(Q39111985)

9 September 2017

Length of uninterrupted CGG repeats determines instability in the FMR1 gene (English)

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9 September 2017

Eichler EE

1

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9 September 2017

Holden JJ

2

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9 September 2017

Popovich BW

3

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9 September 2017

Reiss AL

4

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9 September 2017

Snow K

5

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9 September 2017

Thibodeau SN

6

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9 September 2017

Richards CS

7

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9 September 2017

Ward PA

8

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9 September 2017

Nelson DL

9

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9 September 2017

language of work or name

English

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publication date

1 September 1994

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9 September 2017

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9 September 2017

8

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9 September 2017

88-94

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9 September 2017

1

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https://scigraph.springernature.com/pub.10.1038/ng0994-88

9 September 2017

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cites work

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

1 reference

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

21 January 2018

1 reference

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat.

21 January 2018

1 reference

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

21 January 2018

1 reference

Detection of full fragile X mutation.

21 January 2018

1 reference

Trinucleotide repeat instability: when and where?

21 January 2018

1 reference

Preferential DNA secondary structure mutagenesis in the lagging strand of replication in E. coli

21 January 2018

1 reference

Instability of short tandem repeats (microsatellites) in human cancers.

21 January 2018

1 reference

Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair

21 January 2018

1 reference

Hypermutability and mismatch repair deficiency in RER+ tumor cells

21 January 2018

1 reference

A tetranucleotide repeat mouse minisatellite displaying substantial somatic instability during early preimplantation development.

21 January 2018

1 reference

The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.

21 January 2018

1 reference

Complex gene conversion events in germline mutation at human minisatellites

21 January 2018

1 reference

Advances in molecular analysis of fragile X syndrome

21 January 2018

1 reference

7 January 2021

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

1 reference

7 January 2021

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

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

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7 January 2021

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

1 reference

7 January 2021

Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation

1 reference

7 January 2021

Frequency and stability of the fragile X premutation.

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7 January 2021

Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation.

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7 January 2021

Evidence of founder chromosomes in fragile X syndrome

1 reference

7 January 2021

Origins of the fragile X syndrome mutation

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7 January 2021

Founder effect in a Belgian-Dutch fragile X population

1 reference

7 January 2021

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

1 reference

7 January 2021

Robust amplification and ethidium-visible detection of the fragile X syndrome CGG repeat using Pfu polymerase

1 reference

7 January 2021

Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability

1 reference

7 January 2021

Simple repeat DNA is not replicated simply

1 reference

7 January 2021

Eukaryotic DNA replication. Enzymes and proteins acting at the fork

1 reference

7 January 2021

Microsatellite instability in cancer of the proximal colon

1 reference

7 January 2021

Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test.

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0994-88

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release_zkehh4tlpbe43k5xy5h6epypny

9 September 2017

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Fatcat

https://api.fatcat.wiki/v0/release/zkehh4tlpbe43k5xy5h6epypny

24 November 2022

mapped directly with Wikidata item

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