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

Author

Andrea Novelletto

published in: Nature Genetics

date of publication: 1993-08-01

language: English

main subject: Huntington's disease

Bibliographic databases:

Cites articles 30

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A sex related factor in the inheritance of Huntington's chorea
1983-11-01

A polymorphic DNA marker genetically linked to Huntington's disease
1984-11-01

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines
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Huntington's disease: two families with differing clinical features show linkage to the G8 probe
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Huntington's disease. Pathogenesis and management
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Homozygotes for Huntington's disease
1988-03-01

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

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Recombination events suggest potential sites for the Huntington's disease gene
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Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox,Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1991-07-01

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
1991-06-01

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
1991-05-01

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

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1992-02-01

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member
1992-02-01

Cloning of the essential myotonic dystrophy region and mapping of the putative defect
1992-02-06

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
1992-05

The Huntington's disease candidate region exhibits many different haplotypes
1992-11-01

Instability versus predictability: the molecular diagnosis of myotonic dystrophy
1992-02-01

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy
1992-03-01

An unstable triplet repeat in a gene related to myotonic muscular dystrophy
1992-05-01

Unstable DNA sequence in myotonic dystrophy
1992-03-01

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene
1992-06-01

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy
1992-12-01

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy
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Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy
1993-07-01

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.
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Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1
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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
1993-02-01

Brief report: reverse mutation in myotonic dystrophy

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