Literature DB >> 5297734

Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy.

A E Emery.   

Abstract

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Year:  1966        PMID： 5297734      PMCID： PMC1012908          DOI： 10.1136/jmg.3.2.92

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  5 in total

1.  Evidence for the absence of detectable linkage between the genes for Duchenne muscular dystrophy and the Xg blood group.

Authors:  J I CLARK; R H PUTTE; R MARCZYNSKI; J D MANN
Journal:  Am J Hum Genet       Date:  1963-09       Impact factor: 11.025

2.  Two families of benign sex-linked recessive muscular dystrophy.

Authors:  P E BECKER
Journal:  Rev Can Biol       Date:  1962 Sep-Dec

3.  Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance.

Authors:  V DUBOWITZ
Journal:  Brain       Date:  1960-09       Impact factor: 13.501

4.  [Myopathy and color blindness; analysis of a pedigree].

Authors:  J FREZAL; J DE GROUCHY; M LAMY; C POGNAN
Journal:  Ann Hum Genet       Date:  1957-03       Impact factor: 1.670

5.  On the classification, natural history and treatment of the myopathies.

Authors:  J N WALTON; F J NATTRASS
Journal:  Brain       Date:  1954       Impact factor: 13.501
  5 in total
  9 in total

1.  Distinction between Duchenne and other muscular dystrophies by ribosomal protein synthesis.

Authors:  V Ionasescu
Journal:  J Med Genet       Date:  1975-03       Impact factor: 6.318

2.  Family in which Duchenne's muscular dystrophy and protan colour blindness are segregating.

Authors:  D N Greig
Journal:  J Med Genet       Date:  1977-04       Impact factor: 6.318

Review 3.  [New data on the genetics and classification of muscular dystrophies].

Authors:  P E Becker
Journal:  Humangenetik       Date:  1972

4.  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

5.  Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness.

Authors:  R Skinner; C Smith; A E Emery
Journal:  J Med Genet       Date:  1974-12       Impact factor: 6.318

6.  X-linked scapuloperoneal syndrome.

Authors:  P K Thomas; D B Calne; C F Elliott
Journal:  J Neurol Neurosurg Psychiatry       Date:  1972-04       Impact factor: 10.154

Review 7.  Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.

Authors:  H Moser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  Linkage studies in a family with X-linked recessive ichthyosis employing a cloned DNA sequence from the distal short arm of the X chromosome.

Authors:  P Wieacker; K E Davies; B Mevorah; H H Ropers
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

9.  X-linked recessive type of pure spastic paraplegia in a large pedigree: absence of detectable linkage with Xg.

Authors:  M Zatz; C Penha-Serrano; P A Otto
Journal:  J Med Genet       Date:  1976-06       Impact factor: 6.318
  9 in total

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