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

Published in: Nature Genetics

Date of publication: 1992-06-01

Language: anglais

Main subject: maladie congénitale

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Cites articles 17

Date

Title

Authors

1960-10-01

Dystrophia myotonica in childhood
1975-07-01

Congenital myotonic dystrophy in Britain. I. Clinical aspects
1975-07-01

Congenital myotonic dystrophy in Britain. II. Genetic basis
1978-10-01

Incidence, severity, and time-course of motoneurone dysfunction in myotonic dystrophy: their significance for an understanding of anticipation
1989-06-01

Anticipation in myotonic dystrophy: fact or fiction?
1989-03-01

Criteria for establishing the validity of genetic recombination in myotonic dystrophy
1990-05-01

Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada)
1991-12-20

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
1991-04-18

Structure and function of telomeres
1991-05-01

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
1991-05-01

Fragile X genotype characterized by an unstable region of DNA.
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
1992-03-01

An unstable triplet repeat in a gene related to myotonic muscular dystrophy
1992-03-01

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

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