Back to search

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

Data up to Jan 2025

Published1992
Citations15
References21

Total Citations Per Year

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

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

1991 • 637 citations

A marker X chromosome.

1969 • 614 citations

The marker (X) syndrome: a cytogenetic and genetic analysis

1984 • 390 citations

Fragile Sites on Human Chromosomes

1986 • 242 citations

Proposed Mechanism of Inheritance and Expression of the Human Fragile-X Syndrome of Mental Retardation

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

The fragile X: progress toward solving the puzzle.

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

The fragile(X) syndrome: The mutation problem

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

Cited By (0)

Loading...
High prevalence of the Fra(X) syndrome cannot be explained by a high mutation rate (1992) – American Journal of Medical Genetics | Metascience Observatory Explorer