Literature DB >> 3100805

Localisation of the gene for Emery-Dreifuss muscular dystrophy to the distal long arm of the X chromosome.

N S Thomas, H Williams, L J Elsas, L C Hopkins, M Sarfarazi, P S Harper.   

Abstract

The linkage relationships of the gene for Emery-Dreifuss muscular dystrophy have been analysed in a large American kindred using DNA probes from different regions of the X chromosome. Close linkage was found with the locus for factor VIII, with no recombinants in 12 opportunities (maximum lod score 4.3), and with locus DXS15 (two recombinants in 17 opportunities, maximum lod score 2.9 at 0 = 10 cM). No linkage was found with probes pERT87 and 754, which are closely linked to Duchenne and Becker muscular dystrophies at Xp21. These results confirm a separate localisation on the distal part of the long arm at q27-28 for Emery-Dreifuss muscular dystrophy and should provide the basis for prenatal diagnosis and improved carrier detection in this disorder if the linkage is confirmed to be close.

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Year:  1986        PMID: 3100805      PMCID: PMC1049843          DOI: 10.1136/jmg.23.6.596

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


  9 in total

1.  Survival in x-chromosomal muscular dystrophy.

Authors:  F E DREIFUSS; G R HOGAN
Journal:  Neurology       Date:  1961-08       Impact factor: 9.910

2.  Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

Authors:  L M Kunkel; K D Smith; S H Boyer; D S Borgaonkar; S S Wachtel; O J Miller; W R Breg; H W Jones; J M Rary
Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

3.  Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness.

Authors:  R Skinner; C Smith; A E Emery
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

4.  Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.

Authors:  J Ott
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

5.  Unusual type of benign x-linked muscular dystrophy.

Authors:  A E Emery; F E Dreifuss
Journal:  J Neurol Neurosurg Psychiatry       Date:  1966-08       Impact factor: 10.154

6.  Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.

Authors:  H M Kingston; N S Thomas; P L Pearson; M Sarfarazi; P S Harper
Journal:  J Med Genet       Date:  1983-08       Impact factor: 6.318

7.  Emery-dreifuss humeroperoneal muscular dystrophy: an x-linked myopathy with unusual contractures and bradycardia.

Authors:  L C Hopkins; J A Jackson; L J Elsas
Journal:  Ann Neurol       Date:  1981-09       Impact factor: 10.422

8.  Application of benefit-to-cost analysis to an X-linked recessive cardiac and humeroperoneal neuromuscular disease.

Authors:  M L Wright; L J Elsas
Journal:  Am J Med Genet       Date:  1980

9.  Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy.

Authors:  C S Brown; N S Thomas; M Sarfarazi; K E Davies; L Kunkel; P L Pearson; H M Kingston; D J Shaw; P S Harper
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

  9 in total
  13 in total

1.  Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.

Authors:  J R Yates; N A Affara; D M Jamieson; M A Ferguson-Smith; I Hausmanowa-Petrusewicz; J Zaremba; J Borkowska; A W Johnston; K Kelly
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

2.  Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosome.

Authors:  N Knoers; H van der Heyden; B A van Oost; H H Ropers; L Monnens; J Willems
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

Review 3.  Diagnosis of genetic disease using recombinant DNA. Supplement.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

4.  Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.

Authors:  J R Yates; J P Warner; J A Smith; F Deymeer; J P Azulay; I Hausmanowa-Petrusewicz; J Zaremba; J Borkowska; N A Affara; M A Ferguson-Smith
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

5.  Mapping of the Emery-Dreifuss gene through reconstruction of crossover points in two Italian pedigrees.

Authors:  G Romeo; L Roncuzzi; S Sangiorgi; M Giacanelli; M Liguori; D Tessarolo; M Rocchi
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

6.  Gene deletions in X-linked muscular dystrophy.

Authors:  M Lindlöf; A Kiuru; H Kääriäinen; H Kalimo; H Lang; H Pihko; J Rapola; H Somer; M Somer; M L Savontaus
Journal:  Am J Hum Genet       Date:  1989-04       Impact factor: 11.025

Review 7.  Molecular analysis of muscular dystrophy.

Authors:  K E Davies; S J Kenwrick; M N Patterson; T J Smith; S M Forrest; H R Dorkins; G S Cross; S B England
Journal:  J Muscle Res Cell Motil       Date:  1988-02       Impact factor: 2.698

8.  Frequent alterations of visual pigment genes in adrenoleukodystrophy.

Authors:  P R Aubourg; G H Sack; H W Moser
Journal:  Am J Hum Genet       Date:  1988-03       Impact factor: 11.025

9.  Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.

Authors:  P Saviranta; M Lindlöf; A E Lehesjoki; H Kalimo; H Lang; V Sonninen; M L Savontaus; A de la Chapelle
Journal:  Am J Hum Genet       Date:  1988-01       Impact factor: 11.025

Review 10.  Emery-Dreifuss syndrome.

Authors:  A E Emery
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

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