Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome

BACKGROUND: Congenital heart disease (CHD) is one of the most common birth defects; however, the mechanisms underlying its development are poorly understood. Recently, heritable genetic factors, including copy number variations (CNVs) and single nucleotide polymorphisms (SNPs), have been implicated...

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Detalhes bibliográficos
Publicado no:Medicine (Baltimore)
Main Authors: Cai, Meiying, Huang, Hailong, Su, Linjuan, Lin, Na, Wu, Xiaoqing, Xie, Xiaorui, An, Gang, Li, Ying, Lin, Yuan, Xu, Liangpu
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer Health 2018
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6320040/
https://ncbi.nlm.nih.gov/pubmed/30558042
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000013617
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