The fragile X premutation: into the phenotypic fold
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Genetics
Reference51 articles.
1. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991
2. The molecular biology of the fragile X mutation;Brown,2002
3. Familial transmission of the FMR1 CGG repeat;Nolin;Am J Hum Genet,1996
4. Epidemiology;Sherman,2002
5. Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel;Toledano-Alhadef;Am J Hum Genet,2001
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2. Fragile X syndrome in the largest world clustering. I. Genetic epidemiology and founder effect outline;American Journal of Medical Genetics Part A;2024-01-02
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