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Ophthalmic Paediatrics and Genetics|August 1, 1984
Retrospective analysis of 58 children with retinoblastomaL Mathew, T D Miale, S Rao, et al.Ophthalmology|January 11, 2001
Perceived and actual performance of daily tasks: relationship to visual function tests in individuals with retinitis pigmentosaJ P Szlyk, W Seiple, G A Fishman, et al.Ophthalmology|August 1, 1994
Clinical features of a previously undescribed codon 216 (proline to serine) mutation in the peripherin/retinal degeneration slow gene in autosomal dominant retinitis pigmentosaG A Fishman, E Stone, L D Gilbert, et al.Journal of Andrology|July 1, 1986
Morphometric analysis of spermatozoa in the assessment of human male fertilityD F Katz, J W Overstreet, S J Samuels, et al.Retina (Philadelphia, Pa.)|January 1, 1987
Magnetic resonance imaging of central nervous system defects in Usher's syndromeL Piazza, G A Fishman, R D Kaplan, et al.Proceedings of the National Academy of Sciences of the United States of America|April 18, 1998
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosisH Morimura, G A Fishman, S A Grover, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|April 17, 1999
Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR geneG A Fishman, E M Stone, S Grover, et al.Ophthalmology|December 1, 1991
Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin geneE M Stone, A E Kimura, B E Nichols, et al.Human Mutation|December 19, 2001
Novel frameshift mutations in CRX associated with Leber congenital amaurosisC Rivolta, N E Peck, A B Fulton, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1992
Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosaG A Fishman, K Vandenburgh, E M Stone, et al.Pageof 21