Pupak Derakhshandeh-Peykar
Department of Medical Genetics, Medical Sciences, University of Tehran, Iran - Medizinisch Genetisches Zentrum (MGZ), Munich, Germany
[ 1 ] - 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 individuals we detected a transition of C to T (CTG-GTT, V205V) in exon 7 of the TBX5 gene. This ...
نویسندگان همکار