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Rare Copy Number Variants in Patients with Congenital Conotruncal Heart Defects
BACKGROUND: Previous studies using different cardiac phenotypes, technologies and designs suggest a burden of large, rare or de novo copy number variants (CNVs) in subjects with congenital heart defects (CHD). We sought to identify disease-related CNVs, candidate genes and functional pathways in a l...
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| Publicado no: | Birth Defects Res |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5407323/ https://ncbi.nlm.nih.gov/pubmed/28398664 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.23609 |
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