Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center-Reference-Cited by-同舟云学术

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

Published:2021-05-31 Issue:7 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Xi Hui¹²^ORCID,Xie Wanqin²^ORCID,Chen Jing¹,Tang Wanglan¹,Deng Xiuli¹,Li Hua¹,Peng Ying¹²^ORCID,Wang Dan¹,Yang Shuting¹,Zhang Yanan¹,Duan Ranhui³^ORCID,Fang Junqun⁴,Wang Hua¹²

Affiliation:

1. Department of Medical Genetics & the Prenatal Diagnosis Center of Hunan Province Hunan Provincial Maternal and Child Health Care Hospital Changsha Hunan China

2. NHC Key Laboratory of Birth Defects for Research and Prevention Hunan Provincial Maternal and Child Health Care Hospital Changsha Hunan China

3. Center for Medical Genetics School of Life Sciences & Hunan Key Laboratory of Medical Genetics Central South University Changsha Hunan China

4. Department of Health Care Hunan Provincial Maternal and Child Health Care Hospital Changsha Hunan China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1711

Reference21 articles.

1. “It's about having the choice”: Stakeholder perceptions of population-based genetic carrier screening for fragile X syndrome

2. Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests

3. A Pilot Study of Fragile X Syndrome Screening in Pregnant Women and Women Planning Pregnancy: Implementation, Acceptance, Awareness, and Geographic Factors

4. Caregiver opinions about fragile X population screening

5. Preconceptional and prenatal screening for fragile X syndrome: Experience with 40 000 tests

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1. Attitudes of medical professionals toward fragile X carrier screening and genetic counseling in China;Journal of Community Genetics;2024-01-26

2. Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation;Cells;2023-09-21