The prevalence of CGG repeat expansion mutation in FMR1 gene in the northern Chinese women of reproductive age-Reference-Cited by-同舟云学术

The prevalence of CGG repeat expansion mutation in FMR1 gene in the northern Chinese women of reproductive age

Published:2019-05-16 Issue:1 Volume:20 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Ma Yinan,Wei Xing,Pan Hong,Wang Songtao,Wang Xin,Liu Xiaowei,Zou Liying,Wang Xiaomei,Wang Xiaorong,Yang Hua,Wang Fengying,Wang Kefang,Sun Lifang,Qiao Xiaolin,Yang Yue,Ma Xiuhua,Liu Dandan,Ding Guifeng,Ma Junqi,Yang Xiuli,Zhu Sainan,Qi Yu^ORCID,Yin Chenghong

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-019-0805-z.pdf

Reference27 articles.

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2. Hagerman R, Hagerman P. Advances in clinical and molecular understanding of the FMR1 premutation and fragile X-associated tremor/ataxia syndrome. Lancet Neurol. 2013;12:786–98.

3. Finucane B, Abrams L, Cronister A, Archibald AD, Bennett RL, McConkie-Rosell A. Genetic counseling and testing for FMR1 gene mutations: practice guidelines of the national society of genetic counselors. J Genet Couns. 2012;21:752–60.

4. Wheeler AC, Bailey DB Jr, Berry-Kravis E, Greenberg J, Losh M, Mailick M, et al. Associated features in females with an FMR1 premutation. J Neurodev Disord. 2014;6:30.

5. Gutiérrez JF, Bajaj K, Klugman SD. Prenatal screening for fragile x: carriers, controversies, and counseling. Rev Obstet Gynecol. 2013;6(1):e1–7.

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