Literature DB >> 3026946

Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers.

E Wilichowski, M Krawczak, E Seemanova, F Hanefeld, J Schmidtke.   

Abstract

A set of nine polymorphic loci defined by DNA probes was studied for linkage with the disease locus in ten families with a history of Duchenne muscular dystrophy (DMD), and three families with a history of Becker muscular dystrophy (BMD). The results confirm DMD and BMD linkage to all marker loci and suggest closer linkage of several probes than hitherto detected. This will be of practical interest for risk calculations in affected families.

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Year:  1987        PMID: 3026946     DOI: 10.1007/BF00273835

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  28 in total

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Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

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Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

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Journal:  Nucleic Acids Res       Date:  1985-01-11       Impact factor: 16.971

7.  Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy.

Authors:  D E Wilcox; N A Affara; J R Yates; M A Ferguson-Smith; P L Pearson
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9).

Authors:  S Fadda; M Mochi; L Roncuzzi; S Sangiorgi; D Sbarra; M Zatz; G Romeo
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

9.  Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families.

Authors:  H Dorkins; C Junien; J L Mandel; K Wrogemann; J P Moison; M Martinez; J M Old; S Bundey; M Schwartz; N Carpenter
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  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

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  5 in total

1.  Linkage relationship between retinoschisis and four marker loci.

Authors:  G Gellert; J Peterson; M Krawczak; B Zoll
Journal:  Hum Genet       Date:  1988-08       Impact factor: 4.132

2.  Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome.

Authors:  R A Lewis
Journal:  Trans Am Ophthalmol Soc       Date:  1989

3.  Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 beta.

Authors:  G de Saint Basile; L D Notarangelo; C Bonaiti-Pellié; M Doussau; O Prolini; I W Craig; A Ugazio; C Griscelli; A Fischer
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

4.  Linkage relationship of X-linked juvenile retinoschisis with Xp22.1-p22.3 probes.

Authors:  P A Sieving; E L Bingham; M S Roth; M R Young; M Boehnke; C Y Kuo; D Ginsburg
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025

5.  X linked spondyloepiphyseal dysplasia: a clinical, radiological, and molecular study of a large kindred.

Authors:  J J MacKenzie; J Fitzpatrick; P Babyn; G B Ferrero; A Ballabio; G Billingsley; D E Bulman; P Strasberg; P N Ray; T Costa
Journal:  J Med Genet       Date:  1996-10       Impact factor: 6.318

  5 in total

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