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Documents Apert syndrome: information for families

Ref: 2019F1683 © GOSH NHS Foundation Trust, December 2019 Page 1 of 3 Apert syndrome: information for families Apert syndrome is a type of complex craniosynostosis named

Documents Apert Syndrome: An Insight Into Dentofacial Features

Review began 08/17/2021 Review ended 08/30/2021 Published 09/05/2021 © Copyright 2021 Jose et al. This is an open access article distributed under the terms of the Creative

Documents Apert Syndrome: A Case Report

CASE REPORT Apert Syndrome: A Case Report Gyanendra Kumar1,AditiGarg2,RamanandVignesh3,JatinderKDhillon4,FarrukhFaraz5 Ab s t r Ac t Introduction: Apert syndrome is one of

Documents An Exploration of the Cognitive, Physical and Psychosocial Development of Children with Apert...

An Exploration of the Cognitive, Physical and Psychosocial Development of Children with Apert SyndromeFull Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=cijd20

Documents Apert Syndrome in the Era of Prenatal Diagnosis

222 DSJUOG Apert Syndrome in the Era of Prenatal Diagnosis 1Florin Stamatian, 2Tunde Kovacs, 3Mariela Militaru, 4Gabriela Caracostea ABSTRACT Apert syndrome is a rare autosomal

Documents Apert syndrome with septum pellucidum agenesis

Singapore Med J 2007; 48(2) : e62C a s e R e p o r t AbstrAct Apert syndrome is character ised by craniosynostosis, associated with maxillary hypoplasia, symmetrical syndactyly

Documents Delleman Syndrome: A Case Report with Emphasis on Neuroimaging Features

Delleman Syndrome: A Case Report with Emphasis on Neuroimaging FeaturesCase Report Volume 3 Issue 1 - September 2017 DOI: 10.19080/IJCSMB.2017.03.555604 Int J cell Sci &

Documents Ectrodactyly/split hand feet malformation

Indian Journal of Human Genetics September-December 2009 Volume 15 Issue 3 Address for correspondence: Dr. Geetanjali Jindal, Department of pediatrics #1203, Sector 32-B,

Documents Low-level trisomy 14 mosaicism in a male newborn with ectrodactyly

Case Report Low-level trisomy 14 mosaicism in a male newborn with ectrodactyly M.A. Rodrigues1, L.F. Morgade2, L.F.A. Dias2, R.V. Moreira1, P.D. Maia3, A.F.H. Sales4 and

Documents Incomplete Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate SyndromeReport of 3 Cases

SAS Journal of Surgery ISSN 2454-5104 SAS J. Surg., Volume-1: Issue-1 (May-Jun, 2015); p-18-20 Available online at http://sassociety.com/sasjs/ Incomplete Ectrodactyly Ectodermal