The fragile X syndrome: no evidence for any recent mutations.

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1991 • 3,422 citations

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1991 • 2,062 citations

Fragile X Genotype Characterized by an Unstable Region of DNA

1991 • 794 citations

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation

1991 • 637 citations

Fragile-X syndrome: unique genetics of the heritable unstable element.

1992 • 201 citations

Evidence of founder chromosomes in fragile X syndrome

1992 • 187 citations

Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.

1992 • 100 citations

Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site

1992 • 89 citations

Hereditary unstable DNA: a new explanation for some old genetic questions?

1991 • 73 citations

High prevalence of the Fra(X) syndrome cannot be explained by a high mutation rate

1992 • 15 citations

Penetrance of Fra(X) gene: Influence of grandparental origin of the gene, mental status of the carrier mother, and presence of a normal transmitting male

1992 • 8 citations