High prevalence of the Fra(X) syndrome cannot be explained by a high mutation rate
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Abstract
References (21)
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
Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome
1991 • 1,482 citations
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1987 • 190 citations
Population incidence and segregation ratios in the Martin‐Bell syndrome
1986 • 186 citations
Prevalence of the fragile‐X syndrome in mentally retarded boys in a Swedish county
1986 • 94 citations
Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site
1992 • 89 citations
Recombination and amplification of pyrimidine‐rich sequences may be responsible for initiation and progression of the Xq27 fragile site: An hypothesis
1986 • 67 citations
New polymorphic DNA marker close to the fragile site FRAXA
1990 • 55 citations
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1990 • 39 citations
Transmission of the marker X syndrome trait by unaffected males: Conclusions from studies of large families
1984 • 35 citations
Mutation and selection in the marker (X) syndrome A hypothesis
1984 • 29 citations
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1986 • 20 citations
Fragile X families in a Northern Swedish county ‐ a genealogical study demonstrating apparent paternal transmission from the 18th century
1988 • 12 citations
Investigation of the segregation of the fragile X mutation in daughters of obligate carrier women
1988 • 10 citations
Multipoint linkage analysis of DXS369 and DXS304 in fragile X families
1991 • 9 citations
Validation of linkage‐based DNA‐diagnosis of fragile X gene carriers with the CGG repeat probe
1992 • 5 citations
Deleted Work
1955 • 0 citations