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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Detalles Bibliográficos
Autores principales: Liu, Yichuan, Chang, Xiao, Glessner, Joseph, Qu, Huiqi, Tian, Lifeng, Li, Dong, Nguyen, Kenny, Sleiman, Patrick M. A., Hakonarson, Hakon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746959/
https://www.ncbi.nlm.nih.gov/pubmed/31552105
http://dx.doi.org/10.3389/fgene.2019.00819

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6746959/
https://www.ncbi.nlm.nih.gov/pubmed/31552105
http://dx.doi.org/10.3389/fgene.2019.00819

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