Deletion of All CGG Repeats Plus Flanking Sequences in FMR1 Does Not Abolish Gene Expression

This publication has 45 references indexed in Scilit:

• Purification of Nuclear Proteins from Human HeLa Cells That Bind Specifically to the Unstable Tandem Repeat (CGG)n in the Human FMR1 Gene
  Published by Elsevier ,1996
• Structure of the leukemia-associated human CBFB gene
  Genomics, 1995
• A de novo deletion in FMR1 in a patient with developmental delay
  Human Molecular Genetics, 1994
• Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream region
  American Journal of Medical Genetics, 1994
• CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the philadelphia chromosome
  Genes, Chromosomes and Cancer, 1994
• An Extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype
  Human Molecular Genetics, 1993
• Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.
  Journal of Medical Genetics, 1991
• Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
  Cell, 1991
• Absence of expression of the FMR-1 gene in fragile X syndrome
  Cell, 1991
• Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
  Published by Elsevier ,1991