Whole-exome sequencing for prenatal diagnosis of fetal anomalies: insights from a Jordanian cohort

Background Congenital anomalies are a heterogeneous disorder that occur during fetal development or infancy. Whole exome sequencing (WES) is a promising diagnostic tool for prenatal diagnosis. This study aimed to evaluate the efficiency of WES in identifying the genetic cause of fetal anomalies amon...

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Bibliographic Details

Published in:	The Journal of Maternal-Fetal & Neonatal Medicine
Main Authors:	Mohammad Shboul, Nadia Badaro, Reem Darweesh, Rajaa Fathallah, Mohammed El-Khateeb, Oqba Al-Kuran
Format:	Article
Language:	English
Published:	Taylor & Francis Group 2025-12-01
Subjects:	Congenital anomalies whole exome sequencing prenatal genetic testing variants gene
Online Access:	https://www.tandfonline.com/doi/10.1080/14767058.2025.2538208