Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy-Reference-Cited by-同舟云学术

Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancy

Published:2020-04-12 Issue:6 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Gao Fei¹²,Huang Wen¹,You Yanjun²,Huang Jie²,Zhao Juan¹,Xue Jin¹,Kang Huaixing¹,Zhu Yingbao¹,Hu Zhengmao¹³,Allen Emily G.⁴,Jin Peng⁴,Xia Kun¹³^ORCID,Duan Ranhui¹³⁵^ORCID

Affiliation:

1. Center for Medical Genetics School of Life Sciences Central South University Changsha Hunan China

2. National Institutes for Food and Drug Control Beijing China

3. Hunan Key Laboratory of Medical Genetics Central South University Changsha Hunan China

4. Department of Human Genetics Emory University School of Medicine Atlanta GA USA

5. Hunan Key Laboratory of Animal Models for Human Diseases Central South University Changsha Hunan China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1236

Reference38 articles.

1. Examination of reproductive aging milestones among women who carry the FMR1premutation

2. Consensus Characterization of 16 FMR1 Reference Materials: A Consortium Study

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

4. Fragile X Newborn Screening: Lessons Learned From a Multisite Screening Study

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