 TO HP'l IN HUMANFROM SINGLE CELLS /CD508G542X IN JEWISH PATIENTSIN 13 NORWEGIAN CYSTIC /DF508IN A FAMILY WITH /KERATIN 14IN A FAMILY WITH FAMILIALIN A JAPANESE FAMILY /GENEIN A MRNA SPLICE DONOR SITEIN AN EYE LENS SPECIFICIN ARAB PATIENTS WITHIN CATALONIANS FROM THE EBROIN CODON 370 OF HUMANIN ECUADOREAN PATIENTS WITHIN HUMAN B HEXOSAMINIDASE BIN HUMAN MINISATELLITES /ANDIN MAN /ORIGIN OF DE NOVOIN MEDIUM CHAIN ACYL COA /NEWIN MITOCHONDRIALIN SOUTH BRITTANYIN THE ACID BETA /POINTIN THE ALDOLASE B GENE FROMIN THE APOLIPOPROTEIN AIN THE HUMAN HAPTOGLOBININ THE MITOCHONDRIAL TRNAIN THE NFI GENE CAUSESIN THE PROTEOLIPID PROTEININ THE TESTIS DETERMININGIN TWO MILDLY AFFECTEDIS RARE IN FAMILIAL ANDMAPS TO CHROMOSOME 12OF ISOVALERYL COA /(TYPE 11)OF RAS ONCOGENE IN HUMANOF THE C KIT (MAST/STEM CELLOF THE MTDNA /DUE TO A POINTOF THE RHODOPSIN GENE IN AON FETAL G GLOBIN GENERESPONSIBLE FOR A HUMANSELECTION EQUILIBRIA AND /NEWSER106 PRO IN THE CYP17 GENESPECIFIC PCR AMPLIFICATIONSPECTRUM IN PATIENTS WITHSPECTRUM IN TWO SIMILARSPECTRUM OF THE RHODOPSINSYSTEM TEST /REFRACTORYSYSTEM TEST FOR THE
MUTATIONAL ANALYSIS OFBASIS OF APRT DEFICIENCYDISEASE /CONCEPT OF SOMATICHETEROGENEITY /WITH HIGHSPECTRA IN /P53 AND K RAS
MUTATIONS /AND A SEARCH FOR/AND NONDELETION/DUPLICATION/CARRIERS OF PHENYLKETONURIA/CARRY THE SAME MISSENSE/FOR DETECTION OF POINT/FOUR COMMON CYSTIC FIBROSIS/INTERACTIONS BETWEEN/MUSCULAR DYSTROPHY/MDX/OF CYSTIC FIBROSIS GENE/THREE NOVEL CYSTIC FIBROSIS/WITH MITOCHONDRIAL POINT/WITH THREE SEPARATEAMONG GERMAN AND /FIBROSISAND A MARCO POLO ALLELE /NEWAND ANALYSIS BY RECOMBINANTAND EVOLUTIONARY /MISSENSEAND MILD HEMOPHILIA BAND POLYMORPHISMS IN /OFASSOCIATED WITH LEBERASSOCIATED WITH LEBER /BASSOCIATED WITH RETINITISAT CODON 373 OF FVIII GENEAT CPG DINUCLEOTIDES ANDAT THE AGOUTI LOCUS /LETHALAT THE KIT AND STEM CELLAT THE NEUROFIBROMATOSIS 1AT THE NF1 LOCUS /OFBY ANALYSIS OF DYSTROPHINBY CHEMICAL MISMATCHBY MEANS OF ASO REVERSE DOTBY RESTRICTION ENZYME /POINTCAN BE TRACED TO PREMEIOTICDEFINE FUNCTIONAL SITESDETECTED WITH SINGLE LOCUSIN A COMPLETE SWEDISH /BIN A HUMAN CHROMOSOMALLY
2599S6361310901119514
28122546436
2552559
10002535820
23292375441
2519280444012102245110722571888107023262268740
26744369691112313406
22779772712451
22641118242510171084972
234128142811201049059318935
9992423662
280810451073
112553
89931047281810912921005610
226715
2426221974104797319
279823111064100323442246193
263270186
1022973109727941068223925669914
10892814184910072817525
281010052536
IN A LARGE SAMPLE OF CYSTICIN ALPORT SYNDROME /CONTAINSIN AUTOSOMAL DOMINANTIN BOHEMIA AND MORAVIA /GENEIN BURKITT LYMPHOMAS /P53IN CHICAGO AREA CYSTIC /CFTRIN CIRCULATING /OF SOMATICIN DIFFERENT DOMAINS OF THEIN FAMILIES FROM A /FIBROSISIN FIVE PROVINCES OF SOUTHIN FRENCH CANADIANS /DISEASEIN GENE FOR FIBRILLAR /WITHIN HIGH AND LOW RISKIN HPRT CDNA USING THE PCRIN HUMAN BREAST CARCINOMASIN HUNAN CHINA BY PCRIN ITALY FREQUENCY ANDIN MALES WITH CONGENITALIN MAMMALIAN CELLS /INDUCEDIN MAN AND PROSPECTIVE /ANDIN PATIENTS WITH /SCREEN FORIN PATIENTS WITH BONE ANDIN PELIZAEUS MERZBACHERIN RENAL TUMORS /OF P53IN SPAIN /OF CYSTIC FIBROSISIN THE ALPHA 1 /OF POINTIN THE CARBONIC ANHYDRASEIN THE CFTR GENE BY /OFIN THE COL1A1 GENE OF TYPEIN THE DYSTROPHIN GENE ININ THE FACTOR Vil GENE ININ THE FIX GENE /FOR POINTIN THE G6PD MOLECULE ANDIN THE GENE ENCODING THE AIN THE GLUCOCEREBROSIDASEIN THE HPRT LOCUS IN LESCHIN THE HUMAN APRT GENEIN THE HUMAN SRY GENE ANDIN THE HUMAN TISSUE /POINTIN THE INSULIN RECEPTOR GENEIN THE ORNITHINE /OF POINTIN THE RB AND P53 GENESIN THE REFLECTION OF THEIN THE RETINOBLASTOMA GENEIN THE TYPE IV COLLAGEN A5IN THE TYROSINE /POINTIN THE UROPORPHYRINOGEN IIIIN TORONTO /CYSTIC FIBROSISIN TUMORIGENESIS /OF POINTIN TWO HEMOPHILIA A PATIENTSIN TYPE IA OCULOCUTANEOUSIN UNSELECTED PROGENY OFINDUCED AT THE HPRT LOCUSINTRODUCED BY TARGETED /GENELEADING TO ARYLSULFATASE AOF FACTOR Vil GENE /POINTOF LDL RECEPTOR GENE /NEWOF THE GENE FOR FAMILIALOF THE P53 GENE IN HUMANOF THE RHODOPSIN GENE /ANDOF TYPE II PROCOLLAGEN GENEON DIFFERENT NORMAL /GENETHAT CAUSE MALE SEXUALTHAT INFLUENCE LIPID ANDTWO FAMILIES WITH A LOWUSING A MULTIPLEX /FIBROSISUSING DENATURING GRADIENTUSING NONRADIOACTIVE SINGLEUSING PCR MEDIATED SITEWITHIN THE CYSTIC FIBROSISWITHIN THE CYSTIC FIBROSISWITHIN THE PORPHOBILINOGEN
MUTATOR GENOTYPES AND THE CONCEPT OFMUTES HELD AMONG 87,521 HAIKOU CITYMYB /MAPS TO 6021 Q22 AND IS LINKED TO
PROTO ONCOGENE IN CHICKENS WITHMYC AMPLIFICATION AND CHROMOSOME LP /N
AND C FOS EXPRESSION IN HUMAN /CC FOS AND C RAS ONCOGENE HOMOLOGSEXPRESSION AND PROLONGED /CONCOGENE /THE DOMAIN OF THE HUMANRELATED SEQUENCE /OF A NOVEL
MYCN AMPLIFIED DOMAIN IN /OF THEMYELIN PROTEOLIPID PROTEIN GENE /FORMYELOBLASTIC LEUKEMIA PATIENTS /ACUTEMYELODYSPLASTIC SYNDROME /12 IN
SYNDROME/A MALE WITHSYNDROME /WITH PRIMARYSYNDROMES /AND IN
MYELOGENOUS LEUKEMIA /IN AN ACUTELEUKEMIA /IN CHRONICLEUKEMIA /IN CHRONICLEUKEMIA /WITH ACUTELEUKEMIA /WITH CHRONICLEUKEMIA PATIENTS BY
MYELOGRAM A NEW PRENATAL DIAGNOSTICMYELOD DISORDERS /AND 7 IN MALIGNANT
LEUKEMIA /IN CHRONICLEUKEMIA /OF T(8;21) IN ACUTELEUKEMIA AND IN /IN CHRONICML 1 CELL LEUKEMIA MCL 1 HAS
MYELOMA /BCL2 GENE IN HUMAN MULTIPLEMYELOMENINGOCELE /IN INFANTS WITH
AND GENOMICMYE C LEUKEMIA TO WITHIN 1
577
4632405237827032594182925412359284011172289
44970281321828201078106
25342816232326051101132510746801020985347958
22839842531067101810532538223847248510572553360588194507530
2261249510022318280725592503285994980591
25779
462797267
268222199310081105997100925511044292
277713072590584
24132569918
25702186219311011358133413471381617137013271649139613795861194258113511342617
25891674768
26531709
Permuted Title Index
MYELOPROnFERATIVE DISORDERS /INSYNDROME AT 21011.2
MY0BLAST THERAPY PROLIFERATIVEMYOBLASTS /OF TRANSPLANTED HUMAN
GRAFTED INTO MOUSE SKELETALMYOCARDIAL INFARCTION ITOMYOCLONIC EPILEPSY TO HLA /OF JUVENILEMYOCLONUS EPILEPSY /IN PROGRESSIVEMYOGENIC LINEAGE /OF THEMYOMETRIAL CONTRACTURES AND TECHNICALMYOPATHIES /AND RNA IN MITOCHONDRIAL
/GENE THERAPY IN INHERITEDTHE KING SYNDROME CLINICAL
MYOWITHY AND CARDIOPATHY A NEWENCEPHALOPATHY LACTICIMPLICATIONS FORWITH ENCEPHALOPATHY LACTICWITH EXCESSIVE AUTOPHAGY
MYOPIA/REFRACTIVE ERROR IN PRIMARYAND RETINAL DETACHMENTS IN THE
MYOSIN REGULATORY LIGHT CHAIN ISOtONIC DYSTROPHY
DYSTROPHY /ANTICIPATION INDYSTROPHY /GENES FORDYSTROPHY AND CLOSELY LINKEDDYSTROPHY FAMILIES REVEALSDYSTROPHY GENE /CLONING THEDYSTROPHY GENE /CONTAINS THEDYSTROPHY GENE IN /OF THEDYSTROPHY GENE IS CONTAINEDDYSTROPHY GENE REGION /HUMANDYSTROPHY GENE REGION /OF THEDYSTROPHY ILLUSTRATING SOMEDYSTROPHY IN ITALY AND SPUNDYSTROPHY IN THE SPANISHDYSTROPHY LOCUS /MAP OF THEDYSTROPHY LOCUS AND FOUR DNADYSTROPHY MULTIGENERATIONALDYSTROPHY OBSERVATIONS ONDYSTROPHY POPULATION
MZ TWIN STUDY /A DISCORDANTTWINS DISCORDANT FOR RED GREEN /IN
13721348
2121
248810952041
763261128242742469835
1017244743718878951443216421152407228728482848404
237022222036S8640510431984187523101916778403
2036909
2231
N
NADH DEHYDROGENASE ACTIVITY AND /INAGALAND INDIA /AMONG THE AO NAGAS
INDIA /STUDIES IN AO NAGASNAGAS NAGALAND INDIA /AMONG THE AO
NAGALAND INDIA /STUDIES IN ADNAGER ACROFACIAL DYSOSTOSIS A CASENAIL PATELLA SYNDROME /GENE IN
PATELLA SYNDROME STUDY OF 37NARCOLEPSY /GENETIC EPIDEMIOLOGY OF
/HETEROGENEITY IN FAMILIALNASAL ALAR INDENTATIONS A DOMINANTLY
OBSTRUCTION /IN NEONATES WITHNASCENT POLYPEPTIDE IN THE BALB/CBYJNASU /(MEMBRANOUS UPODYSTROPHYNATI AND NAT2 LOCI /AT THENAT2 LOCI /AT THE NAT1 ANDNATION'S SCHOOLS /EDUCATION IN THENATIONAL FAMILIAL BRAIN TUMOR REGISTRY
GENETICS PROGRAMS /ORIENTEDGENETICS SERVICESHEALTH SERVICE /ORIENTEDHIGH RISK REGISTRY FOR WOMENSOCIETY OF GENETIC /THETREND TOWARD PERFORMING /A
NATIONALITIES OF SICHUAN CHINA /LISUNATIONALITY IN CHINA /GROUP A MINORITYNATIONS /GENETIC SERVICES DEVELOPING
ITO GENETIC SERVICES DEVELOPEDNATIVE AMERICANS (U.S.A.) /AND
AMERICANS OF THE SOUTHWEST /INKINDRED /IN A BRITISH COLUMBIA
NATRIURETIC FACTOR GENE IN FAMILIALNATURAL COURSE OF MEDIUM CHAIN ACYL
HISTORY /OF THE PHENOTYPE ANDHISTORY BASED ON 39 /ANDHISTORY OF ANGELMAN SYNDROMEHISTORY OF PRADER WILLIHISTORY OF RECURRENT NONHISTORY OF THE NONLETHALHISTORY OF TRISOMY 14MUTATIONS AND ANALYSIS BY /OFPRENATAL SCREENING OFSELECTION ASSOCIATED WITH
NATURALLY OCCURRING SOMATIC AND /122NECK/CELL CARCINOMAS OF THE HEAD AND
/CELL CARCINOMAS OF THE HEAD ANDA POSSIBLE PRIMARY CHROMOSOMALARE CYTOGENETICALLY STABLE INCANCERS /ORAL CAVITY AND HEAD AND
NEGATIVE ELECTRORETINOGRAM OF ALANDFAMILY /DXS52 IN A FRAGILE XFOLLICULAR B NON HODGKINRESULTS /ALSO LEAD TO FALSESELECTION MANIFESTED BY THE
NEOANTIGENE GENE PROMOTER /HUMAN 17 1ANEONATAL CARDIOMYOPATHY AND RENAL
51327492868274928686561996746
27712019663905459873549549394615S30S301506081814122627891856
3837
2867267619091037475717676170169704173215193103
288025531319138513941393583810
19801392106026212465536
CONVULSIONS IN A /FAMILIALPROGEROID SYNDROME WITHSEIZURES AUTOSOMAL DOMINANTSHORT LIMB DWARFISM WITH
NEONATE WITH THE CHARGE ASSOCIATION /ANEONATES /HAVING G 6 PD DEFICIENCY
FROM 35 TO 42 WEEKS GESTATIONFROM FIRST COUSIN MARRIAGESWITH NASAL OBSTRUCTION /IN
NEOPLASIA 1 REGION OF CHROMOSOME 112A ITO MULTIPLE ENDOCRINETYPE 1 AND BCL 1 LOCITYPE 1 GENE /ENDOCRINETYPE 1 GENETIC ANDTYPE 1 REGION OF CHROMOSOMETYPE 2 /MULTIPLE ENDOCRINETYPE 2A /MULTIPLE ENDOCRINETYPE 2A /MULTIPLE ENDOCRINETYPE 2A GENE /ENDOCRINETYPE 2A REGION /ENDOCRINETYPE 2B GENE TO CHROMOSOME
NEOPLASIAS /SUFFERING FROM DIFFERENTWITH THE T(10;14)(024;Q11)
NEOPLASTIC EVOLUTION NONRANDOM /VITRONEPHRITIS /IN A FAMILY WITH HEREDITARYNEPHROMEGALY AND DISTINCTIVE FACIESNEPHROPATHY (GLYCOGEN STORAGE DISEASENEPHROSIS /IN NONLETHAL CONGENITAL
DETECTION OF INDEX CASESNEPHROTIC SYNDROME POSSIBLE FINNISHNERVE GROWTH FACTOR INJECTION /OF THENERVOUS SYSTEM AND DEVELOPMENTAL
SYSTEM HEREDITARY DISEASES INSYSTEM HEREDITARY DISEASES INSYSTEM ISOLATING THE GENESSYSTEM MALFORMATIONS /CENTRALSYSTEM MANIFESTATIONS IN
NETHERLANDS /HUNTINGTON DISEASE IN THE/MUSCULAR ATROPHY FROM THEUNDER SPECIAL AIN THE
NEU IN BREAST AND OVARIAN CANCER /CLAXOVA SYNDROME /CHOLESTEROL IN
NEURAL CREST /FOR INVOLVEMENT OF THERETINA SPECIFIC GENE ENCODES ARETINA SPECIFIC GENE OF /HUMANTUBE DEFECTS AND DOWN SYNDROMETUBE OR VENTRAL WALL DEFECTS
NEURINOMAS OF NEUROFIBROMATOSIS TYPENEUROANATOMY OF THE FRAGILE X SYNDROMENEUROBLASTOMA /COMMONLY DELETED IN
/RAS GENE ACTIVATION INCELL LINES AND DURINGIN A CHILD WITH DUPPATIENTS AND THEIR /OFTUMORS /LP DELETIONS IN
NEUROBLASTOMAS USING YEAST ARTIFICIALNEUROCRISTOFATHY REPORT OF 17 CASES /ANEUROFIBROMAS /SYNDROME WITH PLEXIFORMNEUROBR TOSIS /CAUSES CLASSICAL
/OF SEGMENTAL/STUDY OF TYPE 2NON RECKLINGHAUSEN/VON RECKLINGHAUSEN1 AND /IN NOONAN1 AND A CEREBRAL A1 IN SEARCH OF THE1 LOCUS IN NOONAN1 PATIENTS /1 AND1 PATIENTS AN1 PATIENTS FOLLOWED1 RELATED LOCUS ON2 CLINICAL2 LENS FINDINGS INGENE /OF THE TYPE 1GENE /RECKLINGHAUSENGENE AND RELATED /1NOONAN SYNDROMEREGISTRIESTYPE 1 AT THE DNATYPE 1 GENE /THETYPE 1 IN YOUNG /OFTYPE 2 /INTYPE 2 LOCUS ON /THETYPE 2 PATIENTS ANDTYPE I /PATIENT WITH
NEUROLOGICAL PHENOTYPES AMONG MUT ANDNEUROMUCU DISEASES /COUNSELING INNEURON SPECIFIC ENOLASE ACTIVIIES /OF
SPECIFIC HUNTINGTON DISEASE /ASPECIFIC PROMOTER OF A /THE
NEURONAL ACETYLCHOLINE RECEPTOR /5CEROID LIPOFUSCINOSIS TO THEDIFFERENTIATION INDUCED BYRECOGNmON MOLECULE /AS A
NEURONS BY RETROGRADE AXONAL TRANSPORTNEUROOPHTHALMIC INVOLVEMENT /ANDNEUROFATHOLOGICAL FINDINGS IN THENEUROFATHY /LEBER HEREDITARY OPTIC
/LEBER HEREDITARY OPTICAND EVIDENCE FOR /OPTICMUTATION SPECIFIC PCRPARTLY DETERMINED BY AN XWITH AGENESIS OF CORPUSWITH HIGHLY INFORMATIVE
NEUROPSYHATRIC DISORDERS /GENE IN
833114576165068217789121164905209019822184612102559519501956234021452170198213122251314693792846851118311602533842
2692272830386861617671093272
259691368224592308117
113725858282215602
242013291388584
2193815702108481822910282602997322229999
1090830232867680698
2133233963535628182372742
20092169258522325111735257622672335218219352420325248968686651310199731073203219001914979
NEURORETINOPTHY /HEREDITARY OPTICNEUROSPORA /IN DIFFERENT SPECIES OFNEUTRAL ALLELES REGIONS OF ABRUPT /AS
MUTATIONS IN THE GENE /AND 3POLYMORPHISMS IN ANDHRA /ANDPROTEASE IN DUCHENNE MUSCULAR
NEUTROPIL CHEMOTAXIS AND BOMBAYNEVOID HYPERMELANOSIS AN ADDITIONALNEVUS SYNDROME /IN BASAL CELL
SYNDROME /MELANOMA/DYSPLASTICSYNDROME IN CHINESE FAMILIES
NEWBORN BIRTH DEFECTS RATES INLIVER BY HEPATOCELLULAR /ORSCREENING /CLINICALLY AND BYSCREENING /IDENTIFIED BYSCREENING FOR PHENYLKETONURIASCREENING PROGRAM BY /IN ASCREENING SCREENING FOR /FORSICKLE CELL SCREENING AND /OFWITH ISODICENTRIC 18 /ON AWITH PARTIAL TRISOMY 22 DUE /AWITH SIGNS OF JACOBSON /IN A
NEWBORNS /FREQUENCY IN ICTERICAND THEIR MOTHERS /MALFORMEDBY INTERPHASE FLUORESCENCEBY PCR /AMBIGUOUS GENITALIAIN BYELORUSSIA AFTER /ANDIN THE CONNECTION WITH /KIEVWITH A RECIPROCAL CHROMOSOME
NEWER METALS USED IN INDUSTRY /BYNEWFOUNDLAND KINDRED LINKED TO /IN ANEWFOUNDLAND'S SOUTH COAST /ONNF 2 NON HIPPEL LINDAU DISEASE ANDNFl A TWIN STUDY AN EXPRESSION IN
GENE CAUSES CLASSICAL /IN THELOCUS /OF MUTATIONS AT THE
NHL OF NON FOLLICLE CENTER CELL /BNICK TRANSLATION /BY IN SITUNIEMANN PICK DISEASE ABNORMALITIES IN
PICK DISEASE COMPLEMENTATIONPICK DISEASE CORRECTION OF /OFPICK DISEASE FIBROBLASTS BYPICK DISEASE TYPE C ANDPICK DISEASE TYPE C AND IPICK MOUSE /ESTERIFICATION IN
NIGHT BLINDNESS MAY BE LINKED WITH GBLINDNESS PHENOTYPE /STATIONARYBLINDNESS PROXIMAL TO DXS7
NIKAWA KUROKI SYNDROME IN FIVE /UPNINGA HUI AUTONOMOUS REGION /INNODAL AND EXTRANODAL LARGE CELLNOMENCLATURE /SYNDROME DELINEATION AND
OF SKELETAL DYSPLASIASNON B THALASSEMIC HAPLOTYPES IN THE
CDF508 CYSTIC FIBROSIS MUTATIONSCENTROMERIC A SATELLITE DNAFOLLICLE CENTER CELL LINEAGE /OFHISPANIC WHITES IN THE SAN LUISHLA LINKED GENES IN TYPE IHODGKIN LYMPHOMA /INHODGKIN LYMPHOMA /IN FOUR CASES OFHODGKIN LYMPHOMA /IN UNTREATEDHODGKIN LYMPHOMAS /FOLLICULAR BJAPANESE PATIENTS /A STUDY OF 13JEWISH INDIVIDUALS PRESUMED TO /23JEWS /AMONG JEWS ANDKETOTIC HYPERGLYCINEMIA BY ASSAYMALIGNANT CELLS DERIVED FROM /INMUSCULAR TRANSCRIPTS PRODUCED BYSYNDROMAL POSTERIOR NUCHAL CYSTIC
NONALLELIC GENETIC HETEROGENEITY /OFGENETIC HETEROGENEITY IN
NONAUTOLOGOUS CELLS /ENCAPSULATEDNONCLEFTIN CRANIOFACIAL SYNDROMESNN1COLLAGEN CANDIDATE GENES FORNONDELETIONIDUPUCAT1ON MUTATIONS /ANDNONDISJUNCTION/FACTOR FOR
/HIGH RISK FOR MEIOTICEVENTS /STAGE OFIN FAMILIAL /SOMATICIN HUMAN OVARIAN /OFIN HUMANS /ORIGIN OFIS INDUCED BY BLOODIS IT A MYTH OR REALITYON HIS MOTHER IllRELEVANCE TO HUMAN
NONDISJUNCTIONAL AND NORMAL MEIOSISNONFULAL ALZHEIMER DISEASE /ANDNONGENETIC CAUSES OF SPONTANEOUS /OFNONHUMAN PRIMATES /VNTR IN HUMANS AND
OINTITTIUAL DOWN SYNDROME INNONINVASIVE APPROACH FOR FETAL CELL
EVALUATION OF ASSYMETRICMOLECULAR GENETICPRENATAL DIAGNOSIS /FOR
NONISOTOPIC IN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONIN SITU HYBRIDIZATION /AND
NONKETOTIC HYPERGLYCINEMIA OR WITHNONLETHAL CONGENITAL NEPHROSIS /IN
SKELETAL DYSPLASIAS /OF THENONLYMPHOCYTIC LEUKEMIA AN ACUTE
LEUKEMIA SUB TYPE M4NONMOLECULAR APPROACHESNONMOSAIC 45,X /PATIENT WITH APPARENT
578
1022256928821067286573168887420031353135926712469468183218271102184317961675141917201568265516361175269927821601256383372930313
108414
13871852798627875
249162779852319288101878692278061814043
27271105185813872689S3213301333136313922341067
35631312228970418852009247034335115
159115771854124541040815771573141940985
2811365
263117501287641101060180
10851640473851173
25821346S831032
Permuted Title Index
NONMUSCLE CULTURED CELLS FROM /GENE INPRODUCTS OF THE DUCHENNE
NONPOLYPOSIS COLON CANCER (LYNCHCOLORECTAL CARCINOMA IN
NONRADIOACTIVE IN SITU HYBRIDIZATIONIN SITU HYBRIDIZATIONPROBES /EMBRYOS USINGSINGLE STRANDED /USING
NONRANDOM ASSOCIATION OF 7Q34 OTERCHROMOSOMAL BREAKPOINTS ANDCHROMOSOME ABNORMALITIES INCHROMOSOME ER 7 CHANGES AS
NONRANDOMLY DISTRIBUTED IN CELIACNONSECTARIAN HOSPITAL /THAN WOMEN AT ANONSENSE 37 MUTATION IN CATALONIANS
MUTATION IN THEMUTATION IN THE NF1 GENE
NONSMOKERS /OF CIGARETTE SMOKERS ANDNONSPECIFIC ALKALINE PHOSPHATASE GENE
CHROMOSOMAL ABERRATIONSMENTAL RETARDATION /IN
NONSYNDROMIC CLEFT LIP AND PALATECLEFT LIP AND PALATE /TOHEARING LOSS /12% HAD
NONTRISOMIC CYTOGENETIC ABNORMALITIESNOONAN NEUROFIBROMATOSIS 1 AND /IN
SYNDROME /GENETIC COUNSELING INSYNDROME ASSOCIATION REPORT OFSYNDROME PHENOTYPE WITH AN
NOR VARIANTS CLINICAL COMPARISONSNORMAL 3 METHYLGLUTACONYL COA /WITH
ACID A GLUCOSIDASE ACTIVITYAND ABNORMAL KARYOTYPE /THEAND MUTANT HUMAN CFTR GENESAND TRIPLOID OPOSSUM FETUSESAND TUMOR CELLS /LEVEL IN HUMANAND UVC REPAIR MUTANT CELLS /INBACKGROUND ALLELES /DIFFERENTBONE MARROW IN ACUTECELL LINE /PATIENT MOSAIC FOR ACELLS BY A DOUBLE LABELINGCOAGULATION STUDIES (F7R) /ANDCONTROLS AND FAMILIES WITHCVS RESULT /FEATURES AND AFETAL OUTCOME CHANCE OR /WITHGENOTYPES /THALASSEMIA AND 306GIRL /IN A PHENOTYPICALLYGROWTH HORMONE (GH) SECRETIONHUMAN AND XERODERMA /PROTECTSHUMAN DNA /TRANSFECTION OFHUMAN FIBROBLASTS VECTOR /OFINDIVIDUALS AS DETERMINED /INKARYOTYPE /THE 4P SYNDROME BUTMALE PHENOTYPE AFTER PRENATALMAMMALIAN ALLELES INTERGENICMEIOSIS /NONDISJUNCTIONAL ANDOR UNCERTAIN CYTOGENETIC /WITHPARENT /INHERITED FROM APARENTS /21 IN CYTOGENETICALLYPARENTS /AFFECTED SIBLINGS OFPERSONS AND FROM PATIENTS WITHPI M4 M5 AND M6 ALPHA /OF THEPOPULATION /IN INDIVIDUALS FROMPULMONARY DEVELOPMENT /INRELATIVES OF ISOLATED CASES
NORRIE DISEASE /DIAGNOSTIC MARKER FORDISEASE /EPISKOPI BLINDNESSDISEASE IN A THREE GENERATIONDISEASE LOCUS ON XP11.3 /OF THE
NORTH AMERICA /AMONG POPULATIONS INAMERICA /DIAGNOSIS COUNSELING INAMERICAN CAUCASIAN AND AFRICANAMERICAN MATERNALCAROLINA MACULAR DYSTROPHY ANCHINA /STORAGE DISEASES INCHINA AND THEIR APPLICATION TOCHINA CARRIER DETECTION BY /INEAST SCOTLAND PREDICTIVE /ININDIA /OF BETA THALASSEMIA ININDIAN HOSPITAL (ALIGARH) /IN A
NORTHEASTERN QUEBEC IS DUE TO A /l INNORTHERN EUROPE /NYHAN FAMILIES FROM
INDIA /CLEFT PALATE INNORTHWESTERN SIBERIA /POPULATIONS OFNORWEGIAN CYSTIC FIBROSIS FAMILIES /13
TWINS /IN VIRGINIAN ANDNOSOLOGY /TOWARD A COMPLETE MOLECULAR
AND DIAGNOSTIC CODING ITSAND INHERITANCE PATTERNOF PETERS PLUS SYNDROMEOF SMITH LEMLI OPITZOPENING COMMENTS /MOLECULAR
NOT1 BOUNDARY CLONES CONTAIN TWO NEWLINKING CLONES ON CHROMOSOME 22
NRS 1 A NOVEL HUMAN NEURAL RETINA /OFNRUI DIGESTION /ELECTROPHORESIS AFTERNTD IN TURKISH CHILDREN /OFNTDS /OF GENETIC FACTORS IN
/OF PREGNANCIES AT RISK FORIN BARQUISIMETO VENEZUELA /OFIN TWIN PREGNANCIES /FOR OPEN
NUCHAL CYSTIC HYGROMA /POSTERIORFLUID PHYSIOLOGIC OR PATHOLOGIC
NUCLEAR EXTRACTS AND IS ASSOCIATEDGENE MODELS AND THEIR
102916
60019912144223016841105150913131438131414491742267411181084129447215245201015101323
124899
1763635660120012175291445236424511354256427971345143913371500517145611351831153214072539225025872546171114502627
85216
16011219840147323972831927
279119452047149021962854389
2798212
20215581114102186010241403269810532678281511072658351140907898679344
219521912308621838
2235117226801214704946
24172781
GENOME /MAPPING OF THE YEASTRDNA DURING LIMB REGENERATIONRNA COMPLEMENTARY DNA
NUCLEATED ERYTHROCYTES FROM MATERNALNUCLEI /GENE SEQUENCES IN INTERPHASE
/REGIONS WITHIN INTERPHASE/TO INTERPHASE AND METAPHASEFIBROBLASTS MALE PRONUCLEI ANDUSING FLUORESCENCE IN SITU
NUCLEIC ACIDS /OF PROTEINS ANDACIDS FOR GENE MAPPING /OF
NUCLEOLAR ORGANIZER REGION ONTO /OFORGANIZER REGIONS IN /ANDORGANIZING REGIONS WITHIN
NUCLEOTIDE ANALOGS TO DETECT SINGLESEQUENCE LEVEL /AT THESEQUENCE OF THE HUMAN /ANDSUBSTITUTION IN THE MAJOR
NUCLEUS /RNA SPLICING IN THE OOCYTENULL ALLELE /I COMMONLY DUE TO COLlAl
MUTATIONS IN A HUMAN /SPONTANEOUSNULLWEST ABSENCE OF DETECTABLE SERUMNUMERICAL CHROMOSOMAL ABNORMALITIES
CHROMOSOME ABERRATIONS /OFCHROMOSOME ABERRATIONS INCLASSIFICATION APPROACH /A
NURSES IN EVERY SETTING /EDUCATION OF
23712892521110181
1716182
215316482518
921132158417162078223422962621317
2464253623261306128313126791773
0
OBESITY /TWIN STUDIES OF HUMANOBJECTIVE ASSESSMENT /CLINODACTYLY AN
DIAGNOSIS OF DYSMORPHOLOGYOBJECTIVES /DISORDERS ORGANIZATION ANDOBUGATE RECOMBINATION BETWEEN THEOBLONGATA CDNA LIBRARIES /AND MEDULLAOBSERVATION OF THE NERVE GROWTH
ON CHROMOSOMALOBSESSIVE COMPULSIVE DISORDER IN A /OFOBSTETRIC CARE AT A CATHOLIC HOSPITALOBSTETRICAL SERVICES OF SCREENING FOROBSTRUCTION /IN NEONATES WITH NASALOBSTRUCTIVE SLEEP APNEA FAMILIAL /OF
UROPATHIES /PROGNOSIS OFOCULAR ALBINISM /ANALYSIS OF X LINKED
ALBINISM /AROUND X LINKEDOCULOCEREBROFACIAL SYNDROME IN A 15OCULOCUTANEOUS ALBINISM /IN TYPE IA
ALBINISM IN SOUTHERNOCULOMOTOR ABNORMALITIES /WITHOESOPHAGEAL ATRESIA AND /GENETICS OF
ATRESIA RENAL DEFECTS ANDFISTULAE AND OESOPHAGEAL
OFFSPRING /AND AN UNBALANCEDBORN AFTER SELF POISONINGIN COUPLES WITH A TRISOMICOF WOMEN WITH HEREDITARY
OH MUTATED HLA HAPLOTYPES IN /OF 21OHDO BLEPHAROPHIMOSIS SYNDROME /OF THEOHIO 1974 1989 /ATLANTA AND SOUTHWESTOLDER /SYNDROME IN WOMEN AGE 35 AND
/SYNDROME IN WOMEN AGE 35 ANDPHENYLKETONURIA PATIENTS /IN
OLIGOGENIC TRAITS BY LINKAGE ANALYSISOLIGOHYDRAMNIOS /CVS AND MIDTRIMESTER
/SECOND TRIMESTERDUE TO RENAL /CAUSE OF
OLIGONUCLEOTIDE TYPING /SPECIFICOLIGONUCLEOTIDES CORRESPONDING TO ITOOLIGOSACCHARIDES /HPLC OF URINARYOLIVER AND MAC FARLANE SYNDROME
SYNDROME /OF ADAMSOLIVOPONTOCEREBELLAR ATROPHY /DOMINANTOMPHALOCELE AND SEVERE OSSIFICATIONONCOGENE /THE DOMAIN OF THE HUMAN MYC
AMPLIFICATION AND LOSS OF /OFAND GENE AMPLIFICATION INC NEU IN BREAST AND OVARIANFAMILY /GENE OF JUN/FOSFROM HUMAN CHROMOSOME 11013HOMOLOGS IN DIFFERENT /C RASIN CHICKENS WITH RESISTANCEIN HUMAN OVARIAN CANCER /RASIN HUMAN PIEBALDISM /PROTOINVOLVEMENT BETWEEN PRIMARYPRODUCT /TO THE AVIAN V MAF
ONCOGENES BY CHROMOSOMAL IN SITUIN HUMAN LUNG CARCINOMA /OF
ONCOGENESIS /REGION 8Q24 LINKED TOAND AGING /FORMOLECULAR PROCESSES /FOROF PRIMARY OVARIAN CANCER
ONSET /METABOLISM AND THE AGE OFADDITIONAL EVIDENCE OF GENOMICALZHEIMER DISEASE /GENE IN EARLYALZHEIMER DISEASE AN EXAMPLE OFAS A COVARIATE /USING AGE ATCEROID LIPOFUSCINOSIS (BATTENDEAFNESS /STUDIES OF EARLYDIABETES OF THE YOUNG TODISORDERS LOW ACCEPTANCE RATE
4018717233541926233325331397271917421215905
2763929
20512014752
23182000514
2646816816144612711553232665763
26861169125055463
1150926718
28342496569769779
1873650
2570217369
25962308260825692590593189618
2459216013132591254625782572233791
2290266719701972
2274
211
DISORDERS THE EXPERIENCE OFDISTRIBUTIONS FROM FAMILY DATAFAMILIAL BREAST CANCER /OF EARLYFOR FAMILIAL OVARIAN CANCER /ATFORM OF FRIEDREICH ATAXIA ISIN FAMILIAL AMYLOID /OF AGE OFIN MACHADO JOSEPH DISEASE /OFMOSAIC FORM OF DOWN SYNDROMEOF HUNTINGTON DISEASE AND /ATPSYCHOSIS IN THE /LATESPINAL MUSCULAR ATROPHIESSPINAL MUSCULAR ATROPHY IN
ONTOGENESIS BY MEANS OF ANALYSIS OFONTOGENY AND PHYLOGENY OF PEROXISOMALONYCHODYSPLASIA A NEW SYNDROME /ANDOOCYTE MATURATION /STUDIES OF HUMAN
NUCLEUS /RNA SPLICING IN THEOOCYTES /POLYSPERMIC HUMAN
AND PREIMPLANTATION EMBRYOSMAY HELP PREDICT REPRODUCTIVE
OPEN NEURAL TUBE OR VENTRAL WALL /OFNTDS IN TWIN PREGNANCIES /FOR
OPITZ SYNDROME /OF THE SMITH LEMLISYNDROME(S) A NUMERICAL /LEMLI
OPOSSUM FETUSES /NORMAL AND TRIPLOIDOPPOSITE DNA STRANDS OF THE PRION /BY
PATTERNS OF X INACTIVATIONOPSISMODYSPLASIA ASSESSMENT OF THEOPTIC ATROPHY SYNDROME /AND
NEUROPATHY /LEBER HEREDITARYNEUROPATHY /LEBER HEREDITARYNEUROPATHY AND EVIDENCE FORNEUROPATHY MUTATION SPECIFICNEUROPATHY PARTLY DETERMINED BYNEURORETINOPATHY /HEREDITARY
OPTIMAL LEVEL OF HETEROZYGOSITY INLOCUS COMBINATION STRATEGIES
OPTIMIZATION OF DNA EXTRACTION FROMOF RETROVIRAL VECTOR
OPTIMIZED PROTOCOL FOR THE DETECTIONORAL CAVITY AND HEAD AND NECK CANCERS
FACIAL DIGITAL SYNDROME TYPEFACIAL DIGITAL SYNDROMES /ON THEFACIAL DIGITAL SYNDROMES TO LUMP
ORANGUTAN /OF MAN CHIMPANZEE ANDORBITS SHORT PHILTRUM SYNDROME /DEEPORCHESTRATION OF GLYCOSAMINOGLYCANORDERING FOR CATESPIN E AND RENIN ONORGAN SPECIFIC ANEUPLOID DIRECTEDORGANIC ACIDS /PLASMA AND URINEORGANIZATION /BY MONOMERIC
/MARKERS AND GENOMICAND A SEARCH FOR /GENEAND LOCALIZATION OF THEAND NUCLEOTIDE SEQUENCEAND OBJECTIVES /DISORDERSOF ALPHOID REPETITIVEOF BASE SEQUENCES IN THEOF CANINE HOMOLOGS OFOF GENETIC SERVICES /ANDOF HUMAN CHROMOSOMES ATPOLYMORPHISM AND /GENERELATIONSHIP OF DNA AND
ORGANIZER REGION ONTO CHROMOSOMEREGIONS IN ALZHEIMER
ORGANOPHOSPHORUS AND CARBAMATE /TOORIENTAL PATIENT WITH PETERS ANOMALYORIENTED NATIONAL GENETICS PROGRAMS
NATIONAL HEALTH SERVICEYEAST ARTIFICIAL CHROMOSOME
ORIGIN /HETEROZYGOTES OF MULTI ETHNIC/IN TUMORS OF MESENCHYMAL/OF DIFFERENT CHROMOSOMALAND NEW MARKERS /PARENTALAND PHENOTYPE OF MOSAICOF A FRAGMENT IN A TURNER /THEOF A FRENCH CANADIANOF ABNORMALITIES OF CHROMOSOMEOF ASHKENAZI /THE SEPHARDICOF CHROMOSOMAL ABNORMALITIESOF CHROMOSOMAL ERROR INFLUENCEOF DE NOVO DUPLICATIONS USINGOF DE NOVO MUTATION IN MANOF GASTRIC CARCINOMA STUDIESOF HUMAN CHROMOSOME 2 ANOF HYDATIDIFORM MOLAR /GENETICOF MAN A CYTOGENETIC MODELOF MARKER/RING CHROMOSOMES INOF MATERNAL DISOMY IN PRADEROF MIXOPLOID DOWN SYNDROMEOF NONDISJUNCTION IN HUMANSOF NORMAL MAMMALIAN ALLELESOF SEX CHROMOSOME ANEUPLOIDYOF SV40 TRANSFORMED CELL LINESOF THALASSEMIA GENES IN ASIANSOF THE ADDITIONAL CHROMOSOMEOF THE EXTRA HAPLOID SETOF THE X CHROMOSOME IN RETTPOPULATION GENETIC ASPECTS OF
ORNITHINE AMINOTRANSFERASEAMINOTRANSFERASE GENE /OFAMINOTRANSFERASE GENE INAMINOTRANSFERASE MODULATIONAMINOTRANSFERASE RELATEDD AMINOTRANSFERASE GENE OF
579
24826612024582820275754"15042660174118852687223394577012403171258362128411371214751679
2451229822317448665131019973107320321022278720621081246810995838313426331729716467
2148117426316942187226722662296354
212022281861149
1640425164311321584539903S30150204185525861714170216001669271215672826363
14111677406
259921479282620172515931428408
262785
5791070415104
222366
194528021057245019312519
Permuted Title Index
D AMINOTRANSFERASE RELATEDTRANSCARBAMYLASE ACTIVITYTRANSCARBAMYLASE CDNA INTOTRANSCARBAMYLASE DEFICIENCYTRANSCARBAMYLASE GENE /THE
ORODENTAL FINDINGS IN AN EGYPTIANOROSOMUCOID SUBTYPING APPLICATION TOORTHOSTATIC INTOLERANCE /IN FAMILIALOSAKA CITY 1948 1990 /HOSPITAL INOSSIFICATION DEFECT /AND SEVEREOSTEOARTHROSIS AND MUTATIONS OF TYPEOSTEOCHONDRODYSPLASIA /NEWOSTEODYSPLASIA WITH TARDY PROGRESSINGOSTEOGENESIS IMPERFECTA /DEFORMING
IMPERFECTA /FORM OFIMPERFECTA /LETHALIMPERFECTA AND /WITHIMPERFECTA BIOCHEMICALIMPERFECTA TYPEIMPERFECTA TYPE III /OFIMPERFECTA TYPE IVIMPERFECTA WITH /DOMINANT
OSTEOGENIC SARCOMA /CASE OF GIANT CELLOSTEOLYSIS EXCLUSION OF THE GENE FROM
FROM EXTENSIVE REGIONS OFOSTEOPATHIA STRIATA WITH CRANIALOSTEOPOROSIS /IMPERFECTA AND
/OF IDIOPATHIC JUVENILEOSTEOSARCOMA /CHILDHOOD AND ADOLESCENTOTHERS /GYRATE ATROPHY AMONG FINNS ANDOTO PALATAL DIGITAL SYNDROME TYPE II
RENAL DYSPLASIA SYNDROME A CAUSEOUTPATIENT POPULATION /IN A CANADIANOUTSIDE REGION 15011 13 /HETEROGENEITYOVARIAN BREAST CANCER /AND SPORADIC
CANCER /130 AND XP IN HUMANCANCER /AT ONSET FOR FAMILIALCANCER /C NEU IN BREAST ANDCANCER /EXPRESSION IN HUMANCANCER /ONCOGENESIS OF PRIMARYCANCER /RAS ONCOGENE IN HUMANCANCER HEPATOCELLULAR /CANCERCANCER LOCUS ON CHROMOSOME 17EPITHELIAL TUMORS /18 INSEROUS ADENOCARCINOMAS /INTERATOMAS USING DNA MARKERSTUMORIGENESIS /BE INVOLVED INTUMORS /REACTIVATION IN HUMAN
OVEREXPRESS S100B PROTEIN /MICE THATOVEREXPRESSED EXOGENOUS STEROID /OFOVEREXPRESSING CUZN SUPEROXIDE /CELLSOVEREXPRESSION IN BARRETT'S /AND P53OVERGROWTH /AND FEATURES OFOVERLAP CLONING IN THE XP22.3 REGIONOVERLAPPING FEATURES /NEW CASES WITH
PHENOTYPES /OF TWOOVULES /INDUCED FROM UNPOLLINATEDOXIDASE /OXIDASE A NOVEL PEROXISOMAL
A NOVEL PEROXISOMAL OXIDASEACTIVITY IN LONG EVANS /LACKSDEFICIENT MICE BY GENE /URATEGENES MARK ACTIVITY STATESIN ALCOHOLICS THEIR FIRST
OXIDATION AND FLAVIN METABOLISM INDEFECTS PROSPECTS FOR /ACIDDISORDERS OVERVIEW AND /ACIDOF FATTY ACIDS IN X /ANDSIMILARITIES AND /B
OXYGEN FREE RADICALS /ACTIVITY TOTENSION EFFECTS ON FANCONITENSION EFFECTS ON FANCONI
215324772472123755982228561037268865046
8448736265344462497450
246449610541065136519292016796
249795772S4933718
27251116603606582
2596241325725933021977257413384102566138941949222292571172320927711538154852752751224932303493497262259516260
222914011418
p
P 450 DEBRISOQUINE LOCUS (CYP2DP8) ONARM BREAKPOINT OF CHROMOSOME 16 /THEDNA ELEMENTS IN SOMATIC CELLS /OFFAMILY ALLELES RESULTING FROM GENE
P,DEL IN A LIVEBORN INFANTP,DUP 0, + REC(7),DUP PDEL 0 IN AP11.2 /46,XX, 18,+1(180)
DELINEATION OF THE CRITICALP1I.4;P13.3 /SEGREGATION OF T(X;16)P11.4022 ASSOCIATED WITH NORRIE /(X)P11:011 IN A FEMALE WITH REPEATEDP11011 /WITH A DE NOVO T(22;22)P13;Q11 PAT IN A FEMALE WITH INGUINALP13;Q11.2 MAT TRANSLOCATION /T(5;10)P13;034 EXPRESSED TO DIFFERENTP14 /PHYSICAL MAP OF CHROMOSOME 1lP12PI4P16 /IN AN INFANT WITH DEL (4)P21 AND K REV1 PROTEINS BY GTPASE /RASP21.2 OF KERATOSIS FOLLICULARISP21032 /WITH PATERNAL INV(7)P22 /OF PDGFA LOCALIZATION TO 7P21P22.2 /DYSPLASIA IN A GIRL WITH DEL(X)P22;Q11 IN A PREGNANCY WITH THEP23;Q35 IN THREE CASES OF CHILDHOODP25;032 IN A BOY WITH LEUKEMOIDP25021 /CEN 021 SEGMENT OF AN INV(3)P36.3 AND THE POTENTIAL ROLE OF HIGH
2035170928192797156515651501170288
1490123093814771429153219680412
1985156521117749531331132116871541
P36.3;024.3 POSSIBLE LOCALIZATION OFP450 GENES APPLICATION IN THEP450C21 IN RELATION TO ITSP49A DETECTS COMPLEX PVUII HAPLOTYPESP53 AND K RAS MUTATIONAL SPECTRA IN
FROM HUMAN TUMORS IS /MUTANTGENE /LOCI AT 17P13 INCLUDING THEGENE IN HUMAN HEPATOCELLULAR /THEGENE IN HUMAN TRANSITIONAL CELLGENE MUTATIONS IN PATIENTS WITHGENES /MUTATIONS IN THE RB ANDGENETIC AND PROTEIN ALTERATIONSMUTATION A COMMON STEP IN HUMANMUTATIONS IN BURKITT LYMPHOMASMUTATIONS IN RENAL TUMORS /OFOVEREXPRESSION IN BARRETT'S /ANDTUMOR AND GERM LINE MUTATIONS IN
P58 A CELL CYCLE REGULATED PROTEINPACIFIC /OF THE COLONIZATION OF THEPACKAGE FOR MULTIPOINT MAPPING OFPACYDERMOPERIOSTMTS IN THREE MALEPAGET DISEASE LOCUS /A PUTATIVEPAINLESS EUGENICSPAINTING CHROMOSOME 22 AND RAPID /FOR
FLUORESCENCE IN SITUPAIR /THE FIRST REPORT OF A SIBLING
ANALYSIS OF THE LINKAGE OF /SIBLINKAGE ANALYSIS WITH MULTIPLEOF DUPLICATED GENES RP1 AND RP2
PAIRING AND ANEUPLOIDY IN MANPATTERN OF HUMAN CHROMOSOME
PAIRS FROM A POLYMORPHIC TRIMERICPALATAL DIGITAL SYNDROME TYPE II THE
FEATURES /DYSGENESIS ANDPALATE /ALPHA WITH CLEFT LIP AND
/ANALYSIS OF CLEFT LIP AND/IN CHILDREN WITH CLEFT/MALFORMATIONS CLEFT LIP AND/PATIENTS WITH CLEFT LIP AND/STUDIES OF CLEFT LIP ANDITO NONSYNDROMIC CLEFT LIP ANDAND MICROGNATHIA IN TWO /CLEFTASSOCIATION AND LINKAGE /ANDIN A BRITISH COLUMBIA NATIVEIN NORTHERN INDIA /CLEFTIN SHANGHAI CHINA /CLEFT
PALEO INDIANS AND SUGGESTS A PRE [THEPALUSTER HALL SYNDROME /SURVIVAL IN
HALL SYNDROME ASSOCIATEDKILLIAN SYNDROME /REGION FOR
PALMAR DERMATOGLYPHICS AND ABO BLOODPALMITOYLTRANSFERASE B DEFICIENCY
DEFICIENCYTYPE 2 /CARNITINE
PALSY /ADULT PRESENTING WITH CEREBRALPAMIDRONATE DISODIUM IN THE TREATMENTPANEL /REDUCED SOMATIC CELL HYBRID
FOR THE PROXIMAL SHORT ARM OFOF RADIATION INDUCED SOMATIC /AOF SOMATIC HYBRIDS USEFUL FOR
PANIC DISORDER /LINKAGE ANALYSIS OFPAPER /SAMPLES COLLECTED ON FILTER
BLOOD SPECIMENS /DRIED FILTERMATRIX /SPECIMENS COLLECTED ON A
PAPILLARY THYROID CARCINOMA BY /7 IN APARACENTRIC INVERSION /FAMILIAL
INVERSION OF 9P /FAMILIALPARACOCCIDIOIDOMYCOSIS INFECTION /WITHPARACRINOPATHY PLEIOTROPY /AS APARADIGM FOR MAPPING FUNCTIONAL /APARALYSIS /OF DOMINANT PERIODICPARAMETERS /AND CALCIUM DEPENDENT
FOR 586 ALPHA THALASSEMIAPARAMETRIC APPROACHES TO THEPARAOXON ON METHODS OF SERUM /OFPARAOXONASE/ARYLESTERASE /OF SERUMPARAPLEGIA /LINKED HEREDITARY SPASTIC
/WITH ATAXIA AND SPASTICWITH MENTAL RETARDATION
PARASITES INTERFERE WITH THE /DIDPARDHIS OF ANDHRA PRADESH SOUTH INDIAPARENCHYMA INDUCED BY PLASMA /TO BRAINPARENT /BORN AFTER SELF POISONING OF
/INHERITED FROM A NORMALSUPPORT GROUPS COME OF AGE!
PARENTAGE TESTING EXPERIENCES FROM APARENTAL ADJUSTMENT TO THE BIRTH OF A
CONSANGUINITY AND FOUNDERIMPRINTING SUGGESTED BY /GENEMOSAICISM IN DOWN SYNDROMEORIGIN AND NEW MARKERSORIGIN OF ABNORMALITIES OFORIGIN OF CHROMOSOMALORIGIN OF DE NOVO MUTATIONORIGIN OF THE EXTRA HAPLOIDORIGIN OF THE X CHROMOSOMETRANSMISSION AND
PARENTS /21 IN CYTOGENETICALLY NORMAL/AFFECTED SIBLINGS OF NORMAL/BOY BORN TO CONSANGUINEOUS/PATIENTS AND THEIRAND CHILDREN CONCORDANT FORARE HAZARDOUS FOR DISJUNCTIONHAVING G 6 PD DEFICIENCY /FOR
PARKINSON DISEASE /DEMENTIA AND
1468254724142872610
244113732429257726052553587S63259413252571218
2128257
20408491929181516491728728
2041202724031578420959933146622422774956775
236969
1013762101519092678270626377067011437185153623825351530957
21362139213220581944118611025771322174815892673743202
23944451831266158054370896367526132866955127116011755274017601746621183517021567363406104
22232757121984089113882742113617782704
DISEASE /VULNERABILITY TODISEASE WITH IDIOPATHIC
PARKINSONISM /(X LINKED DYSTONIASYNDROME LOCUS BY
PAROTID GLAND OF TRANSGENIC MICE /INPARTIAL DELETION OF CHROMOSOME 22 IN
DELETIONS OF CHROMOSOMES 20DIGEST LIBRARIES FROM FLOW /OFEPILEPSY /GENERALIZED ANDHYPOTHALAMIC GONADOTROPINPHYSICAL MAP OF CHROMOSOME 21TRISOMY 21(022.1 OTER) DUE TOTRISOMY 22 DUE TO MEIOSIS IITRISOMY 2031 2035 SECONDARYTRISOMY 5P IN BROTHER ANDTRISOMY 70 DUE TO MEIOTICTRISOMY 70 IN A DE NOVO /OFTRISOMY 80 AND MONOSOMY 20 /OF
PARTICIPATION /TO INCREASE PATERNALIN A PRENATAL
PARTICLE DENSITY AND CONCENTRATION INPARVOVIRUS INFECTION IN PREGNANCY APATCH MISMATCH REPAIR SYSTEM /SHORTPATELLA SUBLUXATION AND /DEFORMATION
SYNDROME /GENE IN NAILSYNDROME STUDY OF 37 CASES
PATELLAE AND DIAPHRAGMATIC /ABSENTPATERNAL AGE AND DOWN SYNDROME A
AGE AND LATE ONSET ALZHEIMERAGE SUGGESTS MECHANISM OFCOMPLEX DOUBLE TRANSLOCATIONDISOMY IN SPORADIC BECKWITHINV(7)(P21032) /WITHLINE OF TRANSMISSION INPARTICIPATION /TO INCREASETRANSLOCATION /20 DUE TO AUNIPARENTAL DISOMY IN
PATERNITY ESTABLISHMENT FOR A CASEPATHOGENESIS /HIV 1 VARIATION IN AIDS
/MOLECULAR BIOLOGY ANDOF A PRIMARY GONADALOF CONJOINED TWINS [THE
PATHOGENETIC DIAGNOSIS /CONCEPT AS APATHOGENIC DIAGNOSTIC AND CLINICALPATHOGENICITY OF FAMILIAL /ANDPATHOLOGIC /FLUID PHYSIOLOGIC ORPATHOLOGIES CYTOGENETIC FINDINGS
INHERENT IN THE METHOD OFPATHOLOGIST TO USE COMPUTERS IN THEPATHOLOGY /AND CARDIOVASCULAR
AND THE CLINICAL PHENOTYPEOF HUMAN B GALACTOSIDASETO HUMANGENETIK HUMAN
PATHOPHYSIOLOGY /IMPLICATIONS FORPATHWAY AMINOLEVULINATE DEHYDRATASEPATHWAYS IN HUMAN CELLS /REPAIRPATTERN /A GIRL WITH XO/XX CHROMOSOMAL
/EXHIBIT A COMPLEX METHYLATIONFORMATION AND GERMLINE /OFFROM A 46,XY FEMALE WITHIN MALIGNANT ASTROCYTOMASOF HUMAN CHROMOSOME 21 INOF PRENATAL SCREENING ANDPROFILES IN DOWN SYNDROMEREVISITED /AND INHERITANCE
PATTERNING GENES IN DROSOPHILA A/FPATTERNS /OF DIFFERENT ASSOCIATION .
IN FORTY GREEK DUCHENNE ANDIN METHODS FOR ANTENATALOF LINKAGE DISEQUILIBRIUM INOF MATRIX GENES DURINGOF NUCLEOTIDE SUBSTITUTIONOF X INACTIVATION IN MZUSING FLUORESCENCE IN SITU
PATTERSON DAVID SYNDROME /OF A CASE OFPAX2 GENE TO 10Q22.1 024.3 /OF HUMANPAY FOR PRENATAL DIAGNOSIS OF /TOPCI MAPS TO 6021 022 AND IS LINKED TOPCR /AMBIGUOUS GENITALIA NEWBORNS BY
/AMPLIFICATION OF VNTR LOCI BY THE/ANALYSIS OF COMMON DISEASES USING/ANEUPLOIDY USING QUANTITATIVE/BY QUANTITATIVE MULTIPLEX/CYTOMETRY AND CONFIRMATION BY/DEFICIENCY OF A CHINESE BY THE/HUMAN CHROMOSOMES USING SHOT GUN/IN LEUKEMIA AND LYMPHOMA USING/IN SEQUENCE TAGGED SITES/INTERSPERSED REPETITIVE SEQUENCE/MUSCULAR DYSTROPHY BY MULTIPLEX/MUTATIONS IN HUNAN CHINA BY/OF CDF508 BY ALLELE SPECIFIC/OF HUMAN GENOMIC DNA BY/PROBES GENERATED BY INTER ALU/SOMATIC AND SPERM CELLS USING/SORTING AND ALU ELEMENT MEDIATED/TRACE HUMAN TISSUES BY THE/USING CHROMOSOME MICRODISSECTION/USING SOUTHERN BLOTTING ANDAMPLIFICATION /HYBRIDS USING ALUAMPLIFICATION AND SEQUENCING OFAMPLIFICATION IN DUCHENNE AND /BYAMPLIFICATION IN JAPANESE /BY THEAMPLIFICATION IS THE METHOD OFAMPLIFICATION OF CODING SEQUENCES
580
230333
204419492444258514072499477645
21191498141914061539142216861402175918462434922
25527701996746640147426672660140690
1565791175914021558287722952641386943859130546994613081216139
1730434284320
2447240924128252436323138613324201134629907S69653229216142336930
26212231200711
2282179913071175252242610691023109
2324177
103121002058112428201099251622474401605250920701110210825051040231310732612
Permuted Title Index
AMPLIFICATION OF YEAST ARTIFICIALAMPLIFICATION OF ZFY AND SRYAMPLIFIED CDNAS /SEQUENCING OF THEAMPLIFIED DNA FRAGMENTS FOR /OFAMPLIFIED MATERIAL /OFAMPLIFIED YEAST ARTIFICIAL /OF IRSANALYSIS FOR SINGLE CELLS /OFAND AN IMPROVED METHOD OF REVERSEAND CHROMOSOMAL MARKERS IN THE /OFAND IN SITU HYBRIDIZATION /BY THEAND MICROCLONING TECHNIQUEAPPROACH TO ALLELE LOSS DETECTIONAPPROACH TO MONITORING OF /RAPIDBASED DNA POLYMORPHISMS USEFUL /OFBASED GENE ANALYSES /PROTEIN ANDBASED MARKERS FOR CHROMOSOME 3BASED MOLECULAR ANALYSIS /OFBASED POLYMORPHISMS /USINGCHARACTERIZATION AND INITIAL /IRSCOUPLED RESTRICTION DIGESTSDENATURING GRADIENT GEL /USINGELIMINATION OF HETERODUPLEX /BYFOLLOWED BY LIGASE MEDIATED GENEFOR RAPID DETECTION OF SINGLE /GAPGENERATED HETERODUPLEXES /BYGENERATION OF HUMAN CHROMOSOME 22IN A PATIENT WITH APPARENT /BYIN COMBINATION WITH CONSTANT /THEIS RELATIVELY LOW IN ISRAELI /ANDLABELED PROBES AND DIGITAL IMAGINGMARKER LINKED TO MYOTONICMAY ALSO LEAD TO FALSE NEGATIVEMEDIATED DNA AMPLIFICATION /BYMEDIATED SITE DIRECTED MUTAGENESISMETHOD /GC RICH DNA USING THE HOTMETHOD FOR THE RAPID ISOLATION OFMICROCLONING IN HUMAN GENETIC /ANDOF DRIED BLOOD /AMERICANS BYOF GUTHRIE BLOOD SPOTS /BY DIRECTOF POOLED GENOMIC DNA SAMPLES /BYPROBES /WITH BIOTINYLATEDPROBES FOR ISOLATION OF HUMAN /ALUPRODUCTS FROM IRRADIATION REDUCEDREACTIONS AS AN INITIALREVEALS MULTIPLE POLYMORPHIC LOCISINGLE STRAND GEL ELECTROPHORESISTECHNIQUES /BY SOUTHERN BLOT ANDTECHNIQUES /SITU HYBRIDIZATION ANDTESTING FOR 11 PREGNANCIES /ANDTO RESOLVE CONFLICTING FETAL SEXWALKING AND JUMPING CLONING
PCRFLPS BY HIGH RESOLUTION /FACTORPD DEFICIENCY NEONATES /HAVING G 6PDGFA LOCALIZATION TO 7P21 P22 /OFPDUARTE HETEROGENEITY OF P FAMILYPECTUS DEFORMITY HYPOTONIA AND SEVEREPEDIATRIC BRAIN TUMORS /OF MALIGNANT
DEPARTMENT OF A SECOND /IN AHOSPITAL IN BRAZIL /IN APOPULATION /IN A HIGH RISK
PEDIGREE /AN EXTENDED MULTIGENERATION/ANALYSIS OF A FAMILY/IN 17 MEMBERS OF ONEANALYSIS /APPROACH TOSEGREGATING A STUTTERING
PEDIGREES /LINKAGE STUDIES USING CEPHFOR LINKAGE ANALYSESIN SPINAL MUSCULAR ATROPHY
PEEL BOWEL SYNDROME /OF APPLEPEIvZAEUS MERZBACHER DISEASE
MERZBACHER DISEASE /CAUSESMERZBACHER DISEASE /INMERZBACHER DISEASE /WITHMERZBACHER DISEASE /WITH
PELVIC LIPOMATOSIS /RENAL ECTOPIA ANDPEMPHIGOID ANTIGENS 1 AND 2 GENESPENETRANCE FORM OF HEREDITARY /A LOW
OF RETINOBLASTOMA GENEOF THE SOTOS SYNDROME GENESPECIFICATION IN GENETIC
PENETRANCES OF AUTOSOMAL DOMINANTPENETRANT DOMINANT CONDITIONSPENTASOMY X (49,XXXXX) /TWO CASES OFPEOPUNG OF THE AMERICAS /AND THEPEPD LOCUS /CLINICAL EXPRESSION AT THEPEPSINOGEN A GENE /OF A HUMANPEPTIDASE D DEFICIENCY /OF PROLIDASEPEPTIDE HYDROLASE GENE /THE RAT ACYLPEPTIDES OF THE RED CELL MEMBRANEPERCENT /GENE HAVE A G+C CONTENT OF 39PERCEPTION AND HEALTH BEHAVIOR INPERCEPTIONS AND PRACTICES AMONG WOMEN
OF RISK OF WOMEN WHO HAVEPERFORMANCE LIQUID CHROMATOGRAPHY
LIQUID CHROMATOGRAPHYOF TRANSABDOMINAL ANDTHROUGH THE TRANSCERVICAL
PERFORMING EARLY AMNIOCENTESIS FORPERICENTRIC AUTOSOMAL INVERSIONS
INV(2) (PL2Q14) A REVISEDINVERSION OF CHROMOSOMEMARKERS /INFORMATIVEREGION OF CHROMOSOME 10REGION OF THE HUMAN Y /THE
PERICENTROMERIC HETEROCHROMATIN BY
2526168523052793251721602525111341511312061131725962059109619781043961
2165252310572513104197610491649103228131098
91104310601627997
253020752532274318402792165623212168989
20992283958136411851691278520841778211127978702191789777
1410996634790
203319691901268327761181971972
11011083235815082387221221787
2086203427911527255
23272408987
22972629282117331754175356557011301130122615151561147719142008198
1598
LOCALIZATION OF LUBAGMARKERS /CHROMOSOME 10
PERIMETERS AND PITFALLS /LABORATORYPERINATAL INFANTS IN NINGXIA HUI
MANIFESTATION OF TRISOMYPRACTICE /IN PRENATAL AND
PERIODIC PARALYSIS /OF DOMINANTPERIODONTITIS /STUDIES OF JUVENILE
/STUDIES OF JUVENILEPERIPHERAL BLOOD LYMPHOCYTES /MRNA IN
BLOOD LYMPHOCYTES INDUCEDLYMPHOCYTES /ALTERATIONS IN
PERITONMS NOT ASSOCIATED WITHPERLECAN TO MOUSE CHROMOSOME /GENE FORPERMANENT BLACK HAIR DYE /OF A
IMPROVEMENT OF /LEADS TOPEROXISOMAL ASSEMBLY DEFECT IN
B OXIDATION SIMILARITIESBIFUNCTIONAL ENZYMEDEFECT IN SIBLINGS WITHDISORDER /NEW VARIANT OFDISORDERS AN UPDATEMEMBRANE PROTEIN CDNA ANDMEMBRANE PROTEINS /OFOXIDASE /OXIDASE A NOVEL
PEROXISOMES /AND CYTOCHEMISTRY OF/BIOGENESIS OF
PERSISTENT CHOROID PLEXUS CYSTSCLOACA IN LANGER GIEDIONMARKER CHROMOSOME IN A /ATHROMBOCYTOPENIA AND
PERSONAL IDENTIFICATION /REPEATS FORRIGHTS EXTEND /HOW FAR DO OUR
PERSONALITY FACTORS IN YOUNG /ANDPHENOTYPES /THE GENES FROM
PERSPECTIVE /DISEASE A WORLD WIDEPERSPECTIVES PSYCHOSOCIAL FACTORS /NEWPERUVIAN MUMMIES /AND PROTEINS FROM
MUMMIES /D4S175 IN ANCIENTPERVASIVE DEVELOPMENTAL DISORDER /ASPETERS ANOMALY AND ASSOCIATED
ANOMALY SHORT LIMBED DWARFISMPLUS SYNDROME FURTHER /OF
PETO AND DERSIMIONIAN LAIRD COCHRANPH POSITIVE ACUTE LYMPHOCYTIC /IN A
SENSITIVE MUTATION ASSOCIATED WITHPHA STIMULATED LUPUS LYMPHOCYTESPHAKOMATOSIS /IN COWDEN DISEASE A NEWPHALANGEAL TYPE WITH SEVERE MENTALPHASE X IRRADIATION IN RELATION TO /G2PHENOL:CHLOROFORM EXTRACTION NERSUSPHENOMENON OF GENOME'S UNSTABILITYPHENOTYPE /A NEW AUTOSOMAL RECESSIVE
/CHEMOTAXIS AND BOMBAY/CONFIRMATION OF THE/ECTRODACTYLY AN EXPANDED/OBSERVATIONS ON THE/OF LACTASE PERSISTENCE/RELATIONSHIP OF GENOTYPE TO/SEGREGATING A STUTTERING/STATIONARY NIGHT BLINDNESS/WITH THE ALAGILLE SYNDROMEAFTER PRENATAL DIAGNOSIS OFAND CONGENITAL MALFORMATIONSAND LINKAGE TO CHROMOSOMEAND MECHANISM OF /OFAND NATURAL HISTORY /OF THEASSIGNMENT BY GENOTYPINGASSOCIATED WITH AN /ABNORMALASSOCIATED WITH DUPLICATIONASSOCIATIONS MATERNAL /ABOUTBY TRANSFER OF HUMANCORRELATIONS /9 KARYOTYPEIN ADULT MALES /WITH GCIN HUMAN MALIGNANT GLIOMAIN TAY SACHS DISEASE /WITHIN TRISOMY 21 /INFLUENCEIN TURNER SYNDROME /TO THEOF A CHONDRODYSPLASIA /AOF MOSAIC TRISOMY 21 /ANDOF RUSSELL SILVER SYNDROMEOF SEX REVERSED MICE /ONOF SINGLE GENE DISORDERSOF THE 4P SYNDROME BUT /THERELATIONSHIPS IN HUMANUNDER COMPLEX MODES OFWITH AN APPARENTLY BALANCED
PHENOTYPES /APOLIPOPROTEIN(A) ISOFORM/ASSOCIATION WITH CLINICAL/BETWEEN CYSTINURIA/EPIDEMIOLOGY OF COMPLEX/OF TWO OVERLAPPING/SUPEROXIDE DISMUTASE/THE GENES FROM PERSONALITY/X PATIENTS WITH ATYPICALAMONG MUT AND MUT PATIENTSAND PARENTAL ORIGIN OF THEEXAMPLE OF COLON CANCERIN SIBLINGS SHARINGOF X LINKED /THE MULTIPLESUGGESTING LITTLE OR NO
PHENOTYPIC AND MOLECULAR NOSOLOGYANOMALIES IN THREE CASESASPECTS OF LQ DELETION ANDCORRELATIONS /DEFECTS AND
2044188816102780114812272394715
268110891352271688718902560423505260487533454128190945527129131128015071662139825061820921S243001760566
2617748885903898129313694364436161079269525081838720688642819403
264731
19698105331450537
19611295717541
14571542452875152926852568283
141189
2461160016782227434
171124192714660567
1001462265715381553S241511511104S58144086411163441555749S73
CORRELATIONS /MOLECULAR ANDCORRELATIONS /MOLECULAR ANDCYTOGENETIC AND MOLECULARDELINEATION IN TWO SIBLINGSDIFFERENTIATION OF HUMANEXPRESSION /FREQUENCY ANDEXPRESSION /PREVALENCE ANDFEATURES OF DOWN SYNDROMEFINDINGS AFTER FETAL DEMISEHETEROGENEITY IN ROMANOPRESENTATIONS [TRISOMY 13SCREENING /BE DETECTED BYVARIATION SEEN WITH
PHENOTYPICALLY NORMAL GIRL /IN APHENOTYPING /OF SERUM CHOLINESTERASEPHENYLALANINE HYDROXYLASE GENE /HUMAN
HYDROXYLASE GENE /HUMANHYDROXYLASE GENE /OF THEHYDROXYLASE GENE ANDHYDROXYLASE LOCUS OFHYDROXYLASE MRNA THE /OFMETABOLISM IN CARRIERS
PHENYLKETONURIA /A KINETIC VARIANT OF/BULGARIAN CLASSICAL/GENE THERAPY FOR/IN ARAB PATIENTS WITH/MOLECULAR BASIS OFAMONG 10,008 CHILDRENAND SICKLE CELL /FORCOLLABORATIVE STUDYFAMILIES IN NORTH /OFIN SOUTHERN EUROPEIN WORLD POPULATIONSMUTATION IN SOUTHMUTATIONS /CARRIERS OFPATIENTS /IN OLDERPREGNANCY OUTCOMEREPORT ON AN /BASIS OF
PHENYLTHIOCARBAMDE TASTING INPHENYTOIN AND MUSCLE AN IN VITRO STUDY
ON INDUCTION OF SISTER /OFPHEOCHROMOCYTOMAS AND /IN RENAL TUMORSPHEVR SYNDROME AN AUTOSOMAL RECESSIVEPHILADELPHIA CHROMOSOME TRANSLOCATION
POSITIVE LEUKEMIA /WITHPHILTRUM SYNDROME /DEEP ORBITS SHORTPHOSPHATASE AND CALCIUM LEVELS WITH
AND HEMOGLOBIN IN BLOODBIOCHEMICAL CONSEQUENCESGENE /HUMAN PROSTATIC ACIDGENE IN SEVERELY AFFECTEDWITH GENE FREQUENCIES
PHOSPHATE DEHYDROGENASE DEFICIENCY OFISOMERASE IN TROPHOBLASTRECEPTOR /OF IGFI/MANNOSE 6SYNTHETASE TYPE TO
PHOSPHOFRUCTOKINASE DEFICIENCY IS APHOSPHOGLUCOMUTASE LOCUS 1 ANDPHOSPHOGLUCONATE DEHYDROGENASE LOCUSPHOSPHOGLYCERATE KINASE 1 VARIANTS INPHOSPHOGLYCOLATE PHOSPHATASE WITH /ANDPHOSPHOLUPID CONTAINING LIPOSOMESPHOSPHORYLASE B KINASE DEFICIENCY [TO
ON CHROMOSOME 14PHOTON EMISSION COMPUTED TOMOGRAPHYPHOTOTHERAPY AND VITAMIN E EFFECT ONPHYLOGENETIC AND STRUCTURE FUNCTION
INFERENCES /ON MTDNAPHYLOGENY EVALUATING INTERSPECIES
OF PEROXISOMAL MEMBRANE /ANDPHYSICAL AND CLASSICAL METHODS FOR
AND FUNCTIONAL MAPPINGAND GENETIC LIMITS OF THEAND GENETIC MAPPING OF HLA FAND INTELLECTUAL MEASURES /OFAND LINKAGE MAPPING OF DNAAND RECOMBINATION MAP OF /ACHARACTERIZATION OF THE /FORDEFINITION OF THE MYOTONICGENETIC MAPS FOR CHROMOSOMESGROWTH AND DEVELOPMENT OFLINKAGE OF ZFY 2,ZFYMAP /HUNTINGTON DISEASE THEMAP OF CHROMOSOMAL REGIONMAP OF CHROMOSOME llP12 P14MAP OF CHROMOSOME 21 BYMAP OF HUMAN CHROMOSOME 17 /AMAP OF HUMAN CHROMOSOME 19 /AMAP OF HUMAN CHROMOSOME 4 /AMAP OF THE DROSOPHILA GENOMEMAP OF THE HUMAN /ISLAND ANDMAP OF THE SHORT ARM OFMAPPING AROUND THE RP2 LOCUSMAPPING IN THE GENE REGIONMAPPING OF A GENE ENCODINGMAPPING OF A NOVEL MYC /ANDMAPPING OF A REGION OFMAPPING OF CHROMOSOME 11QMAPPING OF CHROMOSOME 19 BYMAPPING OF HUMAN CHROMOSOMEMAPPING OF IRS PCR AMPLIFIEDMAPPING OF SENESCENCE LOCUSMAPPING OF THEMAPPING OF THE APC REGIONMAPPING OF THE DISTAL
581
3483491465898263610782731417
16916701424183544
1532580
24322462449
2883111422802426449
102724827404552779182721211142280
2271224265548362302547129225651325817
135125977168952754456
233147226282324126915022031518
26281928506
262852684619796831568261628691679451680376102
21372700211021882071405216327211859298
2212196
21192150176
2185239
21232177197421462128218622151955182
216221602134216922062105
Permuted Title Index
MAPPING OF THE EMERYMAPPING OF THE FRIEDREICHMAPPING OF THE HUMANMAPPING OF THE LANGERMAPPING OF THE MULTIPLE /ANDMAPPING OF THE NORRIE /ANDMAPPING OF THE YEAST NUCLEARMAPPING OF YEAST ARTIFICIALMAPPING STRATEGIES IN THEMAPPING STUDIES ON HUMAN /ANDMAPPING USING YEAST /FORMAPS /RESOLUTION LINKAGE ANDORDERING FOR CATESPIN E ANDTO GENETIC DISTANCES ON /OF
PHYSICALLY MAPS CLOSE TO THE [THATPHYSIOLOGIC OR PATHOLOGIC /FLUIDPHYSIOLOGICAL HOMEOSTASIS DEVELOPMENTPi M4 M5 AND M6 ALPHA ANTITRYPSINPIEBALDISM /PROTO ONCOGENE IN HUMANPIGMENT GENE REGION IN JAPANESE
PROTEINS /HUMAN RED AND GREENPIGMENTARY DEGENERATION OF THE RETINAPIGMENTI /HEREDITARY INCONTINENTIA
/IN A GIRL WITH INCONTINENTIAPIGMENTOSA /COUNSELING IN RETINITIS
/DOMINANT RETINITIS/DOMINANT RETINITIS/DOMINANT RETINITIS/OF X LINKED RETINITISAND MUTATIONS OF THECONSTRUCTION OF TRANSGENICFAMILIES WITH ORNITHINESTRUCTURAL AND FUNCTIONALUSING GC CLAMPED /RETINITIS
PIGMENTOSUM AND COCKAYNE SYNDROMECELLS AGAINST DNA DAMAGE
PILOT STUDY OF MSAFP SCREENING WITHPIROMELLTIC ANHYDRIDE /EXPOSED TOPKD1 GENE AND MOUSE CHROMOSOME 17 [THEPL2014 A REVISED APPROACH TO /INV(2)PLACENTA /TERMINAL REPEATS IN HUMAN
BY HIGH PERFORMANCE LIOUIDUSING INTERPHASE IN SITU
PLACENTAL BIOPSY AN ALTERNATIVE TOINTERACTIONS AIN FETOMARKER FOR FETAL INFECTIONMOSAICISM /CASES OF CONFINEDMOSAICISM AN OVERVIEWMOSAICISM AND CYSTICMOSAICISM IN INTRAUTERINEMOSAICISM IN SPONTANEOUSPROTEINS IN ANEMBRYONIC /OF
PLACENTAS OF CIGARETTE SMOKERS ANDWITH ABERRANT C MYC /15
PLANTS INDUCED FROM UNPOLLINATEDPLASMA /DENSITY AND CONCENTRATION IN
/OF VARIANT TRANSTHYRETIN FROMAMMONIA AND UREA AND INCREASEAND CEREBROSPINAL FLUIDAND HDL COMPOSITION STUDIES /OFAND URINE ORGANIC ACIDSCELL MEMBRANE GLYCOPROTEINGLUTAMIC ACID IN PRIMARY /INHYPEROSMOLALITY /INDUCED BYLIPOPROTEIN(A) /OFOF WOMEN AT HIGH RISK FORPLASMINOGEN ACTIVATOR /ALTEREDPROMOTED ADHERENCE OF HUMAN /IN
PLASMINOGEN ACTIVATOR INHIBITOR 1ACTIVATOR INHIBITOR 1 /THE
PLATE IN HUMAN RETINOIC ACID /ALARPLATELET DERIVED GROWTH FACTOR /HUMAN
DERIVED GROWTH FACTOR A ANDPLATELETS IN HOMOCYSTINURIA /OFPLEIOTROPY HETEROGENEITY OR APLEURAL EFFUSIONS /ANALYSES OFPLEXIFORM NEUROFIBROMAS /SYNDROME WITHPLEXUS CYSTS INDICATIVE OF TRISOMY 18PLEXUSPAPILLOMA AND TRANSLOCATIONPLOIDY ANALYSIS OF IMMUNOLOGICALLY
IN BLADDER TUMORS USINGOF CARCINOMA IN SITU IS
PLP GENE IN A FAMILY WITH PELIZAEUSGENE IN A PATIENT WITH PELIZAEUS
POIKILODERMA A NEW GENODERMATOSISPOINT MUTATION /DEFICIENCY IS A
MUTATION CAUSING HUMAN 21 /NOVOMUTATION IN A MRNA SPLICE DONORMUTATION IN THE ACID BETAMUTATION IN THE HUMANMUTATION OF RAS ONCOGENE IN /OFMUTATION OF THE MTDNA /DUE TO AMUTATION SPECTRUM IN TWOMUTATIONS /FOR DETECTION OFMUTATIONS /WITH MITOCHONDRIALMUTATIONS AT CODON 373 OF FVIIIMUTATIONS BY RESTRICTION ENZYMEMUTATIONS IN THE ALPHA 1 /OFMUTATIONS IN THE FIX GENE /FORMUTATIONS IN THE HUMAN TISSUEMUTATIONS IN THE ORNITHINE /OFMUTATIONS IN THE RETINOBLASTOMAMUTATIONS IN THE TYROSINEMUTATIONS IN TUMORIGENESIS /OFMUTATIONS OF FACTOR VIII GENE
220721782192197612
2196237
2156S3619712189160
214821072399946453
2397189
2320239876919306431016
78
9991939
9799
193123781097293
2539118615991869156124245701209115111611133935288938944364919129491815482434578477572
2759263130747795567
1577241749924172417924
229624158727431374702128013761676164261410832358661518
23752326451
242559335
25539741064279410076809844721057588507
2495994
MUTATIONS OF THE P53 GENE INMUTATIONS WITHIN THE /TWOMUTATIONS WITHIN THE CYSTIC
POINTERS FOR CHROMOSOME IMPRINTING INPOISONING OF PARENT /BORN AFTER SELFPOLAND /OF PRENATAL DIAGNOSIS INPOLUCIES /FETAL SEX SELECTIONPOUCY DEVELOPMENT AND DISTRIBUTIONPOLO ALLELE /NEW MUTATIONS AND A MARCOPOLY(ADP RIBOSYL)ATION /INVERSION FROMPOLYADENYLATED BY ENDOGENOUSPOLYCYSTIC KIDNEY DISEASE /DOMINANT
KIDNEY DISEASE /DOMINANTKIDNEY DISEASE /FOR ADULTKIDNEY DISEASE /OF ADULTKIDNEY DISEASE 1 /CAUSED BYKIDNEY DISEASE AND ITS /FORKIDNEY DISEASE IN ANKIDNEY DISEASE IN ICELANDKIDNEY DISEASE IN ITALIANKIDNEY DISEASE NEWKIDNEY DISEASES /OF
POLYDACTYLY /STUDY OF HUMANAND OTHER ANOMALIES A NEWSYNDROME WITH PSYCHOMOTOR
POLYGENIC ATHEROSCLEROSIS IN /PREVENTSDISEASES /IN MONOGENIC AND
POLYMORPHIC (CA)N DINUCLEOTIDE /OFCYP2D6 GENOTYPESDNA MARKERS OF X028 /SEVENDNA PROBES FROM HUMAN /OFDNA PROBES OF THE 5012FRAGMENT IN THE BETAHUMAN DNA MARKERS /HIGHLYINFORMATION CONTENT OF /OFLOCI IN HUMAN DNALOCI ON CHROMOSOME 20 /TOMARKER (D10S97) TIGHTLYMARKERS /OF INCEST WITHMARKERS TO STUDY THE /NEWPCR BASED MARKERS FORPROBES /16 FAMILIES WITHSITES IN THE FRAGILE XSITES WITHIN THE /OFTRIMERIC AND TETRAMERICTRIMERIC REPEAT /FROM AURINARY METABOLITE
POLYMORPHISM /B ANTIGEN GROUP (X/Y)/GENETICS OF THE CYP2D6/l A POSSIBLE NEW/INHERITED LOW SIGNAL/STRANDED CONFORMATIONALANALYSIS /CONFORMATIONANALYSIS /DISEASE BY DNAANALYSIS INITIALANALYSIS OF THE APP GENEAND EXPRESSION INAND HOMINOID PHYLOGENYAND ITS CLINICALAT THE HUMAN B1 GAMMADIAGNOSTIC MARKER FORIDENTIFICATION /TO RAPIDIN AGING /C2IN FRENCH CANADIANS /DNAIN HORMONE SENSITIVEIN KOREA /DNAIN PREGNANCY INDUCEDIN PRION GENE IN /TTH1111IN SITES CLOSELY LINKEDIN THE KAINGANG AND /HLAIN THE PLASMINOGENIN THE REGION OF THE 5IN TURKEY /RED CELLMETHOD /CONFORMATIONOF THE FRAGILE XOF THE HUMAN GRANULOCYTEOF VNTR LOCUS (D1S80)ON LIPOPROTEIN LIPID /ERULED OUT IN 45 /DNATO THE GENETIC VARIANCE
POLYMORPHISMS (PHOSPHOGLUCOMUTASE(XBAI AND ECORI) OF THE/AND MOUSE STRAIN CAR 2/COUNSELING WITH DNA/OF DINUCLEOTIDE REPEAT/REPEAT SEQUENCE/SIMPLE SEQUENCE REPEAT/USING GT REPEAT/USING PCR BASEDA POTENTIALLY USEFULAMONG HUMAN AND /OF VNTRAND ALLELE FREQUENCIESAND HAPLOTYPESAND LINKAGE DATA FORARE ASSOCIATED WITHAT SHORT TANDEM REPEATDETECTED WITH GC /DNAIN A DELETION PRONE /CAIN ANDHRA PRADESH TRIBESIN BASAL CELL NEVUS /DNAIN EUROPEAN AND OTHERIN GALACTOSEMIA /ANDIN HUMAN GENOMIC DNAIN INFERTILE COUPLESIN PARDHIS OF ANDHRA
2577104410092421271175617841780224625732424249
237117641048998199499819021110226384786720892192
266582
5511959250112232517206220932099
7419562790205719781051103819272506959538986S93275112821105964112298422904251675451907194520352694287819832846657229123172859241718822830280420052360231326891094277526282746252867553
20492110198196124492615111424041979261865
2520978285520031916186
206915602868
IN SARDINIA /MALARIALIN SOUTHERN AFRICAN /DNAIN THE APOLIPOPROTEIN BIN THE GENES ENCODINGIN THE HUMAN DYSTROPHININ THE MYB PROTO /OF AIN THE TRANSCRIBED 3OF DINUCLEOTIDE REPEATSOF SERUM AND RED BLOODON AGAROSE GELSSUPPORT THE SEPHARDICUSEFUL FOR LINKAGE /DNAUSEFUL IN FAMILY STUDIESWITHIN THE CFTR GENEWITHIN THE HUMAN /DNA
POLYNEUROPATHY BY ISOLATION OFI /IN FAMILIAL AMYLOID
POLYPEPTIDE /WITHIN THE TYROSINASEIN THE BALB/CBYJ MOUSE
POLYPLOIDY /A CASE OF YAS A CAUSE OF ABORTION IS
POLYPOSIS BY LINKAGE ANALYSISCOLI /FAMILIAL ADENOMATOUSCOLI GENE /THE ADENOMATOUSGENE /FAMILIAL ADENOMATOUSIN 16 FAMILIES WITHLOCUS (5021 022) CONTAINS
POLYPS /AND A VARIABLE NUMBER OF/EXAMPLE OF COLON CANCER AND
POLYSPERMIC HUMAN OOCYTESPOMBE IMPLICATIONS FOR HUMAN IRONPOMPE DISEASE (TYPE II GLYCOGEN /OF
DISEASE WITH NORMAL ACID APOOLED GENOMIC DNA SAMPLES DELIBERATEPOOLING SCHEMES /MAP USING CLONEPOPLITEAL PTERYGIUM SYNDROME /LETHALPOPULATION /140L IN A DIVERSE U.S.A
/A HIGH RISK MEDITERRANEAN/ABORTIONS IN QATARI/ALLELES IN THE CAJUN/AMPLIFICATION IN JAPANESE/AND AUTISM IN A CHILEAN/BREAST CANCER IN A SWEDISH/DIGIT IN THE SOUTH AFRICAN/DISORDER IN A MEXICAN/DISORDERS AND THE FINNISH/DYSTROPHY IN THE SPANISH/FIBROSIS GENE IN BASHKIR/HEXOSAMINIDASE B/IN A CANADIAN OUTPATIENT/IN A HIGH RISK PEDIATRIC/IN INDIVIDUALS FROM NORMAL/IN JAPANESE/OF ADIPOSITY IN AN INDIAN/PRESSURE IN AN INDIAN/SAMPLE OF THE U.S.A/SCREENING IN THE PREGNANTAND MOLECULAR GENETICS OFBASED AFP ESTRIOL AND HCGBASED REGISTRY /IN A LARGEBASED STUDY /IDEAS FROM ABASED TWIN REGISTRIES TOBETWEEN MYOTONIC DYSTROPHYBLACKS AND MONGOLOIDSCLINICAL AND GENETICDISTRIBUTION /AND THEIREPIDEMIOLOGICAL ANDFROM ANDHRA PRADESH INDIAGENE ANALYSIS /TOGENETIC ASPECTS OF THEGENETIC STUDIES IN AOGENETIC STUDIES OFGENETIC SURVEY IN THEGENETICS AND CYSTICGENETICS OF CHILDHOODGENETICS OF HYPERVARIABLEGENETICS OF THE ALTAIANSGENETICS OF THE D1S7 D2S44GENETICS OF THE D4S139GENETICS OF THE HUMAN MUC1GENETICS OF UIGURS /ONIN COLOMBIA WITH SPECIALIN MALI AFRICA WITH A VERYMICRODIFFERENTIATION /OFOF ANDHRA PRADESH INDIAOF BUDAPEST /IN THE MALEOF SICHUAN CHINA /GENERALOF STATE FARMS IN HAINANOF THE U.S.S.R /MULTIETHNICOF WESTERN INDIA /RETARDEDREFERRED FOR PRENATAL /IN ASAMPLE AS A TEST OF NEWSCREENING FOR CYSTIC /ANDSCREENING OF FOUR MAINSTRUCTURE IN THE GARHWALSTRUCTURE OF TURKMEN SSRSTUDIES OF INV(9)STUDY OF CFTR GENESTUDY OF COUMARINSUGGESTS THE MYOTONICTHE U.S.A PUBLICVARIATION AND INBREEDINGWHICH HAS AN ELEVATED
POPULATIONS /AMONG HUMAN RACIAL/ASSOCIATIONS IN ADMIXED
582
26452633
662398983
259019362094284527892826205910399881968578
275752545914279361876591609
21321051101599S5812582363574529
279252
63719202501400270923131492607669
27195
187523174612725141028315512713272027371834S9318478842668402
2848282320232531989734
285666
286828242857
6268725228502852283628672860276128272865271711662778276828471493666100525118492825287915452703540203618522849284028282758
Permuted Title Index
/DNA IN AFRICAN/EVOLUTION OF WEST AFRICAN/HETEROZYGOSITY IN HUMAN/IN DIFFERENT/IN EUROPEAN AND OTHER/IN HIGH AND LOW RISK/IN SOUTHERN AFRICAN/IN SOUTHERN AFRICAN/JEWISH AND OTHER/OF VARIOUS CAUCASIAN/ON THREE MEDITERRANEAN/PHENYLKETONURIA IN WORLD/PREVALENT AMIDST INBRED/RECESSIVES IN HUMAN/ROUTES OF THE ANCESTRAL/THALASSEMIA IN TWO SOVIET/THREE CANADIAN ABORIGINAL1970 1989 /U.S.AAND MORE PRECISE MAPPINGFALLEN VICTIMS TOIN NORTH AMERICA /AMONGOF ALABAMA AND BETWEENOF CHAMBA HIMACHAL /CASTEOF COLOMBIA GENETIC ANDOF LUNG CANCER VICTIMSOF NORTHWESTERN SIBERIAOF TEXAS U.S.A /ETHNICOF THE U.S.S.R /DIFFERENTOF THE U.S.S.R /IN HUMANOF TIBETIAN YI MIAO ANDOF TURKMEN SSR /INUSING HYPERVARIABLE DNAUSING RFLPS AND /ISRAELIWITH DIFFERENT /IN TWO
PORE AND LINKAGE ANALYSIS /SWEATPORENCEPHALY IN TWO SWEDISH FAMILIESPORK AND HUMAN CDNA PROBES ENCODINGPOROCYSTIC OSTEODYSPLASIA WITH TARDYPORPHOBILINOGEN DEAMINASE GENE IN /THE
DEAMINASE GENE WITHPORPHYRIA /CONGENITAL ERYTHROPOIETIC
/WITH ACUTE INTERMITTENTPORTIONS OF THE PROXIMAL LONG ARM OFPORTUGAL A STUDY OF THE PREVALENCE /INPORTUGUESE PATIENTS /STUDIES IN 14POSITION 175 IN AN A1(I) CHAIN OF /ATPOSMONAL CLONING ]DISEASE GENES BY
CLONING EFFORTS FORCLONING WHERE IT'S BEEN
POSITIONS OF CHROMOSOMES IN /ANDPOSITIVE ACETYLCHOLINESTERASE BAND AT
ACETYLCHOLINESTERASE TESTSACUTE LYMPHOCYTIC LEUKEMIAAFAFP AND ACHE TESTS INANAPLASTIC LARGE CELL /KI 1AND NEGATIVE SELECTIONLEUKEMIA /WITH PHILADELPHIAOCULOCUTANEOUS ALBINISM IN
POSITRON EMISSION TOMOGRAPHY FINDINGSPOSSUM A COMPUTER/LASER VIDEODISKPOST AMNIOCENTESIS QUESTIONNAIRE FOR
MORTEM LIVER SAMPLES FOR THE /OFTRANSLATIONAL PROCESSING OF
POSTAXIAL ACROFACIAL DYSOSTOSISPOLYDACTYLY SYNDROME WITH
POSTERIOR NUCHAL CYSTIC HYGROMAPOSTMORTEM CVS A FURTHER DELINEATION
FIXED TISSUE /ANALYSIS INPOSTNATAL DIAGNOSIS OF /DETECTION AND
LATE X REPLICATION STUDIESMICROCEPHALY AND SHORT
POSTTRANSLATIONAL MODIFICATION ANDPOTENTIAL BENEFIT THE ONE YEAR FOLLOW
CYTOGENETIC MARKER FORGENE SEQUENCES /ISOLATION OFHUMAN ZINC FINGER PROTEININCREASED RISK FOR GENETICMAPPING OF ONE DISEASE /WITHOF ENZYME REPLACEMENTPITFALLS IN THE USE OFROLE OF HIGH RESOLUTION /THEUNIQUE MECHANISM FOR
POTENTIAUTY IN TWO TRIBES OFPOTENTIALLY USEFUL METHOD FOR MAPPINGPOTENTIALS /IN HONG KONG PROBLEMS ANDPOTTER SEQUENCE IN A FETUS WITHPRADER WILLI AND ANGELMAN SYNDROMES
WILLI AND ANGELMAN SYNDROMESWILLI AND ANGELMAN SYNDROMESWILLI CHROMOSOME REGION /OF THEWILLI CHROMOSOME REGION /THEWILLI PATIENT MOSAIC FOR A /AWILLI SYNDROME /DIAGNOSIS OFWILLI SYNDROME /DIAGNOSIS OFWILLI SYNDROME /DISOMY INWILLI SYNDROME /HISTORY OFWILLI SYNDROME /HYPERPYREXIA INWILLI SYNDROME /LOCUS D15S10 INWILLI SYNDROME /PATIENTS WITHWILLI SYNDROME /STANDARDS FORWILLI SYNDROME AND A JUMPINGWILLI SYNDROME FAMILES IOF 20WILLI SYNDROME IN A BOY WITH AWILLI SYNDROMES /ANGELMAN ANDWILLI SYNDROMES /ANGELMAN AND
26392634278723561916970
26332635
423022838
2713
28412876992
28292697
7728062854284428702839610
281565
96527952769271528242883
67904719
232287310442011530104421182731837534
21742157421
21411274939136911651331262125972000227133
1758975492797892704119511198971457782581
1771745
237421441788647
2483135
15411243283324491795142959
1459186023862299143965510561593169649
22191489948
17011035145487
2224
WILLI SYNDROMES IDENTIFIES /ANDWILLI/ANGELMAN REGION /TO THE
PRADESH INDIA /OF CHAMBA HIMACHALINDIA /POPULATION FROM ANDHRAINDIA /POPULATION OF ANDHRASOUTH INDIA /PARDHIS OF ANDHRATRIBES /IN ANDHRA
PRB1 AND PRB2 /RICH PROTEIN GENESPRB2 /RICH PROTEIN GENES PRB1 ANDPRB2/1 FUSION GENE A PRODUCT OFPRE AND POST AMNIOCENTESIS
CLOVIS COLONIZATION OF THE NEW /AECLAMPSIA A PRELIMINARY EXCLUSIONECLAMPSIA/ECLAMPSIA /STUDIES INMRNA OF DROSOPHILA /OF THE MLC ALK
PREALBUMIN AND TOTAL PROTEIN INPREANEMIC DIAGNOSIS IN PATIENTS WITHPRECUNICAL TESTING FOR HUNTINGTONPRECONCEPTION AND PREIMPLANTATION /OFPRECONCEPTIONAL FAMILY HEALTHPRECURSOR DUE TO AN INTRA EXON /MRNA
IN CELLS FROM FINNISHPROTEIN GENE IN JAPANESEPROTEIN LOCUS BY HOMOLOGOUS
PREDICTABLE SPECTRA OF ASSOCIATEDPREDICTING ESSENTIAL HYPERTENSION /TOPREDICTION IN GENETIC COUNSELING /RISKPREDICTIVE MEDICINE FOR LATE ONSET
STUDY /AND IMBALANCE MODE ATESTING AND SEX RATIOTESTING FOR HUNTINGTONTESTING FOR HUNTINGTONTESTING FOR HUNTINGTONTESTING FOR HUNTINGTON /FORTESTING FOR HUNTINGTON /INTESTING FOR HUNTINGTON /OFTESTING IN MULTIPLE /FORTESTING PROGRAM /THROUGH A
PREDISPOSE OF TRISOMY 21 /21 DOES NOTPREDISPOSED TO BREAST CANCERPREDISPOSES FOR SPECIFIC CHROMOSOMALPREDISPOSING FACTOR FOR NONDISJUNCTIONPREDISPOSMON IN FEMALES WITH
TO BREAST CANCERTO MYOCARDIAL /STUDY OF
PREFERENCES OF ENDOGENOUS RETROVIRUSESPREFERENTIAL LOSS OF HLA COMPATIBLEPREFERRED TO EXCLUSIVE PERFORMANCE /ISPREGNANCIES /AND OUTCOME OF
/AND PCR TESTING FOR 11/FOR OPEN NTDS IN TWIN/MSAFP AND HCG IN TWIN/REPEAT MOLAR/TRIMESTER TRISOMY 18AFTER CVS /FOLLOW UPAT RISK FOR NTDS /OFWITH COMPLETE OR MOSAICWITH FETAL US ANOMALIESWITH NORMAL FETAL OUTCOME
PREGNANCY /IN AN IDENTICAL TWIN/MSAFP LEVELS IN TRIPLET/PROTEINS IN ANEMBRYONIC/UNCONJUGATED ESTRIOL IN MIDA CASE OF RESOLVED FETAL /INAFTER PRENATAL DIAGNOSIS /AAND DNA METHYLATION /MOLARAND LIVE FETUS /MOLARINDUCED HYPERTENSION /INLOSS /WITH RECURRENTLOSS AND FREQUENCY OF /OFLOSSES /FIRST TRIMESTERLOSSES THROUGHOUT GESTATIONOUTCOME MAJOR ANOMALIES ANDOUTCOME TWO YEAR FOLLOW UPOUTCOMES OF FAMILIAL /OFREDUCTION /MULTI FETALSCREENING IN ISRAELTERMINATION /ANEUPLOIDY ATWASTAGE ASSOCIATED WITH AWITH THE HISTORY OF LEFT /A
PREGNANT PATIENT GENETIC COUNSELINGPOPULATION /SCREENING IN THEWOMEN IN DENMARK /AMONG
PREIMPLANTATION DIAGNOSIS OF BETA /TODIAGNOSIS OF GENETICDIAGNOSIS THE FIRSTEMBRYO /OF THEEMBRYOS /OOCYTES ANDGENETIC DIAGNOSIS /ANDMOUSE EMBRYOS
PRELINGUAL DEAFNESS /LINKAGE STUDY FORPREMATURE CHROMOSOME CONDENSATION
CORONARY HEART DISEASE /THEPREMATURITY AND CONGENITAL HEART /BYPREMEIOTIC EVENTS /CAN BE TRACED TOPRENATAL AND PERINATAL PRACTICE /IN
AND POSTNATAL LATE XAND/OR HETEROZYGOTEBIASES IN TWIN RESEARCHCARE /GENETICS TO NEW JERSEYCHOICE THE EXPERIENCE OF ACHROMOSOME ANALYSIS FROMCHROMOSOME DIAGNOSIS AND ITSCHROMOSOME DIAGNOSIS IN /OFCOUNSELING FOR ORNITHINE
186817182870734
27172866285522532253225317582637191911562438912696966107
17772351466
10712244713
2736200624815628603001732182218071738177119501745170717332228159180117541095414932113014911185121418339401139125411721219941113514851157919125592217669281154657
154012181195361836914124712761208116312439531246183418481272621161210362107
2239199913201118711
2817122714572504S8517971731149526863591237
CYTOGENETIC DIAGNOSIS OF THECYTOGENETICS VERSUSDETECTION /OVER 17 YEARS INDETECTION AND POSTNATALDETECTION OF A DENOVODETECTION OF A TRUE MOSAICDETECTION OF ANEUPLOIDY INDETECTION OF TRISOMY 8DIAGNOSES /ABNORMALITY INDIAGNOSIS /A PREGNANCY AFTERDIAGNOSIS /AMNIOCENTESIS FORDIAGNOSIS /AND ACHE TESTS INDIAGNOSIS /AND SUCCESSFULDIAGNOSIS /APPLICATION TODIAGNOSIS /FOR NONINVASIVEDIAGNOSIS /HYBRIDIZATION INDIAGNOSIS AIN UTERO FORDIAGNOSIS /NEW CONCEPTS INDIAGNOSIS /OF WOMEN WHO HAVEDIAGNOSIS /PSEUDOMOSAICISM INDIAGNOSIS A COMPARISON OFDIAGNOSIS A TRUE GENETIC AINDIAGNOSIS AFTER AGE 30DIAGNOSIS AFTER CVS /STUDY ONDIAGNOSIS AND INCIDENCE ATDIAGNOSIS AND MANAGEMENT OFDIAGNOSIS AND PERINATALDIAGNOSIS BY FLUORESCENCE INDIAGNOSIS EXPERIENCE INDIAGNOSIS FOR TRISOMY 21 /OFDIAGNOSIS FREQUENCY CLINICALDIAGNOSIS IN DUCHENNE /ANDDIAGNOSIS IN FINNISH /OFDIAGNOSIS IN HONG KONG /ANDDIAGNOSIS IN POLAND /OFDIAGNOSIS IN SOUTH CHINA /ANDDIAGNOSIS MAY MODIFY /ANOMALYDIAGNOSIS OF 3DIAGNOSIS OF 46,XX/46,XYDIAGNOSIS OF ADIAGNOSIS OF A GENETIC /FORDIAGNOSIS OF A RAPIDLYDIAGNOSIS OF ALPHA /ANDDIAGNOSIS OF ANDIAGNOSIS OF APPLE PEELDIAGNOSIS OF CHROMOSOMALDIAGNOSIS OF CHROMOSOMAL /FORDIAGNOSIS OF CHROMOSOMAL /INDIAGNOSIS OF CHROMOSOME /FORDIAGNOSIS OF COMPLEX /THREEDIAGNOSIS OF CONGENITALDIAGNOSIS OF CYSTIC FIBROSISDIAGNOSIS OF CYSTIC HYGROMADIAGNOSIS OF DANDY WALKER /OFDIAGNOSIS OF DUCHENNEDIAGNOSIS OF FETAL /FORDIAGNOSIS OF FRAGILE XDIAGNOSIS OF FRAGILE X /FORDIAGNOSIS OF FRASER SYNDROMEDIAGNOSIS OF FRYN SYNDROMEDIAGNOSIS OF INV DEL (6)DIAGNOSIS OF LYSOSOMAL /ANDDIAGNOSIS OF MUCOLIPIDOSESDIAGNOSIS OF NON KETOTICDIAGNOSIS OF NUMERICAL /FORDIAGNOSIS OF OTO PALATALDIAGNOSIS OF POMPE DISEASEDIAGNOSIS OF SICKLE CELLDIAGNOSIS OF SPINAL MUSCULARDIAGNOSIS OF SPONGYDIAGNOSIS OF THE SKELETALDIAGNOSIS OF TRIOSEDIAGNOSIS OF TRIPLOIDY /INDIAGNOSIS OF X LINKEDDIAGNOSIS OF X LINKED /FIRSTDIAGNOSIS PATIENTS /STUDY OFDIAGNOSIS USING FETAL CELLSDIAGNOSTIC PROGRAM IN CHINADIAGNOSTIC SERVICES /OFDIAGNOSTIC SERVICES LOCAL /OFDIAGNOSTIC TESTING OF THEDIAGNOSTIC TOOL /A NEWDIAGNOSTICS ON MATERNAL AGEGENETIC DIAGNOSIS IN THE /OFGENETIC DIAGNOSIS OF 1303GENETICS NEEDS ASSESSMENTHEMOGLOBINOPATHY SCREENING /AIDENTIFICATION OF CHROMOSOMEIDENTIFICATION OF FRAGILE XIDENTIFICATION OF SMALLPROGNOSIS OF OBSTRUCTIVE /TOREPAIR /NOT AMENABLE TOREVEALING OF MULTIPLE /INSCREENING /RATIOS USED INSCREENING AND DIAGNOSIS OFSCREENING FOR CYSTICSCREENING FOR CYSTIC FIBROSISSCREENING FOR DOWN SYNDROMESCREENING OF ABNORMALSCREENING OF TRISOMY 21SCREENING PROGRAM USING /ASCREENING THAN WOMEN AT ASEX RATIO A STUDY ON 1089STUDIES TRUE INCREASE OR /BYTESTING FOR ADULT ONSET
583
1259169112118979531170111
14851159176612261165535
111460
1719114S531753162617811162114612341475274114817241625182584
978104638817563911178121714501519666127711201650118191117991615127914081108100411426891207182311981038652119215035584425631283933574177412235731260126992396812631752115
1265181218011239119412681802122017901846118916881714929119218371216113418411842942103108
1242174211991168211
Permuted Title Index
TESTING FOR ADULT POLYCYSTICULTRASONOGRAPHIC FINDINGS IN
PRENATALLY /ABNORMALITIES DIAGNOSEDBY MOLECULAR ANALYSISDETECTED 5P/10P TRISOMYDETECTED CASES /INDETECTED FRAGILE X FEMALESDETECTED YQ REARRANGEMENTSDIAGNOSED ANEUPLOIDY AT /OFDIAGNOSED CASE OF /OF ADIAGNOSED CHILDREN WITH /OFSHOW NO INCREASED RISK FORWITH AN AFFECTED LIVEBORN
PRESENTATION /DYSPLASIA VARIEDOF GAUCHER DISEASE /MILDOF TEN NEW CASES A
PRESENTATIONS /TRISOMY 13 PHENOTYPICOF DUCHENNE TYPE
PRESSURE AND BODY MASS INDEX /OF BLOODIN AN INDIAN POPULATIONIN THE AFRICAN GREEN MONKEYIN TWINS /BLOODWITH AGE /OF SYSTOLIC BLOOD
PRESYMPTOMATIC AND PRENATAL TESTINGDIAGNOSIS OF FAMILIALDIAGNOSIS OF WILSONDNA TESTING FORPREDICTIVE TESTING FORTESTING FOR HUNTINGTONTESTING FOR HUNTINGTONTESTING IN HUNTINGTONTESTING IN HUNTINGTON
PREVALENCE AND PHENOTYPIC EXPRESSIONAT BIRTH OF CONGENITALOF BETA ALLELE OF THEOF CYSTIC HYGROMA BYOF GOITER /WITH A VERY HIGHOF MALFORMATIONS DURINGOF MUTATIONS IN THEOF THE B THALASSEMIA /HIGHOF VITAMIN D DEPENDENCYRATE OF PSEUDOMOSAICISM IN
PREVALENT AMIDST INBRED POPULATIONSPREVENTED BY A SPECIFIC SHORT PATCHPREVENTION PROGRAM FOR DUCHENNEPREVENTS POLYGENIC ATHEROSCLEROSIS INPRIMARY AND SECONDARY CONSTRICTION /OF
BILIARY CIRRHOSIS /ANDCHROMOSOMAL EVENT /A POSSIBLECOMPONENTS OF BODY /FORCONGENITAL GLAUCOMA /OFCONGENITAL GLAUCOMA FROM /ONGASTRIC ADENOCARCINOMA /INGENERALIZED AND PARTIAL /INGLAUCOMA /GENETIC FACTORS INGONADAL TUMOR WITH A /OF AHEALTH CARE THROUGH A FAMILYHEPATOCELLULAR CARCINOMA /OFHEPATOCELLULAR CARCINOMA /WITHHEPATOCYTES OF THE SPARSE FURHYPEROXALURIA TYPE I /OFLUNG ADENOCARCINOMAS /IN EIGHTMYELODYSPLASTIC SYNDROME /WITHMYOPIA /REFRACTIVE ERROR INNODAL AND EXTRANODAL LARGEOVARIAN CANCER /ONCOGENESIS OFSEX DETERMINATION IN MICE /INSQUAMOUS CELL CARCINOMAS OFSTRUCTURE AND LINKAGE /GENESTRUCTURE OF THE TYPE IV
PRIMATES NNTR IN HUMANS AND NONHUMANANALYZED BY MOLECULAR /AND
PRIMED IN SITU LABELING OF NUCLEICPRIMER EXTENSION A NOVEL QUANTIFIABLEPRIMERS THAT ALLOW SPECIFIC AND /ALUPRIMING REACTIONS FOR PROBE LABELINGPRINCIPAL FOR THE DISSEMINATION OFPRINT AND GENETIC STUDY OF CONGENITALPRION ALLELES FROM AN INDIVIDUAL WITH
GENE IN FAMILIAL CREUTZFELDT /INPROTEIN GENE LOCUS /OF THEPROTEINS IN FIBROBLASTS AND
PRO IN THE CYP17 GENE CAUSES 17APRO23HIS /OF THE HUMAN RHODOPSIN GENEPROBABILTIES FOR NORMAL RELATIVES OFPROBANDS /FAMILY MEMBERS OF AUTISTIC
/RELATIVES OF EPILEPTICWITH A CHROMOSOME 20P /INWITH AN ADDITIONAL MARKERWITH LPL DEFICIENCY /SEPARATEWITH OSTEOGENESIS IMPERFECTA
PROBE /HYBRIDIZATION WITH A COSMID/X CENTROMERE BIOTINYLATED DNAHYBRIDIZED IN SITU /SPECIFIC DNAISOLATED FROM A Y LIBRARYLABELING AND SYNTHESIS /FORMAPPING BY FLUORESCENCE IN SITUP49A DETECTS COMPLEX PVUIIPOOL TECHNIQUE /SPECIALSET /CHROMOSOME 21022.3 SPECIFICSPECIFIC FOR PAINTING /22
PROBES /16 FAMILIES WITH POLYMORPHIC/AND CHROMOSOME SPECIFIC/AND Y SPECIFIC A SATELLITE DNA/BY CHROMOSOME SPECIFIC DNA
17648351248166114291718114191011631412213124712578784361467142479527072720678
269327291764105199017671732210301175117682731268872211682827103
1018267426981613713
25521794192
15635421394264976462812994776911386151
226513972472132
13361381895618
25724321315228624052631185792974
251625142732700
23902291229810001045799
279162587716641404470
2497151616981676991251420872872251516341649105183
17251721
/CDNA AND GENOMIC CLONE/CENTROMERIC SATELLITE DNA/EMBRYOS USING NONRADIOACTIVE/HYPERVARIABLE MULTILOCUS DNA/IN SITU HYBRIDIZATION WITH DNA/TO CHROMOSOME SPECIFIC/TO CHROMOSOME SPECIFIC DNA/WITH BIOTINYLATED PCR/WITH SATELLITE DNAANALYSIS /CYTOGENETIC AND DNAAND DIGITAL IMAGING /LABELEDAND HTF SPECIFIC CLONESAND PCR IS RELATIVELY LOW INARE USEFUL IN CHARACTERIZINGAS EVIDENCED BY APPARENT /LOCUSBY DIGITAL IMAGE PROCESSINGDETECTION OF ONCOGENE /SPECIFICENCODING GLUTARYL COA /CDNAFOR CYTOGENETIC ANALYSES OFFOR HUMAN CHROMOSOMES 8 10 ANDFOR IN SITU HYBRIDIZATION WITHFOR ISOLATION OF HUMAN COSMIDFOR PRENATAL DIAGNOSIS OFFOR THE ROLE OF GLUTATHIONEFROM HUMAN TRANSCRIBED /DNAGENERATED BY INTER ALU PCRIN A GIRL WITH SHORT STATUREIN ELUCIDATION OF A Y;15IN IDENTIFYING THE IDIOPATHICIN PRENATAL AND PERINATAL /DNAIN THE REGION OF THE /OFIN THE VICINITY OF THE SPINALOF SINGLE COPY GENESOF THE 5Q12 Q14 REGION /DNATO PREDICT STERILITY IN /AND 7TO THE PRADER WILLI/ANGELMANUSED AS RFLP MARKERS FOR /DNAUSING GC CLAMPED DENATURINGWITHIN AND AMONG POPULATIONSWITHIN CHROMOSOME SUBBANDSWITHIN SELECTED SUBREGIONS BY
PROBING THE FUNCTION OF THE CYSTICPROCESS IN INFERTILE MALES /ON MEIOTIC
IN THE MOUSE /X INACTIVATIONOF ONTOGENESIS BY MEANS OFOF PRENATAL GENETIC DIAGNOSIS
PROCESSED WITH IN SITU CULTURE ANDPROCESSES /FOR ONCOGENESIS MOLECULAR
IN PROGRESSING MUSCULARPROCESSING (TYPE II) MUTATION OF
/PROBES BY DIGITAL IMAGEDEFECTS AND PHENOTYPICOF OVEREXPRESSED EXOGENOUS
PROCOLLAGEN (COL2A1) IN TRANSGENIC /11FROM PROBANDS WITH /TYPEGENE (COLlAl) /IN A TYPEGENE /MUTATIONS OF TYPE II
PRODUCT /REVEALS A PUTATIVE PROTEIN/TO THE AVIAN V MAF ONCOGENECC ESSENTIAL FOR DEVELOPMENTOF UNEQUAL AND HOMOLOGOUS /ATHROUGH MICRO ENCAPSULATED
PRODUCTS FROM IRRADIATION REDUCED /PCROF GENE EXPRESSION AS ANOF THE DUCHENNE MUSCULAR
PROFESSIONAL CODE OF ETHICS THE /AEDUCATION IN GENETICS INEDUCATION IN GENETICS INEDUCATION IN GENETICS INEDUCATION IN HUMANGENETICS EDUCATION AND
PROFESSIONALS /WHILE EDUCATING HEALTHPROFICIENCY TESTING IN THEPROFILE AND PATERNITY ESTABLISHMENT
OF CYCLOPHOSPHAMIDE INOF UTERINE SARCOMAS A STUDY
PROFILES ACCOUNT FOR THE RP2 AND RP3IN DOWN SYNDROME /PATTERNIN HUMAN ORAL CAVITY AND
PROFOUNDLY DEAF CHILDREN ATTENDINGPROGENITORS /IN HUMAN HEMATOPOIETICPROGENY OF MUTAGENIZED HUMAN SOMATICPROGERIA AND A WOMAN WITH GROLL /WITHPROGEROID SYNDROME WITH ELASTINPROGNATHISM ABNORMAL EARS MENTALPROGNOSIS IN PRENATALLY DETECTED CASES
OF OBSTRUCTIVE UROPATHIESOF PRENATALLY DIAGNOSED
PROGNOSTIC IMPLICATIONS OF CHROMOSOMEIMPLICATIONS OF KARYOTYPEINDICATORS OFMOLECULAR DIAGNOSIS OF
PROGRAM /OF INDEX CASES THROUGH MSAFP/RESULTS FROM AN AUSTRALIAN/THROUGH A FAMILY PLANNING/THROUGH A PREDICTIVE TESTING/WITH A MASTERS LEVELAND TEXT IN TEACHINGBY MOLECULAR ANALYSIS OF DNADISEASES /IN THE COMPUTERFOR AUTOMATIC CONSTRUCTION OFFOR DOWN SYNDROME PRELIMINARYFOR DUCHENNE MUSCULARIN CHINA /PRENATAL DIAGNOSTICIN CUBA /DISEASES CONTROL
1123166616842871128116671708165617041079
91S771098162228101697217232216351635199
23211283453
250122471653169321171227221721012085122391017182630205928542066205824181193146
22331802122825788134901697S73492
2461249710654696
2459240022532470216857616
18143273293303313331777180428775381335193962958323
248428079501145710171892921313581332768109611831749151
17451779137
110227882060174917941265
INCREASES THE VALUE OFOF GENETIC HEALTH EDUCATIONTO PERFORM A HOMOGENEITY TESTUSING MSAFP HCG AND UE3
PROGRAMMING APPROACH TO PEDIGREEPROGRAMS /CELL SCREENING AND TREATMENT
/ORIENTED NATIONAL GENETICS/USING THE LINKAGEIN THE U.S.A /SERVICES
PROGRESS IN CLONING THE MYOTONICIN GENOME SCAN FOR LINKAGEIN MULTIPLEXING AND OPTIMALIN THE SEARCH FOR THE GENEINTO THE GENETICS OF MOODTOWARD ITS ISOLATION AS A
PROGRESSING DEMENTIA (MEMBRANOUSMUSCULAR DYSTROPHIES /IN
PROGRESSIVE BILATERAL NASAL ALARCONE DEGENERATION TO XP1 1DEFORMING OSTEOGENESIS /INENCEPHALOPATHY WITH EDEMAINTRACRANIAL TERATOMAMYOCLONUS EPILEPSY /IN
PROHIBITIN IS THE MAMMALIAN /PROTEINPROJECT /KINGDOM HUMAN GENOME MAPPING
GENES GENETIC EDUCATION OFPROLIDASE (PEPTIDASE D) DEFICIENCY /OFPROLIFERATION /AND PROLONGED
IN C ELEGANS /GERMLINEKINETICS OF LEUKEMIC
PROLIFERATIVE IMMUNOLOGICAL ANDPROLINE RICH AND DNA BINDING DOMAINS
RICH PROTEIN GENES PRB1 ANDPROLYMPHOCYTIC LEUKEMIA /IN B CELL
LEUKEMIA TERMINATINGPROMOTED ADHERENCE OF HUMAN /IN PLASMAPROMOTER /AND ANALYSIS OF ITS INTERNAL
/HUMAN 17 1A NEOANTIGENE GENE/OF THE HUMAN COMPLEMENT C4A GENE WHICH ESCAPES XMUTATION ON FETAL G GLOBINOF A CANDIDATE HUNTINGTONOF A FIBROBLAST SPECIFIC /THEREGION FOUND IN HP2 1MODREGIONS /FACTOR A AND B CHAINSHOWS ALLELE SPECIFIC /1
PROMOTERS /HAS TWO TRANSCRIPTIONALPROMOTION /APPROACHES FOR HEALTH
/HEALTH EDUCATION ANDPRONE REGION OF DYSTROPHIN /A DELETIONPRONENESS [TO DNA REPAIR AND CANCERPRONUCLEI AND METAPHASE CHROMOSOMESPROPER FORMATION OF 3 MRNA ENDS /THE
MITOTIC SEGREGATION /ANDPROPHASE /CHROMOSOME 21 IN MEIOTICPROPHYRIA MUTATIONS USING DENATURINGPROPORTION OF GENE DELETIONS DETECTED
OF HUMAN CHROMOSOME 3OF NEW MUTATIONS CAN BE
PROPORTIONS DUE TO X LINKED AND /OFPROSAPOSIN GENE /OF THE HUMAN
SIALIDASE IN FIBROBLASTSPROSAPOSINE GENE /EXPRESSION OF THEPROSPECTIVES OF GENETIC AND /SYNDROMEPROSPECTS FOR CELL TRANSPLANTATION
FOR MOLECULAR ANALYSISFOR NONINVASIVE PRENATALFOR SCREENING /DEFECTSFOR THALASSEMIA SCREENINGOF PRENATAL DIAGNOSIS IN
PROSTATE ADENOCARCINOMA /GENE IN HUMANCARCINOMA /ALTERATIONS IN
PROSTATIC ACID PHOSPHATASE GENE /HUMANCANCER /ABNORMALITIES IN
PROTAMINE 1 AND 2 CDNAS /OF HUMANPROTEASE IN DUCHENNE MUSCULAR /NEUTRALPROTECTION FROM SEVERE MALARIA /WITHPROTECTS NORMAL HUMAN AND XERODERMAPROTEIC FRACTIONS (COMPATIBLE WITHPROTEIN /OF IN VITRO TRANSLATED
/OF THE MURINE HOX 1.2ALTERATIONS IN ARCHIVAL /ANDAMELOGENIN IS EXPRESSED FROMAN ANIMAL MODEL FOR INHERITEDAND DNA VARIATION IN SOUTHERNAND PCR BASED GENE ANALYSESBINDING AND PROPER MITOTICCDNA AND INITIAL STUDIES INCDNA BANK /OF HUMANCONTAINING PROLINE RICH AND /AELECTROMORPHS /GROUPS ANDFROM SUBARACHNOID SPACES TOGENE AND RELATED PSEUDOGENESGENE CAUSES PELIZAEUSGENE IN JAPANESE FAMILIALGENE LOCUS /OF THE PRIONGENE MUTATIONS IN PELIZAEUSGENES PRB1 AND PRB2 /RICHGENES USING NONRADIOACTIVE INGROUP SPECIFIC COMPONENTIMPLICATIONS FOR DOWN SYNDROMEIN CLOSE PROXIMITY TO THEIN NEONATES FROM 35 TO 42KINASE /A CELL CYCLE REGULATEDLEVELS /1 AT THE DNA RNA AND
584
184617721970124220331796S3020951798404187720622991221028738136637036268661277
762400205417739879183241337
212288225313041366499
24602465246724402423233523992425241524172409153
1772978845215324451663420100810982198281780223654952439766424
254160
262392104626061340233113002457731
261825399502309222658723672268258
10961663190
2512228828429552276972107122981101225321442262419
2332912
212828181791
Permuted Title Index
LOCUS BY HOMOLOGOUS /PRECURSORMOLECULAR CLONING /SIGNAL 1OF E COLI /OF CYSTINE BINDINGPOLYMORPHISMS IN PARDHIS OFPRODUCT /REVEALS A PUTATIVEPRODUCTS OF GENE EXPRESSIONPROHIBITIN IS THE MAMMALIANS DEFICIENCY A POSSIBLE CAUSESTUDIES /AND IN VITROT AND IDENTIFICATION OF A CPG
PROTEINASE INHIBITOR IN DOWN SYNDROMEPROTEINS /AND STABILITY OF MUTANT
/BY GTPASE ACTIVATING/HUMAN RED AND GREEN PIGMENT/OF MITOCHONDRIAL IRON SULFUR/OF PEROXISOMAL MEMBRANE/THE FOLDING AND FUNCTION OFAND NUCLEIC ACIDS /OFBY GTPASE ACTIVATING PROTEINSDURING DEVELOPMENT /BINDINGDURING EPITHELIAL /FILAMENTENCODED BY OPPOSITE DNA /TWOFROM GENE SEOUENCES AND SITEFROM PERUVIAN MUMMIES /ANDGENE RESULT IN TWO ENTIRELYIN ANEMBRYONIC PREGNANCYIN FIBROBLASTS AND /PRIONIN HUMAN COCHLEA /OF GIN PATIENTS WITH HEREDITARYSTRUCTURE FUNCTION AND ROLE
PROTEOUPID PROTEIN GENE CAUSES /THEPROTEIN GENE MUTATIONS IN
PROTEOLYTIC PEPTIDES OF THE RED CELLPROTEUS SYNDROME THREE NEW CASES WITH
SYNDROME WITH PLEXIFORMPROTO ONCOGENE C NEU IN BREAST AND /OF
ONCOGENE IN CHICKENS WITH /MYBONCOGENE IN HUMAN PIEBALDISM
PROTOCOL FOR PRESYMPTOMATIC TESTINGFOR THE DETECTION OF CDF508TO IDENTIFY TRISOMY 18 USING
PROTOBONCOGENE A CANDIDATE FOR THE /RETPROTOPORPHYRIA /IN ERYTHROPOIETICPROVIDERS /OF SCREENING PERCEIVED BYPROVINCE CHINA /STATE FARMS IN HAINAN
OF COSENZA ITALY /IN THEPROVINCES OF SOUTH CHINA /IN FIVEPROVINCIAL IMPACT /DIAGNOSTIC SERVICESPROVIRUS ANCHORED SINGLE SITEPROXIMAL 100 AND CHARACTERIZATION OF
60 DELETION RESULTING FROM ADNA MARKERS RN1 AND VK23 /OFINTERSTITIAL 180 DELETIONLONG ARM OF HUMAN CHROMOSOMELONG ARM OF THE HUMAN X /THELONG ARM OF THE X CHROMOSOMEREGION OF MOUSE CHROMOSOME 7SHORT ARM OF CHROMOSOME 17SHORT ARM OF CHROMOSOME 17SPINAL MUSCULAR ATROPHY FROMTO DXS7 /NIGHT BLINDNESSTO THE FRAGILE X SITE /CONTIGTUBULOPATHY DIABETES /OFX CHROMOSOME SHORT ARM /THEXP LOCI LONG RANGEXO /MARIE TOOTH DISEASE ON
PROXIMITY TO THE SPINAL MUSCULARPRP GENE /MUTATION AT CODON 200 OF THEPSEUDO POMPE DISEASE WITH NORMALPSEUDOACHONDROPLASIA STATUS OF THEPSEUDOAUTOSOMAL REGION /OF THE
REGION /WITHIN THE X YREGION IN TOURETTE
PSEUDOCLEFTS FURTHER CONFIRMATION OFPSEUDOCONTIGUOUS SYNDROMESPSEUDOGENES /GENE ADH5 AND RELATED
/PROTEIN GENE AND RELATEDARE DISPERSED THROUGHOUT
PSEUDOHERMAPHROOMSM WITH 45,X/46,XPSEUDOHYPERALDOSTERONISM (LIDDLEPSEUDOHYPOMRATHYROIDISM EXHIBITINGPSEUDOLEPRECHAUNISM MASKED BYPSEUDOMOSAICISM IN AMNIOTIC FLUID
IN EARLY AMNIOCENTESESIN PRENATAL DIAGNOSISTRUE MOSAICISM AND
PSEUDOFMPILLEDEMA /ASSOCIATED WITHPSEUDOXANTHOMA ELASTICUM AND /WITHPSORIASIS VULGARIS TWO LINES OFPSYCHIATRIC DIAGNOSIS AND CHROMOSOME
ILLNESS AND WOLFRAMPROBLEMS DEPRESSION AND
PSYCHIATRY AND GENETIC COUNSELING INPSYCHOMETRIC TESTING /THE VALUE OFPSYCHOMOTOR RETARDATION SOMATIC /WITHPSYCHOSIS IN THE VELOCARDIOFACIALPSYCHOSOCIAL FACTORS INVOLVED IN
IMPACT OF PRESYMPTOMATICISSUES IN A SUPPORT
PTER IN AN ADULT PRESENTING WITH /8P23SYNDROME OF LINEAR SKIN LESIONS
PTERYGIA CONGENITAL HEART ANOMALIESPTERYGIUM SYNDROME /LETHAL POPLITEALPUBERTAL GENU VALGUM /HEREDITARYPUBERTY /HAPLOTYPES IN DISORDERS OF
22442309448
286696
57624001158193
2334159524612
2398482945S462518
12120
22432298247566
235991910002338465286972
11012629771702
25962590189
176810991238234722141846276827271117181220742170147019081425218421182015186019982139109318782159502
2260217320072332100052948
203423601895834713
2284227619731506839824711
1221161316261228630686
276575779055417361738892
174117601732176615301494817637651665
/SHORT STATURE AND DELAYEDPUBUC /FOR EDUCATION OF THE MEDICAL
/POPULATION THE U.S.AACCESS TO GENETICS INFORMATIONAWARENESS OF HUMAN GENETICS KHEALTH IMPACT OF GENETIC /ANDHEALTH ISSUES IN APPROACHINGNEED TO UNDERSTAND GENETICSPOLICY DEVELOPMENT AND /AND
PULMONARY DEVELOPMENT /IN NORMALPULSE FIELD ELECTROPHORESIS AFTER /BYPULSED FIELD GEL ELECTROPHORESIS /BYPULVERIZATION OF CHROMOSOMES INPUNCTATA DUE TO AN INHERITED X Y
IN AN INFANT WITH DEL (4)REPORT OF A BOY WITH X
PURE GONADAL DYSGENESIS /AND 46,XYX LINKED HEREDITARY SPASTIC
PURGED AUTOLOGOUS BONE MARROWPUTATIVE CHOROIDEREMIA GENE AND /THE
GENES IDENTIFIED NEAR THEPAGET DISEASE LOCUS /APROTEIN PRODUCT /REVEALS AR(21) CASE ALSO FOUND TO BEZINC FINGER GENES ON HUMAN
PVUII HAPLOTYPES /P49A DETECTS COMPLEXRFLP AT THE LIPOPROTEIN LIPASE
PYRIMIDINE DIMER FORMATIONPYRROUNE 5 CARBOXYLATE REDUCTASE BYPYRUVATE DEHYDROGENASE ElA SUBUNITS
165339618521777206149
17883951780927621
21191297902804902
2238708
136711
S77192996
1690227228722656254022792416
Q0 /OF CHROMOSOME 4 AND ISO (4P),ISO 4HETEROCHROMATIN AND CARDIOVASCULARHETEROCHROMATIN REGIONS /CHROMOSOMALHETEROMORPHISMS IN TWO SAMPLES OFIN A LIVEBORN INFANT ASSOCIATED
Q,+REC(7),DUP PDEL 0 IN A LIVEBORN011.1013 /WITH 46,XX,DEL(14)0112;024 IN A NEWBORN WITH SIGNS OF012 MARKERS /OF EIGHT CHROMOSOME 22011012;011.2 COMPLEMENT013/1 REGION OF CHROMOSOME 11 (11012
OTER IN TWO T(14;18) NEGATIVE013,5034 OTER 11022,23 XPTER AND /5011013;011 PAT /15, + DER(22),T(15;22)014 REGION /DNA PROBES OF THE 5012015 021 OF CHROMOSOME 5 WITH /TO BAND02.1 /MARFAN SYNDROME LOCUS ON 1501.5021 /OVER A 350 KB REGION IN 9013
32 IN A PH POSITIVE ACUTE /OF 1QOF CHROMOSOME 5 WITH FLUORESCENCE024 /IS LOCATED ON CHROMOSOME 12SEGMENT OF AN INV(3)(P25021) /CEN
021.1 /ATAXIA REGION AT 9013021022.1 /210 DELETION DEL(21)022 AND IS LINKED TO MYB /MAPS TO 6021
CONTAINS THE GENE MUTATED IN022.1 OTER DUE TO A DUPLICATION ON023 025 AND MOUSE CHROMOSOME 3 BY /4024/IS LOCATED ON CHROMOSOME 12(021
/SEQUENCE CLUSTERED AT X022.3OF CHROMOSOME 16 /GENE TO BAND
024.3 /OF HUMAN PAX2 GENE TO 10022.1024;011 TRANSLOCATION /THE T(10;14)025 AND MOUSE CHROMOSOME 3 BY /4 (023027.2 PRESENT IN ONLY 1 OF 685 CASES028;011 TRANSLOCATION /WITH A T(X;14)032.3033.2 WITH POTENTIAL MAPPING OF033;034 NONRANDOM ASSOCIATION OF042.3;P12.2 MAT /1,+DER (1) T(1;12)QATARI POPULATION /ABORTIONS INOLL2 DUE TO A 45,X, Y, /(15CENOT SYNDROMES /THE INHERITANCE OF LONGQT(ROMANO WARD) SYNDROME GENE FROMOTER /NONRANDOM ASSOCIATION OF 7034
/OF BULLOUS DYSTROPHY TO X02411022,23 XPTER AND CHROMOSOME 19DUE TO A DUPLICATION ON THEDUE TO MATERNAL TRANSLOCATIONHNCDNA LIBRARY HIGHLY ENRICHEDIN TWO T(14;18) NEGATIVE
QUADRUPLETS /RELATIVES OF TRIPLETS ANDQUAUTATIVE VARIANTS OF HUMAN SERUMQUALITY BAND SCORING /THREE YEARS OF
OF G BANDED METAPHASES /OF THEOF TWO BOYS WITH PROGERIA AND
QUANTIFIABLE METHOD FOR DETECTION OFQUANTIFICATION OF DIFFERENT GENE /ANDQUANTIFYING URINARY GLYCOSAMINOGLYCANQUANTITATION OF HETEROPLASMY IN A /ANDQUANTITATIVE AND QUALITATIVE VARIANTS
EVALUATION OF TRISOMY 7MULTIPLEX PCR /BYPCR /ANEUPLOIDY USINGTRAITS /FOR MAPPING OFTRAITS USING CHICKENS AS
QUEBEC /WITHIN A FAMILY OF EASTERNIS DUE TO A FOUNDER EFFECT
QUESTIONNAIRE BASED STUDY /COMMUNITY A
15821730157928231565156514831720195414542090139220431533122321711109
811369217121641687217814651307101
1498186721641658217222822251867161226046471509144014001454843
219715091990204314981329252113922666546180416189509741815774375461322102310692068208020022698334
FOR COUNSELING EFFICACYQUOTIENT AMONG FRAGILE X MALES
R
R(18) SYNDROME /IN A PATIENT WITHR(21) CASE ALSO FOUND TO BE 180 BYRABBIT MODEL FOR CRANIOSYNOSTOSISRABBITS LEADS TO PERMANENT /DEFICIENTRACE /EFFECTS OF MATERNAL WEIGHT AND
AND WEIGHT ON HCG AND UE3 LEVELSON MSAFP AND AFAFP MEASUREMENTS
RACES /DIFFERENTIATION OF HUMANRACIAL GROUPS /CAUCASIAN AND HISPANIC
GROUPS /CAUCASIAN AND HISPANICPOPULATIONS /AMONG HUMAN
RADIAL DYSPLASIA /DEFECTS ANDLIMB DEFECTS WITH /DEFECTS AND
RADIATION AND CHEMICALS AND TO /OFCAN ALTER GENE EXPRESSIONSEFFECTS OF THE CHERNOBYLHYBRID CONTAINING 20 CM OFHYBRID IN THE REGION AROUNDHYBRID MAP OF 24 LOCI ONHYBRID MAP OF HUMANHYBRID MAP OF THE PROXIMALHYBRID MAPPING ANDHYBRID MAPPING IN PROXIMALHYBRIDS /CHROMOSOMES USINGHYBRIDS /CHROMOSOMES USINGHYBRIDS AND SIMPLE SEQUENCEHYBRIDS AND YEAST /USE OFHYBRIDS FROM A MARKED HUMANHYBRIDS FROM CHROMOSOME 14INDUCED SOMATIC CELL /OFREDUCED HYBRIDS /17 USINGREDUCED HYBRIDS CONTAININGREPAIR GENE XRCC5 BY /HUMAN
RADIATIONS /LOW LEVEL ELECTROMAGNETICRADICALS /ACTIVITY TO OXYGEN FREERADIO FREQUENCY RADIATION CAN ALTER
ULNAR SYNOSTOSIS GENERALIZEDRADIOLOGIC CORRELATION /ANDRADIOSENSITIVITY ATAXIA /AND LOWRADON AND ASBESTOS EXPOSURE AND THERAJMAHAL HILLS BIHAR INDIA /TRIBES OFRAMBAM HASHARON SYNDROME OF MENTALRANDOM GENETIC DRIFT IN A BRAZILIAN
PRIMING REACTIONS FOR PROBE /OFRANDOMLY SELECTED LARGE 20 KB DNARANGE MAPPING OF THE X CHROMOSOME
ORGANIZATION OF ALPHOID /LONGRESTRICTION ENZYME MAPPING /LONGRESTRICTION MAP OF HUMAN /A LONGRESTRICTION MAP OF THE DOUBLERESTRICTION MAPS /XP LOCI LONG
RAPID AND INFORMATIVE ASSAY FORAND SEMI AUTOMATED DETECTION OFDETECTION OF MITOCHONDRIALDETECTION OF POINT MUTATIONS INDETECTION OF SINGLE ALPHA /FORDETERMINATION OF SEQUENCESDIAGNOSIS OF ANEUPLOIDY INDIAGNOSIS OF FANCONI ANEMIA ANDIDENTIFICATION OF THE 9:22 /ANDIN SITU HYBRIDIZATION METHODSISOLATION OF DNA PROBES WITHINISOLATION OF LARGE NUMBERS OFMETHOD FOR SIMULTANEOUSMETHOD TO SCREEN FOR MUTATIONSPCR APPROACH TO MONITORING OFPHYSICAL MAPPING OF IRS PCRPOLYMORPHISM IDENTIFICATION /TOSCREENING FOR CODING REGIONSEQUENCE INDEPENDENT /FOR THESEQUENCING OF CDNAS FOR TYPESEX ASSIGNMENT IN AMBIGUOUSSITE SPECIFIC SCREENING OF THE
RAPIDLY ADHERING AMNIOTIC FLUID CELLSIDENTIFYING GENES OR MARKERSPROGRESSIVE INTRACRANIAL /OF A
RAPP HODGKIN SYNDROME USING MULTIPLERARE 6Q11 + HETEROMORPHISM CYTOGENETIC
CASE OF GIANT CELL OSTEOGENIC /ACOMPARED TO MUTATION /GENES ISFAMILY WITH DOMINANT INHERITANCEFORM OF CONGENITAL HEART DISEASEIN FAMILIAL AND NONFAMILIAL /ISINHERITED DEFECT OF THE KREBS /AVARIANT OF X LINKED DOMINANT
RAS GENE ACTIVATION IN NEUROBLASTOMAGENE MAMMALIAN EXPRESSION CLONINGSMUTATIONAL SPECTRA IN /P53 AND KONCOGENE HOMOLOGS IN DIFFERENT /CONCOGENE IN HUMAN OVARIAN CANCERP21 AND K REVI PROTEINS BY GTPASE
RAT/REPEATS SHARED IN MOUSE ANDACYL PEPTIDE HYDROLASE GENE [THEBONE MARROW CELLS IN VIVO AND /INCHROMOSOME 7/ARM 120 ANDDEVELOPMENT BY NONRADIOACTIVE IN
585
17582672
151716909314231140114412242636283628522828817816256225762816214020142208S892184S132170158
2040211020652149216521322150211818912422222925767737946776102833688283525142630210921202219214213612173978110510222495976
20971636160916491279205820751009232325962160203527842053249711751092117320801277166615811365262780814142811447824602
2592610
256959312
16452297130118702230
Permuted Title Index
EMBRYONAL CELLS /OF THELIVER /TRANSPLANTED INTOMOUSE AND CHICKEN REVEALS HIGHLY
RATE IN ADVANCING MATERNAL AGEIN AMNIOCENTESIS BY /REPUNCTUREIN FAMILIES WITH HUNTINGTONMODULATED MICROWAVE AND RADIOOF CFTR MUTATIONS IN CHICAGOOF CHROMOSOME 10 IN BALANCEDOF LOSS OF HETEROZYGOSITY ONOF MEIOTIC AND SOMATIC /INCREASEDOF PSEUDOMOSAICISM IN EARLY
RATES IN JEFFERSON COUNTY ALABAMAOF CHROMOSOMAL ABERRATIONS ANDOF SPONTANEOUS INTRACHROMOSOMAL
RATIO /PREDICTIVE TESTING AND SEXA STUDY ON 1089 INDUCED /SEXAND DIFFERENCE MEASUREMENT INAND HYPERHAPLOIDY FREQUENCY INDISTRIBUTION AMONG FAMILIES IN
RATIOS USED IN PRENATAL SCREENINGRATS /ACTIVITY IN LONG EVANS CINNAMON
/IN LONG EVANS CINNAMONRAUCHER LEUKEMIA VIRUS TRANSFORMEDRAUTENSTRAUCH SYNDROME /THE WIEDEMANNRAY AND MAGNETIC RESONANCE IMAGING /X
HYBRID ANALYSIS /TRANSFER AND XINDUCED CHROMATID DAMAGE IN CELLSINDUCED CHROMOSOME ABERRATIONS IN
RAY/OLIGODACTYLY SYNDROME AND THERB (6.16) TRANSLOCATION IN MALE
AND P53 GENES /MUTATIONS IN THEGENE PARENTAL IMPRINTING SUGGESTED
RB(6.16) TRANSLOCATION EVIDENCE FORRB1 GENE USING CONSTANT DENATURANT
LOCUS IN Li FRAUMENI SYNDROME ARDNA CLONED IN YEAST ARTIFICIAL /HUMAN
DURING LIMB REGENERATION IN THEREACTION AND RECURRENT FEVERREACTIONS AS AN INITIAL DELETION
FOR PROBE LABELING ANDREACTIVATION IN HUMAN OVARIAN TUMORS
OF GENES ON THE INACTIVEREACTIVE GENETIC COUNSELING /THAN
PROTEIN IN CLOSE PROXIMITYREACTOR ACCIDENT /OF THE CHERNOBYLREAGENTS /HUMAN CHROMOSOME 13 MAPPINGREARRANGED CHROMOSOMES /OF TERMINAL
HUMAN CHROMOSOME ANDREARRANGEMENT /OF A COMPLEX CHROMOSOME
/T(6P;130) CHROMOSOMEANALYSIS IN LEUKEMIAIN A MOTHER AND THEIN FOUR CASES OF NONIN MAMMALIAN CELLSIN SPERMS NOT INVOLVINGRESPONSIBLE FORWITHIN THE 5.8 KB MAJOR
REARRANGEMENTS /4P DELETIONS AND/AT RISK FOR CHROMOSOME/FOR STRUCTURAL/OF COMPLEX CHROMOSOMAL/SPECIFIC CHROMOSOMALAND EXTRA MARKERBY FLUORESCENT IN SITUCOMMON TO PATIENTSDETECTED PRENATALLYFREQUENTLY INVOLVINGIN THE A5(IV) COLLAGENIN TWO PATIENTS WITHWITHOUT 45,X MOSAIC /YQ
REASONING OF M S GENETIC COUNSELORSREBIRTH OF THE MARSHALL SYNDROME (MIMREC DEL(5) IN ONE EXTENDED FAMILY /AND
DUP(5) AND REC DEL(5) IN ONERECALLED AGE AT MENOPAUSE A TWIN STUDYRECCURRENCE RISK OF A TRISOMIC 21RECEPTOR (C KIT) GENE COMPLEX /FACTOR
/OF IGFIVMANNOSE 6 PHOSPHATEA MAST/STEM CELL GROWTHAS A MODIFYING GENE IN /D2B JUNCTIONAL DIVERSITY /CELLB3 SUBUNIT GENE (GABRB3) TODEFICIENT RABBITS LEADS TODNA POLYMORPHISM RULED OUTGENE (VDR) ARE COLOCALIZEDGENE /5 HYDROXYTRYPTAMINElAGENE /IN THE INSULINGENE /NEW MUTATIONS OF LDLGENE AND MAPPING OF THE GENEGENE DEFECT IN X LINKEDGENE IN MALIGNANT /RYANODINEGENE ISOLATED FROM THEGENE MUTATION IN ECUADOREANGENE ON HUMAN CHROMOSOME 21GENE ON MEANS VARIANCES ANDGENE PRIMARY STRUCTURE ANDGENE REGION /GLUCOCORTICOIDGENE TO IDENTIFY FUNCTIONALGENE WITHIN THE X Y /FACTORGENES /IN T CELLGENES IN MULTIPLE SCLEROSISIMPAIRS GROWTH HORMONELOCUS IN MEXICAN AMERICANSLOCUS STUDIES OF ASSOCIATION
13142485261212041621211
25761829118825741245161326712816254886011992236159426961216512438134181425551891845153188915832553621155228031892215812891321989
251413892452208
2332360
2209165523011422142110311632133325561707157213701651116740714082228
841679473124713381011244791018218551453145327551553229615022296979224023924231094187018824859801907
9542923849691968515
228621232682236027841917245528011076
MAPS TO DISTAL 11 P /DOPAMINEMEDIATED TERATOGENS /OFMUTATIONS THAT CAUSE MALEON HUMAN ERYTHROCYTESPROTO ONCOGENE IN HUMANRFLP DATA AND MUSCLE BIOPSYSTUDY IN ONE CASE OF THESUBUNITS /ACETYLCHOLINE
RECEPTORS AND BINDING PROTEINS DURINGIN ABSTINENT ALCOHOLICS /A2
RECESSIVE AUTOSOMAL DISORDER /PROBABLYCHONDRODYSPLASIA PUNCTATADYSTROPHIC EPIDERMOLYSISECTODERMAL DYSPLASIAFORM /OF THE AUTOSOMALFORM LETHAL POPLITEAL /THEHYDROTIC ECTODERNALINHERITANCE /WITH AUTOSOMALINHERITANCE /WITH AUTOSOMALINHERITANCE /X LINKEDMULTIPLE CONGENITALPHENOTYPE /A NEW AUTOSOMALSENSORINEURAL DEAFNESS ANDSPASTIC ATAXIA OF /AUTOSOMALSYNDROME /A NEW AUTOSOMALSYNDROME /THREE SIBS A NEWSYNDROME OF PTERYGIASYNDROME OR A VARIANT OFSYNDROME SECONDARY TO
RECESSIVES IN HUMAN POPULATIONSRECIPIENTS /AND IN RENAL TRANSPLANTRECIPROCAL CHROMOSOMAL TRANSLOCATION
CHROMOSOME TRANSLOCATION /ATRANSLOCATION /A BALANCEDTRANSLOCATION /DE NOVOTRANSLOCATIONS ANDTRANSLOCATIONS USING /OF
RECIRCULATION OF THE AMNIOTIC FLUIDRECOGNMON MOLECULE /AS A NEURONALRECOMBINANT CHROMOSOME RESULTING FROM
CLONES /WITHIN 7000CYTOKINES /CELLS USINGDYSTROPHIN IN MDX /OFEXPRESSION AND IN VITROFIBROBLASTS /ENCAPSULATEDHUMAN GLUCOCEREBROSIDASEMETHYLMALONYL COA MUTASEREPORTER GENE FOR THERETROVIRAL VECTORS /USING
RECOMBINATION /ALU ALU/ARTIFICIAL CHROMOSOME/LOCUS BY HOMOLOGOUS/MITOTICAND LINKAGE /ANALYSIS OFBASED ASSAY /USING ABETWEEN THE WILSONIN A WERNER SYNDROMEIN EMBRYONIC STEM CELLSMAP OF CHROMOSOME 18MAP OF THE MOUSE XOF A COMPLEX CHROMOSOMEWITHIN THE CEN Q21
RECONSTITUTION OF GLUCOSYLCERAMIDASERECONSTRUCTED BY MOLECULAR /EVOLUTIONRECONSTRUCTING HUMAN HISTORY FROMRECONSTRUCTION AND FURTHER STUDY OF
EXPERIMENTS BASED ONRECONSTRUCTIONS OF FIBROBLASTS /INRECOVERING DNA AND PROTEINS FROMRECOVERY OF DNA FROM ANCIENT BONESRECRUITMENT OF LENS CRYSTALLINS NEWRECULTIVATING THE OLD CELLS /BYRECURRENCE OF DELl 1 P15 IN A FAMILY
OF TWINNING AND FAMILIALOF WOLF HIRSCHHORN
RECURRENT ABORTIONS /IN 902 CASES OFFEVER /REACTION ANDLETHAL OSTEOGENESISMECONIUM PERITONITIS NOT /OFNON SYNDROMAL POSTERIOR /OFNONSENSE MUTATION IN THEPOINT MUTATIONS OF FACTORPREGNANCY LOSS /WITHTRANSLOCATIONS IN NONTRISOMY 21 /OF FAMILIES WITH
RECURRING MUTATIONS AT CPGRECYCLING OF BIOTIN /TRANSPORT ANDRED AND GREEN PIGMENT PROTEINS /HUMAN
BLOOD ENZYMES IN THE CENTRAL /ANDCELL ABO ANTIGEN AND SERUMCELL ACID PHOSPHATASE AND /OFCELL ENZYME AND SERUM PROTEINCELL MEMBRANE BAND 3 IN JAPANESECELL POLYMORPHISM IN TURKEYCELL POLYMORPHISMS ARE ASSOCIATEDCROSS YOGYAKARTA BRANCHGREEN COLOR VISION DEFICIENCY /FORGREEN VISUAL PIGMENT GENE REGION
RED/GREEN COLOR VISION DEFECTS /HUMANREDUCED EXPRESSION OF FETAL HEPATIC
HYBRIDS /17 USING RADIATIONHYBRIDS CONTAINING PORTIONSHYBRIDS TO ISOLATE REGIONLEVELS OF AN ESSENTIAL FATTYRADIATION HYBRID IN THE /AND A
19031291267
2858189
1911751
21821205177699021927812780637648839849689879720788
2004882890817814846
284159017571601117013211562171512663251589219824682480193
24812483532
129124902549
1822442554188425071926254825032188195114221687526
264131518
21212141566
2502166
16211572266616611270132144688770410849941540133017131068479239828455752754286626292830261827542231232024191205215021182168913
2014
SOMATIC CELL HYBRID PANELREDUCING BIRTHS WITH DOWN SYNDROME IN
THE GENETIC INTERVAL AND /TOREDUCTASE ACTIVITY METHIONINE
BY COMPLEMENTATION INDEFICIENCY IDENTIFICATIONDEFICIENCY THERMOLABILITYGENE OF THE YEAST /FERRICIN PHYSIOLOGICALPROBES FOR THE ROLE OF
REDUCTION /MULTI FETAL PREGNANCYOF EXPRESSION IN SMALL CELL
REFERENCE CENTER /YEAR REPORT FROM ATO CYSTIC FIBROSIS /WITH
REFERRAL TO A CENTER PROVIDING /FORREFERRALS FOR GENETICS SERVICESREFINED LOCATION OF THE HUNTINGTON
MAPPING AND EXCLUSION AS THEMAPPING OF SCAl ON CHROMOSOME
REFINEMENT OF THE PERICENTROMERICREFLECTED AND WIDE SPREAD REPEATS IN
IN CYTOGENETIC ABNORMALITIESREFLECTION OF THE CHERNOBYL REACTORREFRACTIVE ERROR IN PRIMARY MYOPIAREFRACTORY MUTATION SYSTEM TEST
MUTATION SYSTEM TEST FORREGENERATION IN THE PRESENCE AND /LIMBREGION (4P16.3) /HUNTINGTON DISEASE
(VILLA CLARA) OF CUBA /CENTRAL/A Y LIBRARY DETECTS THE YQ0 1/ANALYSIS OF THE LOCUS CONTROL/CONE DEGENERATION TO XP11/DISSECTED DEFINED CHROMOSOME/DNA PROBES OF THE 5012 014/ENDOCRINE NEOPLASIA TYPE 2A/GIEDION SYNDROME CHROMOSOME/GLUCOCORTICOID RECEPTOR GENE/HUMAN MYOTONIC DYSTROPHY GENE/HUMAN X INACTIVATION CENTER/IN NINGXIA HUI AUTONOMOUS/IN THE HUNTINGTON DISEASE/INFORMATION ON THE 1P34 1P36.1/ISOLATION OF A CDNA IN THAT/MOLECULAR ANALYSIS OF THE XQ28/OF THE FRAGILE X/OF THE MYOTONIC DYSTROPHY GENE/OF THE PRADER WILLI CHROMOSOME/OF THE PSEUDOAUTOSOMAL/OVERLAP CLONING IN THE XP22.3/PHYSICAL MAPPING OF THE APC/RFLPS IN THE APOAI CIII GENE/SITES IN THE FRAGILE X/THE HUMAN CHROMOSOME 7Q22 32/THE HUNTINGTON DISEASE/THE PRADER WILLI CHROMOSOME/WITHIN THE X Y PSEUDOAUTOSOMAL11022.3 23.1 /AT D GENE TO THE15Q11 13 /HETEROGENEITY OUTSIDE4035 /MAP OF CHROMOSOMAL5 TRANSCRIBED REGION AND CDNAS8024 LINKED TO ONCOGENESISALLELES AND CORONARY ARTERYAMONG NEW MUTANTS /CANDIDATEAND CDNAS OF ALTERNATIVEAND PROGRESS TOWARD ITSAND SUSCEPTIBILITY TO INSULINAROUND X LINKED OCULAR ALBINISMASSOCIATED WITH CRI DU CHATAT 9013 Q21.1 /ATAXIABY EXON AMPLIFICATIONCONTAINING THE VON /A 600 KBDOWNSTREAM OF A GLOBIN GENE INENRICHING THE REGION WITHFOR PALLISTER KILLIAN SYNDROMEFOR SPINAL MUSCULAR ATROPHYFOR THE 180 SYNDROME /CRITICALFOR THE HUNTINGTON DISEASE GENEFOR THE HUNTINGTON DISEASE GENEFOR THE PRADER WILLI ANDFOR THE TRISOMY 18 SYNDROMEFOUND IN HP2 lMOD INDIVIDUALSGENE BETWEEN AN2 AND FSHB /WAGRGENE SEGMENTS FUNCTIONAL ANDHARBORING SCIDXI /OF X013IMPLICATIONS FOR DELETIONIN 9Q13 021 /OVER A 350 KBIN AN ACUTE MYELOGENOUSIN DIGEORGE SYNDROME /CRITICALIN JAPANESE /PIGMENT GENEIN TOURETTE SYNDROMEIN YEAST ARTIFICIAL /MOUSE SXRIS TIGHTLY LINKED TO THEOF 40 /ON THE SUBTELOMERICOF CHROMOSOME 10 /PERICENTRICOF CHROMOSOME 11 (11012 013) /1OF CHROMOSOME 11 IN UREMIC /1OF CHROMOSOME 19013.3 /A 350 KBOF CHROMOSOME 1 P36 COMMONLY /AOF CHROMOSOME 21 THAT CAUSESOF COMMON ALLELIC LOSSES ON 3POF CUBA /DISEASE IN THE WESTERNOF DELETION IN LUNG CANCEROF DNA /BY AN UNSTABLEOF DYSTROPHIN /A DELETION PRONEOF HUMAN CHROMOSOME 15 /WILLI
586
213626862371501
2279193501
23634534531276224
2675273218091783208819961993204424332433608959931047128982
2845991338703172812232170197
2123S8697
2780233622022088178374405238620342092220624041038219222102299236023011116221224322591714
23482432102
27112014216821782383213311252218143721461672227123961860169524252241262322211718
81137086
2320189518592005204220082090595
203622152106260718272243799782392
Permuted Title Index
OF HUMAN CHROMOSOME 19013.3 /AOF HUMAN CHROMOSOME 21OF HUMAN CHROMOSOME 4 /GENEOF HUMAN GENES /3 UNTRANSLATEDOF INTEREST /A GENOMICOF MOUSE CHROMOSOME 7 /PROXIMALOF THE 5 HYDROXYTRYPTAMINElAOF THE FACIOSCAPULOHUMERAL /THEOF THE FACTOR VIII GENE BY AOF THE HUMAN Y CHROMOSOMEOF THE MOUSE Y CHROMOSOME /SXROF THE TCR B CHAIN LOCUS IN /KBOF THE Y CHROMOSOME IN THEON CHROMOSOME 10 /USHER TYPE IION CHROMOSOME 21 STUDY OF FIVEON HUMAN CHROMOSOME 16P /AON THE ACTIVE AND INACTIVE X /5ONTO CHROMOSOME 40TER IN TWORESPONSIBLE FOR THE WOLFSEOUENCE VARIATION IN SOUTHERNSPECIFIC CDNAS USING YEAST /OFSPECIFIC CLONE LIBRARIES FROMSPECIFIC COSMID YEAST /ISOLATESPECIFIC LIBRARIES USINGSPECIFIC SEQUENCE TAGGED SITESSUBSTITUTIONS IN T CELL /CODINGSUGGESTS A SECOND SEXSURROUNDING THE MARFAN /OF THEWITH FURTHER MARKERS /THEWITH GENETIC LINKAGE TO THEWITH YEAST ARTIFICIAL /DISEASE
REGIONAL ASSIGNMENT OF AF8T TO HUMANASSIGNMENT TO XP22.2 P21.2CHARACTERISTICS OF NERVOUSGENETIC FAMILY REGISTERLOCALIZATION OF 75 /ANDLOCALIZATION OF CHROMOSOMEMAPPING OF THEMAPPING ON CHROMOSOMES X 4 5
REGIONS /CHROMOSOMAL 0 HETEROCHROMATIN/COSMID WALKING IN ADJACENT/DNA FROM HUMAN CENTROMERIC/ENCODED BY LARGE GENOMIC/FACTOR A AND B CHAIN PROMOTER/FOR HYPERVARIABLE DNA/IN UNSTABLE CHROMOSOME3P 1 1p 130 17P AND 170 INAND OVER 60% OF THE GENOMEFOR 23 FEATURES OF DOWNIN ALZHEIMER DISEASE ELDERLYINVOLVED IN SEGMENTAL ANEUSOMYOF ABRUPT CHANGE IN SURNAMESOF HUMAN CHROMOSOMES REVEALEDOF HUMAN PROTAMINE 1 AND 2OF HUMAN RDNA CLONED IN YEASTOF MAMMALIAN CHROMOSOMES INOF THE LONG ARM OF CHROMOSOMEON CHROMOSOMES 50 AND 110ON HUMAN CHROMOSOMES 2 13 ANDWITHIN INTERPHASE NUCLEI
REGISTER BEYOND SURVEILLANCEIN ENGLAND AND WALESOF CONGENITAL MALFORMATIONSOF SELECTED INHERITEDOPPORTUNITY FOR ACTIVE
REGISTERS FOR FOLLOW UP AND RESEARCHREGISTRIES /NEUROFIBROMATOSIS
OF CONGENTIAL ANOMALIESTO GENETIC EPIDEMIOLOGY
REGISTRY /FAMILIAL BRAIN TUMOR/IN A LARGE POPULATION BASED/LYMPHOPROLIFERATIVE DISEASE/USING DATA FROM A TUMORA NEED FOR PREANEMIC /ANEMIAFOR WOMEN WITH FAMILY /RISKIN INDIA PRELIMINARY RESULTSOF ABNORMAL KARYOTYPESOF PRENATAL CHROMOSOME
REGRESSIVE LOGISTIC MODELS FORLOGISTIC MODELS IN LINKAGEMODELS /DEVELOPMENTS IN
REGULATED PROTEIN KINASE /A CELL CYCLEREGULATION /OF TRANSCRIPTIONAL
AND EVOLUTIONARY MECHANISMSIN THE PROCESS OFOF A HUMAN PEPSINOGEN AOF C MYC AND C FOS /FACTORSOF GENES /THE DEVELOPMENTALOF HUMAN B GLOBINOF HUMAN PHENYLALANINEOF LIVER SPECIFICOF MURINE CATALASE GENEOF PATTERNING GENES INOF RAS P21 AND K REVIOF THE ALPHA1OF THE DUCHENNE MUSCULAR
REGULATORY ELEMENTS INVOLVED IN /CISLIGHT CHAIN IS LOCATED ONMECHANISM OF THE FACTOR IXROLE OF CALCIUM ACTIVATED
REID CABRAL CHILDREN'S HOSPITALREINVESTIGATION AND LINKAGE ANALYSISREJECT AMNIOCENTESIS FOLLOWING /TORELATION TO ASTHMA AND KIDNEY DISEASES
TO CALCIUM AND CALCIUM /IN
237020572384193623211860188222171002198
2343100
22252155143018692428113217272635202177
2168207021092784234111092218S772204210419852692208
22162116143185
157921131682201
2415219421312567200015281584
56288215632457215849
2016203020201716949357726784208
24793563554026158841082600698608776358359
27861963S582128118
26192233240824132437118A246224302448S6912
2411S7
243821642437731733
204717422752445
TO DNA REPAIR AND CANCER /INTO FACIOSCAPULOHUMERAL /INTO FAMILY HISTORY OF CANCERTO GENETIC AND /INTO INSULIN LIKE GROWTH /INTO ITS DEFICIENCY /IN
RELATIONAL DATABASE FOR A GENETICS /ARELATIONSHIP BETWEEN AGE AT ONSET OF
BETWEEN CLINICALBETWEEN DEXTROMETHORPHANBETWEEN DNA /GENETICBETWEEN PSYCHIATRICBETWEEN THE MOLECULARETHICAL AND LEGAL ASPECTSOF DNA AND GENE CONTENTOF GENOTYPE TO PHENOTYPEOF PHYSICAL TO GENETICTO EUGENICS IN BRITAINTO INFANTILE SLEEP APNEAWITH IMMUNORESPONSIVENESS
RELATIONSHIPS /JOSEPH DISEASE LINKAGEIN HUMAN RED/GREENOF THE LOCI FOR TYPE
RELATIVE RISK ESTIMATION IN GENETICRELATIVES /THEIR MATERNALLY RELATED
AND ASSOCIATED HERITABILITYAND UNRELATED CONTROLOF A NEW AUTOSOMAL /ANDOF EPILEPTIC PROBANDSOF INDEX CASES AN INDICATOROF ISOLATED CASES AFFECTEDOF PATIENTS WITH PRIMARYOF TRIPLETS AND QUADRUPLETS
RELEASING FACTOR PCRFLPS BY HIGHRELIABILITY OF DNA TESTS IN FORENSIC
OF OTHER FOLATE SENSITIVEOF PRECONCEPTION AND
REMODELING LEGAL STANDARD SETTING FORRENAL ADYSPLASIA WITH MULLERIAN
AGENESIS /DIAGNOSIS OF BILATERALAGENESIS WITH TRACHEOESOPHAGEALCARCINOMA CELL LINE BY /A HUMANCELL CARCINOMA /3P IN SPORADICCELL CARCINOMA /DECREASED INCELL CARCINOMA AND UTERUS CANCERCELL CARCINOMAS /OFCELL TUMOR BREAKPOINTS IN /OFDEFECTS AND RADIAL LIMB /ATRESIADIPEPTIDASE GENE TO BAND 024 OFDYSORGANOGENESIS /ANDDYSPLASIA SYNDROME A CAUSE OFDYSPLASIA URETHRAL VALVES ANDECTOPIA AND PELVIC LIPOMATOSISFAILURE /WITH END STAGE CHRONICHYPOPLASIA/DYSPLASIA /DUE TOMALFORMATIONS /ASSOCIATED WITHTRANSPLANT PATIENTS WITH SKINTRANSPLANT RECIPIENTS /AND INTUMORS PHEOCHROMOCYTOMAS AND /IN
RENEWED LINKAGE SEARCH FOR ANRENIN ON CHROMOSOME 1 USING TWO COLORRENPENNING SYNDROME AND LINKAGE TOREPAIR /NOT AMENABLE TO PRENATAL
ACTIVITIES OF HUMAN TRIPLOIDAND CANCER PRONENESS /TO DNAAND IMMUNOLOGIC ANALYSIS /DNADEFECT /ASSOCIATION WITH DNADEFECT IN XP A IDENTIFICATIONDEFECT OF FANCONI ANEMIA CELLSDEFICIENCY POSSIBLE DIAGNOSTICENZYMES /OF A FAMILY OF DNAEVOLUTION AND ITS CONSEQUENCESGENE ERCC 1 /OF THE MURINE DNAGENE ERCC4 /MB OF THE EXCISIONGENE XRCC5 BY SOMATIC CELLIN HUMAN CELLS /MISMATCHIN NORMAL AND UVC REPAIR /DNAIN THE DOMAIN OF THE HUMAN MYCMETHYLTRANSFERASE GENE /DNAMUTANT CELLS ARE THE FUNCTIONSPATHWAYS IN HUMAN CELLSSYSTEM /SHORT PATCH MISMATCH
REPARATIONAL AND IMMUNOLOGICAL /DNAREPARATIVE PROCESSES IN PROGRESSINGREPEAT AT THE CYTOCHROME P 450
CORRELATES WITH X INACTIVATIONCYTOGENETIC STUDIES IN A HIGHLOCI WITHIN AND BETWEEN FOURMARKER DXS548 FOR PRENATAL /CAMOLAR PREGNANCIESPOLYMORPHISM AT THE HUMAN B1POLYMORPHISM IN HORMONEPOLYMORPHISM IN THE REGION OFPOLYMORPHISMS /OF DINUCLEOTIDEPOLYMORPHISMS /SIMPLE SEQUENCEPOLYMORPHISMS /USING GTSEQUENCE POLYMORPHISMSUNITS AND SINGLE STRANDED
REPEATED ABORTIONS GROUPS AT RISK FORDNA HAVE A BEGINNING AND ANFETAL LOSS /IN A FEMALE WITHSEQUENCES ON CHROMOSOME 22
REPEATS AS LINKAGE MARKERS FORFOR PERSONAL IDENTIFICATIONIN HUMAN GENOME /WIDE SPREAD
845203726951222144224142079266022723366
75743418161643
312107319
274816081995241920312788977
2783493812877
2710279113972686208411031623107209639117992713952607257930213841722816
2172536718917150813027187245925901325198821481104119215758451838816
231422758072270257823251709189125442564257024012564241225527418132035959141065
1038940190719831882
5321101981204927891167264012302166209425062433
IN HUMAN PLACENTA /TERMINALIN THE HUNTINGTON DISEASESHARED IN MOUSE AND RAT
REPETITIVE DNA SEQUENCE HYBRIDIZATIONSEQUENCE CLUSTERED ATSEQUENCE FAMILIES ON HUMANSEQUENCE PCR /INTERSPERSEDSEQUENCES IN HUMAN SPERM
REPLACEMENT OF THE P53 GENE IN HUMANTHERAPY /DISEASE BY ENZYMETHERAPY /OF ENZYMETHERAPY FOR GAUCHER
REPLICATION /ARE DEPENDENT ON DNABY BRDU ANTIBODYDEFECTIVE ADENO /USING ADEFECTIVE MUTANT OF /BY ADEPENDENT TRANSCRIPTIONERRORS /RESULTING FROMOF THE INACTIVE XSTUDIES /POSTNATAL LATE X
REPORTER GENE FOR THE DETECTION OF AREPOSITORY /ITALY DATA BANK AND CELLREPRESENTATIVE SAMPLE OF THE U.S.A /AREPRODUCIBILITY OF MOLECULAR WEIGHTREPRODUCTIVE CHOICES OF WOMEN AT RISK
FUNCTION IN THE /OFGENETIC SERVICES TO NEWHORMONES /AND HUMANOUTCOME IN THE IN VITROPOTENTIALITY IN TWOWASTAGE OF THE MOTHERS
REPUBLIC /IN THE DOMINICANOF GERMANY A REPORT FROM THE
REPUNCTURE RATE IN AMNIOCENTESIS BYRESEARCH /PRENATAL BIASES IN TWIN
AND PATIENT TREATMENT /AIN A REFERRED POPULATIONIN TAIWAN /SERVICE ANDIN THE CLINICAL APPLICATIONLABORATORY /FOR A GENETICSON HERITABILITY OFON POPULATION GENETICS OFON THE HISTOPATHOLOGY OF
RESIDUAL ACTIVITY IN SERA FROMHOST CELLS IN SEX MISMATCHEDMETHYLENETETRAHYDROFOLATE /OF
RESISTANCE CAUSED BY HETEROGENEOUSOF TRISOMIC TRANSGENIC ANDTO A HERPES VIRUS WHICH
RESISTANT RICKETS TOTAL LIPODYSTROPHYRESOLUTION BANDING INCLUDING FRAGILE
CHROMOSOME ANALYSIS /HIGHCHROMOSOME ANALYSIS /HIGHCHROMOSOME ANALYSIS AND INCHROMOSOME BANDING /A HIGHGENETIC AND PHYSICAL /HIGHLINKAGE AND PHYSICAL MAPSLINKAGE MAP OF CHROMOSOME 8LOCALIZATION OF 69 /HIGHLOCALIZATION OF HYBRIDIZEDMAPPING OF CHROMOSOME 9 BYPHYSICAL MAP OF THE SHORTPHYSICAL MAPPING OF THERADIATION HYBRID MAP OFRADIATION HYBRID MAPPINGRESTRICTION MAPPING /HIGH
RESOLVED FETAL HYDROPS /A CASE OFFLUORESCENCE /BY TIME
RESOLVING A MARKER CHROMOSOME BYRESONANCE IMAGING /BY MAGNETIC
IMAGING ABNORMALITIES OFIMAGING APPLICATION TO THEIMAGING EXPOSURE /MAGNETIC
RESPIRATORY CHAIN DYSFUNCTION IN /OFCHAIN ENZYME DEFICIENCIESEPITHELIUM /TO THE
RESPONSE IN LYMPHOCYTES FROM NORMALOF BLOOD LYMPHOCYTES TO G2TO LOW DOSE OF XRAYS IN
RESPONSES IN THE ENZYMOPATHIES AND INOF SICKLED ERYTHOROCYTES TO
RESPONSIVE MULTIPLE ACYL COAPSYCHIATRIC PROBLEMS /DIET
RESTRICTION DIGESTS /PCR COUPLEDENDONUCLEASE BANDING /OFENDONUCLEASES UTILITY /BYENZYME ANALYSIS /BY DUALENZYME DIGESTION /BYENZYME MAPPING AROUNDFRAGMENT MELTING /SPECIFICMAP OF HUMAN CHROMOSOMEMAP OF THE DOUBLE MINUTESMAPPING /HIGH RESOLUTIONMAPS /XP LOCI LONG RANGE
RET PROTOONCOGENE A CANDIDATE FOR THERETARDATION (MASA SYNDROME) IN XQ28
/AND SEVERE GROWTH/ASSOCIATED WITH MENTAL/ASSOCIATED WITH MENTAL/IN NONSPECIFIC MENTAL/INTRAUTERINE GROWTH/OF GENES CAUSING MENTAL/TRANSLOCATIONS AND MENTAL2 /(MEGALOCORNEA MENTALA NEW SYNDROME /MENTAL
587
242482
164521991658212020581281242955355524831375163324921681245623461557145712912654273725241850121317401196128428331164146018021621S8578473418102479207927342860925468
1668501485
22292590891163015051541163216201971160
20482144206622012177237S8921702084922
104116678991433908
2555S10503S91147326952542484
2127497554
2523161125281120100722192449214213612084217323471925736521756520115220151409624888
Permuted Title Index
AND A CHARACTERISTICAND CEREBELLAR ATROPHYAND CHROMOSOME ANALYSISAND HYPERCOAGULABILITY AAND NORMAL COAGULATIONAPHASIA SHUFFLING GAITASSOCIATED WITH A /MENTALCONFIRMATION OF /GROWTHCYTOGENETIC AND DNAGENETIC COUNSELING WITHIN CARRIERS OF COMPLEXIN DOWN SYNDROME ININ THREE SIBS A NEWIN TWO MALE SIBLINGSIS NOT EXPLAINED BYLINKED TO DXS369 AT XQ27REPORT OF SECOND CASESHORT LIMBED DWARFISMSOMATIC ANOMALIES ANDSYNDROME DELINEATION OF ASYNDROME THE DEEP ORBITSSYNDROME WITHSYNDROME WITH /MENTALSYNDROME WITH FACIOWITH ATAXIA AND SPASTIC
RETARDED CHILDREN /IN MENTALLYCHILDREN /IN MENTALLYCHILDREN AND IN FETAL BLOODPATIENTS EXAMINED BY HIGHPATIENTS IN HAVANA /MENTALLYPOPULATION OF WESTERN INDIASCHOOL CHILDREN IN TAIWAN
RETICULOCYTES PROSPECTS FOR MOLECULARRETINA /ATROPHY OF THE CHOROID AND
/HIGHLY EXPRESSED IN THE HUMANAND GROWTH DISTURBANCES /OF THESPECIFIC GENE ENCODES A /NEURALSPECIFIC GENE OF JUN/FOS
RETINAL DETACHMENTS IN THE SMITH /ANDSTRUCTURE AND DEVELOPMENT
RETINMS PIGMENTOSA /COUNSELING INPIGMENTOSA /DOMINANTPIGMENTOSA /DOMINANTPIGMENTOSA /DOMINANTPIGMENTOSA /OF X LINKEDPIGMENTOSA AND MUTATIONS OFPIGMENTOSA CONSTRUCTION OFPIGMENTOSA FAMILIES WITHPIGMENTOSA STRUCTURAL ANDPIGMENTOSA USING GC CLAMPED
RETINOBLASTOMA CARRY THE SAMEGENE /EXPRESSION OF THEGENE /MUTATIONS IN THEGENE /THE HUMANGENE HYPERVARIABILITYGENE MUTATIONS TWO /OFHETEROGENEITY /ISPATIENTS /STUDIES IN
RETINOBLASTOMA'S MUTATION /GENERETINOIC ACID /INDUCED BY
ACID /PRESENCE AND ABSENCE OFACID EMBRYOPATHY /IN HUMANACID INDUCED CDNA FROM A
RETINOID EMBRYOPATHYRECEPTORS AND BINDING
RETINOPATHY CANDIDATE GENE IMPLICATEDIN INSULIN DEPENDENT /TO
RETRIEVER MUSCULAR DYSTROPHY /GOLDENRETROGRADE AXONAL TRANSPORT /BYRETROSPECTIVE ANALYSIS OF MATERNAL
EVALUATION /ASTUDY /A COMPARATIVESTUDY ON THE IMPACT OF
RETROTRANSPOSITION EVENT IN MAN /FOR ARETROTRANSPOSON EXPRESSION IN HUMAN /1RETROVIRAL GENE TRANSFER OF HUMAN
GENES GENETIC MARKERS ANDLONG TERMINAL REPEATS INMEDIATED GENE TRANSFER /BYSEQUENCES /HUMAN ENDOGENOUSTRANSDUCTION OF HUMANTRANSGENE EXPRESSION INVECTOR TRANSDUCTION OF /OFVECTORS /USING RECOMBINANT
RETROVIRALLY INSERTED DOMINANT /OFRETROVIRUS IS ESSENTIAL FORRETROVIRUSES /OF ENDOGENOUSRETT SYNDROME /CHROMOSOME MOSAICISM IN
SYNDROME /COMPUTED TOMOGRAPHY INSYNDROME /IN A PATIENT WITHSYNDROME /OF THE X CHROMOSOME INSYNDROME SEARCH FOR THE
REVI PROTEINS BY GTPASE ACTIVATING /KREVEALING OF MULTIPLE CONGENITALREVERSAL AND MULTIPLE ABNORMALITIES
OF THE CLINICALREVERSE BANDS /OF GIEMSA AND
DOT BLOT /BY MEANS OF ASODOT BLOT HYBRIDIZATION /OFMUTATION FROM HP^2 TO HP'l INTRANSCRIPTASE ACTIVITYTRIIODOTHYRONINE /FACTORS AND
REVERSED MICE /ON PHENOTYPE OF SEXREVERSION /DOG MODEL WITH NO SOMATICREVERSION/SUPPRESSION IN DUCHENNE
773668
27688821500737143094410796756871442890870117419467106888926247168798526469634805191285163075414931854254125192273769
245923081443
101016
78
9991939
9799
193123781097221
258458825752624221260361362024201289924228826812010
2670967
248911551631117717352278258024722187242424912337248424852468249020962444414783683
206522232293
121837
88553165718491113440188
14422227464
2319
REVISITED /AND INHERITANCE PATTERNRFLP ANALYSIS OF HLA COMPLEX /BY DNA
AT THE LIPOPROTEIN LIPASE LOCUSBAND SHARING AMONG INDIVIDUALSBASED ASSOCIATION STUDIES /ANDDATA AND MUSCLE BIOPSY /RECEPTORLINKAGE ANALYSIS /BY MEANS OFMARKERS FOR ESTABLISHING GENETICMARKERS IN FOURTEEN DANISHVARIANTS AT THE /EFFECTS OF
RFLPS /USING CLOSELY LINKEDAND HAPLOTYPES IN THE SB GLOBINAND HYPERVARIABLE /MAP USINGBY DENATURING GRADIENT GEL /HHAIBY PCR AMPLIFICATION ININ THE APOAI CIII GENE REGION
RFV MARKER LOCI AROUND THE VON HIPPELMARKER LOCI ON CHROMOSOME 3P
RHABDOMYOSARCOMA ASSOCIATED T(2;13)RHEUMATOID ARTHRITIS AND AUTOIMMUNE
ARTHRITIS IN JAPANESE /OFRHINO PHALANGEAL TYPE WITH SEVERERHIZOMELIC CHRONDRODYSPLASIA PUNCTATA
SHORTENING CLEFT PALATERHMAP A COMPUTER PACKAGE FORRHODOPSIN GENE (PRO23HIS) /THE HUMAN
GENE /AND MUTATIONS OF THEGENE AMONG PATIENTS WITHGENE IN A JAPANESE FAMILYMUTATIONS ASSOCIATED WITHMUTATIONS IN AUTOSOMAL
RHOMBENCEPHAUC ALAR PLATE IN HUMANRIBBING TYPE WITH RHIZOMELICRIBOFLAVIN RESPONSIVE MULTIPLE ACYLRIBOSOMAL RNA GENES BY LOW LEVEL /OF
RNA MULTIGENE FAMILY /HUMANRIBOSYL ATION /INVERSION FROM POLY(ADPRICA /DISEASE IN A SMALL TOWN IN COSTARICHARD III /ASSOCIATION OF KINGRICHTER SYNDROME AND /TERMINATING INRICKETS /EXHIBITING HYPOPHOSPHATEMIC
/THE HISTOPATHOLOGY OF FETALIN A RURAL AREA OF COLOMBIATOTAL LIPODYSTROPHY /RESISTANT
RIDOMILL ON HUMAN CELLS IN VITRORIGHTS EXTEND /HOW FAR DO OUR PERSONALRIGIDITY AND VERY EARLY ONSET /WITHRING CHROMOSOME 11 SYNDROME /WITH
CHROMOSOME 13 LACK OF A DISTINCTCHROMOSOME 20 AND POSSIBLECHROMOSOME 21 DERIVED FROM HERCHROMOSOME INCLUDING PROBABLY A
RING/PLATE /IN THE METAPHASERINGCHROMOSOME (20) MOSAIC /OF ARISE OF SYSTOLIC BLOOD PRESSURE WITHRISK /GENETIC DISEASE OR ENVIRONMENTAL
AN EPIDEMIOLOGIC APPROACHAND PCR TESTING FOR 11 /ATCALCULATION AND GERMLINECHINESE FAMILIES /IN 221 HIGHCUTOFF FOR PRENATAL DIAGNOSIS OFESTIMATION FOR PRESYMPTOMATIC /ONESTIMATION IN GENETIC /RELATIVEFAMILIES AVOID EARLY CHD DEATHSFOR ABNORMAL OUTCOME /INCREASEDFOR ADDITIONAL MALFORMATIONS INFOR CHROMOSOME REARRANGEMENTS /ATFOR CORONARY HEART DISEASE /THEFOR CYTOGENETIC ABNORMALITY INFOR GENETIC DISEASE /INCREASEDFOR HAVING AN AFFECTED CHILD /ATFOR HUNTINGTON DISEASE /ATFOR MALIGNANT HYPERTHERMIAFOR MEIOTIC NONDISJUNCTION /HIGHFOR NTDS /OF PREGNANCIES ATGROUPS /IN 40 PATIENTS IN 5 HIGHIN LEFT FLOW DEFECT FAMILIESMEDITERRANEAN POPULATION /A HIGHOF A TRISOMIC 21 OFFSPRING INOF ANEUPLOIDY IN TWIN GESTATIONSOF CONGENITAL CARDIOVASCULAROF FETAL DOWN SYNDROME /THEOF HUMAN CANCER AND TOXICITYOF SEIZURES TO FIRST DEGREEOF WOMEN WHO HAVE PRENATAL /OFPATIENTS IN BRAZIL NINE YEARPEDIATRIC POPULATION /IN A HIGHPERCEPTION AND HEALTH BEHAVIORPERCEPTIONS AND PRACTICES AMONGPERSONS WHO REQUESTED TESTING /ATPOPULATIONS /IN HIGH AND LOWPREDICTION IN GENETIC COUNSELINGREGISTRY FOR WOMEN WITH FAMILYSPECIFICATION BY ULTRASOUNDTO A COMMON DISEASE HAVING /OF
RISKS AND PRENATAL DIAGNOSIS AEXPERIENCE WITH 2556 CASES /REALIN MOOD DISORDERS /MORBIDITYOF CONGENITAL CARDIOVASCULAR
RN1 AND VK23 USED IN THE DIAGNOSIS OFRNA AND PROTEIN LEVELS /1 AT THE DNA
COMPLEMENTARY DNA /NUCLEARGENES BY LOW LEVEL /OF RIBOSOMALIN MITOCHONDRIAL MYOPATHIES /ANDMULTIGENE FAMILY EXHIBIT A
907110826562871275319111021263019232690101228832021265210402404605
2161370
26638761079804762
2040799
98
9991097237892476249724222436257386512671366824925725891
2561182079113981416146213241369158015192729666270811851191601182317512788164
12479561167427113717881850227698157711728062650250155311462321127428877175326751410173317543019702006608122527381781118027452650190828182521242224272436
SPLICING DEFECT IN B THAL GENE /OFSPLICING IN THE OOCYTE NUCLEUSTRANSCRIPTS IN HUMAN EMBRYONAL
ROBERT REID CABRAL CHILDREN'S HOSPITALROBERTS SYNDROME /DYSPLASIA IN
SYNDROME ISOLATION ANDROBERTSONIAN TRANSLOCATION (13014Q) /A
TRANSLOCATION /T(140210)TRANSLOCATION ON MEIOTICTRANSLOCATION RESULTINGTRANSLOCATION T (22:22)
ROBINOW SYNDROME FOURTEEN CASES WITHROBOTIC HARVESTING /SITU CULTURE ANDROCHESTER COLLABORATION /NEW HAVEN ANDROD MONOCHROMACY TO CHROMOSOME 14 /OFRODENT CELL MUTANTS AS MODELS FOR
SOMATIC CELL HYBRIDS /IN HUMANROKITANSKY KUSTER HAUSER SYNDROMEROLES OF Y CHROMOSOMAL GENES INROMI A RETINOPATHY CANDIDATE GENEROMANO WARD SYNDROME /HETEROGENEITY IN
WARD SYNDROME GENE FROM /QTROOTEDNESS AND OTHER STIGMATA A NEWROUTE /THROUGH THE TRANSCERVICAL
1700 CASES /BY TRANSABDOMINALROUTES OF THE ANCESTRAL POPULATIONSROUTING OF LYSOSOMAL A GLUCOSIDASERP1 AND RP2 LOCATED IMMEDIATELY /GENESRP2 AND RP3 FORMS OF X LINKED /FOR THE
LOCATED IMMEDIATELY UPSTREAM OFLOCUS IN XP1 1.23 /AROUND THE
RP3 FORMS OF X LINKED RETINITIS /ANDRRNA GENES /AND APE EVOLUTION THROUGHRURAL AREA /IN A SOUTH AFRICAN
AREA OF COLOMBIA /RICKETS IN ARUSSELL SILVER SYNDROME /PHENOTYPE OFRUVALCABA MYHRE SMITH SYNDROMERYANODINE RECEPTOR GENE IN MALIGNANT
RECEPTOR RFLP DATA AND
S
S100B PROTEIN IMPLICATIONS FOR DOWNSACCHAROMYCES CEREVISIAE /INSACRAL DEFECT WITH ANTERIOR
DYSGENESIS /FAMILIALSAGUENAY EXCLUSION OF THE ARSACS GENESALINE /INFUSION OF THE UTERUS WITHSAUVARY AMYLASE GENE AMY1C IN /HUMANSALLA DISEASE A FREE SIALIC ACID /INSALT VERSUS PHENOL:CHLOROFORM /BYSAMPLE AS A TEST OF NEW STRATEGY FOR
ENRICHED FOR FAMILIAL COMBINEDOF CYSTIC FIBROSIS PATIENTS INOF FRAGILE X CASES /AN EGYPTIANOF THE U.S.A POPULATION
SAMPLES /LOSS DETECTION IN TUMORACHIEVED BY FILTRATION ANDCOLLECTED ON FILTER PAPERDELIBERATE HETERODUPLEX /DNAFOR THE PRESENCE OF THE /LIVEROF THE BRAZILIAN POPULATION
SAMPUNG /OF THE AMNIOTIC FLUID DURING/STUDIES OF CHORION VILLUSAND SEGREGATION ANALYSISINFUSION OF THE UTERUS WITHON MTDNA PHYLOGENETICTO DETECT LINKAGE FOR TWOTO GENETIC ANALYSES /OF GIBBS
SAN LUIS VALLEY COLORADO /IN THELUIS VALLEY COLORADO /IN THE
SANTIAGO CHILE /ECONOMIC STRATA INSARCOMA /CASE OF GIANT CELL OSTEOGENICSARCOMAS /WITH BONE AND SOFT TISSUE
A STUDY OF 12 CASES /UTERINESARDINIA /MALARIAL POLYMORPHISMS INSATELUTE ASSOCIATION AND NUCLEOLAR
CLONES FROM THE CENTROMEREDNA /EVOLUTION OF ALPHADNA /IRREGULARITIES IN ALPHADNA EXIST IN CHIMPANZEE ANDDNA FAMILIES /OF HUMANDNA FAMILIES ON CHROMOSOMEDNA IN THE CHROMOSOMES OFDNA INTO SIMIAN CHROMOSOMESDNA ON THE STABILITY OF ANDNA PROBES /AND Y SPECIFIC ADNA PROBES /CENTROMERICDNA PROBES /WITHDNA PROBES FOR HUMAN /ALPHADNA PROBES IN PRENATAL ANDDNA SEQUENCES AT 2021 AND /ADNAS /CENP B AND CENTROMERICSUBTELOMERIC AND TELOMERICSUPRACHROMOSOMAL FAMILY
SATELLITES AN UNRECOGNIZEDASSOCIATIONS OF
SATURATION MAPPING OF THE REGIONMAPPING OF THE REGIONMAPPING OF USHER TYPE II
SAUDI ARABIAN DUCHENNE MUSCULAR /THREE
588
2305317
2454733861
238817031647119315691230636122819412077297
2501142043310
6702197814113012532876581
24031939240319741939165
18087251678907429
1911
4192279195388020041287244420132508100527244638222737131712661186279297528231266S15S58128728692718278
266926892881136526051335264515842213264016392626169622341729166316461725166617041635122718584121645169416021222110921682155958
Permuted Title Index
SBY /SPY AND A NEW Y LINKED GENEA CANDIDATE FOR HYA AND SPY FROM
SCAl AND D6S89 AND D6S109 IN ITALYON CHROMOSOME 6P /MAPPING OF
SCALE ANALYSIS OF XQ13 REGION /LARGEMUTATIONS AT THE /LARGE
SCAN FOR LINKAGE IN SCHIZOPHRENIASCAVENGER RECEPTOR GENE PRIMARY /HUMANSCHACHTER SYNDROME (HYPOTELORISMSCHEINKER DISEASE IN THE INDIANASCHEMES /MAP USING CLONE POOLINGSCHISIS MALFORMATIONS AND TWINNING ASCHIZOPHRENIA /AND MODELS FOR
/DEAMINASE GENE WITH/GENETIC LOCI IN/IN PATIENTS WITH/SCAN FOR LINKAGE IN/SITES ASSOCIATED WITH/STUDIES APPLICATION TOA DISCORDANT MZ TWIN /INAND BECKER MUSCULAR /OFAT XP21 OR AN EFFECT OFEXCLUSION OF 5011 /INEXCLUSION OF CANDIDATEWITH MARKERS OF /OFWITHIN A FAMILY OF /AND
SCHIZOSACCHAROMYCES POMBE /THE YEASTSCHOOLS /EDUCATION IN THE NATION'S
IN SOUTHERN AFRICA A FIRMSCHWANNOMA CELL LINE /IN A MALIGNANT
IN A PATIENT WITHSCHWARTZ JAMPEL SYNDROME /IN THESCIDXI /OF XQ13 REGION HARBORINGSCIENCE AND TECHNOLOGY STUDY /OF
AS A WAY OF KNOWINGETHICS AND PUBLIC POLICY
SCIENCES /THE DIVISION OF BIOMEDICALSCLEROSIS /AMYCTROPHIC LATERAL
/AMYOTROPHIC LATERAL/CONCORDANT FOR MULTIPLE/GENES DETERMINING TUBEROUS/IN PATIENTS WITH SYSTEMIC/OF AUTISM AND TUBEROUS1 WITHIN 9034 AND TESTS OFA FOLLOW UP STUDY /MULTIPLEAND THEIR CLINICAL RELEVANCEDEMENTIA AND PARKINSONGENETICS HETEROGENEITY WITHIS DETERMINED BY /MULTIPLELOCALIZATION OF TUBEROUSREPORT OF A PATIENT WITHSUSCEPTIBILITY AIN MULTIPLETO CHROMOSOME 21 /LATERALUSING GT REPEAT /IN TUBEROUS
SCORING /EXPERIMENTS BASED ON BINARY/THREE YEARS OF QUALITY BANDTECHNIOUE /MAXIMUM LIKELIHOOD
SCOTLAND PREDICTIVE TESTING AND SEXSCREEN FOR MUTATIONS IN PATIENTS WITHSCREENED FOR THE FRAGILE X SYNDROMESCREENING /21 AFTER SEROLOGICAL
/BANDING INCLUDING FRAGILE X/BE DETECTED BY PHENOTYPIC/CLINICALLY AND BY NEWBORN/DEFECTS PROSPECTS FOR/EVOLUTION OF THALASSEMIA/IDENTIFIED BY NEWBORN/PROSPECTS FOR THALASSEMIA/RATIOS USED IN PRENATAL/TECHNIQUES IN THALASSEMIAAND COUNSELING /FOR GENETICAND DIAGNOSIS OF DOWNAND PRENATAL DIAGNOSIS INAND PRENATAL DIAGNOSIS INAND PRENATAL DIAGNOSIS OFAND TREATMENT PROGRAMS /CELLBY CONVENTIONAL CYTOGENETICCHROMOSOME 22 ENRICHED /BYDIAGNOSIS COUNSELING INFOR AUTOSOMAL DOMINANTFOR BASE MUTATIONS IN HPRTFOR CODING REGION /RAPIDFOR CYSTIC FIBROSISFOR CYSTIC FIBROSISFOR CYSTIC FIBROSISFOR CYSTIC FIBROSIS AMONGFOR CYSTIC FIBROSIS INFOR DE NOVO MUTATIONS IN /TOFOR DNA SEOUENCE VARIATIONFOR DOWN SYNDROMEFOR DOWN SYNDROMEFOR DOWN SYNDROMEFOR DOWN SYNDROMEFOR DOWN SYNDROME DETECTIONFOR DOWN SYNDROME IN WOMENFOR DOWN SYNDROME IN WOMENFOR DOWN SYNDROME THE /MSAFPFOR DOWN SYNDROME USING /ONFOR DOWN SYNDROME WITH /OFFOR FETAL CHROMOSOMAL /INFOR FETAL DOWN SYNDROME INFOR INBORN ERRORS OFFOR NEURAL TUBE DEFECTS ANDFOR OPEN NTDS IN TWIN /MSAFPFOR PHENYLKETONURIA AND
18592343193719932221
99187722867101896
52915123
20112064638187714052753909
205020502043203019862002236339423
26002232894
2221123439817801782191019382742202215978631913759
19152704142100
1913796191780
1981212118042700860232316121825163018354682623861832392121638520911343883911120179616712251389249
2813278425197018421848184128072792307308309S6494211691250182812031215115518441843117
12141827
FOR POINT MUTATIONS IN THEFOR SEQUENCES NEAR THEFOR THALASSEMIA AND HB S INFOR THE FRAGILE X SYNDROMEFOR TRISOMY 21 FIRST YEARFOR VON HIPPEL LINDAUHETEROZYGOTES OF MULTIIN A HETEROGENEOUSIN ISRAEL /PREGNANCYIN SOUTHEAST ASIAIN THE PREGNANT POPULATIONMETHOD FOR DUCHENNEOF A FAMILY /AND BIOCHEMICALOF ABNORMAL CONCEPTUSESOF AMINOACIDOPATHIES INOF FOUR MAIN CYSTICOF GONOSOMAL ABNORMALITIESOF HEMOGLOBIN E IN ACHANGOF HEMOGLOBIN VARIANTS /TOOF SOUTH AFRICAN /DNAOF THE F508 CYSTIC FIBROSISOF THE WHOLE ESSENTIALOF TRISOMY 21 BASED ONON MENTALLY RETARDED SCHOOLPERCEIVED BY PROVIDERS /OFPROGRAM BY MOLECULARPROGRAM FOR DOWN SYNDROME /APROGRAM INCREASES THE VALUEPROGRAM USING MSAFP HCG ANDPROTOCOL TO IDENTIFY /OF ASCREENING FOR INBORN ERRORSSTRATEGIES BY SIMULATIONSTECHNIQUE FOR RAPID /TUMORTHAN WOMEN AT A /PRENATALTHE USE OF FREE BETAUSING AFFECTEDS ONLYUSING MSAFP HCG ANDWITH DRIED BLOOD SPOT /MSAFPWITH MSAFP HCG AND UE3
SEA DOUBLE ALPHA DELETIONS /DETECTSEASONAL VARIATION OF SEMEN IN THESECOND CASE /RETARDATION REPORT OF
CASE OF FRYNS SYNDROMEENZYME OF THE HEME /THEFAMILY /102150 REPORT OF AGENE ON HUMAN CHROMOSOMES 8 /OFHIT /1 IN SEARCH OF THELEVEL GENERAL HOSPITAL OF A /ALOCUS FOR MARFAN SYNDROME /APRENATAL DIAGNOSIS OF CYSTICSEX DETERMINING GENE IN HUMANSTRIMESTER OLIGOHYDRAMNIOSTRIMESTER TRISOMY 18 /HCG INTRIMESTERS GENETIC DIAGNOSIS A
SECONDARY CONSTRICTION REGIONS OF /ANDMALNOURISHED CHILDREN /INTO A PATERNAL COMPLEX /2035TO PHOSPHORYLASE B KINASE
SECRETED H Y SEROLOGICAL ANTIGEN ANDSECRETION /ANTIDIURETIC HORMONE
/NORMAL GROWTH HORMONE (GH)OF HUMAN FACTOR IX THROUGH
SECTIONED BY JUMP SIZE /LIBRARYSECTIONS FROM STAINED HISTOLOGICALSEGMENT OF AN INV(3)(P25021) /CEN 021
OF THE LONG ARM OF CHROMOSOMESEGMENTAL ANEUSOMIES /OF AUTOSOMAL
ANEUSOMY /INVOLVED INANEUSOMY IN PROBANDS WITH AANEUSOMY OF 15011013 IN THENEUROFIBROMATOSIS /OF
SEGMENTS FUNCTIONAL AND EVOLUTIONARYWITHIN THE UNTRANSLATED /DNA
SEGREGANTS /DIFFERENTIAL MATURATION OFSEGREGATING A STUTTERING PHENOTYPESEGREGATION /AND PROPER MITOTIC
ANALYSIS /SAMPLING ANDANALYSIS AND SIMULATIONANALYSIS FOR THEANALYSIS INCORPORATINGANALYSIS OF 146 ASTHMATICANALYSIS OF BREAST CANCERANALYSIS OF CLEFT LIP ANDANALYSIS OF ESOPHAGEALANALYSIS OF FACIALANALYSIS OF MUTATEDANALYSIS OF SKIN COLOR INANALYSIS OF SMOKINGANALYSIS OF USHER SYNDROMEAND CENTROMERESAND LINKAGE ANALYSIS OF ABETWEEN A BALANCED 2;18IN AN INSERTIONAL /MEIOTICIN LYMPHOCYTES OFIN NORMAL INDIVIDUALS ASOF A FAMILIAL BALANCEDOF CHROMOSOMES IN SPERMOF HIGH BLOOD PRESSURE INOF T(X;16)(P11.4;P13.3)
SEIP SYNDROME AND ANTIMULLERIANSEIZURE DISORDERS /HISTORY DATA ONSEIZURES AUTOSOMAL DOMINANT DISORDER
TO FIRST DEGREE RELATIVES OFSELECTABLE MARKERS IN HUMAN /DOMINANTSELECTION /AFFECTING THE 3 SPLICE SITE
984165439018501847112218551852120838718349891025103480
184914801856565103610921002108
18541846110217491846124212381843183024951742310S3212331186114018391166710
15202409667
23142221789188111422341926113911771563664
1406846105659
140724812175622168714621464
56166459
81826232457155219691663S58276611102648789277
27746018034372764
712750318
27142002117115542546142140767888
891272376187720961112
A METHOD FOR THE SELECTIVEAGAINST TRISOMY 16 MOUSEASSOCIATED WITH BIRTH WEIGHTEQUILIBRIA AND APPLICATIONSFOUNDER EFFECT AND GENE /OFIN HYPODIPLOID LYMPHOCYTESINTENSITY IN A MUSLIM /ANDMANIFESTED BY THE DISTINCTPOLICIES /FETAL SEX
SELECTIVE AMPLIFICATION OF COINCIDENTAND NEUTRAL POLYMORPHISMSCLONAL LOSS AND SUBSEQUENTISOLATION OF CDNAS ENCODEDLOSS OF CHROMOSOME 7MISCARRIAGE RATE INPERFORMANCE OFSCREENING OF GONOSOMAL
SELENIUM LEVELS IN SERUM AND /ZINC ANDSELF HEALING SQUAMOUS EPITHELIOMA
POISONING OF PARENT /BORN AFTERSEWEN IN THE MALE POPULATION OF /OFSEW AUTOMATED DETECTION OF NON /AND
AUTOMATED PROBE MAPPING BYSEMIMICRO DIAGNOSTIC METHOD FORSEMINAL PLASMA AND CEREBROSPINAL FLUIDSENESCENCE LOCUS ON HUMAN CHROMOSOMESENILE DEMENTIA IN ADULT TWINS /ANDSENSE AND ANTISENSE RAS GENE /OFSENSITIVE CALCIUM CHANNEL SUBUNITS IN
FRAGILE SITE EXPRESSION ASLIPASE /IN HORMONEMETHOD FOR TRISOMY 8 /AMUTATION ASSOCIATED WITH /PH
SENSMVITY ACETALDEHYDE TOXICITY ANDAFTER BONE MARROW /MMCTO DNA CROSSLINKINGTO GAMMA IRRADIATION
SENSORIMOTOR NEUROPATHY WITH AGENESISSENSORINEURAL DEAFNESS AND CONGENITALSENSORY NEUROPATHY WITH HIGHLY /ANDSEPARATE CHROMOSOMES FOR /GENOME AND
MUTATIONS /WITH THREEPROBANDS WITH LPL DEFICIENCY
SEPARATED AMNIOCYTES IN RELATION TOSEPARATING GEL ELFCTROPHORESIS /STRANDSEPARATION GEL ELECTROPHORESIS /STRANDSEPHARDIC ORIGIN OF ASHKENAZI /THESEQUENCE /AND ISOLATED LISSENCEPHALY
/OF A NOVEL MYC RELATEDAMPLIFICATION IN TUMORS OFANALYSIS OF MULTIPLE IGKANALYSIS OF THE DYSTROPHINANALYSIS OF THE HPRT GENE INANALYSIS REVEALS A PUTATIVECHROMOSOMAL LOCALIZATION ANDCLUSTERED AT XQ22.3 024COMPARISON OF THE APO B 3COMPONENTS OF HUMAN /SIMPLEDIFFERENCES IN CONTEMPORARYEVOLUTION AND TISSUEFAMILIES ON HUMAN CHROMOSOMEHYBRIDIZATION TO CONSTRUCTIN A FETUS WITH PRENATALLYIN CHROMOSOMAL DNA FROM AINDEPENDENT AMPLIFICATION OFLEVEL /AT THE NUCLEOTIDEOF 180 KB COMPRISING THEOF 2 ADULT PATIENTS WITH GM1OF THE HUMAN PLATELETPCR /INTERSPERSED REPETITIVEPOLYMORPHISMS /REPEATPOLYMORPHISMS IN HUMAN /DNAREPEAT POLYMORPHISMS /SIMPLESIMILARITY TO THE RAT ACYLSPECIFIC OLIGONUCLEOTIDETAGGED SITES FOR LONG RANGETAGGED SITES FOR PHYSICALTAGGED SITES PCR /INTOGGED SITES DEVELOPED FROMVARIATION BY PCR OF POOLEDVARIATION IDENTIFIED INVARIATION IN SOUTHERN /REGIONVARIATION IN THE RB1 GENEVARIATION INTO SITES CUT BYWHICH PARTICIPATES IN THE
SEQUENCES /BY EXPLORING MICROSATELLITE/BY THREE HIGHLY CONSERVED/CLONING OF CORRECTING DNA/FOR MAPPING FUNCTIONAL/FROM ANCIENT AND MODERN DNA/HIGHLY CONSERVED DNA/HUMAN ENDOGENOUS RETROVIRAL/ISOLATION OF POTENTIAL GENE/OF ENOLASE CODING DNA/TO SPLICE SITE CONSENSUS/TWO AMPLIFIED DYSTROPHINAND SITE SPECIFIC /FROM GENEAND THE EVOLUTION OF /ALUAND WALKING IN YEAST /OFARE READILY CAPABLE OF GENEAT 2021 AND 9013 /DNAAT THE FRAGILE X LOCUSAT XP11.2 BY TWO COLORFLANKING MICROSATELLITES /OFFROM SOMATIC CELL HYBRID
589
201143228802808S4
1624282226211784205
285513272011396120411301480829598
1271116611052087578572
213468
2592218016231983216436
24101522225023881900788
191421941003470445103925192826
582186258626232357255096
2214165826311696262223792120219914292395205322342575451229620582049206921102297283421092189210021222792471
2635280325282445209318652274202315
261223372374263824961087247
2625203
26111858236121532097205
Permuted Title Index
FROM TERMINAL 21Q22.3 ANDFROM THE PROXIMAL XIN A PATIENT WITH PRADERIN HUMAN SPERM USINGIN INTERPHASE NUCLEI /GENEIN SUBJECTS WITH SEXIN THE CENTROMERIC /OF BASEIN THE CYSTIC FIBROSIS GENEINTO X IN AN XX MALE SHOWNINVOLVED IN KIDNEY /OFNEAR THE CENTROMERE OF /FORON CHROMOSOME 22 /REPEATEDON THE HUMAN CHROMOSOMES BY.PRESENT AT THE BROKEN ENDSPRESENT WITHIN 7000/3PRODUCED IN HUMAN RODENTREGULATING CELL TYPE /DNARELATED TO CFTR /HUMAN DNATO INTERPHASE CELL NUCLEITO ISOLATE YEAST ARTIFICIAL
SEQUENCING /ELECTROPHORESIS AND DIRECTAND CHARACTERIZATION OFIN A FAMILY WITH 61 /DNAOF CDNAS FOR TYPE I /RAPIDOF LARGE CLONED FRAGMENTSOF SERUM /CDNA CLONING ANDOF TGFA DNA FROM PATIENTSOF THE HPRT GENE 5 REGIONOF THE PCR AMPLIFIED CDNASOF YEAST ARTIFICIAL /ANDTHE HUMAN GENOME SCIENCE
SEQUENTIAL SAMPLING TO DETECT LINKAGESER106 PRO IN THE CYP17 GENE CAUSESSERA FROM PATIENTS WITH PROFOUND ANSERINE FOR GLYCINE Al 901 /CAUSED BY A
FOR GLYCINE SUBSTITUTION AT /ASUBSTITUTION FOR A2(1) GLY 922
SEROLOGICAL ANTIGEN AND MULLERIAN /H YSCREENING /21 AFTER
SEROTONIN MAY AFFECT EXPRESSION OFSEROUS ADENOCARCINOMAS /IN OVARIANSERPENTINE FIBULA UNUSUAL FACIESSERUM Al ANTITRYPSIN AS A RESULT OF A
AND ERYTHROCYTE OF DUCHENNE /INAND RED BLOOD ENZYMES IN THE /OFANTIBODY TITERS IN DUODENAL /ANDBIOCHEMICAL SCREENING FOR DOWNBUTYRYLCHOLINESTERASE /OF HUMANCERULOPLASMIN LACKS OXIDASE /AlCHOLESTEROL LEVELS OF KOREANCHOLINESTERASE PHENOTYPING /OFCHOLINESTERASE VARIANTS WITH /OFDOWN SYNDROME SCREENING THE USEHCG AND FETAL VENTRAL WALLHCG IN PRENATAL DIAGNOSIS OFHCG IN SECOND TRIMESTER TRISOMYHCG PROSPECTIVE STUDY /MATERNALIMMUNOGLOBULINS IN TWIN FAMILIESLEVELS OF HDL C IN BABOONS /ONMARKERS IN MID TRIMESTER /USE OFMARKERS IN SCREENING FOR FETALPARAOXONASE/ARYLESTERASE /OFPROTEIN POLYMORPHISMS IN /ANDSCREENING FOR FETAL DOWN
SERVICE /NEW SOUTH WALES GENETICS/ORIENTED NATIONAL HEALTHAND RESEARCH IN TAIWANUPDATE COMPUTERIZED DATABASE
SERVICES /AND ORGANIZATION OF GENETIC/COMPREHENSIVE GENETICS/NATIONAL GENETICS/PROBLEMS CONFRONTING GENETIC/REFERRALS FOR GENETICS/SOCIAL ASPECTS OF GENETICBY CYSTIC FIBROSIS CENTERSDEVELOPED NATIONS [TO GENETICDEVELOPING NATIONS /GENETICFROM DISEASE ORIENTEDIN A SOUTH AFRICAN RURAL AREAIN DEVELOPING COUNTRIESIN SOUTH AFRICA RESULTS ANDINTO PRIMARY HEALTH CARELOCAL IMPACT /DIAGNOSTICOF SCREENING FOR DOWNPROGRAMS IN THE U.S.APROVINCIAL IMPACT /DIAGNOSTICTO NEW IMMIGRANTS FROM THIRDWHILE EDUCATING HEALTH /AND
SET/CHROMOSOME 21Q22.3 SPECIFIC PROBE/ORIGIN OF THE EXTRA HAPLOID
SEVERE CHILDHOOD DEAFNESS ONFORM OF OSTEOGENESIS /WITH AGROWTH RETARDATION /ANDHYPERHIDROSIS /TEETH ANDHYPOPHOSPHATASIA /ININSULIN RESISTANCE CAUSED BYINTRAUTERINE GROWTH RETARDATIONMALARIA /WITH PROTECTION FROMMENTAL RETARDATION CYTOGENETICMENTAL RETARDATION IN TWO MALEOSSIFICATION DEFECT /ANDPRE ECLAMPSIA A PRELIMINARY /TOSWALLOWING PROBLEMS IN A /AND
SEVERELY AFFECTED SUBJECTS /GENE INMENTALLY RETARDED PATIENTS
2113226017011281181
16852228261216922252165421661652165521982501245323662153214510572299105924972505543
236924282305278517W02718104546810654741054105
1825625133888323268292645575308546512
269158053931018269231139108
2644269012081155543
286618441800150
18101793149
1809S3018061783152
17693738
S30180818031792151
18011215179818121740177716341047294967368414564851152261810798706501919800472754
SEX ASSIGNMENT IN AMBIGUOUS GENITALIACHROMOSOME ABNORMALITIES /WITHCHROMOSOME ABNORMALITIES /WITHCHROMOSOME ANEUPLOIDY AND /OFCHROMOSOME ANEUPLOIDY USING /OFCHROMOSOME ANOMALIES /DYSPLASIA INCHROMOSOME COMPLEMENTS /ABNORMALCHROMOSOMES /MARKERS DERIVED FROMDEPENDENT PENETRANCES OFDETERMINATION /CELLULAR BASIS OFDETERMINATION /THE ROLE OF SRY INDETERMINATION /TO MAMMALIANDETERMINATION AND DOSAGE ANDETERMINATION IN MICE /IN PRIMARYDETERMINATIONS PRENATAL /FETALDETERMINING GENE IN HUMANS /SECONDDETERMINING REGION OF THE Y /THEDISTRIBUTIONS IN PARENTS ANDIDENTIFICATION OF MANIFOLD TRACEINVERSION /LEAD TO CONDITIONAL XYLIMITED AUTOSOMAL DOMINANT TRAITMISMATCHED BONE MARROW TRANSPLANTOF THE CARRIER /DEPENDING ON THERATIO /PREDICTIVE TESTING ANDRATIO A STUDY ON 1089 INDUCEDRATIO AND HYPERHAPLOIDY FREQUENCYRATIO DISTRIBUTION AMONG FAMILIESREVERSAL AND MULTIPLEREVERSED MICE /ON PHENOTYPE OFSELECTION POLICIES /FETALSTEROID HORMONES /AMONGSTEROID HORMONES AND DIETARY /MALE
SEXUAL MALDEVELOPMENT IN MAN /MALESFI I JUMPING LIBRARY SECTIONED BYSHAFTS /DNA ISOLATED FROM HUMAN HAIRSHANGHAI CHINA /CLEFT PALATE INSHIFTING NUCLEOTIDE ANALOGS TO DETECTSHORT ARM /THE PROXIMAL X CHROMOSOME
ARM ABERRATIONS IN HUMAN D G /OFARM INHERITED FROM AN /ON THEARM MARKERS /RELATED AND OTHER XARM OF CHROMOSOME 1 MAKES DNAARM OF CHROMOSOME 17 /PROXIMALARM OF CHROMOSOME 17 /PROXIMALARM OF CHROMOSOME 5 /MAP OF THEARM OF CHROMOSOME 8 /OF THECHAIN ACYL COA DEHYDROGENASELIMB DWARFISM WITH DYSMORPHICLIMBED DWARFISM AND DISTINCTLIMBED DWARFISM DEFECTIVEPATCH MISMATCH REPAIR SYSTEMPHILTRUM SYNDROME /DEEP ORBITSROOTEDNESS AND OTHER STIGMATA ASTATURE AND DELAYED PUBERTYSTATURE ASSOCIATED WITHSTATURE CATARACT AND MENTALSTATURE IN FIVE FAMILIES A /ANDTANDEM REPEAT LOCI WITHIN AND
SHORTENING CLEFT PALATE ANDIN FETUSES WITH DOWN
SHOT GUN PCR /HUMAN CHROMOSOMES USINGSHUFFLING GAIT AND ADDUCTED THUMBSSIALIC ACID STORAGE DISORDER /A FREESIALIDASE IN FIBROBLASTS OFSIALIDOSIS PATIENTS /IN FIBROBLASTS OFSIB DEPENDENCE IN ANALYSIS OF /AND SIB
PAIR ANALYSIS OF THE LINKAGE OFPAIR LINKAGE ANALYSIS WITH /OFSIB DEPENDENCE IN ANALYSIS OF /AND
SIBERIA /POPULATIONS OF NORTHWESTERNSIBLING PAIR /THE FIRST REPORT OF ASIBLINGS /DELINEATION IN TWO
/DISTINCTIVE FACIES IN TWO/RETARDATION IN TWO MALENALVES AND SIRENOMELIA INA NEW SYNDROME /GESTALT INBY TWO DIFFERENT MECHANISMSOF NORMAL PARENTS /AFFECTEDSHARING UNBALANCED /INWITH PSEUDOXANTHOMA /TWOWITH THE ALAGILLE SYNDROME
SIBS /HUNTINGTON DISEASE AND IN THEIRA NEW RECESSIVE SYNDROME [THREEA NEW SYNDROME /IN TWO MALEWITH AUTOSOMAL RECESSIVE /MALEWITH HYPER HYPOPIGMENTATION
SICHUAN CHINA /GENERAL POPULATION OFCHINA /LISU NATIONALITIES OF
SICKLE CELL ANEMIA THE CININNATI /OFCELL CENTER EXPERIENCECELL DISEASE /MINOR ELEMENTS INCELL DISEASE AND OTHER /OFCELL DISEASE IN THE WESTERNCELL SCREENING AND TREATMENT
SICKLED ERYTHOROCYTES TO GRADED MOLARSIGNAL 1 PROTEIN MOLECULAR CLONING
POLYMORPHISM /INHERITED LOWSILVER AMPLIFIED IN SITU /BY
SYNDROME /PHENOTYPE OF RUSSELLSIMAN CHROMOSOMES RESULTS IN ANTOSIMPLEX /WITH EPIDERMOLYSIS BULLOSA
MUTATION MAPS TO CHROMOSOME 12VIRUS TYPE 1 /MUTANT OF HERPES
SI MPSON GOLABI BEHMEL SYNDROME /THESIMULATED ANNEALING IN CHROMOSOME /OF
1175213168585
1069881145516992034431S94430
2236432169123412225274225091190223716681153860119915942696
882227178427392767267
2115250027062078226015371498193119351998213921771585459650903688
25527168141653171289078265762758177737
201349549526432041202726432815728898792870917773
155184014406865331765890821849668
27782769177417742127250418271796212723091282209616781663225720101681735
SIMULATION STUDIES /ANALYSIS ANDSTUDIES OF SEQUENTIALSTUDY /LINKAGE ANALYSIS A
SIMULATIONS /SCREENING STRATEGIES BYSIMULTANEOUS ANALYSIS OF MULTIPLE /FOR
DETECTION ANDDETECTION OF FOUR COMMONDETECTION OF FOUR CYSTICVISUALIZATION OF /CLEARER
SINGAPORE /DYSTROPHY PATIENTS IN/IN THE DRAVIDIAN INDIANS IN
SINGLE ALPHA GLOBIN GENE DELETIONS /OFAMPLIFICATION BY PCR REVEALSBASE DIFFERENCES /TO DETECTCELLS APPLICATION TO /FORCELLS APPLICATIONS TOWARD /FROMCOPY GENES /PROBES OFCOPY HSV 1 TK GENE /INTEGRATEDEXTRACELLULAR AMINOACIDGENE DEFECTS IN CHILE /OFGENE DISORDERS /PHENOTYPE OFGENE DISORDERS AND THE FINNISHGENE WITH LARGE ALLELE EFFECTSGENE WITH LARGE ALLELIC /OF AGIANT MARKER CHROMOSOME /WITH AHUMAN CHROMOSOME HYBRIDS /FROMLINKAGE GROUP /4 YIELD ALOCUS PROBES AS EVIDENCED BYLOCUS PROBES WITHIN AND AMONGMUTANT ALLELE ACCOUNTS FOR THEPHOTON EMISSION COMPUTEDREARRANGED HUMAN CHROMOSOME /ASIDED PCR METHOD FOR THE RAPIDSITE CLEAVAGE OF THE MOUSESTRAND CONFORMATIONSTRAND CONFORMATIONSTRAND CONFORMATION /WITH THESTRAND GEL ELECTROPHORESIS /PCRSTRANDED CONFORMATION /BYSTRANDED CONFORMATIONALSTRANDED MOBILITY /UNITS AND
SINHALESE AND TAMILS OF SRI LANKA [THESINONAAL TRACT /LEIOMYOSARCOMA OF THESIPPLE SYNDROME WITH LICHENSIRENOMELIA IN SIBLINGS NALVES ANDSISTER /PROBLEMS IN A BROTHER AND
[TRISOMY SP IN BROTHER ANDCHROMATID EXCHANGECHROMATID EXCHANGE ANDCHROMATID EXCHANGE FREQUENCYCHROMATID EXCHANGE IN /OFCHROMATID EXCHANGES /OFCHROMATID EXCHANGES AND HUMANCHROMATID EXCHANGES IN CERTAINCHROMATID EXCHANGES IN HUMANCHROMATID EXCHANGES IN MOUSECHROMATID INTERCROSSINGS AND
SISTERS WITHOUT ELEVATED SWEAT SODIUMSITE /CONTIG PROXIMAL TO THE FRAGILE X
/MUTATION IN A MRNA SPLICE DONOR/STUDIES AROUND THE FRAGILE/THE APOLIPOPROTEIN B GENE VNTR20 BASE PAIRS FROM A POLYMORPHICAT 3P14 AND INCREASES THECLEAVAGE OF THE MOUSE GENOMECONSENSUS SEQUENCES /TO SPLICEDIRECTED MUTAGENESIS /MEDIATEDEXPRESSION AS AN INDICATION OFFOR THE HUNTINGTON DISEASE GENEFOUND IN THE PLP GENE IN AFRA(X)(Q27.2) PRESENT IN ONLY IFRAXA /CONTIG AROUND THE FRAGILEFRAXA /CONTIG AROUND THE FRAGILEHOMOLOGY WITH LYSOZYME /ACTIVEIN A HUTTERITE KINDRED WITH XMOLECULAR AND GENETIC /FRAGILE XMUTATION IN THE ALDOLASE B GENEOF 2013 /CLOSE TO THE FRAGILEOF THE FRAGILE X SYNDROME /XOF THE ORNITHINE /AT A MSPIPREFERENCES OF ENDOGENOUSSELECTION /AFFECTING THE 3 SPLICESPECIFIC MUTAGENESIS /ANDSPECIFIC SCREENING OF THE F508USING LASER MICRODISSECTION
SITES /INTERCROSSINGS AND FRAGILEARE DEPENDENT ON DNA REPLICATIONASSOCIATED WITH SCHIZOPHRENIABY APHIDICOLIN AND METHOTREXATECLOSELY LINKED WITH THE CYSTICCUT BY RESTRICTION /INTODEVELOPED FROM CLONED FRAGMENTSEXPRESSION IN LYMPHOCYTES FROMFOR LONG RANGE MAPPING OF THE XFOR PHYSICAL MAPPING USINGIN THE FRAGILE X REGIONIN UNTREATED NON HODGKININ YQ12 /INDUCED COMMON FRAGILEOF DNA METHYLATION IN GENOMICOF HIV RETROVIRAL GENESOF HUMAN LYSOSOMAL A GLUCOSIDASEPCR /IN SEQUENCE TAGGEDWITHIN THE COLLAGENASE GENE ANDWITHIN THE TYROSINASE
SIZE /LIBRARY SECTIONED BY JUMP
590
27662718189918301009181104799320851040287397620992078252512102085253624552659434
52729273613772081197126102854489683
23012075207498422902604228396411052789287513627439178001539160413021568158625651196284325431341631281421592326376669591705207424969971623188423581612378238952844137522642147159255941411122471092S77631137514051559231725282122139021092189103813631564244921875682100192752521752121
Permuted Title Index
AND SEQUENCE COMPARISON OF THEMARKERS IN SCHIZOPHRENIA A /FETALOF THE PROBLEM /SYNDROME THE
SKELETAL ANOMALIES CAUSED BY /ANDDYSPLASIAS /DIAGNOSIS OF THEDYSPLASIAS /NOMENCLATURE OFDYSPLASIAS /OF THE NONLETHALDYSPLASIAS /TWO FETUSES WITHFINDINGS REPORT OF TWO CASESINVOLVEMENT THE FACIOMUSCLE /GRAFTED INTO MOUSEMUSCLE OF PATIENTS WITH /INSYNDROME /THE FACIO CUTANEOUS
SKELETON /DEVELOPMENT OF THE HUMANAND LENS TO ESTIMATE GENETICDYSPLASIA IN ROBERTS SYNDROME
SKIN /IN BASAL CELL CARCINOMAS OF THECANCER HLA ASSOCIATIONS INCANCERS DO NOT HAVE /WITHCOLOR IN A GENETIC ISOLATE /OFLESIONS MICROPHTHALMIA AND
SKULL (TYPE II) A NEW ENTITYSLEEP APNEA /RELATIONSHIP TO INFANTILE
APNEA FAMILIAL AGGREGATION OFSLIDES /FROM STAINED HISTOLOGICALSMOKE INHALATION AND EMBRYONIC GROWTHSMOKERS /ABERRATIONS IN CIGARETTE
AND NONSMOKERS /OF CIGARETTESMOKING ASSOCIATED MALIGNANCIES /OF
EXPOSURE /AND THE ABSENCE OFSMOOTH MUSCLE DYSTROPHIN /OFSNURPOSOMES RNA SPLICING IN THE /ANDSOCIAL ACCEPTANCE /ADVANCES AND
ASPECTS OF GENETIC SERVICESPROBLEMS /COUNSELING AND
SOCIETAL DECISION MAKING ABOUT /FORSOCIETY OF GENETIC COUNSELORSSOCIO ECONOMIC STRATA IN SANTIAGO /LOWSOCIOLOGICAL IMPLICATIONS OF GENETICSODIUM LEVELS /WITHOUT ELEVATED SWEAT
LITHIUM COUNTERTRANSPORT TO /ONSOFT TISSUE SARCOMAS /WITH BONE AND
TISSUE TUMORS /OF BONE ANDSOFTWARE FOR GRAPHIC DISPLAYS OFSOUD TUMORS FACT OR FICTION /OF HUMANSOLUBLE SUPEROXIDE DISMUTASE /WITHSOLUTIONS OF TRACE AND MINOR ELEMENTSSOMATIC AND GERMINAL MUTATIONS IN THE
AND SPERM CELLS USING PCRANOMALIES AND AUTOSOMALCELL HYBRID DNAS /FROMCELL HYBRID MAPPING PANEL FORCELL HYBRID PANEL /REDUCEDCELL HYBRIDIZATION MICROCELLCELL HYBRIDS /IN HUMAN RODENTCELL HYBRIDS AND COSMIDS FORCELL HYBRIDS CARRYING /INDUCEDCELL HYBRIDS CONTAINING ACELLS /OF MUTAGENIZED HUMANCELLS REDUCES THE LIFESPAN OFCONDITIONS AND MENTAL STATESGENE THERAPY /ORGENE THERAPY FOR /TOWARDGENE THERAPY OF HEMOPHILIA BHYBRIDS USEFUL FOR X027 28 /OFMECHANISMS IN HUMAN /FROMMOSAICISM AS OBSERVED INMOSAICISM FOR A FACTOR IXMOSAICISM SUMMARY AND WHATMUTAGENESIS SEQUENCE ANALYSISMUTATION AND SEGREGATION INMUTATION AT THE GLYCOPHORIN AMUTATIONAL DISEASE /CONCEPT OFMUTATIONS IN CIRCULATING /OFMUTATIONS IN THE HUMAN APRTNONDISJUNCTION IN FAMILIALP53 GENE MUTATIONS IN /ANDREVERSION /DOG MODEL WITH NOREVERSION/SUPPRESSION IN
SONOGRAPHIC AND RADIOLOGIC CORRELATIONMARKERS IN PRENATAL
SORTED CHROMOSOMES CONSTRUCTION /FROMCHROMOSOMES FOR X CHROMOSOMEHUMAN CHROMOSOMES /FROM FLOWHUMAN CHROMOSOMES USING SHOT
SORTING AND ALU ELEMENT MEDIATED PCRSOTOS SYNDROME GENE /PENETRANCE OF THE
SYNDROME THE SIZE OF THE PROBLEMSOUTH AFRICA RESULTS AND EXPERIENCES
AFRICAN HYPERLIPIDEMICS FOR /OFAFRICAN POPULATION /DIGIT IN THEAFRICAN RURAL AREA /IN AAMERICA TESTING MODELS OF /OFASIAN ORIGIN POPULATION GENETICAUSTRALIA /OF HEMOPHILIA A INBRITTANY /MUTATION INCHINA /AND PRENATAL DIAGNOSIS INCHINA /IN FIVE PROVINCES OFCOAST /ON NEWFOUNDLAND'SINDIA /PARDHIS OF ANDHRA PRADESHWALES GENETICS SERVICE /NEWWEST INDIA /AMONG SOME TRIBES OF
SOUTHEAST ASIA /SCREENING INASIAN MITOCHONDRIAL DNA
SOUTHEASTERN STATES /AND BETWEEN THE
26319091726981260
43173
1526856646
2488486646930
2562861
2583590592
27641494900
27482763622
129625371294
71610
2443317435152
1770181318142881
252814273626053711898372155321272553440892205
213921361891250117222132232128072819277224692482249420581588289
2599291
255025462535292
2541253812452605464
2319794942216721222499177
1605787172
1792103666918082865
66281227123911117729
286618002862387
26102844
U.S.A. THREE YEARS OFSOUTHERN AFRICA /AND DNA VARIATION IN
AFRICA A FIRM DIAGNOSIS OFAFRICAN BLACKS EXCLUSION OFAFRICAN POPULATIONS /INAFRICAN POPULATIONS /INBLOT ANALYSIS AND FLUORSCENTBLOT AND PCR TECHNIQUES /BYBLOT AUTORADIOGRAPHS /OFBLOTTING AND PCR /USINGCALIFORNIA MEDICAL CENTER /OFEUROPE /PHENYLKETONURIA INITALY /ELLIPTOCYTOSIS INTHAILAND /BETA THALASSEMIA IN
SOUTHWEST (U.S.A.) /AMERICANS OF THEOHIO 1974 1989 /ATLANTA AND
SOVIET EXPERIMENT GENETICS EUGENICSMULTIPURPOSE REGISTER OF /FIRSTPOPULATIONS /THALASSEMIA IN TWO
SPI AND THE 1,25 DIHYDROXYVITAMINETRANSCRIPTION FACTOR GENE (SPI)
SPACER ELEMENTS /FACTOR IX FUNCTION ASSPACES TO BRAIN PARENCHYMA INDUCED BYSPAI/65 HEREDITARY ELLIPTOCYTOSIS INSPAIN /MYOTONIC DYSTROPHY IN ITALY AND
/OF CYSTIC FIBROSIS MUTATIONS INSPANISH CHILDREN /SYNDROME IN FIVE
POPULATION /DYSTROPHY IN THEPOPULATION EPIDEMIOLOGICAL /A
SPANNING THE DIASTROPHIC DYSPLASIASPARSE FUR MOUSE /HEPATOCYTES OF THESPASMS AND DYSMORPHIC FEATURESSPASTIC ATAXIA OF CHARLEVOIX SAGUENAY
DIPLEGIA /ATAXIA ANDPARAPLEGIA /LINKED HEREDITARYPARAPLEGIA /WITH ATAXIA ANDPARAPLEGIA WITH MENTAL /OF
SPATZ DISEASE ANTEMORTEM DIAGNOSIS BYSPECIES /OF DNA VARIATION IN THE HUMAN
OF NEUROSPORA /IN DIFFERENTVARIATION /IN LIGHT OF WITHIN
SPECIFIC A SATELLITE DNA PROBES /AND YALPHOID SEQUENCES TO ISOLATEAND EFFICIENT AMPLIFICATIONAND HYPOXIA INDUCIBLE /TYPEANEUPLOID DIRECTED /ORGANCDNA CLONES EXPRESSED INCDNA ENCODING A NEW MEMBERCDNA USING PROBES GENERATEDCDNAS USING YEAST ARTIFICIALCHROMOSOMAL REARRANGEMENTSCLONE LIBRARIES FROM FLOWCLONES /PROBES AND HTFCOMPONENT /PROTEIN GROUPCOSMID YEAST ARTIFICIALDIFFERENTIAL BINDING TODNA LIBRARIES /CHROMOSOMEDNA LIBRARIES /CHROMOSOMEDNA LIBRARY /BY A CHROMOSOMEDNA PROBE HYBRIDIZED IN SITUDNA PROBES /BY CHROMOSOMEDNA PROBES /TO CHROMOSOMEDNA PROBES FOR CYTOGENETICENOLASE ACTIVITIES /OF NEURONEXPRESSION OF A HUNTINGTONEXPRESSION OF THEFOR PAINTING CHROMOSOME 22GENE ENCODES A BASIC/LEUCINEGENE EXPRESSION /WITH SPERMGENE OF JUNIFOS ONCOGENEGENETIC SYNDROMES WAS /OFHUNTINGTON DISEASE CANDIDATEINTER ALU PCR PROBES FORINTERACTION OF A HUMANISOCHROMOSOME IN A CHILDLIBRARIES USING CHROMOSOMELIBRARY /WITH CHROMOSOMEMUTAGENESIS /AND SITEOLIGONUCLEOTIDE TYPINGPAINTING FLUORESCENCE INPCR /OF CDF508 BY ALLELEPCR AMPLIFICATION IS THEPOLYMORPHISMS SUPPORT THEPROBE ISOLATED FROM A Y /YPROBE SET /CHROMOSOME 21Q22.3PROBES /AND CHROMOSOMEPROBES /TO CHROMOSOMEPROBES BY DIGITAL IMAGEPROBES DETECTION OF ONCOGENEPROBES FOR PRENATALPROBES IN A GIRL WITH SHORTPROBES IN ELUCIDATION OF APROBES TO THE PRADER /1SQPROMOTER OF A CANDIDATEPROTEIN AN ANIMAL MODEL FORREGULATION OF HUMAN /TISSUEREPETITIVE SEQUENCEREPETITIVE SEQUENCES INRESTRICTION FRAGMENT MELTINGSCREENING OF THE F508 CYSTICSEQUENCE TAGGED SITES FORSEQUENCE TAGGED SITES FOR /21SEQUENCES IN SUBJECTS WITHSHORT PATCH MISMATCH REPAIRTRANSCRIPT THAT PHYSICALLY
180425823
20002633263518679585861110114322801063235426762686321726992187018702632955106319841074692
187519891918247285220041987708963675899312
2569167
17252145251624531174252723802247202
2228177S7722622168241716771715154216761721170816352576239124391649245924162308
2322672321412145620701644247
283417281099107328269911634
83166716972171283165316931718233522682462165812812449109221092189168525522399
TRANSCRIPTION /OF LIVERTRANSCRIPTS FROM THE XIST /XTRANSLOCATIONS BY IN SITUVARIANCES AND COVARIANCES ONX CENTROMERE BIOTINYLATED /AYEAST ARTIFICIAL CHROMOSOME
SPECIFICATION AND CNS DEVELOPMENTBY ULTRASOUND /RISKIN GENETIC LINKAGE
SPECIFICITY AN ENDOGENOUS RETROVIRUSSPECIMENS /DRIED FILTER PAPER BLOOD
COLLECTED ON A PAPER MATRIXPROCESSED WITH IN SITU
SPECTRA IN EPIDEMIOLOGICALLY DIVERSEOF ASSOCIATED GENOMIC ERRORS
SPECTRUM CONCEPT AS A PATHOGENETICIN PATIENTS WITH /MUTATIONIN TWO SIMILAR TUMOROF CFTR MUTATIONS IN A LARGEOF CYSTIC FIBROSIS MUTATIONSOF NONGENETIC CAUSES OFOF THE RHODOPSIN GENE AMONG
SPERM /OF CHROMOSOME LESIONS IN HUMANAGE SEX RATIO AND HYPERHAPLOIDYCELLS USING PCR /SOMATIC ANDCHROMOSOME ABNORMALITIES /HUMANIN CARRIERS OF THE MURINE /OFOF MEN HETEROZYGOUS FOR /INOOCYTES AND PREIMPLANTATIONSPECIFIC GENE EXPRESSION /WITHUSING FLUORESCENCE IN SITUUSING FLUORESCENCE IN SITU
SPERMATIDS /GENE EXPRESSED INSPERMATOZOA USING CHROMOSOME /IN HUMANSPERMS NOT INVOLVING CHROMOSOME 21 /INSPHINGOUPID ACTIVATOR PROTEINS
ACTIVATOR PROTEINS GENESPINA BIFIDA /FOR ADULTS WITHSPINAL AND BULBAR MUSCULAR ATROPHY
MUSCULAR ATROPHIES /FOR THEMUSCULAR ATROPHIES /OF THEMUSCULAR ATROPHIES /ONSETMUSCULAR ATROPHY /PEDIGREES INMUSCULAR ATROPHY /REGION FORMUSCULAR ATROPHY /THE GENE FORMUSCULAR ATROPHY CONFIRMATIONMUSCULAR ATROPHY FROM THEMUSCULAR ATROPHY GENE WOBBLERMUSCULAR ATROPHY IN FINLANDMUSCULAR ATROPHY LOCUS /OF THEMUSCULAR ATROPHY LOCUS /OF THEMUSCULAR ATROPHY LOCUS /TO THEMUSCULAR ATROPHY REGION /OF THEMUSCULAR ATROPHY USING /OF
SPINDLE /TRIPLOID EMBRYOS THE TRIPOLARSPINE FORAMEN MAGNUM AND CORDSPINOCEREBELLAR ATAXIA /EFFORTS FOR
ATAXIA AND SPASTICATAXIA GENE ISATAXIA LOCUS TO A 6
SPINULOSA DECALVANS /FOLLICULARISSPIROMETRIC MEASUREMENTS WITH GC /OFSPLICE ACCEPTOR OF ORNITHINE /AT A
DONOR SITE /MUTATION IN A MRNASITE CONSENSUS SEQUENCES /TOSITE FOUND IN THE PLP GENE INSITE MUTATION IN THE ALDOLASESITE SELECTION /AFFECTING THE 3
SPLICING DEFECT IN B THAL GENE DIRECTIN THE OOCYTE NUCLEUS /RNAIN THE PROPOSED CATALYTICMUTATION IN ARAB PATIENTSMUTATION RESPONSIBLE FOR A /AOF DYSTROPHIN MRNA PRECURSOROF PHENYLALANINE HYDROXYLASEOF THE MLC ALK PRE MRNA OF
SPLIT /DIGITAL SYNDROMES TO LUMP OR TOHAND ON THREE OF THEM
SPONDYLOEPIPHYSEAL DYSPLASIA ANALYSISDYSPLASIA CONGENITA
SPONGY DEGENERATION OF BRAIN CANAVANSPONTANEOUS ABORTION /CAUSES OF
ABORTION /COUNSELING INABORTION /MOSAICISM INABORTIONS /DEFECTS INABORTIONS /INABORTIONS /OF HUMANABORTIONS IN QATARIABORTUSES WITH ABNORMALCHROMOSOME ABERRATIONSIN VITRO NEOPLASTICINTRACHROMOSOMAL /RATES OFINTRACHROMOSOMAL MITOTICMUTATION AT 5NULL MUTATIONS IN A HUMANSISTER CHROMATID /OF
SPONTANEOUSLY TRANSFORMED /INSPORADIC BECKWITH WIEDEMANN SYNDROME
CASES /IN 9 FAMILIES AND 16CASES /TYPE 2 PATIENTS ANDCASES OF X LINKED DISEASESOVARIAN BREAST CANCER /ANDRENAL CELL CARCINOMA /3P IN
SPOT [THE DYSTROPHIN GENE DELETION NOTSAMPLES COLLECTED ON FILTER PAPER
591
243097
3682738169821673111225208624441102577122861071385911
255346310743658
1566159444016291552407362
241611841281186283
17072862359173795
1943123918852776214618862018109318642687210121122332221812231590744
215719872052200119852685280223262496235822641112230531798740662
235122802438633636
1121522573365366364S75363916140014791449131425482554255225362843143890676
25851111603
260723571186
Permuted Title Index
SPREAD OF G551 D AND DELTAF508 INOF MODERN PEOPLE /DNA AND THEOF NEW VARIANTS ACROSS THEREPEATS IN HUMAN GENOME /WIDE
SPY AND A NEW Y LINKED GENE SBYFROM THE SXR REGION OF THE MOUSE
SQUAMOUS CARCINOMAS OF THE HEAD ANDCELL CARCINOMAS OF THE HEADCELL CARCINOMAS OF THE HEADCELL CARCINOMAS OF THE HEADCELL CARCINOMAS OF THE LUNGEPITHELIOMA (FERGUSON SMITH
SRI LANKA /THE SINHALESE AND TAMILS OFSRY CAN LEAD TO CONDITIONAL XY SEX /IN
GENE AND 46,XY PURE GONADAL /HUMANGENE IN COS CELLS /OF THEIN SEX DETERMINATION /THE ROLE OFIS THE TESTIS DETERMINING FACTORSPECIFIC SEOUENCES IN SUBJECTS
SSR /IN POPULATIONS OF TURKMENHEREDITARY INHABITANTS /OF TURKMEN
STABILITY OF AN EPISOMAL COSMID IN AOF DNA PREPARED BY SALT /FOROF MUTANT PROTEINS /AND
STAGE CHRONIC RENAL FAILURE /WITH ENDOF NONDISJUNCTION EVENTS
STAINED HISTOLOGICAL SLIDES /FROMSTAINING TECHNIOUES /USING SPECIALSTALK ANOMALY PRENATAL DIAGNOSIS MAYSTANDARD SETTING FOR GENETIC /LEGALSTANDARDS FOR ANTHROPOMETRIC /SELECTED
FOR PRADER WILLI SYNDROMESTATES/AND BETWEEN THE SOUTHEASTERN
/AND TRAINING IN THE UNITED/IN BRITAIN AND THE UNITED/SURNAMES IN FOUR VENEZUELANAND MAY PREDICT VULNERABILITYSEEN IN TWINS /AND MENTAL
STATION CATASTROPHE /CHERNOBYL ATOMICSTATIONARY NIGHT BLINDNESS MAY BE
NIGHT BLINDNESS PHENOTYPENIGHT BLINDNESS PROXIMAL
STATISTICAL ANALYSIS OF MUTABILITYCOMPARISONS OF SIX VNTRMODELS FOR EVALUATING THE
STATISTICALLY SIGNIFICANT CLINICALLYSTATURAL HYPOTROPHY MADELUNG'SSTATURE AND DELAYED PUBERTY /SHORT
ASSOCIATED WITH MATERNALCATARACT AND MENTAL /SHORTIN FIVE FAMILIES A COMMON
STATUS OF AN X LINKED HPAII SITE 20OF GENES ON THE MOUSE ANDOF THE SEARCH FOR MOLECULAROF UNFERTILIZED OOCYTES MAY
STEM CELL FACTOR LOCI MAY BE INVOLVEDCELL TRANSPLANTATION /IN UTEROCELLS /A 1 LOCUS IN EMBRYONICCELLS /B1 GENE IN EMBRYONICCELLS /IN MOUSE EMBRYONICCELLS DERIVATION AND PROPERTIESCELLS TO PRODUCE A MOUSE MODELCELLS USING RECOMBINANT CYTOKINESRESPONSES IN THE ENZYMOPATHIES
STEP IN HUMAN CANCER /A COMMONSTERILITY IN PRENATALLY DETECTED YOSTEROID HORMONE STUDY /THE CANCER AND
HORMONES /AMONG SEXHORMONES AND DIETARY INTAKESULFATASE IN SV 40 /EXOGENOUSSULFATASE PROMOTER A GENE /THE
STICKLER SYNDROME NARIABILITY OFSTIGMATA A NEW AUTOSOMAL RECESSIVESTILLBORN FETUS /HUMAN CHIMERISM IN ASTIMULATED LUPUS LYMPHOCYTES /PHASTIMULATING FACTOR CYTOKINE THERAPY
FACTOR RECEPTOR GENESTOMACH ALDEHYDE DEHYDROGENASE GENESTORAGE DISEASE IN CHORIONIC VILLI
DISEASE XI GSD XI ANDISEASES /TRANSPLANTATION FORDISEASES IN NORTH CHINADISORDER (PSEUDO POMPEDISORDER /A FREE SIALIC ACIDIN MUCOPOLYSACCHARIDOSIS TYPE
STORY /WILMS TUMOR A DIFFERENTSTRAIN CAR 2 POLYMORPHISMS /AND MOUSESTRAND CONFORMATION POLYMORPHISM
CONFORMATION POLYMORPHISMCONFORMATION POLYMORPHISMGEL ELECTROPHORESIS ANALYSISSEPARATING GEL ELECTROPHORESISSEPARATION GEL ELECTROPHORESIS
STRANDED CONFORMATION POLYMORPHISMCONFORMATIONAL POLYMORPHISMMOBILITY POLYMORPHISMS ON
STRANDS OF THE PRION PROTEIN GENE /DNASTRATA IN SANTIAGO CHILE /ECONOMICSTRAUSSLER SCHEINKER DISEASE IN THESTRENGTH /ARE THE FUNCTIONS OF IONICSTRESS AND INSTITUTIONAL FETAL SEXSTRIATA WITH CRANIAL SCLEROSIS REPORTSTROKE /OF FAMILIAL AGGREGATION OF
DUE TO HEREDITARY CYSTATIN CLIKE EPISODES /ACIDOSIS AND
2703168
264224331859234313931319138513941315598
2875119022382393S942393168527152879164625082461302165462216281178209709948
2844333319
28642303277228061928810187827952829112775877016531712890782959
242148
12842566155
246324352493
2925032468484S63910277
273927674922440906814937443619
23602304574846156558529
2013467304
2528984229028042283103925199641105278922982881189625641784796
274410261017
LIKE EPISODES ANALYSIS OF /ANDLIKE EPISODES USING DENATURING
STROMA WITH RESPECT TO THE ASSUMEDSTRUCTURAL ANALYSIS OF CFTR
ANALYSIS OF THEANALYSIS OF THE MYCNAND FUNCTIONAL STUDIESCHROMOSOMAL ABNORMALITIESCHROMOSOME ABNORMALITIESCHROMOSOME ABNORMALITIESDEFECT IN TYPE COLLAGENGENE ENCODING HUMAN /OF THEGENE MUTATIONS IN THE /llPROPERTIES OF A YEASTREARRANGEMENTS /FOR
STRUCTURALLY ABNORMAL X AND Y /OFINTACT MEMBERS OF A /FOR
STRUCTURE AND DEVELOPMENT /RETINALAND EMBRYONIC EXPRESSION OFAND FUNCTION OF 21AND LINKAGE LOCALIZATIONAND MAPPING OF THE A LAND MUTATIONS LEADING TOAND STABILITY OF MUTANTCHROMOSOMAL LOCALIZATIONFUNCTION ANALYSIS OF /ANDFUNCTION AND ROLE ININ THE GARHWAL HIMALAYASIN TWO POPULATIONS WITHIN VNTR ALLELE FREQUENCYMAPPING BY IN SITU /FINEOF HUMAN STOMACH ALDEHYDEOF THE GENE CODING HUMANOF THE HUMAN PROSAPOSIN GENEOF THE PUTATIVEOF THE TYPE IV COLLAGENOF TURKMEN SSR HEREDITARYUSING SURNAMES IN FOUR
STUDENTS /AMONG VIETNAMESESTUTTERING PHENOTYPE /SEGREGATING ASTYLE ON RISK PERCEPTION AND HEALTHSUB TYPE M4 /NONLYMPHOCYTIC LEUKEMIASUBARACHNOID SPACES TO BRAIN /FROMSUBBANDS /PROBES WITHIN CHROMOSOMESUBCELLULAR LOCALIZATION ANDSUBCUNICAL MARKER ANTINEUTROPHIL /ASUBFAMILY BUT DISPLAY LITTLE HOMOLOGYSUBJECTIVE SOMATIC CONDITIONS ANDSUBLUXATION AND ONYCHODYSPLASIA A NEWSUBMICROSCOPIC 4P DELETION DETECTED /A
DELETION CAUSING WOLFSUBPOPULATIONS USING TWO /IN DIFFERENTSUBREGION OF CHROMOSOME 6P /TO A 6 CMSUBREGIONAL LOCALIZATION AND LARGESUBREGIONS BY INTERSPERSED REPETITIVESUBSEQUENT CLONAL EVOLUTION IN /ANDSUBSTANCE THE SAME /INHIBITINGSUBSTITUTION AT CODON 574 OF TYPE II
AT POSITION 175 IN ANFOR A2(1) GLY 922 /SERINEIN A TYPE PROCOLLAGENIN SRY CAN LEAD TO /ACIDIN THE HUMAN GROWTHIN THE MAJOR /NUCLEOTIDEOF GLUTAMATE FOR GLYCINEOF VALINE FOR GLYCINE IN
SUBSTITUTIONS IN T CELL RECEPTOR GENESSUBSTRATE /BIOPSY USING MALTOSE AS A
OXIDATION AND FLAVINSUBTELOMERIC AND TELOMERIC REPEATS
REGION OF 40 /ON THESUBTRACTIVE HYBRIDIZATION /BYSUBTYPE /ASTHMATIC FAMILIES BY ASTHMASUBTYPES GENETICS BEHAVIOR AND BRAIN
OF ALPORT SYNDROME /DIFFERENTOF ATTENTION DEFICITOF BF'F BY ISOELECTRIC /TWO
SUBTYPING APPLICATION TO POPULATIONSUBUNIT CLASS HIGHLY EXPRESSED IN THE
GENE (GABRB3) TO THE /B3GENE AFFECTING THE 3 SPLICE /BGENE IDENTIFIED BY DIRECT DNAOF HEXOSAMINIDASE A IN 35 TAY
SUBUNITS /ACETYLCHOLINE RECEPTORASSOCIATION WITH AN UNUSUALIN HUMANS /CALCIUM CHANNEL
SUCCESSIVE PREGNANCIES WITH NORMAL /INSUCCINATE DEHYDROGENASE DEFICIENCY
SYNTHETASE LOCUS ON 90 32 34SUDDEN INFANT DEATH SYNDROME AN /AND
INFANT DEATH SYNDROME AND ITSINFANT DEATH SYNDROME PATIENTS
SUFFERING FAMILIAL BREAST CANCERFROM DIFFERENT NEOPLASIAS
SUGARBEET PLANTS INDUCED FROM /OFSUICIDE IN PATIENTS WITH HUNTINGTONSULFATASE ACTIVITY ON LYMPHOBLASTOID
GENE IN JEWISH PATIENTSIN SV 40 TRANSFORMED HUMANPROMOTER A GENE WHICH
SULFATE AS A FIRST TRIMESTERSULFUR PROTEINS /OF MITOCHONDRIAL IRONSULPHASALAZINE IN HUMAN LYMPHOCYTE /OFSUPERNUMERARY MARKER CHROMOSOMES
MARKER CHROMOSOMES AND
9774371264S51198
219323781218130315884961462102041340710852337
102325241422862345285246
23082616286
282567
282854
230423552365
112405287928648861969173313469552066S51277322342772770
166114882871200122212058132710547453410541065119024552621522446
27845744971645204222527891957194673
28382856227323921112105910672182241621801135482
214097527482377596131215481765500
2255492
24401251482
28091467
TOES IN TWO BABIES FROMSUPEROXIDE ANION GENERATION AN IN
DISMUTASE ACTIVITY TO /CUZNDISMUTASE PHENOTYPES
SUPPRESSION HYBRIDIZATION /IN SITUOF CELL GROWTH IN A HUMANOF IMMORTALIZATION INOF TRANSFORMED PHENOTYPEOF TUMORIGENICITY BY
SUPPRESSOR GENE /DISRUPTION OFGENE BY FLUORESCENCE INGENE IN EPENDYMOMA /TUMORGENE LOCUS /LINDAU TUMORGENE ON CHROMOSOME 9 INGENE REGIONS 3P IIP 130GENES AND HEREDITARY TUMORGENES CHARACTERIZATION OFLOCI AT 17P13 INCLUDINGLOCUS AT 3P21 /A TUMOR
SUPRACHROMOSOMAL FAMILY CHARACTERIZEDSUBFAMILY BUT
SUPRESSION BY ECBALLIUM ELATERIUMSURFACE ANTIGEN GENE MAPS NEAR THE
MARKERS IN FIRST DEGREE /CELLSURNAMES AS NEUTRAL ALLELES REGIONS
GEOGRAPHICAL DISTRIBUTION ININ FOUR VENEZUELAN STATES
SURROUNDING THE ARGININO SUCCINATETHE GLYCEROL KINASE ANDTHE MARFAN SYNDROME LOCUS
SURVEILLANCE /REGISTER BEYONDOF CONGENITAL ANOMALIESOF GERMINAL MUTATIONS IN
SURVEYING OF CANDIDATE GENES FOR /CDNASURVIVAL IN PALLISTER HALL SYNDROMESURVIVOR WITH TRISOMY 18 /LONG TERMSURVIVORS /IN CHILDREN OF ATOMIC BOMBSUSTAINED RETROVIRAL TRANSGENESV 40 TRANSFORMED HUMAN FIBROBLASTSSV40 TRANSFORMED CELL LINES /ORIGIN OF
TRANSFORMED HUMAN FIBROBLASTS /OFSWALLOWING PROBLEMS IN A BROTHER ANDSWEAT PORE AND LINKAGE ANALYSIS
SODIUM LEVELS /WITHOUT ELEVATEDSWEDEN /U.S.A AND UPPSALA COUNTYSWEDISH FAMILIES /PORENCEPHALY IN TWO
PATIENTS WITH ACUTE /GENE INPOPULATION /BREAST CANCER IN APOPULATION SAMPLE AS A TEST
SWINE CLASS II GENES IN BONE MARROWSXR REGION IN YEAST ARTIFICIAL /MOUSE
REGION OF THE MOUSE Y CHROMOSOMESYMBOUC LANGUAGE FOR PENETRANCESYMMETRICAL FATHER MOTHER AND SIB SIBSYMPTOMS /FAMILIAL AGGREGATION OFSYNCHRONIZATION OF BONE MARROWSYNDROMAL POSTERIOR NUCHAL CYSTIC /NONSYNDROME (5P15.2) USING IRS PCR /CHAT
(DEL(17)(P1 1.2)) DELINEATION(HYPOTELORISM SMALL CUPID(MIM 27268)(MIM NUMBER 154780) /MARSHALL(MIM' 102150) REPORT OF A(MPS VI) BY BONE MARROW /LAMY(PSEUDOLEPRECHAUNISM) MASKED/12 IN MYELODYSPLASTIC/13 LACK OF A DISTINCT/A CANDIDATE GENE FOR MARFAN/A MALE WITH MYELODYSPLASTIC/A NEW AUTOSOMAL RECESSIVE/A NEW DOMINANTLY INHERITED/A SECOND LOCUS FOR MARFAN/AFFECTED BY FRAGILE X/ANALYSIS IN ANGELMAN/ANALYSIS OF USHER/ANALYSIS OF VAN DER WOUDE/AND A 45,XO TURNER/AND CEREBELLAR ATROPHY NEW/AND FROM PATIENTS WITH DOWN/AND ONYCHODYSPLASIA A NEW/AND OPTIC ATROPHY/ANDROGEN INSENSITIVITY/ANHYDRASE 11 DEFICIENCY/BRAIN IN THE 1802 MONOSOMY/BRAIN MORPHOMETRY IN USHER/CANDIDATE GENE FOR LOWE/CARCINOMA IN BLOOM/CASE OF BRACHMANN DE LANGE/CASES WITH INFANTILE MARFAN/CAUSING WOLF HIRSCHHORN/CHOLESTEROL IN NEU LAXOVA/CHROMOSOME 21 IN DOWN/CHROMOSOME MOSAICISM IN RETT/CLINIC FOR MARFAN/CLINICAL FEATURES OF DOWN/COMPUTED TOMOGRAPHY IN RETT/CONFIRMATION OF A NEW/CONTAINS MUTATIONS IN ALPORT/CONTIGUOUS GENE DELETION/CRITICAL REGION FOR THE 180/CRITICAL REGION IN DIGEORGE/DEEP ORBITS SHORT PHILTRUM/DEFICIENT GLYCOPROTEIN/DELETION ANALYSIS IN THE 3P/DIAGNOSIS OF FRAGILE X
592
74787222291553216013952601256824292587217
1391605
25832567303
2553137325881694223413012372625288228822864214022201109949
2756360
22877061469506
2485492579
2598800904
28142671719104460710052490185923432086264327631638704
2168170271068185566756171113341416
9413478828261881500154927502350239566814737708664411020143385023525971496727148891341578317874186838342405144316728671618778511981491
Permuted Title Index
/DIAGNOSIS OF PRADER WILLI/DIAGNOSIS OF PRADER WILLI/DIFFERENT SUBTYPES OF ALPORT/DISOMY IN ANGELMAN/DISOMY IN PRADER WILLI/DNA IN KEARNS SAYRE/DNA LIGASE DEFECT IN BLOOM/DYSPLASIA IN ROBERTS/ECTODERMAL DYSPLASIA/EVENTRATION A NEW/FACIES MIXED DEAFNESS/FIBRILLIN GENE FOR MARFAN/FRAGILE X/FROM PATIENTS WITH DOWN/GENE IN NAIL PATELLA/GENE LOCI IN TOURETTE/GENETIC COUNSELING IN NOONAN/GESTALT IN SIBLINGS A NEW/HEART BLOCK IN DOWN/HEART DISEASE AND TURNER/HETEROGENEITY IN ROMANO WARD/HISTORY OF PRADER WILLI/HYPERPYREXIA IN PRADER WILLI/ICHTHYOSIS AND KALLMANN/IMPLICATIONS FOR DOWN/IN A FAMILY WITH CROUZON/IN A PATIENT WITH R(18)/IN A PATIENT WITH RETT/IN BASAL CELL NEVUS/IN CHILDREN WITH DOWNAIN FAMILIES WITH FRAGILE X/IN MILLER DIEKER/IN THE BECKWITH WIEDEMANN/IN THE SCHWARTZ JAMPEL/IN THE VELOCARDIOFACIAL/IN TWO MALE SIBS A NEW/INITIAL STUDIES IN ZELLWEGER/INSTABILITY FACIAL ANOMALIES/INSTABILITY IN THE FAMMM/INTERSTITIAL 180 DELETION/JEWISH PATIENTS WITH HUNTER/KIDNEY DISEASE AND DOWN/LEADING TO THE KEARNS SAYRE/LETHAL POPLITEAL PTERYGIUM/LI FRAUMENI/LINKAGE STUDIES OF ALPORT/LINKAGE TO THE FRAGILE X/LOCUS D15S10 IN PRADER WILLI/MANIFESTATION OF TRISOMY/MARKERS FOR THE FRAGILE X/MEASUREMENTS IN FRAGILE X/MELANOMA/DYSPLASTIC NEVUS/MENTAL RETARDATION A NEW/MOLECULAR GENETICS OF ALPORT/NATURAL HISTORY OF ANGELMAN/NEURAL TUBE DEFECTS AND DOWN/NEW CASE TORIELLO CAREY/OF A WOMAN WITH KEARNS SAYRE/OF ADAMS OLIVER/OF APPLE PEEL BOWEL/OF CHROMOSOME 21 AND DOWN/OF GILLES DE LA TOURETTE/OF PATIENTS WITH HUNTER/OF THE DELETION 3P25/OF THE FRAGILE X/OF THE GENE FOR WERNER/OF THE GENES FOR USHER/OF THE OHDO BLEPHAROPHIMOSIS/OF THE SMITH LEMLI OPITZ/OF THE X CHROMOSOME IN RETT/ONSET MOSAIC FORM OF DOWN/ORIGIN OF MIXOPLOID DOWN/PATIENTS WITH PRADER WILLI/PATTERN PROFILES IN DOWN/PHENOTYPE OF RUSSELL SILVER/PHENOTYPIC FEATURES OF DOWN/PIGMENTOSUM AND COCKAYNE/PRENATAL DIAGNOSIS OF FRASER/REGION FOR PALLISTER KILLIAN/REGION IN TOURETTE/ROKITANSKY KUSTER HAUSER/SCREENED FOR THE FRAGILE X/SCREENING FOR DOWN/SCREENING FOR DOWN/SCREENING FOR DOWN/SCREENING FOR DOWN/SPECIAL EMPHASIS ON USHER/SPORADIC BECKWITH WIEDEMANN/STANDARDS FOR PRADER WILLI/STUDIES OF DIGEORGE/STUDY OF JOHANSON BLIZZARD/SURVIVAL IN PALLISTER HALL/THE DIAGNOSIS OF FRAGILE X/THE FACIO CUTANEOUS SKELETAL/THE RISK OF FETAL DOWN/THE SIMPSON GOLABI BEHMEL/THE WIEDEMANN RAUTENSTRAUCH/THREE PATIENTS WITH ALPORT/THREE SIBS A NEW RECESSIVE/TO THE PHENOTYPE IN TURNER/TRANSLOCATION IN A TURNER/UNDERREPORTED DOMINANTNARIABILITY OF STICKLER/WHITE MATTER DISEASE A NEW/WITH PRIMARY MYELODYSPLASTIC
6551056194
1558159399529586181264088393
171153119962072176377314631414670169649805419
14471517206520036998541673767894174182119064413161425225514441115637271381S77221911481894709135388838217011775522877911814161924220010668281975S8763751
22231504142814896291678417293652
1437189514201612307308309S642761
9094857
723706
1908646
1127735814101189089
1514782906645
1381
/WITH RING CHROMOSOME 11/WITH SIGNS OF JACOBSON/WOMAN WITH GROLL HIRSCHOWITZ/X SITE OF THE FRAGILE X2MB DISTAL TO D4S43A CAUSE OF OLIGOHYDRAMNIOSA COMMON CAUSE OF INFANTA FAMILY WITH THREE AFFECTEDA LINKAGE STUDY /LI FRAUMENIA NEUROCRISTOPATHY REPORT OFA STUDY OF 13 NON JAPANESEA STUDY OF 522 INFORMATIVEAN ANALYSIS OF POST MORTEMAN AUTOSOMAL RECESSIVE /PHEVRAN UPDATED STUDY /IN DOWNAND A JUMPING TRANSLOCATIONAND ALZHEIMER DISEASE /DOWNAND ANIRIDIA EVIDENCE FORAND ANTIMULLERIAN HORMONEAND ASSOCIATED TUMORS INAND DIAGNOSTIC APPLICATIONSAND DYSMEGAKARYOPOIESISAND GOLTZ SYNDROME /AICARDIAND ISOLATED LISSENCEPHALYAND ITS RELATIONSHIP TOAND ITS VARIATION /TRENAUNAYAND LINKAGE TO XQ21AND SMALL MARKER CHROMOSOMESAND THE ASSOCIATION OFAND THE IDENTIFICATION OF /XASSOCIATED WITH A /OF FRYNSASSOCIATED WITH AN /HALLASSOCIATION REPORT OF AASSOCIATION WITH 8Q DELETIONAT 21011.2BE DETECTED BY PHENOTYPICBUT NORMAL KARYOTYPE /THE 4PCELLS /OF BLOOMCHARACTERIZING PART OF THECHROMOSOME REGION /GIEDIONCLINICAL AND GENETIC /TUMORCLINICAL FINDINGS SUGGESTINGCONFIRMATION OF THE PHENOTYPECONGENITAL DIAPHRAGMATICCONSORTIUM /THE WAARDENBURGCONTIGUOUS A CASE OF BOTHCORRELATION BETWEEN FAMILYCORROBORATIVE REPORT /MYHRECYTOGENETIC CONFIRMATION /18PDELINEATION AND NOMENCLATUREDELINEATION OF A NEW ENTITYDETECTION /SCREENING FOR DOWNDETERMINATION OF ACCURACY /XDIAGNOSIS AND LEARNING ABOUTDUE TO A SUBMICROSCOPIC 4PEVIDENCE FOR AN X LINKEDFAMILES /OF 20 PRADER WILLIFAMILIES /INHIBITOR IN DOWNFAMILIES USING DATA FROM AFIBROBLAST LINE /IN A WERNERFOURTEEN CASES WITH SPECIALFURTHER CLINICAL DELINEATIONFURTHER PHENOTYPIC /PLUSGENE /PENETRANCE OF THE SOTOSGENE FROM CHROMOSOME 6 ATGENE IS NOT ALLELIC TO THEGENE LINKAGE MAPPINGGENE ON XP BETWEEN DXS146GENES /MAPPING THE ZELLWEGERIDENTIFICATION OF A3 AND A5IDS GENE /STUDY OF HUNTERIMMUNOHISTOPATHOLOGY ANDIMPACT OF GENETIC COUNSELINGIMPLICATION FOR HUNTINGTONIN 29 KINDREDS SUGGESTS AIN A 15 YEAR OLD GIRLIN A BOY WITH A SUBTLE /WILLIIN A CHILD WITH 46,XY DELIN A PATIENT PRESENTING ASIN A SURVEY OF CONSECUTIVEIN A THIRD WORLD COMMUNITYIN A TURKISH MALE INFANTIN AN IRANIAN FAMILY WITHIN CHINESE FAMILIES /NEVUSIN FIVE SPANISH CHILDRENIN LIBYA /DOWNIN MAINE 1980 TO 1989 /DOWNIN MENTALLY RETARDED /XIN METROPOLITAN ATLANTA ANDIN MONGOLIA /DOWNIN ONE PATIENT /CAUSES DOWNIN RELATION TO INSULIN LIKEIN THE LOUISIANA ACADIANIN TWO HIGHLY ASCERTAINEDIN TWO SIBLINGS BY TWO /DOWNIN WOMEN AGE 35 AND OLDERIN WOMEN AGE 35 AND OLDERIN WOMEN LESS THAN 35 YEARSIN XQ28 /RETARDATION (MASAIS CAUSED BY DEFECTS ATISOLATION AND /ROBERTSLINKAGE SEARCH UPDATE NEWLINKAGE TO NINE X /ALPORTLOCUS /TO THE FRAGILE XLOCUS BY ANALYSIS OF LINKAGE
13981720950159217277184578401892815234147497581712051701845767891
218137713661448
582748641
1104145188910381520701635150713481835171116892362197
19346986421192
791448196169416501406249421259133
166175310351595600
2548636737898787
2197609
2045191220893831042345
185024422317521454827748
27601478797
14711359692
17501134149326861497210614422023269715511169125018441925
7923881941192320051949
LOCUS ON 1501.5 02.1 /MARFANLOCUS TO 5031.3 5033.3LOCUS WITH 10 DNA MARKERS ONLYMPHOBLASTS /IN ZELLWEGERMEDICAL GENETIC COUNSELINGMOLECULAR ANALYSIS OFNO EVIDENCE FOR /MARFANNOSOLOGY AND INHERITANCEOBSERVED IN 17 MEMBERS OFOF CONGENITAL /IN A NEWOF CRANIOFACIAL MALFORMATIONOF LINEAR SKIN LESIONS /PTEROF MENTAL RETARDATION SHORTOF MULTIPLE EPIPHYSEALOF PROXIMAL TUBULOPATHY /IN AOF PTERYGIA CONGENITAL HEARTOF SEVERE INSULIN RESISTANCEON CHROMOSOME 21 /OF DOWNON XP22.3 /GENE FOR KALLMANNOR A VARIANT OF THEPATIENTS /SUDDEN INFANT DEATHPATIENTS WITH AND WITHOUTPHENOTYPE /WITH THE ALAGILLEPHENOTYPE WITH AN APPARENTLYPOSSIBLE FINNISH TYPEPRELIMINARY RESULTS FROM ANPRENATAL DIAGNOSIS AND /DOWNPROBABLY RECESSIVE /FARLANEPROSPECTIVES OF GENETIC ANDREGISTER IN ENGLAND AND WALESSCREENING BY CONVENTIONALSCREENING THE USE OF FREESCREENING USING MSAFP HCGSCREENING WITH MSAFP HCG ANDSEARCH FOR THE MOLECULARSECONDARY TO PHOSPHORYLASE BSEGREGATION ANALYSIS ANDSTATISTICALLY SIGNIFICANTSTUDY OF 37 CASES /PATELLASUPPORT FOR GENOMICTHE DEEP ORBITS SHORTTHE FIRST REPORT OF A /FACIESTHE IMPACT OF ASSAY VARIANCETHE SIZE OF THE PROBLEMTHREE NEW CASES WITH /PROTEUSTYPE 1 /TO EHLERS DANLOSTYPE 2 A FAMILY UNLINKED TOTYPE I /GENE FOR WMRDENBURGTYPE I /OF WMRDENBURGTYPE AND II CLINICAL ANDTYPE CORROBORATIVE FAMILYTYPE II THE DIAGNOSTICUPDATE /CRANIOSYNOSTOSISUSING MOLECULAR TECHNIQUESUSING MSAFP AND AGE /FOR DOWNUSING MULTIPLE CENTROMERICUSING X AND Y SPECIFIC AWITH ADDITIONAL SKELETALWITH ASSOCIATED /ANOMALYWITH AUTOSOMAL RECESSIVEWITH CRANIOFACIALWITH ELASTIN FIBERSWITH EXTRAMICROCHROMOSOME /XWITH FACIO CUTANEOUSWITH LICHEN AMYLOIDOSIS AS AWITH MATERNAL AGE AND THREEWITH MICROCEPHALY INFANTILEWITH PLEXIFORM NEUROFIBROMASWITH PSYCHOMOTOR RETARDATION
SYNDROME(S) A NUMERICAL /LEMLI OPITZSYNDROMES /AND ENDOCRINOLOGICAL
/AND IN MYELODYSPLASTIC/AND LEARNING ABOUT/ANGELMAN AND PRADER WILLI/ANGELMAN AND PRADER WILLI/MODELS FOR HUMAN BREAKAGE/NONCLEFTING CRANIOFACIAL/OF HURLER AND HUNTER/ON THE ORAL FACIAL DIGITAL/PRADER WILLI AND ANGELMAN/PRADER WILLI AND ANGELMAN/THE INHERITANCE OF LONG OT/UPDATE OF CLEFTINGIDENTIFIES CONSERVATION OFIN THE HUMAN NERVOUS SYSTEMINCREASED SPONTANEOUSIS SYNTENIC TO THE PROXIMALOF MAN /INSTABILITYPREDICTABLE SPECTRA OFTO LUMP OR TO SPLIT /DIGITALWAS REACHED IN 8% OF THEWITH XP22.3 DELETION /BOTH
SYNDROMOLOGY /THE USE OF COMPUTERS INSYNEXIN (ANNEXIN VII) GENE /THE HUMANSYNOSTOSIS GENERALIZED HYPOTONIASYNTENIC HUMAN AND MURINE CHROMOSOMAL
TO THE PROXIMAL REGION OF IISSYNTENY BETWEEN A REGION ON HUMAN
IN MICE AND POSSIBLE ANIMALSYNTHASE ACTIVITY AND METHYLCOBALAMIN
DEFICIENCY /CYSTATHIONINE BGENE CAUSING CONGENITAL /111RAPID METHOD TO SCREEN FOR /B
SYNTHESIS /FOR PROBE LABELING ANDOF ALPHA SATELLITE DNA
593
11091933188350517701664
7790779073687014946887625028174851528229481423771116533660116017491475769766357
16713101233114022938462766758746
15967167281828172771
2025107727
10528316859333391695120316661725856721839879114514866467431215852702892679122261713387
222429734328234259
14598433401868303
25541860157471363323
1448135
2266773
1861186018691868501
2300530
232325141635
Permuted Title Index
SYNTHETASE LOCUS ON 90 32 34TYPE I TO ANONYMOUS DNA
SYNTHETIC MOLECULARLY DEFINED /OFSYSTEM (VACARES) 1987 BIRTH COHORT
/CELLS WITH CONFLUENCED CULTURE/INTERACTION WITH THE ABO BLOOD/SHORT PATCH MISMATCH REPAIR/USING CHICKENS AS A MODELAND DEVELOPMENTAL ANOMALIES INCOMPUTER PROGRAM FOR AUTOMATICFOR EFFICIENT GENETIC ANALYSESFOR MEDICAL GENETICSFOR SYNDROME DIAGNOSIS ANDFOR THE MOLECULAR GENETIC /AHEREDITARY DISEASES IN /NERVOUSHEREDITARY DISEASES IN B.S.S.RIN CLINICAL GENETICSISOLATING THE GENES FOR VONMALFORMATIONS /CENTRAL NERVOUSMANIFESTATIONS IN COWDENTEST /REFRACTORY MUTATIONTEST FOR THE SIMULTANEOUS
SYSTEMATIC ANALYSIS OF PROTEINSEARCH OF THE GENOME FOR
SYSTEMATICALLY ASCERTAINED EUROPEANSYSTEMIC LUPUS ERYTHEMATOSUS /WITH
MALFORMATIONS /AND ASSOCIATEDMAPPING AND SEQUENCING OFSCLEROSIS /IN PATIENTS WITH
SYSTEMS CONCEPT /AND FUNCTIONSIN DYSMORPHOLOGY APPROACHES
SYSTOLIC BLOOD PRESSURE WITH AGE /OF
2140203120027301575265125522080842206010411811133191
269227287503038686169931047576194020432733885
27851597121138
2729
T
T(22:22) (P11:011) IN A FEMALE WITHAND IDENTIFICATION OF A CPG ISLANDCELL LEUKEMIA /NEW TRANSLOCATION INCELL LEUKEMIA IN AN ATAXIA /OFCELL RECEPTOR B JUNCTIONAL DIVERSITYCELL RECEPTOR GENES /INCELL RECEPTOR GENES IN MULTIPLE /ANDGENE ON CHROMOSOME 190 /TROPONINLYMPHOCYTES NIRUS WHICH INFECTSMUTATION AT A MSPI SITE OF THE /C TO
T(10;14XQ24;011) TRANSLOCATION /THET(11;19) ACUTE LEUKEMIAS /INT(13;21) /WITH AN APPARENTLY BALANCEDT(14;18) NEGATIVE FOLLICULAR NONT(14Q21Q) BY FLUORESCENT IN SITU /NOVO
ROBERTSONIAN TRANSLOCATIONT(1;12) (Q42.3;P12.2) MAT /1, + DER (1)T(22;22XPIQ1I) /WITH A DE NOVOT(2;13) TRANSLOCATION BREAKPOINTT(2;5XP23;C35) IN THREE CASES OFT(2;7XP25;Q32) IN A BOY WITHT(5;10XPI3;QII.2) MAT TRANSLOCATIONT(5;7)(Q33;34) NONRANDOM ASSOCIATIONT(6;9) TRANSLOCATION IN ACUTE /OF THE
TRANSLOCATION IN ANLL /OF THET(6P;13Q) CHROMOSOME REARRANGEMENTT(8;21) IN ACUTE MYELOID LEUKEMIA /OFT(X;14X)Q2;Ql11) TRANSLOCATION /WITH AT(X;16)(P1I.4;PI3.3) /SEGREGATION OFTA ON PHENOTYPE OF SEX REVERSED MICETABBY (TA) ON PHENOTYPE OF SEX /OFTACHYCARDIA AND APPARENT AUTOSOMALTAGGED SITES FOR LONG RANGE MAPPING
SITES FOR PHYSICAL MAPPINGSITES PCR /IN SEQUENCE
TAIWAN /DISEASE ENDEMIC AREA IN/OF ALPHA THALASSEMIA IN/RETARDED SCHOOL CHILDREN IN/SERVICE AND RESEARCH IN
TALUS AND CALCANEUS A NEW AUTOSOMALTAILS OF SRI LANKA /THE SINHALESE ANDTANDEM DUPLICATION OF THE SHORT ARM
REPEAT LOCI WITHIN AND BETWEENREPEATS FOR PERSONALTRIPLICATION OF 10(021 32) IN
TANDELY REPEATED DNA HAVE A /DOESTAPETOCHORIDAL DEGENERATION /WITHTAGS DIGESTION /REVEALED BYTARDY PROGRESSING DEMENTIA /WITHTARGET FOR ANTI GLOMERULAR BASEMENTTARGETED CORRECTION OF A DEFECTIVE /OF
DISRUPTION OF THEHOMOLOGOUS RECOMBINATION INTO MACROPHAGES
TASTING IN PATIENTS WITH THYROIDTAY SACHS ALLELE /TO CARRY A CLASSICAL
SACHS D1 VARIANT /A LATE INFANTILESACHS CARRIERS DETECTION AMONGSACHS CHROMOSOMES FROM 23 NON /35SACHS DISEASE /OF JEWISH INFANTILESACHS DISEASE ALLELES IN THE /OFSACHS DISEASE AND ADULT GM2 /OFSACHS DISEASE CHARACTERIZATION OFSACHS DISEASE IN CHINA TWO NEWSACHS DISEASE IN NEW ENGLAND /FORSACHS DISEASE MUTATIONS IN FRENCH
1230233413572604224027841917236825905592251323660139216341647144093837013311321142915092582125
142113422604
8822272227781
2109218921001383103418541810738
28751585
65250613692640
111563873383
2487243525035525471067494461106724462709
3283
224617882289
SACHS DISEASE ONE GENERATION /OFSACHS SCREENING IN THE PREGNANT
TCR B CHAIN LOCUS IN CONJUNCTION WITHTEACH DYSMORPHOLOGY TO AN AVERAGE /TOTEACHER TRAINING /GENETICS K 12 LEADTEACHING DYSMORPHOLOGY TO HOUSESTAFF
HUMAN GENETICS IN THETHE PATHOLOGIST TO USE
TECHNICAL ADVANCES AND SOCIALDIFFICULTY OF TRANSCERVICAL
TECHNIQUE /CHROMOSOME BANDING/MAXIMUM LIKELIHOOD SCORING/PCR AND MICROCLONING/SPECIAL PROBE POOLAN ALTERNATIVE FORM OFASSOCIATION MAPPING ANDFOR GENOME ANALYSISFOR RAPID DETECTION OFIMPROVEMENT /DETERMINATIONIN ITALIAN HEMOPHILIA BON HISTONE DEPLETED
TECHNIQUES /AND MOLECULAR GENETIC/BY IN SITU HYBRIDIZATION/BY SOUTHERN BLOT AND PCR/SITU HYBRIDIZATION AND PCR/USING SPECIAL STAININGAND FLUORESCENCE IN SITUAND IN SITU HYBRIDIZATIONAND IN SITU HYBRIDIZATIONAND OUTCOME /DIAGNOSISFOR ISOLATING GENES /ANDIN THALASSEMIA SCREENING
TECHNOLOGIES /EVOLUTION AND NEW/HARNESSING NEWIN PRACTICE /HEALTH CARE
TECHN&LOGY /DNA DIAGNOSTICFOR THE DEVELOPMENT AND /INSTUDY /OF SCIENCE ANDTO FIND NEW POLYMORPHIC
TEETH AND SEVERE HYPERHIDROSISTELANGIECTASIA GENE(S) TO A CM /ATAXIA
GROUP D CELLS BY MICROIN ITALY DATA BANK ANDIS FLANKED BY THELOCUS /NEAR THE ATAXIALYMPHOBLASTS /ATAXIAPATIENT WITH A /ATAXIAUSING BIVARIATE BRDU
TELEPHONE COUNSELING FOR PARENTS /ANDTELOMERE FUSION THAT MAPS CLOSE TO
SEQUENCES IN A PATIENT WITHSEQUENCES PRESENT AT THE /OFTELOMERE FUSION THAT MAPS
TELOMERES /CHROMOSOMEFUNCTION ON REINTRODUCTION
TELOMERIC REPEATS SHARED IN MOUSE ANDSITE FOR THE HUNTINGTON /A
TEMPERATURES AS A TEST FOR STABILITYTEMPORAL BONE CT FINDINGS /HAND ANDTENSION EFFECTS ON FANCONI ANEMIA
EFFECTS ON FANCONI ANEMIATERATOGEN /MELLITUS AS A HUMAN
INFORMATION SERVICE UPDATETERATOGENESIS IN 12 PATIENTS /OFTERATOGENS /OF RECEPTOR MEDIATEDTERATOLOGY /META ANALYSIS IN CLINICALTERATOMA /PROGRESSIVE INTRACRANIALTERATOMAS USING DNA MARKERS /OVARIANTERATOTHANASIA AND THE PREVALENCETERBUTALNE SULFATE AS A FIRST /OFTERM CULTURE /LYMPHOCYTES IN LONG
EVALUATION OF THE LEUKEMIC CLONEFOLLOW UPS /ISSUES AND LONGINBREEDING ON THE FREQUENCIES OFMETABOLIC CONTROL /AND LONGPLACENTA USING INTERPHASE IN /ASURVIVOR WITH TRISOMY 18 /LONG
TERMINAL 21022.3 AND COSMID WALKINGDELETION OF THE LONG ARM OFDELETION XQ24 IN A WOMANDELETIONS OF BAND 1P36DELETIONS OF CHROMOSOME 14REARRANGED CHROMOSOMES /OFREPEATS IN HUMAN PLACENTA
TERMINATED A PREGNANCY AFTER PRENATALTERMINATING IN RICHTER SYNDROME ANDTERMINATION /ANEUPLOIDY AT PREGNANCY
OF PRIMER EXTENSION ATERRIER A NEW DOG MODEL WITH NO /FOXTEST/REFRACTORY MUTATION SYSTEM
AND CLINICAL OBSERVATION OF THEAPPLIED IN PATIENTS WITH ACUTEAPPLIED TO TWINS /MEMORYFOR MUCOPOLYSACCHARIDOSISFOR STABILITY OF DNA PREPARED BYFOR THE SIMULTANEOUS DETECTIONIN PRENATAL REVEALING OF /THE AFPOF BYELORUSSIAN CHILDRENOF HUNTINGTON DISEASE /OF THE DNAOF NEW STRATEGY FOR THE GENETICUSING AGE AT ONSET AS A COVARIATE
TESTING /AT RISK PERSONS WHO REQUESTED/CONFIDENTIALITY IN GENETIC/FATHER WAS UNAVAILABLE FOR/THE CASE FOR POSTPONING
20718341001362061373341394351128162027002061251513202088163724951604265216331671130395813641628166714551695S83S13385S34S271802
5153
12342057841294
23012654196719556772604160917782147170116552147236
24981645188425087961401141867417931295129112931277410103
12511624586
1141284152412091469211314811420153817261655242417661366116397446499325331344S85577
250810471837280611001005197030139
28771822
/THE VALUE OF PSYCHOMETRICAND POPULATION SCREENING FORAND SEX RATIO /PREDICTIVEASSESSING GENETIC 10 ANDASSIGNMENT IN MALKNANTEXPERIENCES FROM A COMMERCIALFOR 11 PREGNANCIES /AND PCRFOR ADULT ONSET DISORDERS LOWFOR ADULT POLYCYSTIC KIDNEYFOR HUNTINGTON DISEASEFOR HUNTINGTON DISEASEFOR HUNTINGTON DISEASEFOR HUNTINGTON DISEASEFOR HUNTINGTON DISEASEFOR HUNTINGTON DISEASEFOR HUNTINGTON DISEASE AFOR HUNTINGTON DISEASE IN THEFOR HUNTINGTON DISEASE THEFOR HUNTINGTON DISEASE THEIN HUNTINGTON DISEASEIN HUNTINGTON DISEASEIN MULTIPLE ENDOCRINEIN THE SOUTHEASTERN U.S.A.LEGAL AND ETHICAL ISSUES WITHLINKAGE TO HLA /MENINGOCELEMODELS OF POPULATION /AMERICAOF CHILDREN FOR GENETICOF FAMILY MEMBERS IN THE /XOF THE SPINAL MUSCULARPROGRAM /THROUGH A PREDICTIVE
TESTIS /ALL GERM CELL TUMORS OF THE/OF CARCINOMA IN SITU OF THEDETERMINING FACTOR EVIDENCEDETERMINING FACTOR MAPPING ONDETERMINING REGION SUGGESTS ASECRETED H Y SEROLOGICAL /ARE
TESTS IN FORENSIC PRACTICE /OF DNAIN PRENATAL DIAGNOSIS /AND ACHEIN THE THIRD TRIMESTEROF LINKAGE TO 110 AND 140 /AND
TETRAMERIC TANDEM REPEATS FOR /ANDTETRANUCLEOTIDE REPEAT POLYMORPHISM
REPEAT SEQUENCE /ANDTETRAPLOIDY UNDER PROLONGED HYPOTONICTETRASOMY 12P /DIAGNOSED CASE OF
18P SYNDROME CYTOGENETIC9P A TISSUE SPECIFIC
TEXAS U.S.A /ETHNIC POPULATIONS OFTEXT IN TEACHING DYSMORPHOLOGY TO /ANDTG N(AG)M MICROSATELLITE REFLECTS /ATGFA DNA FROM PATIENTS WITH CLEFT LIPTHAI FAMILIES TOWARD GENETIC /OFTHAILAND /BETA THALASSEMIA IN SOUTHERN
/HOSPITAL BANGKOKTHAL GENE DIRECT SEQUENCING OF THE /BTHALASSEMA /DIAGNOSIS OF BETA
72 BETA THALASSEMIA ANDALLELES IN U.A.E /OF BAND 306 NORMAL GENOTYPESAND HB S IN THE EAST /FORBY DUAL RESTRICTION /ALPHABY PCR GENERATED /TO BGENE AMONG AFRICAN /B ZEROGENE IN VARIOUS ETHNICGENES IN ASIANS /ORIGIN OFIN LAOTIANS AND ITSIN NORTH INDIA /OF BETAIN SOUTHERN THAILAND /BETAIN TAIWAN /OF ALPHAIN THE DRAVIDIAN INDIANSIN TWO SOVIET POPULATIONSMAJOR IN A HIGH RISK /OFMAJORS OUTCOME OF 39MUTATIONS IN FIVE /OF BMUTATIONS IN HUNAN CHINANONSENSE 37 MUTATION IN /BPROMOTER MUTATION ON /A B +RESULTING FROM COMPOUND /BSCREENING /EVOLUTION OFSCREENING /PROSPECTS FORSCREENING /TECHNIOUES INSCREENING AND PRENATALSCREENING AND PRENATALSCREENING DIAGNOSIS /BSCREENING HETEROZYGOTESSCREENING IN SOUTHEAST
THALASSEMHO L- E DISEASE INTHALASSEMIC HAPLOTYPES IN THE /NON BTHANATOPHORIC DYSPLASIA WITHTHEORETICAL ACCEPTABILITY OF PRENATALTHERAPY /DISEASE BY ENZYME REPLACEMENT
/OF ENZYME REPLACEMENT/OR SOMATIC GENE/STIMULATING FACTOR CYTOKINEAN INTERVENTION MODEL WITHFOR ADA DEFICIENCY AND CANCERFOR GAUCHER DISEASE USINGFOR HEMOPHILIA B EXPRESSIONFOR HEPATIC DEFICIENCIES IN AFOR PHENYLKETONURIA /GENEGENETICIST INVOLVEMENT /ANDIN GAUCHER DISEASE /OF ENZYMEIN INHERITED MYOPATHIES /GENEIN LDL RECEPTOR DEFICIENTINDUCED CHANGES IN THE /OF
594
173825188018361911274011852111764210301966173217711807300176717381822175117681950180440
195328659511610123917456141318239316652341105
110311659391913250619072049157614121650145665137
2800236917642354124923051272183127991831390112010492743S4
10701072102423541034287399225011851117282026742423107038639238538839138918553877932727900182555355524696191816S91248324742478248218135564244231337
Permuted Title Index
OF CYSTIC FIBROSIS AND A 1OF FABRY DISEASE /STUDIES ANDOF HEMOPHILIA B /SOMATIC GENEOF MUT METHYLMALONIC ACIDURIAPROLIFERATIVE IMMUNOLOGICAL
THERMOLABIUTY OF RESIDUAL /DEFICIENCYTHORACIC FUSION KLIPPEL FEIL ANOMALYTHROMBOCYTOPENIA AND ANEMIA IN ANTHUMB AND MENTAL RETARDATION (MASATHUMBS SYNDROME FURTHER CLINICALTHYMIDINE KINASE GENE BY CELL FUSIONTHYMUS WITH LIP PSEUDOCLEFTS FURTHERTHYROID /AND CONGENITAL ABSENCE OF THE
CARCINOMA BY FLUORESCENT INCARCINOMA IS NOT LINKED TODISEASE /IN PATIENTS WITHDISEASE IN FAMILIES
THYROXINE BINDING AND TRANSIENTTIBETIAN YI MIAO AND LISU /OFTIBIA HYPOPLASIA POLYDACTYLY ANDTIMING OF PREGNANCY LOSSES THROUGHOUTTISSUE /ANALYSIS IN POSTMORTEM FIXED
AND ITS CLINICAL APPLICATIONCULTURE CYTOGENETIC ANALYSISDISORDERS /HERITABLE CONNECTIVEDISORDERS ORGANIZATION ANDDYSPLASIA /AND CONNECTIVEEXPRESSION OF THE DMD LIKE /ANDNONSPECIFIC ALKALINE /THE HUMANOF TWIN GESTATION /AND FETALSARCOMAS /WITH BONE AND SOFTSPECIFIC EXPRESSION OF ASPECIFIC ISOCHROMOSOME IN A /ASPECIFIC REGULATION OF HUMANSPECIFIC RESTRICTION FRAGMENTSPECIFICITY AN ENDOGENOUS /OFTUMORS /OF BONE AND SOFT
TISSUES/IN HEARING FROM AUDITORYBY THE PCR /TRACE HUMANIMPROVE LIFE QUALITY OF TWOIN A PHENOTYPICALLY NORMALOF A PRENATALLY DIAGNOSED /INTOWARD A COMPLETE MOLECULAR
TITERS IN DUODENAL ULCERS /ANTIBODYTK GENE /INTEGRATED SINGLE COPY HSV 1TOBACCO SMOKE INHALATION AND /MATERNALTOCOLYTIC AGENT IN PATIENTS /TRIMESTERTOE LENGTH OF HAN AND ZHUANG /ON THETOES IN TWO BABIES FROM SAME FATHERTOGGED SITES DEVELOPED FROM CLONEDTOLUENE EMBRYOPATHY ELUCIDATION OFTOMOGRAPHIC STUDY ON 26 BRAZILIAN /ANDTOMOGRAPHY FINDINGS IN PERSONS AT
IN RETT SYNDROME /COMPUTEDTONGUE MOVEMENTS IN INDIVIDUALS FROMTOPOISOMERASE 1 AS A CANDIDATE GENETORIELLO CAREY SYNDROME /NEW CASETORONTO /CYSTIC FIBROSIS MUTATIONS INTORSION DYSTONIA GENE AND LOCI ON /THETOURETTE SYNDROME /GENE LOCI IN
SYNDROME /OF GILLES DE LASYNDROME /REGION INSYNDROME GENE LINKAGE MAPPINGSYNDROME LINKAGE SEARCHSYNDROME SEGREGATION /DE LA
TOWN IN COSTA RICA /DISEASE IN A SMALLTOXICITY /RISK OF HUMAN CANCER AND
AND THE ROLE OF CYTOSOLICTOXICOSIS /ON INHERITED CANINE COPPERTRACE AND MINOR ELEMENTS IN SICKLE /OF
ELEMENTS AND FETAL CONGENITALHUMAN TISSUES BY THE PCR
TRACED TO PREMEIOTIC EVENTS /CAN BETRACHEO OESOPHAGEAL FISTULAE ANDTRACHEOBRONCHIAL DEFECTS /ASSOCIATEDTRACHEOESOPHAGEAL ABNORMALITIES AND
FISTULA /ATRESIA ANDTRACHEOMALACIA PECTUS DEFORMITYTRACT /LEIOMYOSARCOMA OF THE SINONASALTRADMONAL CYTOGENETIC TECHNIQUES /OF
HERBAL MEDICINES /AFRICANTRAINING /GENETICS K 12 LEAD TEACHER
ADOPTION WORKERS IN GENETICSAN ASSESSMENT OF CURRENTIN THE UNITED STATES /AND
TRAIT /A DOMINANTLY INHERITEDWITH VARIABLE EXPRESSION
TRAITS /FOR MAPPING OF QUANTITATIVE/VARIANCE OF NINE LIPID AND APOAND DISEASES /TO MULTIFACTORIALBY LINKAGE ANALYSIS /OLIGOGENICUSING CHICKENS AS A MODEL
TRANSABDOMINAL AND TRANSCERVICAL CVSAND TRANSCERVICAL CVSAPPROACH FOR CVS /THECVS /150 CASES OFCVS IN THE EVALUATIONROUTE 1700 CASES /BY
TRANSACTING FACTOR MUTANT CELL LINE /ATRANSCARBAMYLASE ACTIVITY IN MURINE
CDNA INTO PRIMARYDEFICIENCY /ORNITHINEGENE /THE ORNITHINE
TRANSCERVICAL CVS /DIFFICULTY OFCVS /PATIENTS UNDERGOING
S912475249453221
50183213981925737
246683478813221888547
2663853
2769720361111910811278352354879
2379472
164126052391145624622449244437126
250995015321412351575
2536129612512851747
21221295707227683
28311874755
22612353207219241895204519412766865428
241018712127129025092817816721927
2646870136214552557206
17761762333663
223720682775S9563
2080113012561138126211521253246624772472123755911281251
CVS /TRANSABDOMINAL ANDCVS IS PREFERRED TO /ANDROUTE /THROUGH THE
TRANSCRIBED 3 UNTRANSLATED REGION OFFROM A CPG ISLAND 5 OFREGION AND CDNAS OF /5SEQUENCES FROM TERMINALSEQUENCES PRODUCED IN
TRANSCRIPT THAT PHYSICALLY MAPS CLOSETRANSCRIPTASE ACTIVITY /REVERSETRANSCRIPTION /OF LIVER SPECIFIC
AND IMMUNOLOGICALAPPLICATION TO THEDEPENDENT ANDFACTOR GENE (SP1) ANDFACTORS CREATES HOT /OFFACTORS INFACTORS THAT CONTROLOF RIBOSOMAL RNA GENESOF THE HISTONE H2A GENE
TRANSCRIPTIONAL ACTIVITY OFCONTROL AND GENETICSPROMOTERS /HAS TWOREGULATION /OFREGULATION OFREGULATION OF A HUMANREGULATION OF THEREGULATION OF THE
TRANSCRIPTIONALLY INACTIVE /TUMORS ISTRANSCRIPTS /AND CDNAS OF ALTERNATIVE
FROM THE XIST LOCUS OFIN AN EXTENDED COSMIDIN HUMAN EMBRYONAL /RNAOF THE DYSTROPHIN GENE INPOLYADENYLATED BYPRODUCED BY THE 3 END OF
TRANSDUCTION AND EXPRESSION OF THEOF HUMAN ADENOSINEOF MURINE HEMATOPOIETICOF ORNITHINE /MEDIATED
TRANSFECTED FIBROBLASTS STABLY /INTRANSFECTION /STUDIED BY DNA
OF CULTURED HUMANOF NORMAL HUMAN DNA
TRANSFER /BY RETROVIRAL MEDIATED GENEAND EXPRESSION OF THE HUMANAND INTERPHASE CYTOGENETICSAND X RAY HYBRID ANALYSISAS AN APPROACH TO THE /GENEFLAVOPROTEIN AND EDHGENTRANET /OF GENEMOLECULAR CLONING OF /BY GENEOF A SINGLE REARRANGED HUMANOF CHROMOSOME 9 /MEDIATEDOF HUMAN CHROMOSOME 18 /BYOF HUMAN CHROMOSOME 6 /BY THEOF HUMAN ORNITHINE /GENEOF RECOMBINANT METHYLMALONYLTO THE RESPIRATORY EPITHELIUM
TRANSFORMATION OF NORMAL HUMANTRANSFORMED CELL LINES /ORIGIN OF SV40
CELLS /LEUKEMIA VIRUSCELLS OVEREXPRESSING CUZNHUMAN FIBROBLASTS /OF SV40HUMAN FIBROBLASTS /SV 40LYMPHOBLASTOID CELL LINESPHENOTYPE IN HUMAN /OF
TRANSFORMING GENE /THE MOUSE MDM2GROWTH FACTOR ALPHA GENEGROWTH FACTOR ALPHA TOGROWTH FACTOR ALPHA WITHGROWTH FACTOR B1 GENE IN
TRANSGENE EXPRESSION IN HEPATOCYTESTRANSGENES /AND TO IDENTIFY EFFECTS OF
/METHYLATION OF X LINKEDTRANSGENIC AND TRANSFORMED CELLS
CUZNSOD MICE DISPLAYMICE /ATHEROSCLEROSIS INMICE /DYSTROPHIN IN MDXMICE /FACTOR IX GENE INMICE /IN PAROTID GLAND OFMICE PRODUCES A PHENOTYPEMICE THAT CARRY A MUTANTMICE THAT OVEREXPRESS
TRANSIENT CIRCULATING BLASTS IN AEUTHYROID HYPERTHYROXINEMIAMYELOPROLIFERATIVE SYNDROME
TRANSITION AT A SPLICE ACCEPTOR OF /GGFROM ENDOREDUPLICATION TO
TRANSITIONAL CELL CARCINOMA /IN HUMANTRANSLATED PROTEIN /OF IN VITROTRANSLATION /BY IN SITU NICKTRANSLATIONAL CONTROL OF ORNITHINE
PROCESSING OF /POSTTRANSLOCATION (130140) /A ROBERTSONIAN
(9P22P 9022Q) IN A MALE(X;17) /AND(Y;11)(Q11.2;Q24) IN A/200 TRISOMY UNBALANCED/20 DUE TO A PATERNAL/A BALANCED RECIPROCAL/A DE NOVO UNBALANCED/AUTOSOMAL CHROMOSOMAL/DETERMINES A SUBTLE/ELUCIDATION OF A Y;15
125611301130193621542432211325012399188
243023091029241218702540119326242224561710S712409118S6924082411S7
24412432
97239624541029242422692471248424682477236424062476225024912492208918912486264
2479227423012568875
26012472532S912587579
13412229259849214382568136110151013224224352485256216602229418192
248024872444246179941961985313482802157625772309165224504921703134713761720749
140211701470146814171693
/FEMALES WITH XIY/NOVO COMPLEX FOUR WAY/SYNDROME AND A JUMPING/T(14Q21Q) ROBERTSONIAN/T(5;10)(P13;Q11.2) MAT/THE T(10;14)(Q24;Q11)/TRISOMY 70 IN A DE NOVO/UNBALANCED CHROMOSOME/WITH A T(X;14)(Q28;Q11)/WITH X;3 BALANCED1,+DER (1) T(1;12)14;16 DIFFERENT14;18 AND 8024 /OF46,XY, /UNBALANCED46,XY,T(1 :7)(P22;Q11)9;11 IN BECKWITHAND A CURRENT /X YAND SCHIZOPHRENIA /2;18BETWEEN CHROMOSOMES 6BREAKPOINT CLONING INBREAKPOINT IN A /OF ABREAKPOINTS /BY CLONINGCHROMOSOMES /OF X YEVIDENCE FOR /RB(6.16)EXPERIENCES WITH 100HETEROZYGOTE ANALYZEDIN A CHILD BY IN SITUIN A GIRL WITH /AUTOSOMEIN A PRADER WILLI /15;18IN A TURNER SYNDROMEIN ACUTE NONLYMPHOCYTICIN ANLL /OF THE T(6;9)IN CASE OF BRACHMANN DEIN CHRONIC MYELOGENOUSIN CHRONIC MYELOIDIN FOUR GENERATIONS ANDIN LYMPHOMAS /(11;18)IN MALE CARRIERS /(6.16)IN T CELL LEUKEMIA /NEWINHERITED FROM A NORMALINVOLVING 4 CHROMOSOMESOF NUCLEOLAR ORGANIZERON CHROMOSOME 22 /EWINGON MEIOTIC PROCESS INPRENATAL AND POSTNATALRESULTING IN FETALT (22:22) (P11:011) INT(2;5)(P23;Q35) INT(2;7)(P25;Q32) IN AT(5;7)(Q33;Q34)WITH BREAKPOINTS ON
TRANSLOCATIONS /10 IN BALANCED/INVERSIONS ANDAND DUPLICATIONSAND IMBALANCE MODE AAND MENTAL RETARDATIONBY IN SITU /AND CRYPTICBY IN SITU /SPECIFICIN NON HODGKIN LYMPHOMAINVOLVING ACROCENTRICUSING CHROMOSOME
TRANSMISSION /AUTOSOMAL DOMINANTAND ANTICIPATION OF AGEFREQUENCIES OF THE NITROIN HUNTINGTON DISEASE /OFOF ADIPOSITY IN AN /ANDOF DELETED MITOCHONDRIALOF SEGMENTAL /FAMILIAL
TRANSPEPTIDASE GENES TO HUMANTRANSPLANT FOR MUCOPOLYSACCHARIDOSIS
PATIENTS WITH SKIN CANCERSRECIPIENTS /AND IN RENALSTUDIES /BONE MARROW
TRANSPLANTATION /BONE MARROW/BONE MARROW/IN UTERO BONE MARROW/IN UTERO STEM CELLNI BY BONE MARROWAND GENE THERAPY INFOR METABOLIC DISEASEFOR STORAGE DISEASESIN CANINE /BONE MARROWIN TYPE 1 GAUCHEROR SOMATIC GENETO FANCONI ANEMIA
TRANSPLANTED HUMAN MYOBLASTS /OFINTO RAT LIVER
TRANSPORT /BY RETROGRADE AXONAL/OF LYSOSOMAL MEMBRANEACTIVATION AND OXIDATION OFAND RECYCLING OF BIOTINDISORDERS (CONDITIONS NOTOF ASPARTYLGLUCOSAMINIDASEOF PROTEIN FROM /BARRIEROF VITAMIN B12 /LYSOSOMAL
TRANSPOSITION OF P DNA ELEMENTS INTRANSPOSONS /CLONED FRAGMENTS USINGTRANSSEXUAL MALES /ABNORMALITIES INTRANSTHYRETIN FROM PLASMA /OF VARIANT
VARIANT ASSOCIATED WITHVARIANT ASSOCIATED WITHVARIANTS /FOR TWO
TRANSVAGINAL CVS AND MIDTRIMESTERTREACHER COLLINS SYNDROME IN A CHILD
COLLINS SYNDROME LOCUS TO
595
1458154717011647142922516867012604147214401153133315339531596902200215023702600124
14411552175711711717643143915142582125149616491351144662315831357160114061132208311931457156912301331132115091329118815561706156214091673368133016021715781
27571583791
2713228818
2130564592590166813671607154155561424157156
247355724691522
2124852489281516479261466955476
281925051206578853960
274711508271933
Permuted Title Index
TREATED FAMILIAL MEDITERRANEAN FEVERWITH 4 /IN PATIENTSWITH GRANULOCYTE COLONY
TRENAUNAY SYNDROME AND ITS VARIATIONTREND TOWARD PERFORMING EARLYTRIAD /ISSUES IN CASE OF CURRARINOTRIAL OF A SCREENING PROTOCOL TO
OF DIETOTHERAPY IN FUMARASETRIBAL POPULATION OF ANDHRA PRADESH
POPULATIONS OF NORTHWESTERN /INTRES /IN ANDHRA PRADESH
OF RAJMAHAL HILLS BIHAR INDIAOF SOUTH WEST INDIA /AMONG SOME
TRICENTRIC X CHROMOSOME IDENTIFIED BYTRICHO RHINO PHALANGEAL TYPE I WITHTRICHOMEGALY PIGMENTARY DEGENERATIONTRIENES /INCREASED CONJUGATEDTRUNDOIHYROMME /FACTORS AND REVERSETRIMERIC AND TETRAMERIC TANDEM
REPEAT CORRELATES WITH XTRIMESTER /AND UE3 LEVELS IN THE MID
[TESTS IN THE THIRDAMNIOCENTESIS /BY MIDAMNIOCENTESIS NERSUS MIDAND EARLY SECOND PRENATALCVS /FOLLOWING FIRSTHCG AND UNCONJUGATED /MIDHUMAN PLACENTAS OF /FIRSTOLIGOHYDRAMNIOS /SECONDPREGNANCY LOSSES /FIRSTPREGNANCY SCREENING IN /MIDTOCOLYTIC AGENT IN PATIENTSTRISOMY 18 PREGNANCIES
TRIMESTERS GENETIC DIAGNOSIS A /SECONDTRIMETHOPRIM AND DNA LINKAGE ANALYSES
ON CHROMOSOMAL /OFTRINUCLEOTIDE AND TETRANUCLEOTIDE /OFTRIOSE PHOSPHATE ISOMERASE IN /OFTRIPLE HELICAL DOMAIN OF TYPE Il/THE
NOR VARIANTS CLINICALTRIPLET GESTATION /OF MSAFP IN
PREGNANCY /MSAFP LEVELS INTRIPLETS AND QUADRUPLETS /RELATIVES OFTRPLICATION OF 10(021 32) IN A PHTRIPLOID CELLS WITH CONFLUENCED /HUMAN
EMBRYOS THE TRIPOLAR SPINDLEOPOSSUM FETUSES /NORMAL AND
TR>PLOIDY /IN PRENATAL DIAGNOSIS OF/OF CLINICALLY SUSPECTEDFETAL PHENOTYPES AND
TPOLAR SPINDLE /TRIPLOID EMBRYOS THETRUPTERYGIUM HYPOGLAUCUM (LEVEL) HUTCHTRISOMIC 21 OFFSPRING IN COUPLES WITH
CHILD ASSOCIATED WITH /WITH ATRANSGENIC AND TRANSFORMED
TRISOMY /RELEVANCE TO HUMAN10 IN A CONFINED PART OF A12 IN CHRONIC LYMPHOCYTIC /OF13 /IN TRISOMY 18 AND13 PHENOTYPIC PRESENTATIONS14 MOSAICISM /HISTORY OF15 A CASE REPORT /MOSAIC15 PLACENTAS WITH ABERRANT C16 DETECTED BY MID TRIMESTER16 MOUSE FETUSES /AGAINST18 /LONG TERM SURVIVOR WITH18 /PLEXUS CYSTS INDICATIVE OF18 AND TRISOMY 13 /IN18 PREGNANCIES /TRIMESTER18 SYNDROME USING MOLECULAR18 USING MSAFP UE3 AND HCG21/21 DOES NOT PREDISPOSE OF21 /AND PHENOTYPE OF MOSAIC21 /CARDIAC HISTOLOGY IN21 /IN 98 FETUSES WITH21 /INFLUENCE PHENOTYPE IN21 /OF FAMILIES WITH RECURRENT21 A PREDISPOSING FACTOR FOR21 AFTER SEROLOGICAL SCREENING21 BASED ON MATERNAL SERUM /OF21 DUE TO A DE NOVO T(140210)21 FIRST YEAR EXPERIENCE IN21 IN CYTOGENETICALLY NORMAL21(022.1 OTER) DUE TO A22 DUE TO MEIOSIS Il/PARTIAL2031 2035 SECONDARY TO A5 /REPORT OF A CASE OF MOSAIC5 MOSAICISM DETECTED5P IN BROTHER AND SISTER7 IN A PAPILLARY THYROID /OF70 DUE TO MEIOTIC /PARTIAL70 IN A DE NOVO TRANSLOCATION8 AND GENETIC COUNSELING /FOR8 DETECTION IN BONE MARROWS8 MOSAICISM /HEART DEFECTS IN8 MOSAICISM IN AN IDENTICAL80 AND MONOSOMY 20 DUE TO A9P ARISING FROM A DERIVATIVEDUE TO A T(5;10)(P13;011.2)OF CHROMOSOMES 6P AND 130SYNDROME /MANIFESTATION OFUNBALANCED TRANSLOCATION /200
TRNA LEU(UUR) GENE ASSOCIATED WITHTRNALEU(UUR) MUTATION IN /THE MTDNATROPHOBLAST AND STROMA WITH RESPECT
15541367619641122617611238562
271728152855283328621698107976944314422506959114493992012411142112
11971294926119512081251113911771487253720491269522120012611157266613691575159024519231426104
159018531553155322294091209135521414242151482918920143214691280214
113916951238170716009348351411171315911825108
16341847121914981419140612311257153913221422168612022161499148514021555142914211148749
10179771264
CELLS /ISOMERASE INCELLS ISOLATED FROM FIRST
TROPONIN T GENE ON CHROMOSOME 190TRUNCATED TRANSCRIPTS OF THE /OFTTCT DELETION LEADING TO B /41 42TTHIIlI POLYMORPHISM IN PRION GENE INTUBE DEFECTS AND DOWN SYNDROME /NEURAL
OR VENTRAL WALL DEFECTS /NEURALTUBEROUS SCLEROSIS /GENES DETERMINING
SCLEROSIS /OF AUTISM ANDSCLEROSIS 1 WITHIN 9034 ANDSCLEROSIS AND THEIR CLINICALSCLEROSIS GENETICSSCLEROSIS LOCALIZATION OF /INSCLEROSIS USING GT REPEAT /IN
TUBULOMATHY DIABETES MELLITUS ANDTUMOR /AFFECTED WITH MALIGNANT
A DIFFERENT STORY /WILMSAND ASCITIC RAUCHER LEUKEMIAAND GENITOURINARY ANOMALIESAND GERM LINE MUTATIONS IN /P53BREAKPOINTS IN CHROMOSOMAL BANDCELLS /CHROMOSOME ABERRATIONS INCELLS /LEVEL IN HUMAN NORMAL ANDFORMATION IN VON RECKLINGHAUSENINVERSION FROM POLY(ADP /ANDLOCUS WT1 /11P13 WILMSREGISTRY /FAMILIAL BRAINREGISTRY /USING DATA FROM ASAMPLES /LOSS DETECTION INSCREENING TECHNIQUE FOR RAPIDSECTIONS FROM STAINED /OFSUPPRESSOR GENE BY FLUORESCENCESUPPRESSOR GENE IN EPENDYMOMASUPPRESSOR GENE LOCUS /LINDAUSUPPRESSOR GENE ON CHROMOSOME 9SUPPRESSOR GENE REGIONS 3P II PSUPPRESSOR GENES /IN TWO SIMILARSUPPRESSOR GENES AND HEREDITARYSUPPRESSOR LOCI AT 17P13 /OFSUPPRESSOR LOCUS AT 3P21 /ASYNDROME CLINICAL AND GENETICSYNDROMES IN THE HUMAN NERVOUSWITH A 48,XY,+ 7,+1(12P) /GONADAL
TUMORIGENESIS /BE INVOLVED IN OVARIAN/OF POINT MUTATIONS IN/UNDERLYING COLORECTALBY SUBTRACTIVE /KIDNEY
TUMORIGENICITY BY REPLACEMENT OF THETUMORS /13 AND 17 IN HUMAN COLORECTAL
/18 IN OVARIAN EPITHELIAL/ALLELOTYPING OF MALE GERM CELL/LP DELETIONS IN NEUROBLASTOMA/OF BONE AND SOFT TISSUE/OF EXTRAGONADAL GERM CELL/OF MALIGNANT PEDIATRIC BRAIN/REACTIVATION IN HUMAN OVARIANFACT OR FICTION /OF HUMAN SOLIDIN 11 P15.5 /AND ASSOCIATEDIN NEUROFIBROMATOSIS 1 INIS TRANSCRIPTIONALLY INACTIVEOF MESENCHYMAL ORIGIN /INOF THE TESTIS /ALL GERM CELLPHEOCHROMOCYTOMAS AND /IN RENALUSING FLUORESCENCE IN SITU
TURCOT SYNDROME GENE IS NOT ALLELICTURKEY /CHROMOSOME IRREGULARITIES IN
/CONGENITAL GLAUCOMA FROM/RED CELL POLYMORPHISM IN
TURKISH BOY BORN TO CONSANGUINEOUS /ACHILDREN /OF NTD INMALE INFANT /SYNDROME IN APATIENTS /CYCLOPHOSPHAMIDE IN
TURKMEN SSR /IN POPULATIONS OFSSR HEREDITARY INHABITANTS /OF
TURNER MOSAIC IOF A FRAGMENT IN ASYNDROME /AND A 45,XOSYNDROME /HEART DISEASE ANDSYNDROME ITO THE PHENOTYPE INSYNDROME /TRANSLOCATION IN ASYNDROME MEDICAL GENETICSYNDROME SCREENING BY /IN 45,XSYNDROME USING X AND Y /WITH
TWIN /IN ONE MILDLY AFFECTED MALEFAMILIES IIMMUNOGLOBULINS INGESTATION /AND FETAL TISSUE OFGESTATIONS /ESTRIOL LEVELS INGESTATIONS SUPPORTS PRENATAL /INPREGNANCIES /FOR OPEN NTDS INPREGNANCIES /MSAFP AND HCG INPREGNANCY /IN AN IDENTICALREGISTRIES TO GENETIC /BASEDRESEARCH /PRENATAL BIASES INSTUDIES OF HUMAN OBESITYSTUDY /A DISCORDANT MZSTUDY /AGE AT MENOPAUSE ASTUDY /IN EXPRESSION IN NFl ASTUDY IN FAMILIAL MEDITERRANEAN
TWINNING /AND GENETICS OF DIZYGOTICA FAMILIAL ASSOCIATION /ANDAMONG RELATIVES OF TRIPLETSAND FAMILIAL INCIDENCE OF /OF
TWINS /AND MENTAL STATES SEEN IN/AND SENILE DEMENTIA IN ADULT/BLOOD PRESSURE IN
126912942368102910492291117
1137202286319131915142
19131981502135230413412202181722161613542602257312661560013172495622217
1391605
258325672553303137325881934303138625662495113
225224292593257461158437113112191389372
2181222
24412586614132516426092677628
28308918387975382715287916692395141489
151417701671172514842644164111971146121418331485402S854019092755
13858400915266626662772
682693
/CHOLESTEROL LEVELS OF KOREAN/DIETARY INTAKE COMPONENTS IN/DYSTROPHY GENE IN MONOZYGOTIC/FACTORS IN YOUNG MONOZYGOTIC/GROWTH AND DEVELOPMENT OF HUMAN/IN VIRGINIAN AND NORWEGIAN/MEMORY TEST APPLIED TO/STUDIES WITH MONOZYGOTIC/THE PATHOGENESIS OF CONJOINED/TO BLEOMYCIN A STUDY INDISCORDANT FOR RED GREEN COLORHDL CHOLESTEROL /OF SAME AGED
TYPE /SYNDROME POSSIBLE FINNISH1 (CMT 1A) LOCUS WITHIN 17P11.21 /DIAGNOSIS OF GLUTARIC ACIDEMIA1 /MUTANT OF HERPES SIMPLEX VIRUS1 [TO EHLERS DANLOS SYNDROME1 ACIDIC KERATIN /OF A 40K1 AND BCL 1 LOCI /NEOPLASIA1 AT THE DNA RNA AND PROTEIN1 FAMILIES WITH MARKERS FROM THE1 GAUCHER DISEASE /IN1 GENE /ENDOCRINE NEOPLASIA1 GENE [THE NEUROFIBROMATOSIS1 GENETIC AND BIOCHEMICAL1 IN YOUNG CHILDREN PRESENTING1 NEUROFIBROMATOSIS GENE /OF THE1 NEUROFIBROMATOSIS GENE AND /THE1 REGION OF CHROMOSOME 11 IN1A GENE IN DISTAL BAND 17P11.21A IN FIVE FRENCH ACADIAN2 /IN NEUROFIBROMATOSIS2 /MULTIPLE ENDOCRINE NEOPLASIA2 A FAMILY UNLINKED TO /SYNDROME2 DEFICIENCY TWO NEW CASES AND2 LOCUS ON CHROMOSOME 222 NEUROFIBROMATOSIS /STUDY OF2 PATIENTS AND SPORADIC CASES2A /MULTIPLE ENDOCRINE NEOPLASIA2A /MULTIPLE ENDOCRINE NEOPLASIA2A GENE /ENDOCRINE NEOPLASIA2A REGION /ENDOCRINE NEOPLASIA2B GENE TO CHROMOSOME 10 MARKERSA PREVIOUSLY UNREPORTED FEATUREC AND CELL DISEASE /DISEASEC AND CELL DISEASE /DISEASEI /GENE FOR WAARDENBURG SYNDROMEI /IN LATTICE CORNEAL DYSTROPHYI /OF PRIMARY HYPEROXALURIAI /OF WAARDENBURG SYNDROME/PATIENT WITH NEUROFIBROMATOSISAND II CLINICAL AND GENETICALCOLLAGEN AIN THE COLlAl GENE OFCOLLAGEN FROM TWO PATIENTS OFCOLLAGEN IN A CLINICALLY /OFCOMMONLY DUE TO COLIAl NULLCORROBORATIVE FAMILY /SYNDROMEDIABETES /HLA LINKED GENES ININ NORTHEASTERN QUEBEC IS DUEMOLECULAR AND BIOCHEMICALPROCOLLAGEN FROM PROBANDS WITHPROCOLLAGEN GENE (COLlAl) /IN ATO ANONYMOUS DNA MARKERS ONWITH SEVERE MENTAL RETARDATION
IA OCULOCUTANEOUS ALBINISM AINIl/GENE IN TYROSINEMIAII A NEW ENTITY /CLOVERLEAF SKULLII COLLAGEN IN HYPOCHODROGENESISII COLLAGEN PRODUCES LETHAL /OFII DIABETES MELLITUS /GENE INII GLYCOGEN STORAGE DISEASE INII MUTATION OF ISOVALERYL COAII PROCOLLAGEN (COL2A1) IN /HUMANII PROCOLLAGEN GENE /MUTATIONS OFII REGION ON CHROMOSOME 10 /USHERII SONOGRAPHIC AND RADIOLOGICII THE DIAGNOSTIC PROBLEM OF Al1B VON WILLEBRAND DISEASE /FOR
III /ABNORMALmES OF COLLAGENIII /OF OSTEOGENESIS IMPERFECTAIII COLLAGEN /HAPTOGLOBIN ANDIII COLLAGEN AND CARBAMYL /FORIV /KINDRED OF EHLERS DANLOSIV ASSOCIATED WITH SERINEIV COLLAGEN AS GENE LEADING TOIV COLLAGEN A5(IV) CHAIN AND /THEM4 /NONLYMPHOCYTIC LEUKEMIA SUBMUSCULAR DYSTROPHY /OF DUCHENNEOF BULLOUS DYSTROPHY TO X024 OTEROF MAPLE SYRUP URINE DISEASEOF METHYLMALONIC ACIDURIA /CBICON COGNITIVE AND PERSONALITYSPECIFIC AND HYPOXIA INDUCIBLETO THE LONG ARM OF CHROMOSOME 9VI FIBROBLASTSVII COLLAGEN AND BULLOUS /HUMANVII COLLAGEN GENE ON CHROMOSOME 3WITH RHIZOMELIC SHORTENING
TYPING /SPECIFIC OLIGONUCLEOTIDEIN PATIENTS WITH HODGKINOF DINUCLEOTIDE REPEAT /ANDOF HUMAN N ACETYLATIONTHE HUMAN CA3 AND MOUSE STRAINWITH POLYMORPHIC TRIMERIC AND
TYR2G6CYS MUTATION IN THE PROTEOLIPID
596
269127672222921
27212658S8527599431339223139911602039481168120252684218428181998557612
2372102574298
233959519521958200919501077535
216922925851956234021452170198282362779827
1055132
10522232831347496534
2464685S32269883724971065203110792318507900474522722574490
248146
21557949331068350496867
20316971054194
240513467951990105853192124535984672387
73762283413495354525282506972
Permuted Title Index
TYROSiNASE GENE MUTATIONS IN TYPE IAPOLYPEPTIDE /WITHIN THEPOSITIVE OCULOCUTANEOUS
TYROSINE AMINOTRANSFERASE GENE IN [THETYROSINM A /DEFICIENT IN HEREDITARY
11 EFFECTS AND LINKED LOCI11 FAMILY INFORMATIVE
TYPE11 /GENE IN
UNUSUAL COURSE AND EARLY
2318
5252000507
483
452452
507
893
U.A.E /OF B THALASSEMIA ALLELES INU.S.A /ETHNIC POPULATIONS OF TEXAS
/SERVICES PROGRAMS IN THEAND UPPSALA COUNTY SWEDENCOUPLES WITHOUT A PREVIOUSLY /INPOPULATION /140L IN A DIVERSEPOPULATION /SAMPLE OF THEPOPULATIONS 1970 1989PUBLIC /POPULATION THEVETERANS WITH PRIMARY /ON 200
U.S.A. /AMERICANS OF THE SOUTHWEST/HISPANIC AND NATIVE AMERICANSFAMILIES /WITHIN AMERICANTHREE YEARS OF QUALITY BAND
U.S.&R /DIFFERENT POPULATIONS OF THE/IN HUMAN POPULATIONS OF THE/MULTIETHNIC POPULATION OF THE
UDP GAL 4 EPIMERASE DEFICIENCY /OFUE3 /PROGRAM USING MSAFP HCG AND
/THAN 35 YEARS OF AGE HCG AFP ANDAND HCG/TRISOMY18 USING MSAFPEFFECTS OF MATERNAL WEIGHT ANDLEVELS IN THE MID TRIMESTER /AND
UGURS /ON POPULATION GENETICS OFULCERATIVE COLITIS EVIDENCE FROM A /OFULCERS /ANTIBODY TITERS IN DUODENALULNA COMPLEX AN ANALYSIS OF 491 CASESULNAR RAY/OLIGODACTYLY SYNDROME AND
SYNOSTOSIS GENERALIZED /RADIOULTRASONIC EVALUATION OF DYSSEGMENTALULTRASONOGRAPHIC FINDINGS IN 98ULTRASONOGRAPHICALLY DETECTED FIRSTULTRASONOGRAPHY SIGNIFICANT INDICATORULTRASOUND /RISK SPECIFICATION BY
ABNORMALITIES ANAND CARDIOLOGY /CARDIACDETECTION OF ANEUPLOIDDIAGNOSIS AND MSAFP LEVELSFINDINGS /IN ABNORMALVERSUS AMNIOCENTESIS FOR
ULTRAVIOLET DAMAGE AND REPAIR IN THEUNCLASSIFIED CONGENITAL MUSCULARUNCONJUGATED ESTRIOL /MSAFP HCG AND
ESTRIOL IN MID PREGNANCYESTRIOL LEVELS IN TWIN
UNCULTURED FETAL CELLS NEW RESULTS/INUNDERRECOGNIZED INBORN ERROR OF /ANUNDERREPORTED DOMINANT SYNDROMEUNDERSERVED AND ETHNIC MINORITIES /FORUNDERWATER WEIGHING /MEASURED USINGUNDETECTED SUBMICROSCOPIC DELETION /ANUNEQUAL AND HOMOLOGOUS CROSSING OVERUNFERTILIZEDOOCYTES MAY HELP PREDICTUNIDENTIFIED MAJOR GENE ON /OF ANUNIFIED MAJOR GENE MODEL AND /OFUNILATERAL RADIO ULNAR SYNOSTOSISUNIPARENTAL DISOMY IN ANGELMAN
ISODISOMY /14 SUGGESTED BYISODISOMY RESULTING FROMPATERNAL DISOMY IN
UNIQUE MECHANISM FOR PREGNANCYMUTATION CREATING A NEW MSPL /A
UNITED KINGDOM /IN GENETICS IN THEKINGDOM HUMAN GENOME MAPPINGKINGDOM PROTOCOL FORSTATES /AND TRAINING IN THESTATES /IN BRITAIN AND THE
UNITS AND SINGLE STRANDED MOBILITYUNIVERSITY OF SOUTHERN CALIFORNIAUNPOLLINATED OVULES /INDUCED FROMUNRELATED CONTROL INDIVIDUALS /AND
FEMALES WITH X/Y /OF TWOPATIENTS /IN TWO
UNREPORTED FEATURE /TYPE A PREVIOUSLYUNSTABILITY AMONG INDIVIDUALS WITHUNSTABLE CHROMOSOME REGIONS /IN
REGION OF DNA /BY ANUNTRANSLATED REGION OF HUMAN GENES /3
REGIONS OF HUMAN /THEUPDATED STUDY /IN DOWN SYNDROME AN
UPDATING LINKAGE MAPS /METHODS FORUPPSALA COUNTY SWEDEN /U.S.A ANDUPS /ISSUES AND LONG TERM FOLLOWUPSTREAM OF HUMAN COMPLEMENTURACIL ALTERS THE ASYNCHRONOUS /FLUORO
DIRECTED FRAMESHIFT MISMATCHURATE OXIDASE DEFICIENT MICE BY GENEUREA AND INCREASE IN PLASMA GLUTAMICUREMIC HYPERPARATHYROIDISM /11 IN
279965
17982671184119202737269718521381267628671893180496527952847183212421844123811401144286027735752358897737308351195112912251273275276926
124411722570821123312551197111
439782179026491488225312842783206777315582077158890
1243441329
20541768333319
278911431548493145876282318382131379193624571205159
267111412403155725442493477595
URETHRAL VALVES AND SIRENOMELIA INURINARY GLYCOSAMINOGLYCAN EXCRETION
METABOLITE PROFILE OFOLIGOSACCHARIDES /HPLC OF
URINE DISEASE /TYPE OF MAPLE SYRUPDISEASE CORRELATION BETWEENORGANIC ACIDS /PLASMA AND
UROPATHIES /PROGNOSIS OF OBSTRUCTIVEUROPORPHYRINOGEN III SYNTHASE GENEUROTHEUAL CELL LINES ARISING FROMUSHER SYNDROME /ANALYSIS OF
SYNDROME /BRAIN MORPHOMETRY INSYNDROME /OF THE GENES FORSYNDROME /SPECIAL EMPHASIS ONSYNDROME IN THE LOUISIANA /OFSYNDROME TYPE 2 A FAMILY /OFTYPEII REGION ON CHROMOSOME 10
USSR MEDICAL SCHOOL /GENETICS IN THEUTERINE LEIOMYOMA APPLICATION OF /IN A
SARCOMAS A STUDY OF 12 CASESUTERO BONE MARROW TRANSPLANTATION /IN
FOR PRENATAL DIAGNOSIS /INIDENTITY /INMYELOGRAM A NEW PRENATAL /INSTEM CELL TRANSPLANTATION /IN
UTERUS CANCER /CELL CARCINOMA ANDWITH SALINE /INFUSION OF THE
UUR GENE ASSOCIATED WITH /TRNA LEUMUTATION IN MITOCHONDRIAL
UVC REPAIR MUTANT CELLS ARE THE /ANDUZBEKI JEWISH AND A MOSLEM ARAB /IN ANUZBEKISTAN /HEREDITARY DISEASES IN
V
V H4 IS CORRECTED AFTER TRANSFECTIONKAPPA IMMUNOGLOBULIN GENES IN HUMANMAF ONCOGENE PRODUCT/TO THE AVIANMALFORMATION /1 AND A CEREBRAL A
VACARES 1987 BIRTH COHORT /SYSTEMVACTERL (VERTEBRAL DEFECTS ANALVAL ILE IN THE EXON 17 OF THEVALGUM /HEREDITARY PUBERTAL GENUVALDATE THE USE OF DNA TYPING WITHVAUNE FOR GLYCINE IN THE All /OFVALLEY COLORADO /IN THE SAN LUIS
COLORADO /IN THE SAN LUISVALVES AND SIRENOMELIA IN SIBLINGSVAN DER WOUDE SYNDROME /ANALYSIS OFVARIABIUTY IN CLINICAL EXPRESSION
IS CAUSED BY A SERINE FOROF COMPLEMENT RECEPTOR ONOF STICKLER SYNDROME
VARIABLE CLINICAL EXPRESSION AT THECLINICAL EXPRESSION OFEXPRESSION /TRAIT WITHEXPRESSION OF PRIMARYNUMBER OF POLYPS/ANDAREGION GENE SEGMENTS /IGKSITES OF HIV RETROVIRAL /TO
VARIANCE /SYNDROME THE IMPACT OF ASSAYOF NINE LIPID AND APO TRAITS
VARIANCES AND CORRELATIONS OF /MEANSAND COVARIANCES ON THE
VARIANT /A LATE INFANTILE TAY SACHS B19/CASE STUDIES ON UNUSUALASSOCIATED WITH CARDIACASSOCIATED WITH INCREASEDBAND IN TWO FAMILIES /9QH+IN A FAMILY WITH CROUZON /21P+OF GM2 GANGLIOSIDOSIS /WITH B1
OF PEROXISOMAL DISORDER /NEWOF PHENYLKETONURIA /A KINETICOF THE WIEDEMANN /OR AOF VON WILLEBRAND DISEASEOF X LINKED DOMINANT /RAREPHILADELPHIA CHROMOSOMEREPEAT UNITS AND SINGLE /OFTHROUGH THREE GENERATIONS /4TRANSTHYRETIN FROM PLASMA /OF
VARIANTS /ADRENOLEUKODYSTROPHY AND ITS/FOR TWO TRANSTHYRETINACROSS THE HISTONE ARRAY OFAFTER X RAY AND MAGNETICAMONG CHINESE LAOTIANS ANDAT THE LECITHIN/CHOLESTEROLBY DENATURING GRADIENT GELCLINICAL COMPARISONS /NORIN A LARGE MULTI ETHNIC STATEIN CHILDREN OF ATOMIC BOMB /1OF HUMAN SERUM /QUALITATIVEOF T(8;21) IN ACUTE MYELOIDON HUMAN METAPHASE /BANDINGUSING ANION EXCHANGE HIGHUSING SPECIAL STAININGWITH SUSCEPTIBILITY TO
VARIATION /IN LIGHT OF WITHIN SPECIES/TRENAUNAY SYNDROME AND ITSAMONG FAMILIAL /LIPOPROTEINAND DISTANCE ANALYSES INAND INBREEDING EFFECT ON
917 AND MUTATION IN HUMAN577 AT THE PORPHOBILINOGEN538 BY PCR OF POOLED GENOMIC569 IDENTIFIED IN /SEQUENCE1058 IN AIDS PATHOGENESIS /HIV 1524 IN DNA /FOR DETECTION OF263 IN EXPRESSION IN NF1 A TWIN929 IN HUMAN N /GENETIC530 IN PLASMA PROMOTED1383 IN SOME CASTE POPULATIONS2750 IN SOUTHERN AFRICA /AND DNA850 IN SOUTHERN AFRICANS8 IN SUSCEPTIBILITY TO
2761 IN THE GARHWAL HIMALAYAS2023 IN THE HUMAN SPECIES /OF DNA1077 IN THE RB1 GENE USING2155 INTO SITES CUT BY /SEQUENCE335 OF FAMILIAL RISKS OF
1364 OF RED CELL ACID /GENETIC1335 OF SEMEN IN THE MALE154 OF THE TRANSFORMING GROWTH114 SEEN WITH MUTATIONS IN GENE
1819 VARIATIONS IN MONOAMINE OXIDASE GENES1194 IN XQ28 /CHANGES AND DNA155 OF DELTA F 508 FREQUENCY302 VARYING LEVELS OF MOSAICISM IN
1287 NEUROLOGICAL PHENOTYPES AMONG1017 VAS DEFERENS /BILATERAL ABSENCE OF THE977 VASCULAR ABNORMALITIES KLIPPEL
2564 DISEASE /HOMOCYSTINURIA AND998 VATER ASSOCIATION WITH CENTRAL2692 VDR ARE COLOCALIZED ON HUMAN /GENE
VECTOR /ADENO ASSOCIATED VIRALMEDIATED DISRUPTION OFTRANSDUCTION OF MURINE
VECTORS/IN EBV BASED EXPRESSION/USING RECOMBINANT RETROVIRALFOR EFFICIENT TRANSDUCTION
VELOCARDIOFACIAL SYNDROME/IN THE2250 VENEZUELA /OF NTDS IN BARQUISIMETO1857 VENEZUELAN STATES /SURNAMES IN FOUR2459 VENTRAL WALL DEFECTS /HCG AND FETAL732 WALL DEFECTS /NEURAL TUBE OR2730 VENTRICULAR MYOSIN REGULATORY LIGHT816 VERIFICATION OF ORIGIN OFSV40/IN
1071 VERTEBRAL DEFECTS ANAL ATRESIA651 DEFECTS AND RADIAL DYSPLASIA
2506 VETERANS WITH PRIMARY MYELODYSPLASTIC446 VI BY BONE MARROW TRANSPLANTATION
2669 FIBROBLASTS /TYPE2689 FURTHER CHARACTERIZATION OF THE917 VIABIUTY AND EPISTASIS /THAT INCLUDES
2350 VICINITY OF THE SPINAL MUSCULAR /THE858 OF THE SPINAL MUSCULAR /THE
1065 VICTIMS INCLUDING RADON AND ASBESTOS2858 TO CHERNOBYL ATOMIC STATION906 VIDEODISK PROGRAM AND TEXT IN
2327 SYSTEM FOR SYNDROME684 VIETNAM /E DISEASE IN
2237 VIETNAMESE STUDENTS /AMONG764 VII (BETA GLUCURONIDASE DEFICIENCY)599 COLLAGEN AND BULLOUS PEMPHIGOID
2623 COLLAGEN GENE ON CHROMOSOME 32187 GENE /THE HUMAN SYNEXIN (ANNEXIN1828 VILLA CLARA OF CUBA /CENTRAL REGION2775 VILLAGE POPULATION IN MALI AFRICA /A515 VILU BIOPSY USING MALTOSE AS A
2738 VILLUS SAMPLING /STUDIES OF CHORION494 TROPHOBLAST AND STROMA WITH1461 VIRAL BASED GENOMIC LIBRARY OF 150960 VECTOR /ADENO ASSOCIATED853 VIRGINIA CONGENITAL ANOMALIES1513 VIRGINIAN AND NORWEGIAN TWINS/IN1447 VIRIUZATION /OF 46,XY LINE AND NO1059 VIRUS INFECTION /CHRONIC HEPATITIS B454 MEDIATED TRANSDUCTION OF449 TRANSFORMED CELLS /LEUKEMIA814 TYPE 1 /MUTANT OF HERPES SIMPLEX444 WHICH INFECTS T LYMPHOCYTES824 WITH SUPERNUMERARY TOES IN TWO
1351 VIRUSES CAN CAUSE MEIOTIC DAMAGE IN2789 VISION CHANGES AND DNA VARIATIONS IN954 DEFECTS /HUMAN RED/GREEN COLOR578 DEFICIENCIES AMONG VIETNAMESE130 DEFICIENCY /FOR RED GREEN COLOR
2747 VISUAL LOSS IN LEBER HEREDITARY OPTIC2642 PIGMENT GENE REGION IN /GREEN2555 VISUALIZATION BY TIME RESOLVED /AND2679 OF HYBRIDIZED PROBES OF2690 VITAMIN B12 /LYSOSOMAL TRANSPORT OF2073 D BINDING PROTEIN GROUP /THE1200 D DEPENDENCY TYPE IN /OF2701 D DEPENDENT RICKETS IN A /OF506 D RESISTANT RICKETS TOTAL546 E EFFECT ON SISTER CHROMATID
1342 VMUGO RESULTS OF A FAMILY STUDY1611 VITREORETINOPATHY /A GENE FOR X LINKED565 /FAMILIAL EXUDATIVE
1628 VIVO/IN MURINE HEMATOPOIETIC CELL IN539 ACTIVATION OF PLATELETS IN /AN IN167 AND IN VITRO TRANSMISSION AIN641 AND THEIR SUPRESSION BY /CELLS IN
2682 FOOTPRINT ANALYSIS AND GENOMIC2883 GENE THERAPY IN LDL RECEPTOR IEX2649 GPA ASSAY IMPLICATIONS FOR /IN
597
31320112792471
22952793
135494992870258
2635504
2832312
28032528
2650275411662242
442303219017471412511106641
23238681870249225872468247624902471174126802864182611372164579816817
1381561467717
2055210121126102806137133793886
24732387
7322862845
2827574S15126425292492273026581534772
2477134116812590747
137121902419886
22312032232010412085476
22622698725891156827051942857
2471872158313012428423
2546
Permuted Title Index
HYPEROXIA A CYTOGENETIC STUDY /INHYPOXYGENATION A CYTOGENETIC /INSOMATIC MUTATION AT THE /INSOMATIC MUTATIONS IN THE HUMAN
VK23 USED IN THE DIAGNOSIS OF FRAGILEVNTR ALLELE FREQUENCIES WITHIN THE /IN
ALLELE FREQUENCY DISTRIBUTIONSIN HUMANS AND NONHUMAN PRIMATESLOCI AMONG ASIAN BLACK CAUCASIANLOCI AMONG ASIAN BLACK CAUCASIANLOCI AMONG THREE ETHNIC GROUPSLOCI BY THE PCR /AMPLIFICATION OFLOCI IN THREE CANADIAN /OF SIXLOCUS (D1S80) DETECTED BY THE /OFMARKERS /WEIGHT DETERMINATIONS OFPOLYMORPHISMS AMONG HUMAN AND /OFSITE /THE APOLIPOPROTEIN B GENESIZE AND SEQUENCE COMPARISON OFTYPES AND HAPLOTYPES AT THE
VNTRS FOR FORENSIC INVESTIGATIONS /OFVOLE MICROTUS AGRESTIS /IN THE FIELDVOLTAGE EEG TO 20013.2 20013.3 ANDVOLUMES AND POSITIONS OF CHROMOSOMESVON HIPPEL LINDAU DISEASE AND NF 2
HIPPEL LINDAU DISEASE BY DNA /FORHIPPEL LINDAU SYNDROME IN 29 /OFHIPPEL LINDAU TUMOR SUPPRESSORRECKLINGHAUSEN NEUROFIBROMATOSISRECKLINGHAUSEN NEUROFIBROMATOSISRECKLINGHAUSEN NEUROFIBROMATOSISWILLEBRAND DISEASE /FOR TYPE IlBWILLEBRAND DISEASE NARIANT OFWILLEBRAND FACTOR GENE AS A CAUSEWILLEBRAND FACTOR GENE CAUSING A
VP16 INDUCED CHROMOSOMAL INSTABILITYVULGARIS TWO LINES OF EVIDENCE FORVULNERABLITY TO PARKINSON DISEASE
1418140125352538190828442828263128362852283725222829231325242615
662631280131417102028214130311222316051028213326021068444106844467727652303
w
WAARDENBURG SYNDROME CONSORTIUM /THESYNDROME IS CAUSED BYSYNDROME TYPE I /GENE FORSYNDROME TYPE I /OF
WAGR COMPLEXREGION GENE BETWEEN AN2 AND FSHB
WALES /REGISTER IN ENGLAND ANDGENETICS SERVICE /NEW SOUTH
WALK OF 460 KB IN A CANDIDATE REGIONWALKER MALFORMATION IN A FAMILY /DANDYWALKING AND JUMPING CLONING STRATEGY
AND THE IDENTIFICATION OFIN ADJACENT REGIONS /COSMIDIN YEAST ARTIFICIAL /AND
WALL DEFECTS /HCG AND FETAL VENTRALDEFECTS /NEURAL TUBE OR VENTRAL
WASTAGE /A POSSIBLE CAUSE OF FETAL/MARRIAGES DUE TO FETALASSOCIATED WITH A CHROMOSOMEOF THE MOTHERS AND BODY
WEEKS GESTATION /ABNORMALITY AT 28GESTATION /FROM 35 TO 42
WEIGHING /MEASURED USING UNDERWATERWEIGHT /ASSOCIATED WITH BIRTH
ADJUSTMENT ON MSAFP SCREENINGADJUSTMENT ON SCREENING FORAND LEVELS OF B HCG ANDAND RACE /EFFECTS OF MATERNALDETERMINATIONS OF VNTR MARKERSOF OFFSPRING BORN AFTER SELFON HCG AND UE3 LEVELS IN THE
WERNER SYNDROME /OF THE GENE FORSYNDROME FIBROBLAST LINE /IN A
WEST AFRICAN POPULATIONS /EVOLUTION OFINDIA /AMONG SOME TRIBES OF SOUTH
WESTERN INDIA /RETARDED POPULATION OFREGION OF CUBA /DISEASE IN THE
WEYERS ULNAR RAY/OLIGODACTYLYWHITE MATTER DISEASE A NEW SYNDROME
POPULATIONS OF ALABAMA AND /ANDWHITES IN THE SAN LUIS VALLEY COLORADOWHOLE ARM TRANSLOCATION (9P22P 9Q22Q)
ESSENTIAL REGION OF THE FACTORGENOME AND SEPARATE CHROMOSOMES
WHORLED NEVOID HYPERMELANOSIS AN /ANDWIDESPREAD X LINKED DISEASES IN /SOMEWIEDEMANN RAUTENSTRAUCH SYNDROME /THE
SYNDROME /IN THE BECKWITHSYNDROME /SPORADIC BECKWITHSYNDROME AND ANIRIDIASYNDROME AND ASSOCIATEDSYNDROME SUPPORT FOR
WILMS TUMOR A DIFFERENT STORYTUMOR AND GENITOURINARY /WITHTUMOR LOCUS WT1 /11 P13
WILSON DISEASE /AND MANAGEMENT OFDISEASE /THEIR APPLICATION TODISEASE I COPPER AND /MODEL OFDISEASE II SERUM CERULOPLASMINDISEASE IN CHINESE /OFDISEASE LOCUS /LINKED TO THE
797927
1052S1422413571800
23966892785213821132031826113711581236124311641145912
264928801169120312551140252412711144197525482634286214931827889645
2844266913471002219487496581476790767
21811596304220126947
21164385129902373
DISEASE LOCUS AND THE CLOSEWIRE HAIRED FOX TERRIER A NEW DOG /AWISCONSIN USING CDF508 ANALYSIS /INWISKOTT ALDRICH SYNDROME GENE ON XPWOBBLER MAPS CLOSE TO ERBB ON MOUSEWOLF HIRSCHHORN SYNDROME /CAUSING
HIRSCHHORN SYNDROME 2MB DISTALHIRSCHHORN SYNDROME DUE TO A /OFHIRSCHHORN SYNDROME IMPLICATION
WOLFRAM SYNDROME OBSERVED IN 17 /ANDWOLMAN DISEASE SHOWS IT BELONGS TO ANWOMAN WITH GROLL HIRSCHOWITZ SYNDROME
WITH KEARNS SAYRE SYNDROME /Or AWITH ROKITANSKY KUSTER HAUSER /A
WOMEN AGE 35 AND OLDER /SYNDROME INAGE 35 AND OLDER /SYNDROME INAT A NONSECTARIAN HOSPITAL /THANAT HIGH RISK FOR MEIOTIC /OFAT RISK FOR HAVING AN AFFECTEDGENETICALLY PREDISPOSED TO /ININ DENMARK /AMONG PREGNANTLESS THAN 35 YEARS OF AGE HCGRECEIVING OBSTETRIC CARE AT AUNDER AGE 35 /CONSIDERATIONS INWHO HAVE PRENATAL DIAGNOSIS /OFWITH A GENETIC PREDISPOSITIONWITH FAMILY HISTORIES OF BREASTWITH HEREDITARY HEMATOLOGIC /OF
WOMEN'S ACCEPTANCE OF AMNIOCENTESISWORKERS EXPOSED TO PIROMELLITIC /IN
IN GENETICS /TRAINING ADOPTIONWORKSTATION /USING THE BIOMEK 1000WTI /11P13 WILMS TUMOR LOCUS
GENE IN PATIENTS WITH WILMS TUMOR
19264641006191218641488172716612442790
224895022814201169125017421577185017331848184417421201175317546082321744159917762125126220
x
X (49,XXXXX) /TWO CASES OF PENTASOMY(MARTIN BELL) SYNDROME IN AN(P11.4Q22) ASSOCIATED WITH NORRIE(P22.2) /IN A GIRL WITH DEL(027.2) PRESENT IN ONLY 1 OF 685/IN A FEMALE WITH 45,X/46,XR4 5 AND 16 AND THE CLONING OFADRENOLEUKODYSTROPHY /FATTY ACIDS INAND 11 /WITH MARKERS FROM CHROMOSOMEAND A MARKER CHROMOSOME /OF FRAGILEAND Y CHROMOSOME HOMOLOGIES ANDAND Y CHROMOSOMES /ABNORMALAND Y CHROMOSOMES /FROM BOTH THEAND Y CHROMOSOMES SPECIAL PROBEAND Y SPECIFIC A SATELLITE DNAASSOCIATED BREAKPOINT CLUSTERAUTOSOME TRANSLOCATION IN A GIRLBREAKPOINT CLUSTER REGION ISBY FLUORESCENCE IN SITU /CHROMOSOMECASES /AN EGYPTIAN SAMPLE OF FRAGILECENTROMERE BIOTINYLATED DNA PROBECHROMOSOMAL BREAKPOINT IN A PATIENTCHROMOSOMAL RFLP MARKERS IN /TO NINECHROMOSOMECHROMOSOME /ANALYSIS OF THE HUMANCHROMOSOME /GENETIC DEFECT ON THECHROMOSOME /IN PART BY A GENE ON THECHROMOSOME /INDUCTION OF THE FRAGILECHROMOSOME /LONG ARM OF THE HUMANCHROMOSOME /MAP OF THE MOUSECHROMOSOME /OF THE INACTIVECHROMOSOME /ON THE INACTIVE HUMANCHROMOSOME /RANGE MAPPING OF THECHROMOSOME A GENOME STRATEGY TOCHROMOSOME CONTAINS A HIGH /OF THECHROMOSOME GENETIC MAPS FROM /OFCHROMOSOME IDENTIFIED BY IN SITUCHROMOSOME IN RETT SYNDROME /OF THECHROMOSOME INACTIVATION /OF HUMANCHROMOSOME INACTIVATION ANDCHROMOSOME LINKED DISORDER AND WITHCHROMOSOME LINKED FAMILIALCHROMOSOME MAPPING /CHROMOSOMES FORCHROMOSOME MOSAICISM IN RETTCHROMOSOME REACTIVATION IN HUMANCHROMOSOME REPORT OF A FAMILIAL /THECHROMOSOME SHORT ARM /THE PROXIMALCHROMOSOME SPECIFIC CDNA CLONES /OFCHROMOSOME SPECIFIC CDNA USING /ANCHROMOSOME SPECIFIC REPETITIVECHROMOSOMES /ON THE MOUSE AND HUMANCHROMOSOMES /THE ACTIVE AND INACTIVEEXPRESSION /OF LOW LEVEL FRAGILEFEMALES COUNSELING ISSUES AND LONGFREQUENCY IN MENTALLY RETARDEDGENOTYPE IS CHARACTERIZED BY ANIN A 4 YEAR OLD MALE /AND FRAGILEIN AN INSTITUTION FOR MENTALLYIN AN XX MALE SHOWN BY FLUORESCENTINACTIVATION /A GENE WHICH ESCAPESINACTIVATION /DISTAL XP THAT ESCAPESINACTIVATION /GENE ON XP22.3 ESCAPESINACTIVATION /GENES THAT ESCAPEINACTIVATION /METHYLATION AND
152714711490774
1612145218551620381688S291085236725151725S77643200521298221698206519231571179
229375
16232118195115572452210921742015
8516982223145
166024168572122783138915362260252722471658242124281550114112853791415161716922440240223072285147
INACTIVATION /MULTIPLE MECHANISMS OFINACTIVATION /REPEAT CORRELATES WITHINACTIVATION /TO THE PROBLEM OFINACTIVATION CENTER REGION /HUMANINACTIVATION CONFIRMATION BY A /OFINACTIVATION IN MZ TWINS DISCORDANTINACTIVATION PROCESS IN THE MOUSEIRRADIATION IN RELATION TO FAMILYLINKED ADRENOLEUKODYSTROPHY /OFLINKED ADRENOLEUKODYSTROPHY AND ITSLINKED AND AUTOSOMAL DISORDERS NEWLINKED AND AUTOSOMAL INHERITANCE /TOLINKED ANDROGEN INSENSITIVITY /WITHLINKED CHARCOT MARIE TOOTH DISEASELINKED CLASPED THUMB AND MENTAL /OFLINKED CLEFT PALATE IN A BRITISH /OFLINKED COMPLICATED FORM OF SPASTICLINKED CONGENITAL STATIONARY NIGHTLINKED DEAFNESS /GENETICS OFLINKED DEAFNESS AND CHOROIDEREMIALINKED DILATED CARDIOMYOPATHYLINKED DISEASES /MOSAICISM INLINKED DISEASES /SPORADIC CASES OFLINKED DISEASES IN DIFFERENTLINKED DOMINANT /RARE VARIANT OFLINKED DOMINANT HEREDITARY MOTOR /OFLINKED DYSTONIA PARKINSONISMLINKED DYSTONIA PARKINSONISM /OF THELINKED ECTODERMAL DYSPLASIA SWEATLINKED EYE DISEASES /GENES FOR THELINKED FABRY DISEASE /WITH THELINKED GENE COLOR VISIONLINKED GONADAL DYSGENESIS /INLINKED GPD EXPRESSION IN NORMAL ANDLINKED HEREDITARY SPASTIC PARAPLEGIALINKED HPAII SITE 20 BASE PAIRS /ANLINKED HYDROCEPHALUS LOCUS WITH [THELINKED HYDROCEPHALUS TO XQ28 /OFLINKED HYPOHIDROTIC ECTODERMAL /INLINKED HYPOHIDROTIC ECTODERMAL /THELINKED ICHTHYOSIS AND KALLMANN /WITHLINKED INHERITED DYSMYELINATINGLINKED LIVER GLYCOGENOSIS IN XP22LINKED LOCUS /DETERMINED BY ANLINKED LOCUS AT XP21 LINKED TO THELINKED LYMPHOPROLIFERATIVE DISEASELINKED LYMPHOPROLIFERATIVE DISEASELINKED LYMPHOPROLUFERATIVE DISEASELINKED MENTAL RETARDATION LINKED TOLINKED MENTAL RETARDATION SYNDROMELINKED MENTAL RETARDATION SYNDROMELINKED MENTAL RETARDATION WITHLINKED MYOPATHY WITH EXCESSIVE /FORLINKED OCULAR ALBINISM /ANALYSIS OFLINKED OCULAR ALBINISM /AROUNDLINKED PROGRESSIVE CONE /OF ANLINKED RECESSIVE CHONDRODYSPLASIALINKED RECESSIVE INHERITANCELINKED RETINITIS PIGMENTOSA /OFLINKED RETINITIS PIGMENTOSA /OFLINKED SPINAL AND BULBAR MUSCULARLINKED SPINOCEREBELLAR ATAXIA ANDLINKED TRANSGENES /METHYLATION OFLINKED VITREORETINOPATHY /A GENE FORLOCUS /SEQUENCES AT THE FRAGILELOCUS IN THE CONTEXT OF YEASTMALES EVIDENCE FOR GENETIC /FRAGILENEGATIVE FAMILY /DXS52 IN A FRAGILEON DISTRIBUTIONS OF PHYSICAL ANDPATIENTS WITH ATYPICAL PHENOTYPESRAY AND MAGNETIC RESONANCE IMAGINGRAY HYBRID ANALYSIS /TRANSFER ANDRAY INDUCED CHROMATID DAMAGE INRAY INDUCED CHROMOSOME ABERRATIONSREGION /OF THE FRAGILEREGION /SITES IN THE FRAGILEREPLICATION STUDIES /POSTNATAL LATESCREENING /BANDING INCLUDING FRAGILESHORT ARM MARKERS /RELATED AND OTHERSITE /CONTIG PROXIMAL TO THE FRAGILESITE MOLECULAR AND GENETIC /FRAGILESITE OF THE FRAGILE X SYNDROMESPECIFIC TRANSCRIPTS FROM THE XISTSTUDIES WHAT IS PRACTICAL /FRAGILESYNDROME /AFFECTED BY FRAGILESYNDROME /DIAGNOSIS OF FRAGILESYNDROME /FRAGILESYNDROME /IN FAMILIES WITH FRAGILESYNDROME /LINKAGE TO THE FRAGILESYNDROME /MARKERS FOR THE FRAGILESYNDROME /MEASUREMENTS IN FRAGILESYNDROME /OF THE FRAGILESYNDROME /SCREENED FOR THE FRAGILESYNDROME /THE DIAGNOSIS OF FRAGILESYNDROME /X SITE OF THE FRAGILESYNDROME AND DIAGNOSTIC APPLICATIONSSYNDROME AND SMALL MARKER /FRAGILESYNDROME AND THE IDENTIFICATION OFSYNDROME DETERMINATION OF ACCURACYSYNDROME IMPACT OF GENETIC /FRAGILESYNDROME IN MENTALLY RETARDEDSYNDROME LOCUS /TO THE FRAGILESYNDROME WITH EXTRAMICROCHROMOSOMETESTING OF FAMILY MEMBERS IN THEUSING TRIMETHOPRIM AND DNA LINKAGE
598
14895914497
15422231146
2695864130
2808802441
2007192519096751878
241086238511911111965824191420441949904
2531174388619762451708959195920461106112680597119212032753968108212631946716852963188720512014703902689
1931193995
19871680194223613732672198027001511255518918451531374103814571630193121593751592
9716035001198171854S771894709828161219081592377145110381259185014932005148616101487
Permuted Title Index
PSEUDOAUTOSOMAL REGION /WITHIN THETRANSLOCATION AND A CURRENT
Y TRANSLOCATION CHROMOSOMES/OFX/AUTOSOME TRANSLOCATION PRENATAL ANDX/Y POLYMORPHISM /B ANTIGEN GROUP
TRANSLOCATION /FEMALES WITHTRANSLOCATION IN A TURNER SYNDROME
X;14 (028;011) TRANSLOCATION /WITH A TX;16 (P11.4;P13.3) /SEGREGATION OF TX;17 /AND TRANSLOCATIONX;3 BALANCED TRANSLOCATION /WITHX,9 CHROMOSOME /FROM A DERIVATIVEXBAI AND ECORI OF THE /POLYMORPHISMSXERODERMA PIGMENTOSUM AND COCKAYNE/IN
PIGMENTOSUM CELLS AGAINSTXl AN AUTOSOMAL RECESSIVE SYNDROMEGSD XI AN AUTOSOMAL RECESSIVE
XIST GENE CDNA CLONING MAPPING ANDGENE SEQUENCE ANALYSIS REVEALS ALOCUS OF THE HUMAN X /FROM THE
XO/XX CHROMOSOMAL PATTERN /A GIRL WITHXP A IDENTIFICATION OF SECOND GENE ON
BETWEEN DXS146 AND DXS7 /GENE ONIN HUMAN OVARIAN CANCER /130 ANDLOCI LONG RANGE RESTRICTION MAPSTHAT ESCAPES X INACTIVATION /DISTAL
XP11 REGION /CONE DEGENERATION TOXP11.2 BY TWO COLOR FLUORESCENCE INXP11.23 /AROUND THE RP2 LOCUS INXPI1.3 /OF THE NORRIE DISEASE LOCUS ONXP21 LINKED TO THE DYSTROPHIN GENE /AT
OR AN EFFECT OF THE DYSTROPHINSURROUNDING THE GLYCEROL KINASE
XP22 /X LINKED LIVER GLYCOGENOSIS INXP22.2 P21.2 OF KERATOSIS/TO
PTER SYNDROME OF LINEAR SKINXP22.3 /GENE FOR KALLMANN SYNDROME ON
DELETION /BOTH SYNDROMES WITHDELETIONSESCAPES X INACTIVATION /GENE ONREGION /OVERLAP CLONING IN THE
XPTER AND CHROMOSOME 19 IN 15XQ /MARIE TOOTH DISEASE ON PROXIMAL
ISOCHROMOSOME IN CVS AND FETAL/AX013 REGION HARBORING SCIDXI /OFXQ21 /SYNDROME AND LINKAGE TOXQ22.3 024/SEQUENCE CLUSTERED ATX024 28/CHROMOSOME BASED MAPPING OF
IN A WOMAN WITH ROKITANSKYQTER /OF BULLOUS DYSTROPHY TOQTER HNCDNA LIBRARY HIGHLY /HUMANXQ28 LOCUS /CPG ISLANDS AT
XQ27 /RETARDATION LINKED TO DXS369 AT28 MAPPING AND ITS USE IN RAPID
XC23 /CHANGES AND DNA VARIATIONS IN/OF X LINKED HYDROCEPHALUS TO/RETARDATION (MASA SYNDROME) IN/SEVEN POLYMORPHIC DNA MARKERS OF/WITHIN THE G6PD CLUSTER OF BANDDNA /GENE IN A I MB CONTEXTOFLOCUS /CPG ISLANDS AT XQ24REGION/MOLECULAR ANALYSIS OF THE
XRAYS IN DIFFERENT AGE GROUPS OF /OFXRCC5 BY SOMATIC CELL HYBRIDIZATIONXX + INV DUP (15) KARYOTYPE /AND 47
MALE SHOWN BY FLUORESCENT IN SITUMALENESS AND XX TRUEMALES AND TRUE HERMAPHRODITES /INTRUE HERMAPHRODITISM A SEX LIMITED
XY SEX INVERSION /LEAD TO CONDITIONALXYMYY AND FRAGILE X IN A 4 YEAR OLDXYYYY KARYOTYPE /ADULT WITH 49
236090214411457986145815142604
881376147215552746293
25398468462259
9697
82523141912606
21732402703
215319742196753205022201921198514942294144855
2307209220432007164122211104165837314201990252121521946205821902046192519591964204
2152178
25421891152116922237982
2237119014151510
y
LINE BY PCR IN A /OF ACHROMOSOMAL GENES IN MAMMALIAN /OF
CHROMOSOME /DISORDER SHOWING LOSS OF
CHROMOSOME /FACTOR MAPPING ON
CHROMOSOME /LONG ARM OF THE HUMAN
CHROMOSOME /MATURATION GENE TO THE
CHROMOSOME /REGION OF THE HUMAN
CHROMOSOME /SXR REGION OF THE MOUSE
CHROMOSOME BY COMPARATIVE MAPPING
CHROMOSOME HOMOLOGIES AND GENES /AND
CHROMOSOME IN THE ETIOLOGY OF 46,XXCHROMOSOME LONG ARM /EUCHROMATIC
CHROMOSOME OF MEN WITH IDIOPATHIC
CHROMOSOME PCR AND MICROCLONING
CHROMOSOME PROBE P49A DETECTS
CHROMOSOME SPECIFIC POLYMORPHISMS
CHROMOSOME SPECIFIC PROBES IN
CHROMOSOME SPECIFIC PROBES IN A
CHROMOSOMES /ABNORMAL X AND
CHROMOSOMES /FROM BOTH THE X AND
CHROMOSOMES SPECIAL PROBE POOL /AND
IDENTIFIED BY IN SITU HYBRIDIZATION
LIBRARY DETECTS THE Y011REGION /A
LINKED GENE SBY /SPY AND A NEW
MOSAICISM /WITH 45,X/46,X INVPOLYPLOIDY CASE OF
13561665
198
2225
2205
28722826
1085
2367
2515
1476
991
1859
1506
1427
PSEUDOAUTOSOMAL REGION /WITHIN THE XSEQUENCES INTO X IN AN XX MALE /OFSEROLOGICAL ANTIGEN AND MULLERIAN /HSPECIFIC A SATELLITE DNA PROBES /ANDSPECIFIC DNA PROBE HYBRIDIZED INSPECIFIC PROBE ISOLATED FROM A YT(Y;1 5)(Q12;Q1 1.2) COMPLEMENTTRANSLOCATION AND A CURRENT /XTRANSLOCATION CHROMOSOMES /OF X
Y, 15, + DER(Y)T(Y;15)(Q12;Q1 1.2) /45,X,Y11 (Q11.2;Q24) IN A NEWBORN WITHY,15(Q12;Q11.2) COMPLEMENT
TRANSLOCATION /ELUCIDATION OF AYARD EXPERIENCES /GENETICS SCHOOLYEAST 06 METHYLGUANINE/04 /OF A CLONED
ARTIFICIAL CHROMOSOMEARTIFICIAL CHROMOSOME /OF THEARTIFICIAL CHROMOSOME AND CDNAARTIFICIAL CHROMOSOME AT D13S31ARTIFICIAL CHROMOSOME BASED /OFARTIFICIAL CHROMOSOME CLONESARTIFICIAL CHROMOSOME CLONESARTIFICIAL CHROMOSOME CLONES INARTIFICIAL CHROMOSOME CLONINGARTIFICIAL CHROMOSOME CLONINGARTIFICIAL CHROMOSOME CLONINGARTIFICIAL CHROMOSOME CLONINGARTIFICIAL CHROMOSOME CONTIGARTIFICIAL CHROMOSOME CONTIGARTIFICIAL CHROMOSOME CONTIG /AARTIFICIAL CHROMOSOME CONTIG /KBARTIFICIAL CHROMOSOME CONTIG ATARTIFICIAL CHROMOSOME END /OFARTIFICIAL CHROMOSOME LIBRARYARTIFICIAL CHROMOSOME LIBRARYARTIFICIAL CHROMOSOMESARTIFICIAL CHROMOSOMES /22 USINGARTIFICIAL CHROMOSOMES /ASARTIFICIAL CHROMOSOMES/INARTIFICIAL CHROMOSOMES/INARTIFICIAL CHROMOSOMES /INARTIFICIAL CHROMOSOMES /OFARTIFICIAL CHROMOSOMES /OFARTIFICIAL CHROMOSOMES /OFARTIFICIAL CHROMOSOMES /USINGARTIFICIAL CHROMOSOMES /WITHARTIFICIAL CHROMOSOMES A /USINGARTIFICIAL CHROMOSOMES AND /OFARTIFICIAL CHROMOSOMES CONTIGARTIFICIAL CHROMOSOMES DNA /OFARTIFICIAL CHROMOSOMES FROM THEARTIFICIAL CHROMOSOMES FROM THEARTIFICIAL CHROMOSOMES IN XP21ARTIFICIAL CHROMOSOMES NEAR THEARTIFICIAL CHROMOSOMES ON HUMANARTIFICIAL CHROMOSOMES PHYSICALCHROMOSOME INSERTED INTO A /OF ANUCLEAR GENOME /MAPPING OF THESCHIZOSACCHAROMYCES POMBE /THE
YI MIAO AND LISU NATIONALITIES OFYOGYAKARTA BRANCH /RED CROSSYP /STUDIES IN DIFFERENT DICENTRICYQ DELETION MAP AND AZF LOCUS THE USE
IN A PATIENT WITH PHENOTYPE OF /OFREARRANGEMENTS WITHOUT 45,X MOSAIC
Y011 REGION /A Y LIBRARY DETECTS THEY012 /INDUCED COMMON FRAGILE SITES IN
zZELLWEGER CELL LINES /STUDIES OF
SYNDROME /INITIAL STUDIES INSYNDROME GENES /MAPPING THESYNDROME LYMPHOBLASTS /IN
ZERO THALASSEMIA GENE AMONG AFRICAN /BZETA WILL RELIABLY DETECT (SEA) /ANTIZFY 2,ZFY 1,SRYHYA SPY AND A NEW Y
AND SRY SPECIFIC SEQUENCES IN /OFGENE EXPRESSION DURING THE RAT /OFGENE IN HUMAN PROSTATE /OF THESEQUENCE IN CHROMOSOMAL DNA FROM
ZHUANG MINORITIES FAMILY /OF HAN ANDZINC AND SELENIUM LEVELS IN SERUM AND
FINGER GENES /ANALYSIS OF HUMANFINGER GENES MAPPING TO /NOVELFINGER GENES ON HUMAN CHROMOSOMEFINGER PROTEIN GENES USING /HUMAN
ZIPPER MOTIF HOMOLOGOUS TO THE AVIANZYGOSITY DIAGNOSIS AT BIRTH /FORZYGOTE AND THE FETUS DATA FROM THE
NUMBERS
#3P CHROMOSOME VIA MICROCELL FUSION /A06 METHYLGUANINEI04 METHYLTHYMINE DNAI (CMT IA) LOCUS WITHIN 17P11.2 /TYPE(P36.3) AND THE POTENTIAL ROLE OF/CAUSED BY POLYCYSTIC KIDNEY DISEASE
2360 /DIAGNOSIS OF GLUTARIC ACIDEMIA TYPE1692 /MAP AT THE CENTROMERE OF CHROMOSOME105 /MUTANT OF HERPES SIMPLEX VIRUS TYPE
1725 /OF THE MURINE DNA REPAIR GENE ERCC1676 /TO EHLERS DANLOS SYNDROME TYPE991 A NOVEL HUMAN NEURAL RETINA /OF NRS1454 ACIDIC KERATIN /OF A 40K TYPE902 AND11 RELATED TO VARIOUS MALIGNANT1441 AND 2 CDNAS /OF HUMAN PROTAMINE1454 AND 2 GENES /PEMPHIGOID ANTIGENS1720 AND 4 ALLELES IN BULGARIAN1454 AND A CEREBRAL A V MALFORMATION1693 AND BCL1 LOCI /NEOPLASIA TYPE393 AND NEUROFIBROMATOSIS 1 PATIENTS
2401 AND PHOSPHOGLYCOLATE PHOSPHATASE18 ANTICHYMOTRYPSIN GENE /IN THE ALPHA
2057 ANTITRYPSIN DEFICIENCY ADENOVIRUS /A2168 ANTITRYPSIN HAPTOGLOBIN AND TYPE2373 ANTITRYPSIN VARIANTS BY DENATURING373 AS A CANDIDATE GENE FOR FANCONI
1950 AT THE DNA RNA AND PROTEIN LEVELS2160 CELL LEUKEMIA MCL1 HAS SIGNIFICANT2065 DNA NEW COSMIDS FOR HUMAN /USING COT179 ELEMENT IDENTIFICATION AND ANALYSIS
2185 FAMILIES WITH MARKERS FROM THE /TYPE2193 GAUCHER DISEASE /IN TYPE2306 GENE /ENDOCRINE NEOPLASIA TYPE204 GENE/THE NEUROFIBROMATOSIS TYPE
2389 GENETIC AND BIOCHEMICAL SCREENING102 HAS SIGNIFICANT HOMOLOGY TO BCL 2
2159 IN SEARCH OF THE SECOND HIT101 IN YOUNG CHILDREN PRESENTING WITH
2075 LEVELS/ACTIVATOR INHIBITOR2102 LOCI /NEOPLASIA TYPE 1 AND BCL2167 LOCUS IN EMBRYONIC STEM CELLS /A2135 LOCUS IN NOONAN NEUROFIBROMATOSIS 12162 MAKES DNA DIAGNOSTICS POSSIBLE IN
50 MAPPED TO HUMAN CHROMOSOME 4(02349 MAPPING ADDITIONAL INFORMATION ON
203 MB CONTEXT OF XQ28 DNA /GENE IN A2158 MB OF THE EXCISION REPAIR GENE ERCC4200 NEUROFIBROMATOSIS GENE /OF THE TYPE1682 NEUROFIBROMATOSIS GENE AND RELATED2526 OF 685 CASES SCREENED FOR THE /ONLY2189 ON CHROMOSOME 10/HUMAN HEXOKINASE2204 ONCOGENE FROM HUMAN CHROMOSOME 11013202 PATIENTS /1 AND NEUROFIBROMATOSIS185 PATIENTS /IN NEUROFIBROMATOSIS378 PATIENTS FOLLOWED FOR 1577 PATIENT
2785 POSITIVE ANAPLASTIC LARGE CELL /KI2112 PREVENTS POLYGENIC ATHEROSCLEROSIS2114 PROMOTER SHOWS ALLELE SPECIFIC2220 PROTEIN MOLECULAR CLONING /SIGNAL2145 REGION OF CHROMOSOME 11 (11012 013)2156 REGION OF CHROMOSOME 11 IN UREMIC1859 RELATED LOCUS ON CHROMOSOME 15413 RETROTRANSPOSON EXPRESSION IN HUMAN237 SEQUENCES ARE READILY CAPABLE OF
2363 T(1; 12) (042.3;P12.2) MAT/1, + DER2769 TK GENE /INTEGRATED SINGLE COPY HSV2754 USING TWO COLOR FLUORESCENCE IN1683 VARIANTS IN CHILDREN OF ATOMIC BOMB910 VARIATION IN AIDS PATHOGENESIS /HIV1678 WITHIN 9034 AND TESTS OF LINKAGE TO910 1,+DER (1) T(1;12) (Q42.3;P12.2) MAT991 1,25 DIHYDROXYVITAMINE D3 RECEPTOR1564 1SRYHYA SPY AND A NEW Y LINKED GENE
1.6M YEAST ARTIFICIAL CHROMOSOME10 /GENETIC MAPS FOR CHROMOSOMES 5 AND/HUMAN HEXOKINASE 1 ON CHROMOSOME/PERICENTRIC REGION OF CHROMOSOMEAND 12 /FOR HUMAN CHROMOSOMES 8AND 12 ARE BOTH MEMBERS OF THEDNA MARKERS ON 150 RESULTS OF AN1435 IN A CONFINED PART OF A TERM
2089 IN BALANCED TRANSLOCATIONS2069 MARKERS LINKED TO MULTIPLE
2743 PERICENTROMERIC MARKERS /CHROMOSOME18739 SPECIFIC ALPHOID SEQUENCES TO1859 YEAR PERIOD /EASTERN INDIA OVER A1685 YEARS AND 26,000 CASES /IN2230 1%00o CHILDREN UNDER THE AGE OF SIX
100/DEFECTIVE APOLIPOPROTEIN 8
2606 FAMILIES/EXPERIENCES WITH2851s 1000 WORKSTATION /USING THE BIOMEK8529 102150 REPORT OF A SECOND FAMILY8226 10S INDUCED ABORTUSES /A STUDY ON
2251 10;14 (024;011) TRANSLOCATION /THE T2272 I101BDELETION /PATIENTS WITH A2144 DELETION IN THE LDL RECEPTOR /A2459 100 AND CHARACTERIZATION OF NEW2859 100221 024.3 /OF HUMAN PAX2 GENE TO1264 11(1112013) /1 REGION OF CHROMOSOME
/CLOSE TO ERBB ON MOUSE CHROMOSOME/FOR LOCI ON CHROMOSOMES 9 AND/WITH MARKERS FROM CHROMOSOME X ANDAND CHROMOSOME 17 /OF CHROMOSOMECONTAINING THE MULTIPLE ENDOCRINEIN THREE PATIENTS WITH II PIN UREMIC HYPERPARATHYROIDISM
1395 IRRADIATION REDUCED SOMATIC CELL2401 PREGNANCIES /AND PCR TESTING FOR2039 RELATED TO VARIOUS MAUGNANT /1 AND1541 SYNDROME/WTH RING CHROMOSOME998 YEAST ARTIFICIAL CHROMOSOME LIBRARY
599
4812199168123252025230826841350245723871027732
218499
2628680S91867
2073187428182589208224601998557612
237210252589222742
241721842463
99193518672202204
170998
2339161221352608
991090830
1331192
241723092090595
232825802611144025362148506
22951913144018701859101
21632135200616352234188312091186196218882145276011872779103617572125
6671199225
2682515
2170228220901864142
2036201621641723595
2136118613501396
2102
Permuted Title Index
115 MALE PATIENTS WITH INFERTILITY /OF11;18 TRANSLOCATION IN LYMPHOMAS11;19 ACUTE LEUKEMIAS /IN TIIP /DOPAMINE RECEPTOR MAPS TO DISTAL
130 17P AND 170 IN HUMAN BREASTDUPLICATIONS AND FEATURES OF /WITHMARKERS IN AUTOSOMAL DOMINANT /AND
11P12 P14 /PHYSICAL MAP OF CHROMOSOME11P13 WILMS TUMOR LOCUS WT1IIPI5.5/AND ASSOCIATED TUMORS IN
/MAP OF HUMAN CHROMOSOME BAND110 /REGIONS ON CHROMOSOMES 50 AND
/WITH MARKERS OF CHROMOSOMEAND 140 MARKERS /OF LINKAGE TOMARKERS NEAR THE ATAXIA
11012 013 /1 REGION OF CHROMOSOME 1111013/ONCOGENE FROM HUMAN CHROMOSOME
ARE CLOSELY ASSOCIATED WITH BIN THE 90 CASES OF ESOPHAGEAL
11022 23 IN 45 BRITISH FAMILIES24 MARKERS FROM IRRADIATION /OF
11022,23 XPTER AND CHROMOSOME 19 IN11022.3 23.1 /AT D GENE TO THE REGION11023 /TO A CM INTERVAL ON CHROMOSOME
AND 12Q23 /WITH BREAKPOINTS ON12 (013 OTER) IN TWO T(14;18) /DUP
/FOR HUMAN CHROMOSOMES 8 10 AND/MUTATION MAPS TO CHROMOSOMEARE BOTH MEMBERS OF THE DIMERICCASES /UTERINE SARCOMAS A STUDY OFIN CHRONIC LYMPHOCYTIC LEUKEMIA BYIN MYELODYSPLASTIC SYNDROMELEAD TEACHER TRAINING /GENETICS KPATIENTS /OF TERATOGENESIS INYEAR CHROMOSOME RESEARCH IN A
12% HAD NONSYNDROMIC HEARING LOSS12(021 024) /IS LOCATED ON CHROMOSOMEt22 NATURALLY OCCURRING SOMATIC AND12P /DIAGNOSED CASE OF TETRASOMY
CHROMOSOMAL PATTERN FROM A 46,XY120 AND RAT CHROMOSOME 7 /ARM12023/WITH BREAKPOINTS ON 11Q23 AND
OTER DUE TO MATERNAL /WITH DUP13 (P13;011)PAT IN A FEMALE WITH
(032.3033.2) WITH POTENTIAL /DEL/HETEROGENEITY OUTSIDE REGION 15011/IN TRISOMY 18 AND TRISOMY46,XX,INV(13)(P13;Qll)PAT IN AA CASE OF A MICRODELETION DELAND 17 IN HUMAN COLORECTAL TUMORSAND 21 /ON HUMAN CHROMOSOMES 2CASES /DYSOSTOSIS REPORT OFCLONES AND THEIR APPLICATION TODELETIONS HAVE SIMILAR PHENOTYPESLACK OF A DISTINCT SYNDROMEMAPPING REAGENTS /HUMAN CHROMOSOMENON JAPANESE PATIENTS /A STUDY OFNORWEGIAN CYSTIC FIBROSIS FAMILIESPHENOTYPIC PRESENTATIONS /TRISOMY
13.3 USING RADIATION HYBRIDS AND1303 AMNIOCENTESES /DIAGNOSIS OF136 AT RISK PERSONS WHO REQUESTED /OF13:14 ROBERTSONIAN TRANSLOCATION ON13;21 /WITH AN APPARENTLY BALANCED T13,22 ROBERTSONIAN TRANSLOCATION130 17P AND 170 IN HUMAN BREAST /liP
AND XP IN HUMAN OVARIAN CANCERRESULTING FROM A 3:1 SEGREGATION
130140 /A ROBERTSONIAN TRANSLOCATION13033.1 /OF ONE DISEASE LOCUS TO14 (011.1013) /WITH 46,XX,DEL
/PHOSPHORYLASE ON CHROMOSOME/TERMINAL DELETIONS OF CHROMOSOMEBREAKPOINT IN A PATIENT WITH RAPPEXONS AMPLIFIED IN MULTIPLEX /OFIRS PCR CHARACTERIZATION ANDMOSAICISM /HISTORY OF TRISOMYMUTATION IN A FAMILY WITH /KERATINPORTUGUESE PATIENTS /STUDIES INSMALL CELL LUNG CARCINOMAS /OFSUGGESTED BY UNIPARENTAL ISODISOMY
146 ASTHMATIC FAMILIES BY ASTHMA /OF14;16 DIFFERENT BEHAVIOR DEPENDING ON14;18 AND 8024 REARRANGEMENT IN FOUR
NEGATIVE FOLLICULAR B NON /T14P+ MARKER CHROMOSOME /THE CASE WITH140 MARKERS /OF LINKAGE TO 110 AND140210 BY FLUORESCENT IN SITU /NOVO T
ROBERTSONIAN TRANSLOCATION /T140L IN A DIVERSE U.S.A POPULATION15/1 RELATED LOCUS ON CHROMOSOME
/1970 1989 A TWENTY YEAR PERIOD/WILLI REGION OF HUMAN CHROMOSOME/WITH A MARKER CHROMOSOMEA CASE REPORT /MOSAIC TRISOMYAND DETAILED MAPPING OF /6 ANDKARYOTYPE /AND 47 XX + INV DUPMONTHS EXPERIENCE WITH A /FIRSTPATIENTS WITH HEMATOLOGIC /INPLACENTAS WITH ABERRANT C MYCSYSTEMATICALLY ASCERTAINED /19 INYEAR OLD GIRL /SYNDROME IN A
15,+DER(22),T(15;22X013;011)PAT15,+DER(Y)T(Vt15XQ12;011.2) /45,X, Y,150 200 KB INSERTS /GENOMIC LIBRARY OF
152562313231903256717231960196126
218121422030198619131955209026081387604196721082043230129413291392163520102234133513551334206129573423
216425531412138618701329132914776471116214
1477647
2593202069521161116141622092341107142421101220301119366015692567606
14211703647148319791726166610332165215
22578371380207778911531333139215441913163416471920232835923921535148215021521178713099182043752153314542529
CASES COMPARED TO COMPLICATIONSCASES OF TRANSABDOMINAL CVS
154780 /MARSHALL SYNDROME (MIM NUMBER155,223 POPULATION OF STATE FARMS IN1575 GENETIC COUNSELING CASES /OF1577 PATIENT YEARS /FOLLOWED FOR15;18 TRANSLOCATION IN A PRADER WILLI15;22 (013;01 1)PAT /15, + DER(22),TISCEN QLL.2 DUE TO A 45,X, Y,150 RESULTS OF AN INTERNATIONAL /ON
SPECIFIC PROBES TO THE PRADER1501.5 02.1 /MARFAN SYNDROME LOCUS ON1501113 /HETEROGENEITY OUTSIDE REGION
13 DELETIONS HAVE SIMILAR15011013 A DIFFERENCE BETWEEN /DISTAL
IN THE PRADER WILLI AND /OF16 /BREAKPOINTS ON CHROMOSOME
/CLONES TO HUMAN CHROMOSOMES 5 AND/GAMMA IS ENCODED BY CHROMOSOME/GENE MAPS TO HUMAN CHROMOSOME/GENE TO BAND 024 OF CHROMOSOME/LINKAGE MAPS OF HUMAN CHROMOSOMEAND THE CLONING OF LEUKEMIA /5 ANDDETECTED BY MID TRIMESTER /TRISOMYFAMILIES WITH POLYMORPHIC PROBESINVERSION IN ACUTE MYELOMONOCYTICMOUSE FETUSES /AGAINST TRISOMYSPORADIC CASES /IN 9 FAMILIES AND
1677 DELTA [THREE PATIENTS WITH16P AND 160 MAY EXPLAIN LEUKEMIC
CONTAINING THE PKD1 GENE AND160 MAY EXPLAIN LEUKEMIC INVERSIONS17 (P11.2) > DELINEATION OF THE /(DEL
/OF CHROMOSOME 11 AND CHROMOSOME/OVARIAN CANCER LOCUS ON CHROMOSOME/PROXIMAL SHORT ARM OF CHROMOSOME/PROXIMAL SHORT ARM OF CHROMOSOME/THE PKD1 GENE AND MOUSE CHROMOSOME1A NEOANTIGENE GENE PROMOTER /HUMANCASES /A NEUROCRISTOPATHY REPORT OFCOSMID LIBRARY USING FLUORESCENCEIN HUMAN COLORECTAL TUMORS /13 ANDLOCI /AND LINKAGE TO CHROMOSOMEMEMBERS OF ONE PEDIGREE /INOF THE AMYLOID PRECURSOR PROTEINUSING RADIATION REDUCED HYBRIDSYEARS IN PRENATAL DETECTION /OVER
1700 CASES /BY TRANSABDOMINAL ROUTE175 IN AN A1(I) CHAIN OF TYPE
KB REGION OF THE TCR B CHAIN /OF A17A HYDROXYLASE DEFICIENCY /CAUSES17P AND 17Q IN HUMAN BREAST CARCINOMAS
AND P53 OVEREXPRESSION IN /ON17P11.2 /TYPE 1 (CMT 1A) LOCUS WITHIN
/TYPE 1A GENE IN DISTAL BAND17P13 IN MILLER DIEKER SYNDROME AND
INCLUDING THE P53 GENE /LOCI AT170 IN HUMAN BREAST CARCINOMAS /AND
LINKAGE /CANCER EVIDENCE FOR17011.2 DNA MARKERS ANALYSIS /WITH17021 /CLONING OF HUMAN CHROMOSOME18 (P11.2y46,XX, 18,+1(180)
/BY TRANSFER OF HUMAN CHROMOSOME/LONG TERM SURVIVOR WITH TRISOMY/OF ABNORMALITIES OF CHROMOSOME/ON A NEWBORN WITH ISODICENTRIC/PLEXUS CYSTS INDICATIVE OF TRISOMY/RECOMBINATION MAP OF CHROMOSOMEAND TRISOMY 13 /IN TRISOMYBY FLUORESCENCE IN SITU /21 ANDHOMOLOGIES WITH HUMAN CHROMOSOME 50IN OVARIAN EPITHELIAL TUMORSPREGNANCIES [TRIMESTER TRISOMYSYNDROME /IN A PATIENT WITH RSYNDROME USING MOLECULAR ITRISOMYUSING MSAFP UE3 AND HCG /TRISOMYYEARS DIAGNOSTIC ASSESSMENT HAS
18 + 1(180)180 KB COMPRISING THE HUMAN /OF1890 1950/HUMAN GENETICS IN GERMANYISP ASSOCIATED WITH TETRASOMY 18P
SYNDROME CYTOGENETIC CONFIRMATION180/18,+1
AS THE LOCUS FOR SUSCEPTIBILITYBY DNA ANALYSES AND FLUORESCENCEDELETION SYNDROME /INTERSTITIALSYNDROME /CRITICAL REGION FOR THE
1802 MONOSOMY SYNDROME /BRAIN IN THE19 /BY ALUI GIEMSA OF CHROMOSOME
/CONTIG MAP OF HUMAN CHROMOSOME/FINGER GENES ON HUMAN CHROMOSOMEAND 21 LOCI IN FAMILIAL ALZHEIMERBY FLUORESCENCE IN SITU /CHROMOSOMECOSMID CONTIG MAP USING CLONEDNA MARKERS LINKED TO MYOTONICIN 15 SYSTEMATICALLY ASCERTAINEDSTRATEGIES AND RESULTS /CHROMOSOME
1910 1990 /EUGENICS AND LYSENKOISM1948 1990 /HOSPITAL IN OSAKA CITY1950 /HUMAN GENETICS IN GERMANY 18901971 1990 /A 20 YEAR STUDY IN BELGIUM1974 1989 /ATLANTA AND SOUTHWEST OHIO1980 TO 1989 /DOWN SYNDROME IN MAINE1967 BIRTH COHORT /SYSTEM (VACARES)1989 ATLANTA AND SOUTHWEST OHIO 1974
12621262855
276876083014391533145418831718110911161116
8759185
18972103225821722124185920
1051170914326769621556186915561702201619771998213918692465815
215125931961790
1071215012111253534100
10452567257120391952
581373256720266352306150187514691567167512802188214
2156186325741139151716951238
231501257532016501650150119911690142516721433159822032272199218252
19842043176321
268832014752686113427302686
/DOWN SYNDROME IN MAINE 1980 TO/U.S.A POPULATIONS 1970A TWENTY YEAR PERIOD (15) /1970
1990 /20 YEAR STUDY IN BELGIUM (1971/EUGENICS AND LYSENKOISM 1910/HOSPITAL IN OSAKA CITY 1948
190 /DISTANCES ON HUMAN CHROMOSOME/TROPONIN T GENE ON CHROMOSOME
19013.3 /A 350 KB REGION OF CHROMOSOMEWHICH CONTAINS THE MYOTONIC
1:14 (P36.3;024.3) POSSIBLE /46,XY,T1:7 (P22;011) IN A PREGNANCY WITH THE1;12 (042.3;P12.2) MAT /1, + DER (1) TIA GENE IN DISTAL BAND 17P11.2 [TYPE
IN FIVE FRENCH ACADIAN KINDREDSLOCUS WITHIN 17P1 1.2 /TYPE 1 (CMTNEOANTIGENE GENE PROMOTER /HUMAN 17
IMOD INDIVIDUALS AFFECTS EXPRESSION1P34 1 P36.1 REGION /INFORMATION ON THE1P36 COMMONLY DELETED IN NEUROBLASTOMA
EMERGENCE OF TWO OVERLAPPING1P36.1 REGION /INFORMATION ON THE 1P3410 /LOCUS ON HUMAN CHROMOSOME
/USHER TYPE II REGION ON CHROMOSOMEMARKERS /UNLINKED TO CHROMOSOMETHE ROLE OF HIGH RESOLUTION
10(021 32) IN A PH POSITIVE ACUTE /OF2 (PL2014) A REVISED APPROACH TO /INV/(MEGALOCORNEA MENTAL RETARDATION/1 HAS SIGNIFICANT HOMOLOGY TO BCL/IN NEUROFIBROMATOSIS TYPE/MULTIPLE ENDOCRINE NEOPLASIA TYPENON HIPPEL LINDAU DISEASE AND NF13 AND 21 /ON HUMAN CHROMOSOMESA FAMILY UNLINKED TO CHROMOSOME 10ADULT PATIENTS WITH GM1 /SEOUENCE OFAN ANCESTRAL TELOMERE TELOMERECDNAS /OF HUMAN PROTAMINE 1 ANDCLINICAL HETEROGENEITY AND NATURALCYSTATINS MAP TO TWO DIFFERENT LOCIDEFICIENCY TWO NEW CASES AND /TYPEFIRST REPORT OF THE WAARDENBURGGENES /PEMPHIGOID ANTIGENS 1 ANDISOZYME DETERMINE THE ALCOHOLKETOGLUTARATE DEHYDROGENASELENS FINDINGS IN 40 PATIENTS IN 5LOCUS ON CHROMOSOME 22 /TYPEMETHYL BRANCHED CHAIN FATTY ACYLNEUROFIBROMATOSIS /STUDY OF TYPEPATIENTS AND SPORADIC CASES /TYPEPOLYMORPHISMS /AND MOUSE STRAIN CAR
2,ZFY 1,SRYHYA SPY AND A NEW Y /ZFY2.4 MB DUCHENNE MUSCULAR DYSTROPHY20 /KINDRED LINKED TO CHROMOSOME
/OF THE LONG ARM OF CHROMOSOME/TO POLYMORPHIC LOCI ON CHROMOSOME/TWO DIFFERENT LOCI ON CHROMOSOMEAND 21 IN A BOY WITH MULTIPLEAND POSSIBLE ASSIGNMENT OF THEBASE PAIRS FROM A POLYMORPHIC /SITECLONING AND ISOLATION OF POTENTIALCM OF HUMAN DNA SURROUNDING THEKB DNA PROBES USED AS RFLP MARKERSMOSAIC /OF A RINGCHROMOSOMEPRADER WILLI SYNDROME FAMILES /OFYEAR STUDY IN BELGIUM (1971 1990)
200 KB INSERTS /GENOMIC LIBRARY OF 150OF THE PRP GENE /MUTATION AT CODONU.S.A VETERANS WITH PRIMARY /ON
20P DELETION /WITH A CHROMOSOME200 /ADDITIONAL MARKERS ON CHROMOSOME
/WITH SIX MARKERS ON CHROMOSOMEMAY NOT BE ASSOCIATED /DELETIONTRISOMY UNBALANCED TRANSLOCATION
20013.2 20013.3 AND LINKAGE /EEG TO20013.3 AND LINKAGE HETEROGENEITY21 (021Q22.1) /210 DELETION DEL
/21 DOES NOT PREDISPOSE OF TRISOMY/AND PHENOTYPE OF MOSAIC TRISOMY/AS LINKAGE MARKERS FOR CHROMOSOME/CARDIAC HISTOLOGY IN TRISOMY/FAMILIES ON HUMAN CHROMOSOME/HYBRID MAP OF HUMAN CHROMOSOME/IN 98 FETUSES WITH TRISOMY/INFLUENCE PHENOTYPE IN TRISOMY/LATERAL SCLEROSIS TO CHROMOSOME/NEW COSMIDS FOR HUMAN CHROMOSOME/OF DOWN SYNDROME ON CHROMOSOME/OF FAMILIES WITH RECURRENT TRISOMY/ON HUMAN CHROMOSOMES 213 AND/RECEPTOR GENE ON HUMAN CHROMOSOME/REGION OF HUMAN CHROMOSOMEA PREDISPOSING FACTOR FOR /TRISOMYABERRATIONS BY COMPETITIVE IN SITUAFTER SEROLOGICAL SCREENINGAND 18 BY FLUORESCENCE IN SITUAND DOWN SYNDROME /OF CHROMOSOMEBASED ON MATERNAL SERUM HCGBY PULSED FIELD GEL ELECTROPHORESISCASE ALSO FOUND TO BE 180 BY DNADERIVED FROM HER MOTHER /CHROMOSOMEDOES NOT PREDISPOSE OF TRISOMY 21DUE TO A DE NOVO T(140210) BYFIRST YEAR EXPERIENCE IN THEHYDROXYLASE (P450C21) IN RELATION
600
113426973591475321
268821072368203623701468953144019521958203924652425220222151538220221342155107715051369156162425892009195030320201077451
21472457676218353579
238727164478062169527229
258525281859
188331462
742183140714629592374214026301519103514752529100013811664196219651368749
2028202814651707160020949342120S89835141180
2082152817132020196820571591164418252156416108
2119169013241707163418472414
Permuted Title Index
HYDROXYLASE DEFICIENCY EVIDENCEIN A BOY WITH MULTIPLE ANOMALIESIN CYTOGENETICALLY NORMAL PARENTSIN DOWN SYNDROME /CHROMOSOMEIN MEIOTIC PROPHASE /CHROMOSOMELOCI IN FAMILIAL ALZHEIMER DISEASEMARKERS AND OTHER MARKERS INOFFSPRING IN COUPLES WITH AOH MUTATED HLA HAPLOTYPES IN /OFSPECIFIC SEQUENCE TAGGED SITES FORSPECIFIC YEAST ARTIFICIALSTUDY OF FIVE PATIENTS /CHROMOSOMETHAT CAUSES DOWN SYNDROME IN ONETO ACCOMPLISH DIAGNOSIS OF THEUSING VARIOUS METHODS /CHROMOSOME
21(Q22.1 QTER) DUE TO A DUPLICATION2148 CASES /CHROMOSOMES INVOLVED IN21P+ VARIANT IN A FAMILY WITH CROUZON210 DELETION DEL(21)(021022.1)21011.2 /SYNDROME AT21022.3 AND COSMID WALKING IN
SPECIFIC PROBE SET /CHROMOSOME22 ,T(15;22)(Q13;Q11)PAT /15, + DER
/EWING TRANSLOCATION ON CHROMOSOME/NOT1 LINKING CLONES ON CHROMOSOME/OF THE LONG ARM OF CHROMOSOME/REPEATED SEQUENCES ON CHROMOSOME/TO MAPPING OF HUMAN CHROMOSOME/TYPE 2 LOCUS ON CHROMOSOMEAND OTHER HUMAN AUTOSOMESAND RAPID IDENTIFICATION OF THEBY SCREENING CHROMOSOME 22DUE TO MEIOSIS II NONDISJUNCTIONENRICHED LIBRARIES /CHROMOSOMEIN NEURINOMAS OF NEUROFIBROMATOSISPROBE SPECIFIC FOR PAINTINGRESPONSIBLE FOR ISOLATED HEARTSQUAMOUS CELL CARCINOMAS OF THE /OFTUMOR SUPPRESSOR GENE IN EPENDYMOMAUSING YEAST ARTIFICIAL CHROMOSOMESWITH FURTHER APPLICATION TO RAPIDYEARS EXPERIENCE WITH A MASTERS
221 HIGH RISK CHINESE FAMILIES /IN226 BONE LESIONS PATHOGENIC /OF22:22 (P11 :1 1) IN A FEMALE WITH /T22;22 (P110 1) /WITH A DE NOVO T22011 AND ITS CLINICAL CONSEQUENCES
012 MARKERS /OF EIGHT CHROMOSOME23 CASES /DIAGNOSIS OF CYSTIC HYGROMA
FEATURES OF DOWN SYNDROME ON /FORIN 45 BRITISH FAMILIES /1 1Q22NON JEWISH INDIVIDUALS PRESUMED TO
23.1 /AT D GENE TO THE REGION 11022.324 LOCI ON THE LONG ARM OF CHROMOSOME
MARKERS FROM IRRADIATION HYBRIDS250 PREGNANCIES WITH FETAL US /IN2556 CASES /REAL RISKS EXPERIENCE WITH26 BRAZILIAN PATIENTS /STUDY ON
BRAZILIAN PATIENTS /STUDY ON26,000 CASES /IN 10 YEARS AND27268 /SYNDROME (MIM29 KINDREDS SUGGESTS A COMPLEX /IN2;13 TRANSLOCATION BREAKPOINT /T2;18 TRANSLOCATION AND SCHIZOPHRENIA2;,5 (P23;Q35) IN THREE CASES OF /T2;7 (P25;032) IN A BOY WITH LEUKEMOID2A /MULTIPLE ENDOCRINE NEOPLASIA TYPE
/MULTIPLE ENDOCRINE NEOPLASIA TYPE/TO MULTIPLE ENDOCRINE NEOPLASIAGENE /ENDOCRINE NEOPLASIA TYPEREGION /ENDOCRINE NEOPLASIA TYPE
26 GENE TO CHROMOSOME 10 MARKERS /TYPE2MB DISTAL TO D4S43 /SYNDROME2P AND I1 P MARKERS IN AUTOSOMAL20 /DNA MARKERS ON HUMAN CHROMOSOME
DELETION IDENTIFIED IN ONE MILDLYDUE TO A PATERNAL TRANSLOCATION
2013 /CLOSE TO THE FRAGILE SITE OF2021 AND 9013 /DNA SEQUENCES AT2031 2Q35 SECONDARY TO A PATERNAL2035 SECONDARY TO A PATERNAL COMPLEX3 (P25021) /CEN 021 SEGMENT OF AN INV/PCR BASED MARKERS FOR CHROMOSOMENII COLLAGEN GENE ON CHROMOSOMEBETA 4 AND ALPHA 5 NEURONAL /ALPHABP IN FRAME DELETION OF THEBY SOUTHERN BLOT ANALYSIS ANDENCODES A TUMOR SUPPRESSOR LOCUS ATEND OF THE DYSTROPHIN GENE /BY THEEXONS IN A PATIENT WITH DUCHENNE /OFHYDROXYACYL COA DEHYDROGENASE /CHAININ JAPANESE BRAZILIANS /BANDMETHYLADENINE DNA GLYCOSYLASE CDNAMETHYLGLUTACONIC ACIDURIA WITH /OFMETHYLGLUTACONYL COA HYDRATASEMRNA ENDS /THE PROPER FORMATION OFNEUTRAL MUTATIONS IN THE GENE /ANDNOVEL MUTATIONS IN TWO HEMOPHILIA ASEQUENCES PRESENT WITHIN 7000SPLICE SITE SELECTION /AFFECTING THEUNTRANSLATED REGION OF HUMAN GENESVNTR IN HUMANS AND NONHUMAN PRIMATES
30 /PRENATAL DIAGNOSIS AFTER AGE306 NORMAL GENOTYPES /THALASSEMIA AND3234 /SYNTHETASE LOCUS ON 90
237514071219415420199219381553665
218921671430210616542281149812751447146513482113163415332083219114812166199
21692130164922511419225125851649901138513912162203517796011305123093815181954114215281967106723012208210894111807078311187681231370
20021331132119562340198221452170198217271960203114841402214718581406140616871978
7321824491867258822692549263
26292258121712172445106710022198111219362631114618312140
A KARYOTYPIC ASSOCIATION FOR /L022IN A PH POSITIVE ACUTE /OF 1Q(021MENINGIOMAS /AND BEHAVIOR INREGION /THE HUMAN CHROMOSOME 7022
34 /SYNTHETASE LOCUS ON 90 32347 MUTATION OF THE RHODOPSIN GENE IN35 /CONSIDERATIONS IN WOMEN UNDER AGEAND OLDER /SYNDROME IN WOMEN AGEAND OLDER /SYNDROME IN WOMEN AGETAY SACHS CHROMOSOMES FROM 23 NONTO 42 WEEKS GESTATION /FROMYEARS OF AGE HCG AFP AND UE3 /THAN
350 KB REGION IN 9013 021 /OVER AKB REGION OF CHROMOSOME 19013.3 /A
37 CASES /PATELLA SYNDROME STUDY OFMUTATION IN CATALONIANS FROM THE
37,954 PERINATAL INFANTS IN NINGXIA370 OF HUMAN GLUCOCEREBROSIDASE A PH373 OF FVIII GENE CAUSING HEMOPHILIA A39 FETUSES AT RISK AND PCR TESTING /OF
INDIVIDUALS IN 9 FAMILIES AND 16PERCENT /GENE HAVE A G + C CONTENT OF
3:1 SEGREGATION OF A FAMILIAL /FROM A3HYPERVARIABLE REGION ALLELES AND
REGION DOWNSTREAM OF A3P liP 130 17P AND 170 IN HUMAN
IN SPORADIC RENAL CELL CARCINOMAORDERED BY FLUORESCENT IN SITUSYNDROME /DELETION ANALYSIS IN THE
3P13 /BREAKPOINTS IN CHROMOSOMAL BAND3P14 AND INCREASES THE GENETIC /AT3P21 /A TUMOR SUPPRESSOR LOCUS AT
THE COMMON REGION OF DELETION IN3P21.1 /WITHIN HUMAN CHROMOSOMAL BAND
/WITHIN HUMAN CHROMOSOMAL BAND3P23P24.12 /IN A CHILD WITH 46,XY DEL3P25 SYNDROME /OF THE DELETION3P25.1 /AF8T TO HUMAN CHROMOSOME 3PTER3PTER 3P25.1 /AF8T TO HUMAN CHROMOSOME30 VIA SPREADING OF X INACTIVATION /OF3T3 CELL LINE ARE SIMILAR TO THOSE IN
CELLS AND CELLS FROM NIEMANN PICK4 (P14P16) /IN AN INFANT WITH DEL(023 025) AND MOUSE CHROMOSOME 3 BY/A PHYSICAL MAP OF HUMAN CHROMOSOME/GENE REGION OF HUMAN CHROMOSOME/NEAR THE CENTROMERE OF CHROMOSOME5 AND 16 AND THE CLONING OF /XALLELES IN BULGARIAN CLASSICAL /ANDALU BANDING BY FLUORESCENCE IN SITUANALYZED CYTOGENETICALLY ANDAND ALPHA 5 NEURONAL ACETYLCHOLINEAND ISO (4P),ISO 4(Q) /OF CHROMOSOMECHROMOSOMES WITH 6 BREAKPOINTSEPIMERASE DEFICIENCY IDENTIFIED BYHYDROPEROXYCYCLOPHOSPHAMIDE PURGEDVARIANT THROUGH THREE GENERATIONSYEAR OLD MALE /AND FRAGILE X IN AYIELD A SINGLE LINKAGE GROUP
4(0) /OF CHROMOSOME 4 AND ISO (4P),ISO40 PATIENTS IN 5 HIGH RISK GROUPS /IN
TRANSFORMED HUMAN FIBROBLASTS /SV4000 JAPANESE INDIVIDUALS /IN40K TYPE 1 ACIDIC KERATIN /OF A41 42 (TTCT) DELETION LEADING TO B42 (TTCT) DELETION LEADING TO B /41WEEKS GESTATION /FROM 35 TO
4452 PROFOUNDLY DEAF CHILDREN /OF45 ALCOHOLICS /RULED OUT IN
BRITISH FAMILIES /11022 23 INCASES OF CONFINED PLACENTAL /UP OF
45,X /PATIENT WITH APPARENT NONMOSAICMOSAIC /YQ REARRANGEMENTS WITHOUTTURNER SYNDROME SCREENING BY /IN
45,X, Y, 15, + DER(Y)T(Y;15)(012;011.2)45,X/46,X INV (Y) MOSAICISM /WITH45,X/46,XR(X) /IN A FEMALE WITH45,X/46,XY MOSAICISM WITH45,X/47,XY, + 14 /WITH UNUSUAL MOSAICISM45,XO TURNER SYNDROME /AND A450 DEBRISOQUINE LOCUS (CYP2DP8) ON /P450KB YEAST ARTIFICIAL CHROMOSOME AT46,XX INDIVIDUALS FREQUENCY OF THE /IN
MALENESS /IN THE ETIOLOGY OFTRUE HERMAPHRODITE AND A 45,XO
46,XX,47,XX,+MAR AND /MOSAICISM46,XX,DEL(14) (011.1013) /WITH46,XX,INV(13XP13;Q11)1AT IN A FEMALE46,XX/46,XY CHIMERISM /DIAGNOSIS OF46,XY DEL 3P23P24.12 /IN A CHILD WITH
FEMALE WITH MIXED GONADAL /ALINE AND NO VIRILIZATION /OFPURE GONADAL DYSGENESIS /AND
46,XY, /UNBALANCED TRANSLOCATION46,XY,T(1:14XP36.3;024.3) POSSIBLE46,XYT(1:7XP22;011) IN A PREGNANCY460 KB IN A CANDIDATE REGION FOR THE47 XX + INV DUP (15) KARYOTYPE /AND47,XX, + DER(9)T(9;9XP13;034) /AND4U,XXXX /DISEASE IN A PATIENT WITH48,XY, + 7,+ (12P) CHROMOSOMAL PATTERN4600 CVS FIVE YEARS OF INDIAN /OF49 XYYYY KARYOTYPE /ADULT WITH49,XXXXX /TWO CASES OF PENTASOMY X461 CASES /ULNA COMPLEX AN ANALYSIS OF
15201369131021922140999
12011169125010679121844
812036746
26742780436
27941185676
282114217141125256726072161785172217052588224
2138219582710662104210415427986278041867218523841907185
10271656167021821582140618321367954141519711582806492154526841049104991223
109419679351032910167114541506145215341431239520352373780
22252395153214831477145082713861534223815331468953
23961521153214131386114715101527235
4E /BY INITIATION FACTOR EIF4P ,ISO 4(0) /OF CHROMOSOME 4 AND ISO
DELETION DETECTED PRENATALLY BYDELETIONS AND REARRANGEMENTSDELETIONS USING PCR BASED /OFSYNDROME BUT NORMAL KARYOTYPE /THE
4P16 BY FLUORESCENT IN SITU /OF4P16.3 /THE HUNTINGTON DISEASE REGION40 /MUSCULAR DYSTROPHY TO CHROMOSOME
/ON THE SUBTELOMERIC REGION OFMARKERS IN RELATION TO /CHROMOSOMERESULTS OF AN INTERNATIONAL /ON
4035 /DYSTROPHY LOCUS ON/MAP OF CHROMOSOMAL REGION4QTER /MUSCULAR DYSTROPHY GENE ATLINKAGE ANALYSIS OF THE /GENE ON
40TER /MUSCULAR DYSTROPHY GENE AT 4035IN TWO FAMILIES /ONTO CHROMOSOME
5 /CARRYING AN INVERTED INSERTION/LOCI ON THE LONG ARM OF CHROMOSOME/MAP OF THE SHORT ARM OF CHROMOSOME/REPORT OF A CASE OF MOSAIC TRISOMYAND 10 /GENETIC MAPS FOR CHROMOSOMESAND 16 /CLONES TO HUMAN CHROMOSOMESAND 16 AND THE CLONING OF LEUKEMIAAND 7 IN MALIGNANT MYELOID DISORDERSAND REC DEL(5) IN ONE EXTENDED /DUPBCR IN SOME PATIENTS WITH /WITHCARBOXYLATE REDUCTASE BY /PYRROLINECRI DU CHAT DELETION /FOR CHROMOSOMEFLANKING REGION 5 TRANSCRIBED /THEHALF OF THE COL4A5 GENE /THE UNKNOWNHARBORING THE FAMILIAL ADENOMATOUSHIGH RISK GROUPS /IN 40 PATIENTS INHYDROXYTRYPTAMINE1A RECEPTOR GENEIN ONE EXTENDED FAMILY CARRYING ANMARKERS /OF 75 CHROMOSOMEMETHYLCYTOSINE IS PREVENTED BY A /ATMOSAICISM DETECTED PRENATALLY WITHNEURONAL ACETYLCHOLINE RECEPTOROF THE FACTOR VIII GENE /CPG ISLANDREGION ON THE ACTIVE AND INACTIVE XTRANSCRIBED REGION AND CDNAS OFWITH FLUORESCENCE IN SITU
5.8 KB MAJOR BREAKPOINT CLUSTER /THE500 CASES /CYTOGENETIC EVALUATION OF508 FREQUENCY IN EUROPEAN COUNTRIES /F512 SEVERELY MENTALLY RETARDED /OF522 INFORMATIVE FAMILIES IS THERE AN542 MENTALLY RETARDED PATIENTS /IN56 CASES OF MACERATED INTRAUTERINE /OF574 OF TYPE II COLLAGEN IN /AT CODON586 ALPHA THALASSEMIA 72 BETA /FOR5;10 (P13;Q11.2) MAT TRANSLOCATION /T5;7 (033;034) NONRANDOM ASSOCIATION /TSB GLOBIN GENE CLUSTER PHENYLALANINEUP IN BROTHER AND SISTER /TRISOMY5P/1OP TRISOMY DUE TO A /DETECTED5P15.2 USING IRS PCR PRODUCTS FROM50 /HOMOLOGIES WITH HUMAN CHROMOSOME
/MUSCULAR DYSTROPHY TO CHROMOSOMEAND 110 /REGIONS ON CHROMOSOMES
5011 013,5034 OTER 11022,23 XPTER AND5011.2 13.3 USING RADIATION HYBRIDS5012 014 REGION /DNA PROBES OF THE5021 022 CONTAINS THE GENE MUTATED5031.3 5033.3 /SYNDROME LOCUS TO5033.3 /SYNDROME LOCUS TO 5031.36 /BY THE TRANSFER OF HUMAN CHROMOSOME/OF THE DMD LIKE LOCUS ON CHROMOSOME/PRENATAL DIAGNOSIS OF INV DELAND 15 AND DETAILED MAPPING OFAND 7 PROBES TO PREDICT STERILITYAT THE HLA LINKAGE GROUP /CHROMOSOMEBREAKPOINTS /4 CHROMOSOMES WITHCM SUBREGION OF CHROMOSOME 6P /TO APD DEFICIENCY NEONATES /HAVING GPHOSPHATE DEHYDROGENASE DEFICIENCYPHOSPHATE RECEPTOR /OF IGFII/MANNOSETHUS EXCLUDING A PUTATIVE PAGETYEAR STUDY /ABNORMALITY IN BAHRAIN
6.16 TRANSLOCATION EVIDENCE FOR /RBTRANSLOCATION IN MALE CARRIERS
60% OF THE GENOME /REGIONS AND OVER600 KB REGION CONTAINING THE VON /A
KB YEAST ARTIFICIAL CHROMOSOME /A604 CASES /PROSPECTIVE FOLLOW UP OF63 KDA PROTEOLYTIC PEPTIDES OF THE665 CASES SCREENED FOR THE FRAGILE X69 POTENTIAL HUMAN ZINC FINGER /OF69,XXX, 7, 7, + REC(7),DEL PDUP6;9 TRANSLOCATION IN ACUTE /OF THE T
TRANSLOCATION IN ANLL /OF THE T6P /MAPPING OF SCA1 ON CHROMOSOME
/TO A 6 CM SUBREGION OF CHROMOSOME/TO THE MHC ON CHROMOSOMEAND 130 RESULTING FROM A 3:1IN A FAMILY WHERE CLOSE LINKAGE TO
6P21.3 /GENETIC MAPPING OF HLA F ON6P;130 CHROMOSOME REARRANGEMENT /T60 DELETION RESULTING FROM A DE NOVO
IN EIGHT PRIMARY LUNG /DELETION OFIS INVOLVED IN IMMORTALIZATION OF
6011 + HETEROMORPHISM CYTOGENETIC /RARE6021 022 AND IS LINKED TO MYB /MAPS TO
601
2450158216611651961
1711151682
1904204220372012196622122217143
22171132145322082177123121631897185
258114532597227911762432236221328061882145322162552125721822154242824322171137012321747754
147416301149474
18311429150928831539142921681863
782030204321101223101
193319332601237915031502910
2197140620011778232415021929139915521583200021332159125226291612214415652582125
199320011932142120522137142114701336259815811307
Permuted Title Index
7 (P21032) /WITH PATERNAL INV,DEL P,DUP Q, + REC(7),DUP PDEL 0 IN,DUP PDEL 0 IN A LIVEBORN INFANT/ARM 120 AND RAT CHROMOSOME/PROXIMAL REGION OF MOUSE CHROMOSOME/WITH MATERNAL DISOMY FOR CHROMOSOMEAND THE HUMAN MYOTONIC DYSTROPHYCANDIDATE FOR A JUNCTION WITH THECHANGES AS A POSSIBLE GENETIC /ERDERIVED MARKER CHROMOSOMES RESULTSIN A PAPILLARY THYROID CARCINOMA BYIN MALIGNANT MYELOID DISORDERS /ANDIN PATIENTS WITH ACUTE MYELOGENOUSPROBES TO PREDICT STERILITY IN /AND
7, 7, + REC(7),DEL PDUP 0, + REC(7),DUP7,+ REC(7),DEL PDUP 0, + REC(7),DUP /7,7.6KB DELETION IN FRENCH CANADIANS70 KD PEROXISOMAL MEMBRANE PROTEIN7000 RECOMBINANT CLONES /WITHIN71 SEPARATE PROBANDS WITH LPL /OF717 MISSENSE MUTATION IS RARE IN72 BETA THALASSEMIA AND 306 NORMAL
ITALIAN FAMILIES AFFECTED BY /ON75 CHROMOSOME 5 MARKERS /OF7P21 P22 /OF PDGFA LOCALIZATION TO70 DUE TO MEIOTIC RECOMBINATION OF A
IN A DE NOVO TRANSLOCATION /TRISOMYIN SQUAMOUS CELL CARCINOMAS OF THE
7022 32 REGION /THE HUMAN CHROMOSOME
1565 7034 QTER /NONRANDOM ASSOCIATION OF1565 8/LINKAGE MAP OF CHROMOSOME1565 /OF SECOND GENE ON HUMAN CHROMOSOMES1870 /OF THE SHORT ARM OF CHROMOSOME1860 10 AND 12 /FOR HUMAN CHROMOSOMES1712 AND CARRIERS IN HIS FAMILY /OF EXONS86 AND GENETIC COUNSELING /FOR TRISOMY2213 DETECTION IN BONE MARROWS WITH1314 MOSAICISM /HEART DEFECTS IN TRISOMY1396 MOSAICISM IN AN IDENTICAL TWIN1322 NOVEL DELETERIOUS AND 3 NEUTRAL /OF2581 8% OF THE CHILDREN AND A FURTHER 12%1396 85% DETECTION RATE OF CFTR MUTATIONS910 853 OF THE TRIPLE HELICAL DOMAIN OF1565 87,521 HAIKOU CITY PEOPLE /HELD AMONG1565 8;21 IN ACUTE MYELOID LEUKEMIA /OF T2662 8P23 PTER IN AN ADULT PRESENTING WITH190 8P23.1 MINIMAL DYSMORPHIC FEATURES /OF
2198 80 AND MONOSOMY 20 DUE TO A PATERNAL470 DELETION /SYNDROME ASSOCIATION WITH
2811 8024 LINKED TO ONCOGENESIS /REGION1831 REARRANGEMENT IN FOUR CASES OF654 9 /CASE STUDIES ON UNUSUAL VARIANT
2216 /FROM A MARKED HUMAN CHROMOSOME2111 /FROM LINKAGE TO HUMAN CHROMOSOME1422 /MEDIATED TRANSFER OF CHROMOSOME1686 /OF THE LONG ARM OF CHROMOSOME1394 /TYPE TO THE LONG ARM OF CHROMOSOME2192 AND 11 /FOR LOCI ON CHROMOSOMES
1509 BY FLUORESCENCE IN SITU /CHROMOSOME2048 CHROMOSOMES IN 4000 JAPANESE /INV2314 FAMILIES AND 16 SPORADIC CASES /IN1585 IN BASAL CELL CARCINOMAS OF THE SKIN1635 KARYOTYPE PHENOTYPE CORRELATIONS690 MARKERS TO FRIEDREICH ATAXIA WITHIN1202 T(9;9)(P13;034) EXPRESSED TO216 90/YEARS OF INDIAN EXPERIENCES (19841499 CASES OF ESOPHAGEAL CARCINOMAS /THE1485 901 SUBSTITUTION IN A TYPE I /Al1067 902 CASES OF RECURRENT APL'tIlONS /IN
23 922 /SERINE SUBSTITUTIC', FOR A2(1) GLY96 FETUSES WITH TRiSOMY 21 /IN1829 9:22 TRANSLOCATION IN CHRONIC /OF THE522 9;11 IN BECKWITH WIEDEMANN SYNDROME2777 9;9 (P13;034) EXPRESSED TO DIFFERENT1342 9P /FAMILIAL PARACENTRIC INVERSION OF1530 A TISSUE SPECIFIC ISOCHROMOSOME IN1500 ARISING FROM A DERIVATIVE X;91402 INVOLVEMENT IN MELANOMA /CHROMOSOME1507 9P22P 90220 IN A MALE WITH2591 90 /LOCUS AS THE CLASSICAL FORM ON1333 32 34 /SYNTHETASE LOCUS ON1461 9013 /DNA SEQUENCES AT 2021 AND2149 021 /OVER A 350 KB REGION IN2004 Q21.1 /ATAXIA REGION AT
9013;021 IN A PATIENT WITH CHRONIC /OF2568 90220 IN A MALE WITH MYELODYSPLASTIC1512 9034 AND TESTS OF LINKAGE TO 110 AND598 IN ASHKENAZIC JEWS /ON CHROMOSOME142 90H+ VARIANT BAND IN TWO FAMILIES
602
22011545676
25831529189315321147604106512701054835164915961532158914561555223134782021401858
81217813791347191323531513
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