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Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent.

author

Darren G Monckton

published in: American Journal of Human Genetics

date of publication: 1995-01-01

language: English

main subject: myotonic dystrophy

Cites articles 32

Date

Title

Authors

1994-01-01

Myotonic dystrophy reviewed: back to the future?
1994-03-01

Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins

Xavier Estivill i Pallejà
1994-03-01

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy
1994-01-01

Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes.
1994-04-01

Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm

Gert Jansen
1994-02-01

Complex gene conversion events in germline mutation at human minisatellites

Darren G Monckton, John A.L. Armour
1994-01-01

Effects of the sex of myotonic dystrophy patients on the unstable triplet repeat in their affected offspring
1994-03-01

CTG trinucleotide repeat variability in identical twins with myotonic dystrophy

Adolfo López de Munain
1993-06-01

Negative expansion of the myotonic dystrophy unstable sequence
1993-06-01

Mitotic stability of fragile X mutations in differentiated cells indicates early post-conceptional trinucleotide repeat expansion.
1993-12-01

Somatic instability of CTG repeat in myotonic dystrophy
1993-05-01

Myotonic dystrophy: size- and sex-dependent dynamics of CTG meiotic instability, and somatic mosaicism

Jean-Pierre Rabès, Sandrine Luce
1993-06-01

The full mutation in the FMR-1 gene of male fragile X patients is absent in their sperm.
1993-01-01

Explanation for exclusive maternal origin for congenital form of myotonic dystrophy

Grant R Sutherland
1993-01-01

Different sex-dependent constraints in CTG length variation as explanation for congenital myotonic dystrophy

Jean-Pierre Rabès
1993-02-01

Brief report: reverse mutation in myotonic dystrophy

Gert Jansen
1993-09-01

Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy
1992-07-01

Anticipation in myotonic dystrophy: new light on an old problem
1992-04-01

Methylation and mutation patterns in the fragile X syndrome
1992-03-01

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

Antonio Pizzuti
1992-03-01

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

Gert Jansen
1992-09-01

Dynamic mutations: a new class of mutations causing human disease
1992-10-01

Anticipation in myotonic dystrophy. I. Statistical verification based on clinical and haplotype findings
1992-02-01

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

Gert Jansen
1992-02-06

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

John David Brook
1992-09-01

Phenotypic expression of the myotonic dystrophy gene in monozygotic twins
1992-02-01

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

Gert Jansen
1992-05-01

Unstable DNA sequence in myotonic dystrophy

John David Brook
1992-04-01

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

Didier Devys
1992-10-01

Anticipation in myotonic dystrophy. II. Complex relationships between clinical findings and structure of the GCT repeat
1992-10-01

Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype

Robert Winqvist

Article - wd:Q35643691

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