Clinical utility of trio whole exome sequencing in fetuses with ultrasound anomalies

Abstract Introduction Ultrasound scanning anomalies in fetuses are a cause for concern and often necessitate further diagnostic procedures. This retrospective study evaluated the utility of trio whole exome sequencing (trio-WES) in the diagnosis of fetuses with ultrasound anomalies. Methods We inclu...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής

Κύριοι συγγραφείς:	Ziye Zeng, Lan Zhang, Yuqin Zhou, Xue Zhang, Hong Yi, He Li, Yuqi Liu, Jian Li, Qian Chen, Yulin Chen, Guiming Yu, Jing Yi, Yana Zhang, Hua Zhang, Yanling Dong
Μορφή:	Artigo
Γλώσσα:	Inglês
Έκδοση:	BMC 2025-04-01
Σειρά:	Human Genomics
Θέματα:	Trio whole exome sequencing Structural anomalies Dynamic anomalies Soft markers Prenatal diagnosis
Διαθέσιμο Online:	https://doi.org/10.1186/s40246-025-00745-6
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