Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios

Congenital heart defects (CHDs) are a common birth defect, affecting approximately 1% of newborn children in the United States. As previously reported, a significant number of CHDs are potentially attributed to altered copy number variants (CNVs). However, as many genomic variants are rare, a large-...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Liu, Yichuan, Chang, Xiao, Glessner, Joseph, Qu, Huiqi, Tian, Lifeng, Li, Dong, Nguyen, Kenny, Sleiman, Patrick M. A., Hakonarson, Hakon
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6746959/
https://ncbi.nlm.nih.gov/pubmed/31552105
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00819
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