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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Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
Assuntos:
Research Article
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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