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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Detalles Bibliográficos
Autores principales: An, Yu, Duan, Wenyuan, Huang, Guoying, Chen, Xiaoli, Li, Li, Nie, Chenxia, Hou, Jia, Gui, Yonghao, Wu, Yiming, Zhang, Feng, Shen, Yiping, Wu, Bailin, Wang, Hongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705616/
https://www.ncbi.nlm.nih.gov/pubmed/26742958
http://dx.doi.org/10.1186/s12920-015-0163-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705616/
https://www.ncbi.nlm.nih.gov/pubmed/26742958
http://dx.doi.org/10.1186/s12920-015-0163-4

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