Copy number variation analysis in Chinese children with complete atrioventricular canal and single ventricle

BACKGROUND: Congenital heart disease (CHD) is one of the most common birth defects. Copy number variations (CNVs) have been proved to be important genetic factors that contribute to CHD. Here we screened genome-wide CNVs in Chinese children with complete atrioventricular canal (CAVC) and single vent...

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Detalles Bibliográficos
Autores principales: Zhang, Xingyu, Wang, Bo, You, Guoling, Xiang, Ying, Fu, Qihua, Yu, Yongguo, Zhang, Xiaoqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502261/
https://www.ncbi.nlm.nih.gov/pubmed/34627233
http://dx.doi.org/10.1186/s12920-021-01090-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502261/
https://www.ncbi.nlm.nih.gov/pubmed/34627233
http://dx.doi.org/10.1186/s12920-021-01090-y

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