An Electroretinographic and Molecular Genetic Study of X-Linked Cone Degeneration
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference27 articles.
1. Cone dysfunction syndromes;Goodman;Arch. Ophthalmol.,1963
2. Progressive cone degeneration, dominantly inherited;Berson;Arch. Ophthalmol.,1968
3. Sex-difference in progressive cone dystrophy. I;Pinckers;Ophthalmic Paediatr. Genet.,1981
4. Sex-difference in progressive cone dystrophy. II;Pinckers;Ophthalmic Paediatr. Genet.,1981
5. Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus;Fleischman;Arch. Ophthalmol.,1983
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