Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1966 Jun;3(2):92–95. doi: 10.1136/jmg.3.2.92

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

A E Emery
PMCID: PMC1012908  PMID: 5297734

Full text

PDF
92

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BECKER P. E. Two families of benign sex-linked recessive muscular dystrophy. Rev Can Biol. 1962 Sep-Dec;21:551–566. [PubMed] [Google Scholar]
  2. CLARK J. I., PUTTE R. H., MARCZYNSKI R., MANN J. D. Evidence for the absence of detectable linkage between the genes for Duchenne muscular dystrophy and the Xg blood group. Am J Hum Genet. 1963 Sep;15:292–297. [PMC free article] [PubMed] [Google Scholar]
  3. DUBOWITZ V. Progressive muscular dystrophy of the Duchenne type in females and its mode of inheritance. Brain. 1960 Sep;83:432–439. doi: 10.1093/brain/83.3.432. [DOI] [PubMed] [Google Scholar]
  4. FREZAL J., DE GROUCHY J., LAMY M., POGNAN C. Myopathie et daltonisme; analyse d'un pedigree. Ann Hum Genet. 1957 Mar;21(3):237–243. doi: 10.1111/j.1469-1809.1972.tb00285.x. [DOI] [PubMed] [Google Scholar]
  5. WALTON J. N., NATTRASS F. J. On the classification, natural history and treatment of the myopathies. Brain. 1954;77(2):169–231. doi: 10.1093/brain/77.2.169. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES