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

auteur

G Deidda

Enzo Ricci

gepubliceerd in: American Journal of Human Genetics

publicatiedatum: 1998-07-01

taal: Engels

belangrijk thema: facioscapulohumerale dystrofie

Cites articles 18

Date

Titel

Auteurs

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)

G 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

G.W.A.M. 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

Artike - wd:Q34386097

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