Literature DB >> 6139558

Localisation of gene for Becker muscular dystrophy.

H M Kingston, P S Harper, P L Pearson, K E Davies, R Williamson, D Page.   

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Year:  1983        PMID： 6139558     DOI： 10.1016/s0140-6736(83)91252-7

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  15 in total

1.  Becker muscular dystrophy: correlation of deletion type with clinical severity.

Authors:  A M Norman; N S Thomas; H M Kingston; P S Harper
Journal:  J Med Genet       Date:  1990-04       Impact factor: 6.318

2.  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

3.  Isolation of the gene for Duchenne muscular dystrophy.

Authors:  D N Singh
Journal:  Indian J Pediatr       Date:  1988 Mar-Apr       Impact factor: 1.967

4.  Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies.

Authors:  M Claustres; S Tuffery; M P Chevron; M P Jozelon; P Martinez; B Echenne; J Demaille
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

5.  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

6.  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

7.  Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation.

Authors:  C Ingle; R Williamson; A de la Chapelle; R R Herva; K Haapala; G Bates; H F Willard; P Pearson; K E Davies
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

Review 8.  Prenatal diagnosis of Duchenne muscular dystrophy: a three-year experience in a rapidly evolving field.

Authors:  E Bakker; E J Bonten; H Veenema; J T den Dunnen; P M Grootscholten; G J van Ommen; P L Pearson
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

9.  Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus.

Authors:  J A Towbin; D R Wu; J Chamberlain; P D Larsen; W K Seltzer; E R McCabe
Journal:  Hum Genet       Date:  1989-09       Impact factor: 4.132

10.  Human X chromosome markers and Duchenne muscular dystrophy.

Authors:  K E Davies; A Speer; F Herrmann; A W Spiegler; S McGlade; M H Hofker; P Briand; R Hanke; M Schwartz; V Steinbicker
Journal:  Nucleic Acids Res       Date:  1985-05-24       Impact factor: 16.971
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