(Q36265695)

13 August 2017

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title

The fragile X syndrome: isolation of the FMR-1 gene and characterization of the fragile X mutation (English)

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13 August 2017

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B A Oostra

1

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13 August 2017

A J Verkerk

series ordinal

2

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13 August 2017

publication date

1 April 1992

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13 August 2017

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13 August 2017

volume

101

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13 August 2017

issue

7

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13 August 2017

page(s)

381-387

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

13 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FBF00582832

A new DNA marker tightly linked to the fragile X locus (FRAXA).

21 January 2018

1 reference

12 December 2020

New polymorphic DNA marker close to the fragile site FRAXA.

1 reference

12 December 2020

Effects of nucleotides on expression of the folate sensitive fragile sites

1 reference

12 December 2020

Microdissection of the fragile X region.

1 reference

12 December 2020

Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).

1 reference

12 December 2020

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

1 reference

12 December 2020

Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile X.

1 reference

12 December 2020

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome

1 reference

12 December 2020

Limited size of the fragile X site shown by fluorescence in situ hybridization

1 reference

12 December 2020

Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA)

1 reference

12 December 2020

A YAC contig across the fragile X site defines the region of fragility

1 reference

12 December 2020

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The fragile X site in somatic cell hybrids: an approach for molecular cloning of fragile sites.

1 reference

12 December 2020

Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence

1 reference

12 December 2020

Linkage homogeneity near the fragile X locus in normal and fragile X families

1 reference

12 December 2020

The fragile X: progress toward solving the puzzle

1 reference

12 December 2020

New distal marker closely linked to the fragile X locus

1 reference

12 December 2020

Laser microdissection of the fragile X region: identification of cosmid clones and of conserved sequences in this region

1 reference

12 December 2020

Physical map of human Xq27-qter: localizing the region of the fragile X mutation

1 reference

12 December 2020

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Conference report: International Workshop on the fragile X and X-linked mental retardation.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Linear order of new and established DNA markers around the fragile site at Xq27.3.

1 reference

12 December 2020

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

1 reference

12 December 2020

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

1 reference

12 December 2020

Fragile X genotype characterized by an unstable region of DNA.

1 reference

12 December 2020

Report of the committee on cytogenetic markers

1 reference

12 December 2020

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

1 reference

12 December 2020

Relationship between age and IQ among fragile X males: a multicenter study

1 reference

12 December 2020

Isolation of a human DNA sequence which spans the fragile X.

1 reference

12 December 2020

Proposed mechanism of inheritance and expression of the human fragile-X syndrome of mental retardation

1 reference

12 December 2020

Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytes.

1 reference

12 December 2020

A marker X chromosome

1 reference

12 December 2020

Genetic linkage heterogeneity in the fragile X syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male

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12 December 2020

A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardation

1 reference

12 December 2020

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

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12 December 2020

Identifiers

DOI

10.1007/BF00582832

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13 August 2017

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