Genetic Testing and Pregnancy Outcome Analysis of 362 Fetuses with Congenital Heart Disease Identified by Prenatal Ultrasound

BACKGROUND: Congenital heart defects (CHD), as the most common congenital anomaly, have been reported to be associated with chromosomal abnormalities. Currently, patients with CHD are routinely offered karyotyping and chromosomal microarray (CMA) testing, but the genotype-phenotype relationship has...

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Detalles Bibliográficos
Autores principales: Luo, Shiyu, Meng, Dahua, Li, Qifei, Hu, Xuehua, Chen, Yuhua, He, Chun, Xie, Bobo, She, Shangyang, Li, Yingfeng, Fu, Chunyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cardiologia - SBC 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199505/
https://www.ncbi.nlm.nih.gov/pubmed/30133550
http://dx.doi.org/10.5935/abc.20180144

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199505/
https://www.ncbi.nlm.nih.gov/pubmed/30133550
http://dx.doi.org/10.5935/abc.20180144

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