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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Shranjeno v:
Bibliografske podrobnosti
izdano v: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
Jezik:Inglês
Izdano: BioMed Central 2016
Teme:
Research Article
Online dostop: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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