Co-occurring diagnoses amongFMR1premutation allele carriers
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2009.01317.x/fullpdf
Reference32 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. Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox;Fu;Cell,1991
3. Fragile X genotype characterized by an unstable region of DNA;Yu;Science,1991
4. Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat;Ashley;Nat Genet,1993
5. Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations;Primerano;RNA,2002
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