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

Author

Antonio Pizzuti

Published in: Cell

Date of publication: 1991-12-20

Language: anglais

Bibliographic databases:

Cites articles 20

Date

Title

Authors

1984-01-01

The marker (X) syndrome: a cytogenetic and genetic analysis.
1984-01-01

Gene amplification
1985-03-01

Hypervariable 'minisatellite' regions in human DNA.
1985-01-01

Further segregation analysis of the fragile X syndrome with special reference to transmitting males.
1986-01-01

Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county.
1986-01-01

Population incidence and segregation ratios in the Martin-Bell syndrome.
1987-01-01

Random cloning and sequencing by the M13/dideoxynucleotide chain termination method.
1988-03-01

Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA
1989-01

Characterization and expression of a cDNA encoding the human androgen receptor
1990-03-01

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

, ,
1991-02-01

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome
1991-05-01

Molecular cloning and analysis of the fragile X region in man
1991-04

The CEPH consortium linkage map of human chromosome 1
1991-03-01

Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island
1991-06-01

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
1991-05-01

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
1991-08-01

Absence of expression of the FMR-1 gene in fragile X syndrome
1991-05-01

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

, ,
1991-02-01

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis
1991-05-01

Fragile X genotype characterized by an unstable region of DNA.

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