Primary vitreoretinal dysplasia resembling Norrie's disease in a female: association with X autosome chromosomal translocation.-Reference-Cited by-同舟云学术

Primary vitreoretinal dysplasia resembling Norrie's disease in a female: association with X autosome chromosomal translocation.

Published:1986-01-01 Issue:1 Volume:70 Page:64-71
ISSN:0007-1161
Container-title:British Journal of Ophthalmology
language:en
Short-container-title:British Journal of Ophthalmology

Author:

Ohba N.,Yamashita T.

Publisher

BMJ

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Reference15 articles.

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3. Clinical and histopathologic classification of retinal dysplasia;Lahav, M.; Albert, D.M.; Wyand, S.;Am J Ophthalmol,1973

4. Retinal malformations. Aetiological heterogeneity and morphological similarity in congenital retinal nonattachment and falciform folds;Warburg, M.;Br J Ophthalmol,1979

5. Primary vitreoretinal dysplasia transmitted as an autosomal recessive disorder;Ohba, N.; Watanabe, S.; Fujita, S.;BrJ Ophthalmol,1981

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