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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Detalles Bibliográficos
Autores principales: Cai, Meiying, Huang, Hailong, Su, Linjuan, Lin, Na, Wu, Xiaoqing, Xie, Xiaorui, An, Gang, Li, Ying, Lin, Yuan, Xu, Liangpu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320040/
https://www.ncbi.nlm.nih.gov/pubmed/30558042
http://dx.doi.org/10.1097/MD.0000000000013617

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320040/
https://www.ncbi.nlm.nih.gov/pubmed/30558042
http://dx.doi.org/10.1097/MD.0000000000013617

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