Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center

Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center

Abstract Background Fragile X syndrome (FXS) is the most common inherited form of intellectual disability. Prenatal screening of FXS allows for early identification and intervention. The present study explored the feasibility of FXS carrier screening during prenatal diagnosis for those who were not...

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Bibliographic Details
Main Authors: Hui Xi, Wanqin Xie, Jing Chen, Wanglan Tang, Xiuli Deng, Hua Li, Ying Peng, Dan Wang, Shuting Yang, Yanan Zhang, Ranhui Duan, Junqun Fang, Hua Wang
Format: Article
Language:English
Published: Wiley 2021-07-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
carrier screening
FMR1
fragile X syndrome
prenatal diagnosis
Online Access:https://doi.org/10.1002/mgg3.1711

Internet

https://doi.org/10.1002/mgg3.1711

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