(Q45290860)

11 December 2017

title

Huntington's disease: testing the test (English)

1 reference

11 December 2017

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Read AP

1

1 reference

11 December 2017

language of work or name

English

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publication date

1 August 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

4

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11 December 2017

page(s)

329-330

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https://scigraph.springernature.com/pub.10.1038/ng0893-329

11 December 2017

exact match

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cites work

Trinucleotide repeat instability: when and where?

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

Trinucleotide repeat length instability and age of onset in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

A point mutation in the FMR-1 gene associated with fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

Homozygotes for Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

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%2FNG0893-329

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%2FNG0893-329

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

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%2FNG0893-329

Problems in genetic prediction for Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

Exclusion testing for Huntington's disease in pregnancy with a closely linked DNA marker

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

Fragile X syndrome without CCG amplification has an FMR1 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

inferred from DOI database lookup

7 January 2021

based on heuristic

Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-329

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG0893-329

1 reference

Dimensions Publication ID

11 December 2017

1036394996

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1 reference