Direct detection of novel expanded trinucleotide repeats in the human genome (Q34352411)

1 August 2017

title

Direct detection of novel expanded trinucleotide repeats in the human genome (English)

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1 August 2017

Schalling M

1

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1 August 2017

Hudson TJ

series ordinal

2

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1 August 2017

Buetow KH

series ordinal

3

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1 August 2017

Housman DE

series ordinal

4

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1 August 2017

language of work or name

English

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publication date

1 June 1993

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1 August 2017

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1 August 2017

volume

4

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1 August 2017

issue

2

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1 August 2017

page(s)

135-139

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

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0693-135

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

Human genes containing polymorphic trinucleotide repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

Population incidence and segregation ratios in the Martin-Bell syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG0693-135

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

7 January 2021

Genetic disease detection and DNA amplification using cloned thermostable ligase

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

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

https://api.crossref.org/works/10.1038%2FNG0693-135

7 January 2021

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

7 January 2021

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

7 January 2021

Heritable unstable DNA sequences

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

7 January 2021

Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

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%2FNG0693-135

7 January 2021

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

7 January 2021

Survey of human and rat microsatellites.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-135

7 January 2021

Identifiers

DOI

10.1038/NG0693-135

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1 August 2017

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