Literature DB >> 2993155

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

S Fadda, M Mochi, L Roncuzzi, S Sangiorgi, D Sbarra, M Zatz, G Romeo.   

Abstract

A study of linkage between Becker muscular dystrophy and four X chromosome-specific DNA polymorphisms in 17 kindreds has indicated that this gene is located in Xp, as already anticipated by single pedigree analysis. In particular the DXS43 and DXS9 loci, identified by probes D2 and RC8, respectively, are closely linked to each other and are both located at approximately 15 cM from the Becker locus. These linkage data, together with the previously established linkage between Becker and the DXS7 locus identified by probe L 1.28, indicate that the Becker gene is located in the same region where Duchenne has been mapped and also yield information about relative genetic distances among different DNA polymorphisms of the X chromosome.

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Year:  1985        PMID： 2993155     DOI： 10.1007/bf00295664

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


  16 in total

1.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

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.  New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups.

Authors:  M Zatz; S B Itskan; R Sanger; O Frota-Pessoa; P H Saldanha
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

4.  Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes.

Authors:  D Page; B de Martinville; D Barker; A Wyman; R White; U Francke; D Botstein
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

5.  A strategy to reveal high-frequency RFLPs along the human X chromosome.

Authors:  J Aldridge; L Kunkel; G Bruns; U Tantravahi; M Lalande; T Brewster; E Moreau; M Wilson; W Bromley; T Roderick
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

6.  Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

Authors:  D Drayna; K Davies; D Hartley; J L Mandel; G Camerino; R Williamson; R White
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

7.  Clinical trial in Duchenne dystrophy. I. The design of the protocol.

Authors:  M H Brooke; R C Griggs; J R Mendell; G M Fenichel; J B Shumate; R J Pellegrino
Journal:  Muscle Nerve       Date:  1981 May-Jun       Impact factor: 3.217

8.  Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids.

Authors:  L Roncuzzi; S Fadda; M Mochi; L Prosperi; S Sangiorgi; R Santamaria; D Sbarra; D Besana; L Morandi; M Rocchi
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025

9.  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

10.  Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome.

Authors:  C Verellen-Dumoulin; M Freund; R De Meyer; C Laterre; J Frédéric; M W Thompson; V D Markovic; R G Worton
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
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  7 in total

1.  Italian experience regarding the prevention of Duchenne and Becker muscular dystrophies.

Authors:  G Romeo; M Devoto; N Archidiacono; A Ferlini; L Roncuzzi; M A Melis; E Paderi; M Ferrari; S Tedeschi; G Galluzzi
Journal:  Eur J Pediatr       Date:  1988-05       Impact factor: 3.183

2.  Sporadic cases in Duchenne muscular dystrophy. A reappraisal through segregation analysis on 988 sibships.

Authors:  A Russo; G Barbujani; M L Mostacciuolo; F H Herrmann; A W Spiegler; G Galluzzi; G A Danieli
Journal:  Hum Genet       Date:  1987-07       Impact factor: 4.132

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

Authors:  E Wilichowski; M Krawczak; E Seemanova; F Hanefeld; J Schmidtke
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

Review 4.  Diagnosis of genetic disease using recombinant DNA.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1986-05       Impact factor: 4.132

5.  Atypical form of X-linked proximal pseudohypertrophic muscular dystrophy.

Authors:  A W Spiegler; I Hausmanowa-Petrusewicz; J Borkowska; F H Herrmann
Journal:  J Neurol       Date:  1987-04       Impact factor: 4.849

6.  Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.

Authors:  M W Thompson; P N Ray; B Belfall; C Duff; C Logan; I Oss; R G Worton
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

7.  Population data on benign and severe forms of X-linked muscular dystrophy.

Authors:  M L Mostacciuolo; A Lombardi; V Cambissa; G A Danieli; C Angelini
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132
  7 in total

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