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Neuroradiology|April 20, 2000
MRI of the intraorbital optic nerve in patients with autosomal dominant optic atrophyM Votruba, S Leary, N Losseff, et al.Gene Therapy|January 1, 1994
Progressive retinal atrophy: a model for retinitis pigmentosa in companion animalsD R Sargan, P J Clements, A Sohal, et al.The British Journal of Ophthalmology|January 20, 1999
New model of conjunctival scarring in the mouse eyeM B Reichel, M F Cordeiro, R A Alexander, et al.Human Mutation|April 3, 1999
Severe autosomal dominant retinitis pigmentosa caused by a novel rhodopsin mutation (Ter349Glu). Mutations in brief no. 208. OnlineD A Bessant, S Khaliq, A Hameed, et al.American Journal of Human Genetics|May 23, 1998
A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32D A Bessant, S Khaliq, A Hameed, et al.Investigative Ophthalmology & Visual Science|August 31, 2001
Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreousS Khaliq, A Hameed, M Ismail, et al.Journal of Medical Genetics|August 1, 1990
Linkage studies and deletion screening in choroideremiaA F Wright, R L Nussbaum, S S Bhattacharya, et al.Investigative Ophthalmology & Visual Science|July 13, 2000
Evidence for a new locus for X-linked retinitis pigmentosa (RP23)A J Hardcastle, D L Thiselton, I Zito, et al.Molecular Cell|August 14, 1998
GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophyI Sokal, N Li, I Surgucheva, et al.The British Journal of Ophthalmology|January 25, 2005
Posterior polar cataract is the predominant consequence of a recurrent mutation in the PITX3 geneP K F Addison, V Berry, A C W Ionides, et al.Pageof 37