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Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).

published in: American Journal of Human Genetics

date of publication: 1993-11-01

language: English

main subject: myotonic dystrophy

Cites articles 35

Date

Title

Authors

1993-06-01

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

Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy
1993-08-01

No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissues

Vera M. Kalscheuer
1993-06-01

Cheaters sometimes prosper: distortion of mendelian segregation by meiotic drive
1993-05-01

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

Jean-Pierre Rabès, Sandrine Luce
1993-04-01

Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.
1993-02-01

Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.

Ian Macdonald
1993-02-01

Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission.
1993-02-01

Brief report: reverse mutation in myotonic dystrophy

Gert Jansen
1992-05-01

Fragile-X syndrome: unique genetics of the heritable unstable element

Eric J Kremer
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
1992-11-01

Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation

Jean-Louis Mandel
1992-11-01

Presymptomatic diagnosis of myotonic dystrophy

Gert Jansen
1992-11-01

The correlation of age of onset with CTG trinucleotide repeat amplification in myotonic dystrophy
1992-11-01

Minimal expression of myotonic dystrophy: a clinical and molecular analysis
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
1992-02-01

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
1992-06-01

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy
1992-07-01

Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs

Gert Jansen, Wiljan Hendriks
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

Gert Jansen
1992-05-01

Unstable DNA sequence in myotonic dystrophy

John David Brook
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
1991-10-01

Myotonic dystrophy. Predictive value of normal results on clinical examination.
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

Antonio Pizzuti
1990-05-01

Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada)
1989-06-01

Anticipation in myotonic dystrophy: fact or fiction?
1989-10-01

Genomic imprinting and genetic disorders in man.

Wolf Reik
1989-03-01

Criteria for establishing the validity of genetic recombination in myotonic dystrophy

Article - wd:Q35194760

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