Literature DB >> 6086495

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences.

H M Kingston, M Sarfarazi, N S Thomas, P S Harper.   

Abstract

A linkage study in 30 Becker muscular dystrophy (BMD) kindreds using three cloned DNA sequences from the X chromosome which demonstrate restriction fragment length polymorphisms (RFLPs), suggests that the BMD gene is located on the short arm of the X chromosome, in the p21 region. The genes for Becker and Duchenne dystrophies must therefore be closely linked, if not allelic, and any future DNA probes found to be of practical use in one disorder should be equally applicable to the other. The linkage analysis also provides data on the frequency of recombination along the short arm of the X chromosome, and across the centromeric region.

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Year:  1984        PMID: 6086495     DOI: 10.1007/bf00270551

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


  21 in total

1.  Extensions to pedigree analysis I. Likehood calculations for simple and complex pedigrees.

Authors:  K Lange; R C Elston
Journal:  Hum Hered       Date:  1975       Impact factor: 0.444

2.  [A new x-chromosomal muscular dystrophy].

Authors:  P E BECKER; F KIENER
Journal:  Arch Psychiatr Nervenkr Z Gesamte Neurol Psychiatr       Date:  1955

3.  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

4.  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

5.  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

6.  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

7.  The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups.

Authors:  A E Emery; C A Smith; R Sanger
Journal:  Ann Hum Genet       Date:  1969-01       Impact factor: 1.670

8.  Mild and severe forms of X-linked muscular dystrophy.

Authors:  R F Shaw; F E Dreifuss
Journal:  Arch Neurol       Date:  1969-05

9.  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

10.  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

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  36 in total

1.  [Computer experience and further developments in the respiratory function laboratory (author's transl)].

Authors:  R Schindl; K Mayer; K Aigner
Journal:  Med Klin       Date:  1975-11-07

Review 2.  Genetic and clinical correlations of Xp21 muscular dystrophy.

Authors:  K M Bushby
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

3.  2004 William Allan Award address. Cloning of the DMD gene.

Authors:  Louis M Kunkel
Journal:  Am J Hum Genet       Date:  2005-02       Impact factor: 11.025

4.  Phenotypic heterogeneity and the single gene.

Authors:  G K Suthers; K E Davies
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

Review 5.  Medical genetics.

Authors:  M Super
Journal:  Postgrad Med J       Date:  1991-07       Impact factor: 2.401

Review 6.  Improved diagnosis of Duchenne/Becker muscular dystrophy.

Authors:  A H Beggs; L M Kunkel
Journal:  J Clin Invest       Date:  1990-03       Impact factor: 14.808

7.  DNA markers in primate models of human disease.

Authors:  J E Hixson
Journal:  Genetica       Date:  1987-08-31       Impact factor: 1.082

8.  A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional information.

Authors:  M Sarfarazi; H Williams
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

9.  Isolating the gene for Duchenne muscular dystrophy.

Authors:  P S Harper
Journal:  Br Med J (Clin Res Ed)       Date:  1986-09-27

10.  Dystrophin immunohistochemistry in a symptomatic carrier of Becker muscular dystrophy.

Authors:  K Haginoya; K Yamamoto; K Iinuma; T Yanagisawa; Y Ichinohasama; M Shimmoto; Y Suzuki; K Tada
Journal:  J Neurol       Date:  1991-10       Impact factor: 4.849

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