Literature DB >> 2993158

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

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.   

Abstract

The inheritance of seven restriction fragment length polymorphisms detected by DNA probes has been studied in families with Duchenne and Becker muscular dystrophies (DMD and BMD). The probes used have all been mapped to the short arm of the X-chromosome, four being distal and three proximal to the disease loci located within the Xp21 region. Linkage analysis of the DNA polymorphisms in relation to the two disorders showed similar genetic distances. Data obtained from DMD and BMD families have been combined to give more precise values for the different recombination fractions. Combined use of these polymorphic DNA markers will be of practical value in the genetic counselling of women at risk for Duchenne and Becker muscular dystrophy.

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Year:  1985        PMID: 2993158     DOI: 10.1007/bf00295671

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


  19 in total

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Journal:  Nucleic Acids Res       Date:  1982-03-11       Impact factor: 16.971

5.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1984-02       Impact factor: 3.365

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Authors:  R G Worton; C Duff; J E Sylvester; R D Schmickel; H F Willard
Journal:  Science       Date:  1984-06-29       Impact factor: 47.728

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

8.  Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophy.

Authors:  M E Pembrey; K E Davies; R M Winter; R G Elles; R Williamson; T A Fazzone; C Walker
Journal:  Arch Dis Child       Date:  1984-03       Impact factor: 3.791

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

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Authors:  K E Davies; B D Young; R G Elles; M E Hill; R Williamson
Journal:  Nature       Date:  1981-10-01       Impact factor: 49.962

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  24 in total

1.  Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening.

Authors:  A M Norman; M Upadhyaya; N S Thomas; K Roberts; P S Harper
Journal:  J Med Genet       Date:  1989-09       Impact factor: 6.318

2.  A manifesting carrier of Duchenne muscular dystrophy with severe myocardial symptoms.

Authors:  K Kamakura; M Kawai; K Arahata; H Koizumi; K Watanabe; H Sugita
Journal:  J Neurol       Date:  1990-12       Impact factor: 4.849

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

Authors:  N S Thomas; H Williams; L J Elsas; L C Hopkins; M Sarfarazi; P S Harper
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

4.  Detection of Duchenne muscular dystrophy carriers by dosage analysis using the DMD cDNA clone 8.

Authors:  Y P Mao; M Cremer
Journal:  Hum Genet       Date:  1989-01       Impact factor: 4.132

5.  Molecular deletion patterns in Duchenne and Becker type muscular dystrophy.

Authors:  S Liechti-Gallati; M Koenig; L M Kunkel; D Frey; E Boltshauser; V Schneider; S Braga; H Moser
Journal:  Hum Genet       Date:  1989-03       Impact factor: 4.132

6.  Linkage analysis of X linked retinitis pigmentosa in the Irish population.

Authors:  G J Farrar; M T Geraghty; J M Moloney; D J McConnell; P Humphries
Journal:  J Med Genet       Date:  1988-04       Impact factor: 6.318

7.  A multipoint linkage analysis program for X-linked disorders, with the example of Duchenne muscular dystrophy and seven DNA probes.

Authors:  J Clayton
Journal:  Hum Genet       Date:  1986-05       Impact factor: 4.132

8.  The use of flanking markers in prediction for Duchenne muscular dystrophy.

Authors:  H Williams; M Sarfarazi; C Brown; N Thomas; P S Harper
Journal:  Arch Dis Child       Date:  1986-03       Impact factor: 3.791

9.  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

10.  DNA linkage analysis of X-linked retinoschisis.

Authors:  N Dahl; P Goonewardena; J Chotai; M Anvret; U Pettersson
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

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