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Health & Medicine Huntingtons disease

1. Molecular Genetics Lab to the Neurology Clinic 2. Goals • Increase understanding of the neuropathology and clinical presentation of HD• Review basic genetics• Understand…

Education Genetics ppt

1.Genetics2. WHAT IS GENETICS????? The branch of biology that deals with heredity, especially the mechanisms of hereditary transmission and the variation of inheritedcharacteristics…

Documents Organization of Genetics Course Molecular Genetics Cytogenetics Transmission Genetics Population...

Slide 1 Organization of Genetics Course Molecular Genetics Cytogenetics Transmission Genetics Population Genetics Slide 2 Molecular Genetics Identification of DNA as the…

Documents N C Fig. 13-1, Page 307 Gene Expression. Pg. 242 Deoxyribonucleotide.

Slide 1 N C Fig. 13-1, Page 307 Gene Expression Slide 2 Pg. 242 Deoxyribonucleotide Slide 3 DNA Bases Pg. 242 Slide 4 Deoxyribonucleotide A Slide 5 DNA Strand Pg. 244 Slide…

Documents A Physician’s Guide to the Management of Huntington’s Disease Third Edition

Third Edition A Physician’s Guide to the Management of Huntington’s Disease Martha Nance, M.D. Jane S. Paulsen, Ph.D. Adam Rosenblatt, M.D. Vicki Wheelock, M.D.

Documents Presentation and care of a family with Huntington disease in a resource-limited community

Presentation and care of a family with Huntington disease in a resource-limited communityRESEARCH ARTICLE Open Access Presentation and care of a family with Huntington disease

Documents Fragile X Syndrome

CG_CONTENT1389-2029/11 $58.00+.00 ©2011 Bentham Science Publishers Ltd. Fragile X Syndrome 1 , Flora Tassone System, Sacramento, California, USA 2 Department of Biochemistry

Documents Congenital Myotonic Dystrophy

Congenital Myotonic DystrophyReview Article Open Access J Neurol Neurophysiol ISSN: 2155-9562 JNN, an open access journal Neuromuscular Medicine Congenital Myotonic Dystrophy

Documents Molecular and Clinical Characteristics of Myotonic Dystrophy Type 1 in Koreans

2172483 DOI 10.3343/kjlm.2008.28.6.483 1 Molecular and Clinical Characteristics of Myotonic Dystrophy Type 1 in Koreans So Yeon Kim, M.D.1*, Ji Yeon Kim, M.D.2*, Gyoung Pyoung

Documents ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43...

OP-BRCM200064 1..13ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization Tazelaar, G. H. P., Boeynaems, S., De Decker,