Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center

Abstract To evaluate the genetic etiology of fetal dextrocardia, associated ultrasound anomalies, and perinatal outcomes, we investigated the utility of whole exome sequencing (WES) for prenatal diagnosis of dextrocardia. Fetuses with dextrocardia were prospectively collected between January 2016 an...

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Autori principali:	Huili Xue, Aili Yu, Lingji Chen, Qun Guo, Lin Zhang, Na lin, Xuemei Chen, Liangpu Xu, Hailong Huang
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Nature Portfolio 2024-07-01
Serie:	Scientific Reports
Soggetti:	Dextrocardia Prenatal diagnosis Situs inversus totalis Whole exome sequencing Primary ciliary dyskinesia
Accesso online:	https://doi.org/10.1038/s41598-024-67164-w
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