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Genome-wide copy number variant analysis for congenital ventricular septal defects in Chinese Han population
BACKGROUND: Ventricular septal defects (VSDs) constitute the most prevalent congenital heart disease (CHD), occurs either in isolation (isolated VSD) or in combination with other cardiac defects (complex VSD). Copy number variation (CNV) has been highlighted as a possible contributing factor to the...
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| Publicado no: | BMC Med Genomics |
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| Main Authors: | , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4705616/ https://ncbi.nlm.nih.gov/pubmed/26742958 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-015-0163-4 |
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