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Ophthalmic Genetics|March 18, 2006
A G1103R mutation in CRB1 is co-inherited with high hyperopia and Leber congenital amaurosisH Abouzeid, Y Li, I H Maumenee, et al.Ophthalmology|January 1, 1986
Fundus flavimaculatus without maculopathy. A clinicopathologic studyP J McDonnell, J D Kivlin, I H Maumenee, et al.American Journal of Medical Genetics|January 15, 1992
Mitochondrial DNA mutation and heteroplasmy in type I Leber hereditary optic neuropathyD P Zhu, E P Economou, S E Antonarakis, et al.Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1995
Effects of strabismus surgery on refraction in childrenD Denis, J Bardot, F Volot, et al.American Journal of Human Genetics|February 11, 1999
Congenital motor nystagmus linked to Xq26-q27J B Kerrison, M R Vagefi, M M Barmada, et al.American Journal of Human Genetics|November 1, 1983
Linkage analysis in dominant optic atrophyJ D Kivlin, E W Lovrien, D T Bishop, et al.The British Journal of Ophthalmology|June 1, 1981
Prevalence of map-dot-fingerprint changes in the corneaT P Werblin, L W Hirst, W J Stark, et al.American Journal of Ophthalmology|August 15, 1986
Ocular features of the Hagberg-Santavuori syndromeJ B Bateman, M PhilippartArchives of Ophthalmology (Chicago, Ill. : 1960)|March 1, 1985
Spondyloepiphyseal dysplasia congenita. Light and electron microscopic studies of the eyeT G Murray, W R Green, I H Maumenee, et al.Ophthalmic Genetics|April 26, 2000
Microfibril abnormalities of the lens capsule in patients with Marfan syndrome and ectopia lentisE I Traboulsi, J A Whittum-Hudson, S H Mir, et al.Pageof 17