Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

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

Purification of Mouse Immunoglobulin Heavy‐Chain Messenger RNAs from Total Myeloma Tumor RNA

1980 • 2,696 citations

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

1991 • 2,062 citations

Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome

1991 • 1,482 citations

Absence of expression of the FMR-1 gene in fragile X syndrome

1991 • 1,456 citations

Fragile X Genotype Characterized by an Unstable Region of DNA

1991 • 794 citations

A versatilein vivoandin vitroeukaryotic expression vector for protein engineering

1988 • 686 citations

A point mutation in the FMR-1 gene associated with fragile X mental retardation

1993 • 619 citations

Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome

1993 • 387 citations

The human cation-independent mannose 6-phosphate receptor. Cloning and sequence of the full-length cDNA and expression of functional receptor in COS cells.

1988 • 244 citations

Population incidence and segregation ratios in the Martin‐Bell syndrome

1986 • 186 citations

Isolation of Sequences that Span the Fragile X and Identification of a Fragile X-Related CpG Island

1991 • 174 citations

Alternative splicing in the fragile X gene FMR1

1993 • 135 citations

Prevalence of the fragile‐X syndrome in mentally retarded boys in a Swedish county

1986 • 94 citations

Alternative splicing in the fragile X gene FMR1

1993 • 92 citations

Immunocytochemistry of lysosomal hydrolases and their precursor forms in normal and mutant human cells

1984 • 44 citations

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