Incidence of Fragile X Syndrome by Newborn Screening for Methylated FMR1 DNA
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference51 articles.
1. Absence of expression of the FMR-1 gene in fragile X syndrome;Pieretti;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. 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
4. DNA methylation represses FMR-1 transcription in fragile X syndrome;Sutcliffe;Hum. Mol. Genet.,1992
5. Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus;Eberhart;Somat. Cell Mol. Genet.,1996
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