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Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 18, 2003
Macular pigment: quantitative analysis on autofluorescence imagesM Trieschmann, G Spital, A Lommatzsch, et al.
Human Mutation|March 29, 2000
Novel mutations of the RPGR gene in RP3 familiesI Zito, M B Gorin, C Plant, et al.
American Journal of Mental Retardation : AJMR|June 1, 1999
Self-injurious behavior and Prader-Willi syndrome: behavioral forms and body locationsF J Symons, M G Butler, M D Sanders, et al.
BMJ (Clinical Research Ed.)|April 22, 1995
Incidence of acute symptomatic toxoplasma retinochoroiditis in south London according to country of birthR E Gilbert, M R Stanford, H Jackson, et al.
The British Journal of Ophthalmology|September 1, 1989
A point prevalence study of 150 patients with idiopathic retinal vasculitis: 2. Clinical relevance of antiretinal autoimmunity and circulating immune complexesE Kasp, E M Graham, M R Stanford, et al.
American Journal of Human Genetics|January 1, 1991
A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosaC F Inglehearn, R Bashir, D H Lester, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 19, 2000
Familial cavernous hemangioma: An expanding ocular spectrumD Sarraf, A M Payne, N D Kitchen, et al.
Ophthalmology|June 1, 1996
Clinical features of progressive bifocal chorioretinal atrophy: a retinal dystrophy linked to chromosome 6qB F Godley, P A Tiffin, K Evans, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1995
Chromosome 19q cone-rod retinal dystrophy. Ocular phenotypeK Evans, J Duvall-Young, F W Fitzke, et al.
American Journal of Ophthalmology|November 20, 1998
Disturbance of sleep in blindnessH Tabandeh, S W Lockley, R Buttery, et al.
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