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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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Hoofdauteurs: Huili Xue, Aili Yu, Lingji Chen, Qun Guo, Lin Zhang, Na lin, Xuemei Chen, Liangpu Xu, Hailong Huang
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Nature Portfolio 2024-07-01
Reeks:Scientific Reports
Onderwerpen:
Dextrocardia
Prenatal diagnosis
Situs inversus totalis
Whole exome sequencing
Primary ciliary dyskinesia
Online toegang:https://doi.org/10.1038/s41598-024-67164-w
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