Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/9/19/2909/9815107/092909.pdf
Cited by 25 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation alleles;American Journal of Medical Genetics Part A;2019-05-02
2. Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers;Genetics in Medicine;2015-05
3. Heterozygosity for a Hypomorphic Polβ Mutation Reduces the Expansion Frequency in a Mouse Model of the Fragile X-Related Disorders;PLOS Genetics;2015-04-17
4. Fragile X Syndrome: The FMR1 CGG Repeat Distribution Among World Populations;Annals of Human Genetics;2011-12-21
5. Fragile X analysis of 1112 prenatal samples from 1991 to 2010;Prenatal Diagnosis;2011-06-30
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