Inventaire - your friends and communities are your best library - Inventaire

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

Author

Russell G. Snell

James F. Gusella

published in: Nature Genetics

date of publication: 1993-08-01

language: English

main subject: Huntington's disease

Bibliographic databases:

Cites articles 14

Date

Title

Authors

1981-10-01

Factors influencing age at onset and duration of survival in Huntington's chorea
1983-07-01

Huntington's Chorea in the Netherlands The problem of genetic heterogeneity
1983-01-01

Maternal transmission in Huntington's disease

, ,
1984-05-01

The natural history of Huntington disease: possible role of "aging genes".
1984-05-01

Parental transmission in Huntington's disease
1989-11-01

Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene
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

, ,
1991-07-01

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
1991-04-01

Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting
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
1992-02-06

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy
1992-02-01

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy
1993-03

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
1993-07-01

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

Article -

Welcome to inventaire

The library of your friends and communities

you are offline