Literature DB >> 15403126

A pedigree of hereditary progressive muscular dystrophy.

J W BOYES, F C FRASER.   

Abstract

Entities:  

Keywords:  DYSTROPHY

Mesh:

Year:  1949        PMID: 15403126     DOI: 10.1111/j.1469-1809.1949.tb02421.x

Source DB:  PubMed          Journal:  Ann Eugen


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  4 in total

1.  Muscular dystrophy occurring in identical twins.

Authors:  A G BECKETT
Journal:  Br Med J       Date:  1955-02-12

2.  A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.

Authors:  M Upadhyaya; P W Lunt; M Sarfarazi; W Broadhead; J Daniels; M Owen; P S Harper
Journal:  J Med Genet       Date:  1991-10       Impact factor: 6.318

3.  Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias.

Authors:  P W Lunt; D A Compston; P S Harper
Journal:  J Med Genet       Date:  1989-12       Impact factor: 6.318

4.  A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probes.

Authors:  M Upadhyaya; M Sarfarazi; P W Lunt; W Broadhead; P S Harper
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

  4 in total

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