Application of trio-based whole-exome sequencing in fetal ultrasound anomalies: a single-center retrospective study of 454 cases

This study assessed the diagnostic effectiveness of trio-WES compared to CMA in fetuses with ultrasound anomalies and explored optimal prenatal testing strategies. A retrospective review included 454 fetuses who underwent trio-WES and/or CMA between 2020 and 2023. Cases were divided into four groups...

Täydet tiedot

Bibliografiset tiedot

Päätekijät:	Dongyi Yu, Dairong Feng, Jiangbo Qu, Lei Nie, Qian Liu, Lu Gao, Wenzhen An, Na Liu, Yuying Fang
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Frontiers Media S.A. 2025-11-01
Sarja:	Frontiers in Genetics
Aiheet:	fetal ultrasound anomalies prenatal diagnosis whole-exome sequencing microarray analysis chromosome disorders single gene disorders
Linkit:	https://www.frontiersin.org/articles/10.3389/fgene.2025.1662801/full
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