Posterior Segment Neovascularization Associated With Optic Nerve Aplasia von Lee, Brian L., Bateman, J. Bronwyn, Schwartz, Steven D.

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Identification and Functional Consequences of a New Mutation (E155G) in the Gene for GCAP1 That Causes Autosomal Dominant Cone Dystrophy von Wilkie, Susan E., Li, Yang, Deery, Evelyne C., Newbold, Richard J., Garibaldi, Daniel, Bateman, J. Bronwyn, Zhang, Heidi, Lin, Wei, Zack, Donald J., Bhattacharya, Shomi S., Warren, Martin J., Hunt, David M., Zhang, Kang

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A New Locus for Autosomal Dominant Cataract on Chromosome 12q13 von Bateman, J. Bronwyn, Johannes, Meriam, Flodman, Pamela, Geyer, David D, Clancy, Kevin P, Heinzmann, Camilla, Kojis, Tracy, Berry, Rebecca, Sparkes, Robert S, Spence, M. Anne

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Favorable Visual Outcome in Cryptococcal Meningitis von Ferreira, Rosane C., Phan, Greg, Bateman, J. Bronwyn

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Optic Nerve Hypoplasia Secondary to Intracranial Teratoma von Lee, Jivianne T., Hall, Theodore R., Bateman, J. Bronwyn

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Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa von KOJIS, T. L, HEINZMANN, C, FLODMAN, P, NGO, J. T, SPARKES, R. S, SPENCE, M. A, BATEMAN, J. B, HECKENLIVELY, J. R

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Growth of the Human Optic Disk and Nerve During Gestation, Childhood, and Early Adulthood von Rimmer, Steve, Keating, Colleen, Chou, Tina, Christenson, Peter D., Foos, Robert Y., Bateman, J. Bronwyn, Farb, M. Daniel

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Conjunctival Biopsy in Infantile Neuroaxonal Dystrophy von Ferreira, Rosane C., Mierau, Gary W., Bateman, J. Bronwyn

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Autosomal-dominant Anomalies of the Iris Pigment Epithelium von Lee, Brian L., Lamer, Andrea B., Bateman, J. Bronwyn

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Genetics and ophthalmology. 100 years of evolution von Bateman, J.B.

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Vortex vein exit sites : scleral coordinates von LIM, M. C, BATEMAN, J. B, GLASGOW, B. J

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Comparison of Fluorescent Genotyping Methods von Johannes, Meriam, Geyer, D.D., Berry, R., Walter, N.A.R., Sikela, J.M., Bateman, J.B.

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Meningococcal endophthalmitis without concomitant septicemia or meningitis von AUERBACH, S. B, LEACH, C. T, BATEMAN, B. J, SIDIKARO, Y, CHERRY, J. D

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LOCALIZATION OF THE GENE FOR NORRIE DISEASE TO BETWEEN DXS7 AND DXS426 ON XP von LINDSAY, S, THISELTON, DL, BATEMAN, JB, NGO, JT, SPARKES, RS, COLEMAN, M, DAVIES, KE, BHATTACHARYA, SS

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Electroretinograms in autism: a pilot study of b-wave amplitudes von Ritvo, E R, Creel, D, Realmuto, G, Crandall, A S, Freeman, B J, Bateman, J B, Barr, R, Pingree, C, Coleman, M, Purple, R

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Dielectric properties of the system bovine albumin : urea : betaine in aqueous solution von Bateman, J B, Evans, G F, Brown, P R, Gabriel, C, Grant, E H

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Vertical saccades in superior oblique palsy von Stathacopoulos, RA, Yee, RD, Bateman, JB

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Ocular Features of the Hagberg-Santavuori Syndrome von Bateman, J. Bronwyn, Philippart, Michel

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Comparison of measured astigmatic retinoscopies from different lid specula von Shea, Caroline J., Westfall, Kelly Cooper, MacKenzie, Todd, Bateman, J.Bronwyn

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Novel Single-Base Deletional Mutation in Major Intrinsic Protein ( MIP) in Autosomal Dominant Cataract von Geyer, David D., Spence, M. Anne, Johannes, Meriam, Flodman, Pamela, Clancy, Kevin P., Berry, Rebecca, Sparkes, Robert S., Jonsen, Matthew D., Isenberg, Sherwin J., Bateman, J. Bronwyn

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