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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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| Udgivet i: | Rep Biochem Mol Biol |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Varastegan Institute for Medical Sciences
2013
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4757068/ https://ncbi.nlm.nih.gov/pubmed/26989721 |
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