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Archives of Ophthalmology (Chicago, Ill. : 1960)|July 1, 1997
Assessment of the phenotypic range seen in Doyne honeycomb retinal dystrophyK Evans, C Y Gregory, S D Wijesuriya, et al.Eye (London, England)|January 1, 1995
The role of molecular genetics in the prenatal diagnosis of retinal dystrophiesK Evans, C Y Gregory, A Fryer, et al.The British Journal of Ophthalmology|October 1, 1979
A comparative histopathological study of argon and krypton laser irradiations of the human retinaJ Marshall, A C BirdThe British Journal of Ophthalmology|September 1, 1976
Internuclear ophthalmoplegia. An electro-oculographic study of peak angular saccadic velocitiesA C Bird, J LeechThe British Journal of Ophthalmology|September 1, 1995
Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19qK Evans, M al-Maghtheh, F W Fitzke, et al.Genome Research|February 1, 1996
Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypesS D Wijesuriya, K Evans, M R Jay, et al.Human Molecular Genetics|February 1, 1994
Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19M al-Maghtheh, C F Inglehearn, T J Keen, et al.American Journal of Ophthalmology|August 15, 1984
Recurrences of acute posterior multifocal placoid pigment epitheliopathyA L Lyness, A C BirdPageof 188