FMR1 alleles in Tasmania: a screening study of the special educational needs population
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2004.00344.x/fullpdf
Reference59 articles.
1. Identification of a gene (FMR1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome;Verkerk;Cell,1991
2. The fragile X mental retardation protein inhibits translation via interacting with mRNA;Li;Nucleic Acids Res,2001
3. Abnormal dendritic spines in fragile X knockout mouse: maturation and pruning deficits;Comery;Proc Nat Acad Sci USA,1997
4. Length of uninterrupted CGG repeats determines instability in the FMR-1 gene;Eichler;Nat Genet,1994
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