Diagnostic value of ophthalmologic findings in myotonic dystrophy: Comparison with risks calculated by haplotype analysis of closely linked restriction fragment length polymorphisms-Reference-Cited by-同舟云学术

Diagnostic value of ophthalmologic findings in myotonic dystrophy: Comparison with risks calculated by haplotype analysis of closely linked restriction fragment length polymorphisms

Published:1992-01-01 Issue:1 Volume:42 Page:55-60
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Ashizawa T.,Hejtmancik J. F.,Liu J.,Perryman M. B.,Epstein H. F.,Koch D. D.

Publisher

Wiley

Subject

Genetics(clinical)

Reference28 articles.

1. Potassium channel blockers and impulse propagation in murine motor endplate disease

2. (1991) Myotonic dystrophy-the search for the gene: progress, strategies and prospects. In (ed), “Current Neurology”. Chicago, Year Book Medical Publishers, pp 27-62.

3. Early recognition of heterozygotes for the gene for dystrophia myotonica

4. Ocular Changes in Myotonic Dystrophy

5. Über familiäre atrophische Myotonie

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