Literature DB >> 2769721

Linkage analysis of French families with facioscapulohumeral muscular dystrophy.

G Lucotte1, S Berriche, M Fardeau.   

Abstract

Linkage analysis was undertaken in seven French families with facioscapulohumeral muscular dystrophy (FSHD). Six polymorphic DNA probes were studied, including random DNA sequences, coding sequences, and a hypervariable marker. No evidence for linkage of these probes to the disease was detected, and the results exclude probable location of the FSHD gene from three chromosomal regions (16p, proximal 19q, and 21q).

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Year:  1989        PMID： 2769721      PMCID： PMC1015667          DOI： 10.1136/jmg.26.8.485

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


  4 in total

1.  Linkage studies in facioscapulohumeral muscular dystrophy.

Authors:  G W Padberg; E C Klasen; W S Volkers; G G De Lange; A R Wintzen
Journal:  Muscle Nerve       Date:  1988-08       Impact factor: 3.217

2.  Linkage studies in autosomal dominant facioscapulohumeral muscular dystrophy.

Authors:  G Padberg; A W Eriksson; W S Volkers; L Bernini; E Van Loghem; P Meera Khan; L E Nijenhuis; J C Pronk; G M Schreuder
Journal:  J Neurol Sci       Date:  1984-09       Impact factor: 3.181

3.  Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

4.  [Birth and metamorphosis of Landouzy-Dejerine progressive atrophic myopathy].

Authors:  Y Sorrel-Dejerine; M Fardeau
Journal:  Rev Neurol (Paris)       Date:  1982       Impact factor: 2.607
  4 in total
  3 in total

1.  A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.

Authors:  M Upadhyaya; P W Lunt; M Sarfarazi; W Broadhead; J Daniels; M Owen; P S Harper
Journal:  J Med Genet       Date:  1991-10       Impact factor: 6.318

2.  A clinically homogeneous group of families with facioscapulohumeral (Landouzy-Déjérine) muscular dystrophy: linkage analysis of six autosomes.

Authors:  S J Jacobsen; E S Diala; B V Dorsey; M B Rising; R Graveline; K Falls; P Schultz; C Hogan; K Rediker; C D'Amico
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

3.  An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.

Authors:  M Sarfarazi; M Upadhyaya; G Padberg; M Pericak-Vance; T Siddique; G Lucotte; P Lunt
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318
  3 in total

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