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Rare Copy Number Variation Analysis in Chinese Children of Complete Atrioventricular Canal and Single Ventricle 

2021-01-04

Abstract excerpt

<h4>Background: </h4> Congenital heart disease (CHD) is the most common birth defects. Copy number variations (CNVs) have been proved to be important genetic factors that contribute to CHD. Here, we screened pathogenic CNVs in Chinese children with two rare types of CHD, complete atrioventricular canal (CAVC) and single ventricle (SV) . <h4>Methods: </h4>： We screened CNVs in 262 sporadic CAVC cases and 259 sporad...

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Literature Corpus work: 4546a5f9-f391-5cee-b911-2d7d1f0ed24f
DOI: 10.21203/rs.3.rs-136133/v1

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