Literature DB >> 4829421

Detection of heterozygotes for myotonic dystrophy.

S Bundey.   

Abstract

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Year:  1974        PMID： 4829421     DOI： 10.1111/j.1399-0004.1974.tb01669.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  5 in total

1.  Congenital myotonic dystrophy in Britain. II. Genetic basis.

Authors:  P S Harper
Journal:  Arch Dis Child       Date:  1975-07       Impact factor: 3.791

2.  Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q.

Authors:  H G Harley; K V Walsh; S Rundle; J D Brook; M Sarfarazi; M C Koch; J L Floyd; P S Harper; D J Shaw
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

3.  Myotonic dystrophy--early detection and genetic counselling.

Authors:  T Schubert; F Jerusalem; A C Martenet; M Metaxas; M Meyer
Journal:  J Neurol       Date:  1980       Impact factor: 4.849

4.  Myotonic dystrophy- early detection and genetic counselling by T. Schubert et al.

Authors:  S Bundey
Journal:  J Neurol       Date:  1982       Impact factor: 4.849

5.  Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy.

Authors:  K V Walsh; H G Harley; J D Brook; S A Rundle; M Sarfarazi; P S Harper; D J Shaw
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132
  5 in total

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