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American Journal of Ophthalmology|February 15, 1993
Ocular manifestations of the lacrimo-auriculo-dento-digital syndromeG W Heinz, J B Bateman, D J Barrett, et al.Physics in Medicine and Biology|January 1, 1992
Dielectric properties of the system bovine albumin: urea: betaine in aqueous solutionJ B Bateman, G F Evans, P R Brown, et al.Current Eye Research|November 1, 1993
Assignment of tear lipocalin gene to human chromosome 9q34-9qterB J Glasgow, C Heinzmann, T Kojis, et al.Investigative Ophthalmology & Visual Science|July 1, 1987
Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2D J Barrett, J B Bateman, R S Sparkes, et al.American Journal of Ophthalmology|January 1, 1983
Ocular histopathologic studies of neonatal and childhood adrenoleukodystrophyS M Cohen, W R Green, Z C de la Cruz, et al.American Journal of Ophthalmology|December 22, 2000
A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathyJ B Kerrison, N R Miller, F Hsu, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1991
Rhodopsin mutations in autosomal dominant retinitis pigmentosaC H Sung, C M Davenport, J C Hennessey, et al.American Journal of Human Genetics|July 1, 1993
Identification of novel rhodopsin mutations responsible for retinitis pigmentosa: implications for the structure and function of rhodopsinJ P Macke, C M Davenport, S G Jacobson, et al.American Journal of Medical Genetics|January 1, 1992
Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genesF A Collins, D L Murphy, A L Reiss, et al.Ophthalmology|June 1, 1996
Orbital lesions in the blue rubber bleb nevus syndromeC A McCannel, J Hoenig, J Umlas, et al.Pageof 17