Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese cases

Prenatal whole-exome sequencing for fetal structural anomalies: a retrospective analysis of 145 Chinese cases

Abstract Background Whole-exome sequencing (WES) significantly improves the diagnosis of the etiology of fetal structural anomalies. This study aims to evaluate the diagnostic value of prenatal WES and to investigate the pathogenic variants in structurally abnormal fetuses. Methods We recruited 144...

Olles dieđut

Bibliográfalaš dieđut
Váldodahkkit: Yayun Qin, Yanyi Yao, Nian Liu, Bo Wang, Lijun Liu, Hui Li, Tangxinzi Gao, Runhong Xu, Xiaoyan Wang, Fanglian Zhang, Jieping Song
Materiálatiipa: Artihkal
Giella:English
Almmustuhtton: BMC 2023-10-01
Ráidu:BMC Medical Genomics
Fáttát:
Whole-exome sequencing
Prenatal diagnosis
Structural anomalies
Prenatal ultrasonography
Liŋkkat:https://doi.org/10.1186/s12920-023-01697-3

Interneahtta

https://doi.org/10.1186/s12920-023-01697-3

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