A genetic assay of three patients in the same family with Holt-Oram syndrome; a case report

Holt-Oram syndrome (HOS) is a developmental disorder inherited in an autosomal-dominant pattern. Affected organs are the heart and forelimbs with upper extremity skeletal defects and congenital heart malformation. In this study we present three cases of HOS in the same family. In one of these three...

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發表在:Rep Biochem Mol Biol
Main Authors: Ebrahimzadeh-Vesal, Reza, Hosseini, Seyed kianush, Rezakhanlu, Fereshteh, Derakhshandeh-Peykar, Pupak
格式: Artigo
語言:Inglês
出版: Varastegan Institute for Medical Sciences 2013
主題:
Case Report
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC4757068/
https://ncbi.nlm.nih.gov/pubmed/26989721
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