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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Udgivet i:BMC Med Genomics
Main Authors: 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
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2016
Fag:
Research Article
Online adgang: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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