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Article

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

BMC medical genomics - 9 Oct 2021

Zhang Xingyu, Wang Bo, You Guoling, Xiang Ying, Fu Qihua, Yu Yongguo, Zhang Xiaoqing

Abstract excerpt

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 ventricle (SV), since there were scarce researches dedicated to these two types of CHD. METHODS: We screened CNVs in 262...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 34627233
DOI: 10.1186/s12920-021-01090-y
PMCID: PMC8502261

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