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Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects
Genomic disorders and rare copy number abnormalities are identified in 15–25% of patients with syndromic conditions, but their prevalence in individuals with isolated birth defects is less clear. A spectrum of congenital heart defects (CHDs) is seen in heterotaxy, a highly heritable and genetically...
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| Yayımlandı: | Philos Trans R Soc Lond B Biol Sci |
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| Asıl Yazarlar: | , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The Royal Society
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5104505/ https://ncbi.nlm.nih.gov/pubmed/27821535 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1098/rstb.2015.0406 |
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