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A systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this field
The etiology of congenital heart defect (CHD) combines environmental and genetic factors. So far, there were studies reporting on the screening of a single gene on unselected CHD or on familial cases selected for specific CHD types. Our goal was to systematically screen a proband of familial cases o...
Kaydedildi:
Yayımlandı: | Eur J Hum Genet |
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Asıl Yazarlar: | , , , , , , , , , , , , , , , , , , , , , , , |
Materyal Türü: | Artigo |
Dil: | Inglês |
Baskı/Yayın Bilgisi: |
Nature Publishing Group
2016
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Konular: | |
Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4717196/ https://ncbi.nlm.nih.gov/pubmed/26014430 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.105 |
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