(Q45290651)

11 December 2017

title

Trinucleotide repeat instability: when and where? (English)

1 reference

11 December 2017

Nelson DL

1

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11 December 2017

Warren ST

series ordinal

2

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11 December 2017

language of work or name

English

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publication date

1 June 1993

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11 December 2017

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11 December 2017

volume

4

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11 December 2017

issue

2

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11 December 2017

page(s)

107-108

1 reference

https://scigraph.springernature.com/pub.10.1038/ng0693-107

11 December 2017

exact match

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cites work

Questions of expansion

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

Heritable unstable DNA sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

7 January 2021

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

7 January 2021

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

7 January 2021

Segregation of the fragile X mutation from an affected male to his normal daughter

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

7 January 2021

Retreat of the triplet repeat?

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-107

7 January 2021

Identifiers

DOI

10.1038/NG0693-107

1 reference

Dimensions Publication ID

11 December 2017

1039263094

0 references

1 reference