Prenatal chromosomal microarray analysis in a large Chinese cohort of fetuses with congenital heart defects: a single center study

Abstract Background and objectives Congenital heart defect (CHD) is one of the most common birth defects. The aim of this cohort study was to evaluate the prevalence of chromosomal abnormalities and the clinical utility of chromosomal microarray analysis (CMA) in fetuses with different types of CHD,...

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Bibliografiske detaljer

Principais autores:	Qing Lu, Laipeng Luo, Baitao Zeng, Haiyan Luo, Xianjin Wang, Lijuan Qiu, Yan Yang, Chuanxin Feng, Jihui Zhou, Yanling Hu, Tingting Huang, Pengpeng Ma, Ting Huang, Kang Xie, Huizhen Yuan, Shuhui Huang, Bicheng Yang, Yongyi Zou, Yanqiu Liu
Format:	Artigo
Sprog:	Inglês
Udgivet:	BMC 2024-08-01
Serier:	Orphanet Journal of Rare Diseases
Fag:	Congenital heart defects Chromosomal abnormalities Copy number variations Chromosomal microarray analysis Prenatal diagnosis
Online adgang:	https://doi.org/10.1186/s13023-024-03317-4
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