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Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy

author

Giancarlo Deidda

Enzo Ricci

published in: American Journal of Human Genetics

date of publication: 1998-07-01

language: English

main subject: facioscapulohumeral muscular dystrophy

Cites articles 18

Date

Title

Authors

1996-10-01

The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region.
1996-05-01

Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD)
1996-12-01

Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1
1995-01-01

Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter
1995-01-01

The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter

Cisca Wijmenga
1995-01-01

Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35
1994-04-01

Position-effect variegation and the new biology of heterochromatin
1994-01-01

Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions.

Cisca Wijmenga
1994-08-01

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy.

Fiona Francis, Cisca Wijmenga
1994-07-01

4q35 molecular probes for the diagnosis and genetic counseling of facioscapulohumeral muscular dystrophy
1994-10-01

Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD)

Giancarlo Deidda, Andrea Novelletto, Cisca Wijmenga
1993

FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

George W. Padberg
1993-06

Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

Cisca Wijmenga
1993-05-01

No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markers

Suely K Marie, Mariz Vainzof, Maria Rita Passos-Bueno
1993-07-01

Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements

Cisca Wijmenga
1992-09

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

Cisca Wijmenga
1991-01-01

Diagnostic criteria for facioscapulohumeral muscular dystrophy
1988-02-11

A simple salting out procedure for extracting DNA from human nucleated cells

Article - wd:Q34386097

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