Copy number variations in the GATA4, NKX2‐5, TBX5, BMP4 CRELD1, and 22q11.2 gene regions in Chinese children with sporadic congenital heart disease

BACKGROUND: Congenital heart disease (CHD) is a common birth defect originating from both environmental and genetic factors. An overabundance of copy number variations (CNVs) affecting cardiac‐related genes has previously been detected in individuals with CHD. OBJECTIVE: To evaluate if the presence...

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Detalhes bibliográficos
Publicado no:J Clin Lab Anal
Main Authors: Li, Zhetao, Huang, Jiwei, Liang, Biao, Zeng, Dingyuan, Luo, Shiqiang, Yan, Tizhen, Liao, Fengwen, Huang, Jun, Li, Jingwen, Cai, Ren, Deng, Xine, Tang, Ning
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6818592/
https://ncbi.nlm.nih.gov/pubmed/30221396
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.22660
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