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Logo of procrsmedFormerly medchtJournal of the Royal Society of MedicineProceedings of the Royal Society of Medicine
 
Proc R Soc Med. 1971 February; 64(2): 181–184.
PMCID: PMC1812441

Genetic factors in neurological disease. Clinical aspects.

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Full text is available as a scanned copy of the original print version. Get a printable copy (PDF file) of the complete article (625K), or click on a page image below to browse page by page. Links to PubMed are also available for Selected References.

Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • CHANDLER JH, REED TE, DEJONG RN. Huntington's chorea in Michigan. III. Clinical observations. Neurology. 1960 Feb;10:148–153. [PubMed]
  • HEATHFIELD KW, MILLER AB. A FAMILY SHOWING BOTH DYSTROPHIA MYOTONICA AND SPASTIC PARAPLEGIA. Neurology. 1965 May;15:481–485. [PubMed]
  • Stevens D, Parsonage M. Mutation in Huntington's chorea. J Neurol Neurosurg Psychiatry. 1969 Apr;32(2):140–143. [PMC free article] [PubMed]
  • WALTON JN, NATTRASS FJ. On the classification, natural history and treatment of the myopathies. Brain. 1954;77(2):169–231. [PubMed]
  • Warrier CB, Pillai TD. Familial myasthenia gravis. Br Med J. 1967 Sep 30;3(5569):839–840. [PMC free article] [PubMed]

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