Clinical study of single nucleotide polymorphism-based chromosome microarray analysis in the etiological diagnosis of fetal congenital heart disease

Abstract This study investigates the clinical application of single-nucleotide polymorphisms (SNP)-based chromosome microarray analysis (CMA) in the etiological diagnosis of fetal congenital heart disease (CHD). We 5,116 amniotic fluid samples collected through amniocentesis from January 2022 to Dec...

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Autors principals:	Yinxia Zheng, Shuyuan Xue, Guilan Ding, Luhan Zhang, Guifeng Ding
Format:	Artigo
Idioma:	Inglês
Publicat:	Nature Portfolio 2025-11-01
Col·lecció:	Scientific Reports
Matèries:	Pregnant women Fetus Congenital heart disease Single nucleotide polymorphism Chromosome microarray analysis
Accés en línia:	https://doi.org/10.1038/s41598-025-23787-1
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