(Q34357407)

1 August 2017

title

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

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1 August 2017

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4

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1 August 2017

Duyao M

1

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1 August 2017

Ambrose C

2

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1 August 2017

Myers R

3

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1 August 2017

Persichetti F

5

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1 August 2017

Frontali M

6

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1 August 2017

Folstein S

7

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1 August 2017

Ross C

8

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1 August 2017

Franz M

9

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1 August 2017

Abbott M

10

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1 August 2017

language of work or name

English

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publication date

1 August 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

4

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1 August 2017

page(s)

387-392

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Huntington's disease. Pathogenesis and management

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

Homozygotes for Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

Recombination events suggest potential sites for the Huntington's disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

Predictive testing for Huntington's disease with use of a linked DNA marker

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

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%2FNG0893-387

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%2FNG0893-387

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%2FNG0893-387

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

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%2FNG0893-387

7 January 2021

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

Huntington's disease: two families with differing clinical features show linkage to the G8 probe

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

The Huntington's disease candidate region exhibits many different haplotypes

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

Instability versus predictability: the molecular diagnosis of myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

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%2FNG0893-387

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%2FNG0893-387

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

Unstable DNA sequence in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

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%2FNG0893-387

7 January 2021

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

Brief report: reverse mutation in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

Huntington disease: no evidence for locus heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

1 reference

https://api.crossref.org/works/10.1038%2FNG0893-387

7 January 2021

Identifiers

DOI

10.1038/NG0893-387

1 reference

Dimensions Publication ID

1 August 2017

1048577444

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1 reference