Linkage analysis in spinopontine atrophy: Correlation or HLA linkage with phenotypic findings in hereditary ataxia-Reference-Cited by-同舟云学术

Linkage analysis in spinopontine atrophy: Correlation or HLA linkage with phenotypic findings in hereditary ataxia

Published:1987-07 Issue:3 Volume:27 Page:595-602
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bale Allen E.,Bale Sherri J.,Schlesinger Sandra L.,McFarland Henry F.,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics (clinical)

Reference32 articles.

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2. Spino-Pontine Degeneration

3. (1984): A classification for ataxia. In (eds): “The Olivopontocerchellar Atrophies” New York: Raven Press, pp 1-4.

4. (1984): An apology and an introduction to the olivopontocerebellar atrophies. In (eds): “The Olivopontocerebellar Atrophies.” New York: Raven Press, pp 5-12.

5. (1954): “The Spino-Cerebellar Degenerations.” Springfield, Illinois: Charles C. Thomas, pp 19-20.

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1. Autosomal dominant cerebellar ataxia with retinal degeneration;Neurology;1994-08

2. A 17th-century founder gives rise to a large North American pedigree of autosomal dominant spinocerebellar ataxia not linked to the SCA1 locus on chromosome 6;Neurology;1992-11-01

3. Classification and Epidemiology of Cerebellar Degenerations;Foundations of Neurology;1992

4. Dominant Olivopontocerebellar Atrophy Mapping to Human Chromosome 6p;Foundations of Neurology;1992

5. Late onset autosomal dominant cerebellar ataxia a family description and linkage analysis with the hla system;Arquivos de Neuro-Psiquiatria;1991-09