Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene von KLEVERING, B. J, VAN DRIEL, M, DE POL, D. J. R. V, PINCKERS, A. J. L. G, CREMERS, F. P. M, HOYNG, C. B

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Autosomal Recessive Retinitis Pigmentosa and Cone-rod Dystrophy Caused by Splice Site Mutations in the Stargardt's Disease Gene ABCR von Cremers, Frans P. M., van de Pol, Dorien J. R., van Driel, Marc, den Hollander, Anneke I., van Haren, Frank J. J., Knoers, Nine V. A. M., Tijmes, Nel, Bergen, Arthur A. B., Rohrschneider, Klaus, Blankenagel, Anita, Pinckers, Alfred J. L. G., Deutman, August F., Hoyng, Carel B.

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Positional cloning of the gene for X-linked retinitis pigmentosa 2 von Berger, Wolfgang, Pinckers, Alfred J.L.G, Bergen, Arthur A.B, Ropers, H.-Hilger, Fundele, Reinald, Rosenberg, Thomas, Feil, Silke, Hinzmann, Bernd, Kirschner, Renate, van Duijnhoven, Gerard, Dong, Juan, Rosenthal, André, Cremers, Frans P.M, Schwahn, Uwe, Hemberger, Myriam, Lenzner, Steffen

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Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type von BERGEN, A. A. B, SAMANNS, C, SCHUURMAN, E. J. M, VAN OSCH, L, VAN DORP, D. B, PINCKERS, A. J. L. G, BAKKER, E, GAL, A, VAN OMMEN, G. J. B, BLEEKER-WAGEMAKERS, E. M

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The 2588G→C Mutation in the ABCR Gene Is a Mild Frequent Founder Mutation in the Western European Population and Allows the Classification of ABCR Mutations in Patients with Starga... von Maugeri, Alessandra, van Driel, Marc A., van de Pol, Dorien J.R., Klevering, B. Jeroen, van Haren, Frank J.J., Tijmes, Nel, Bergen, Arthur A.B., Rohrschneider, Klaus, Blankenagel, Anita, Pinckers, Alfred J.L.G., Dahl, Niklas, Brunner, Han G., Deutman, August F., Hoyng, Carel B., Cremers, Frans P.M.

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Positional Cloning of the Gene for X-Linked Retinitis Pigmentosa 3: Homology with the Guanine-Nucleotide-Exchange Factor RCC1 von Roepman, Ronald, van Duijnhoven, Gerard, Rosenberg, Thomas, Pinckers, Alfred J. L. G., Bleeker-Wagemakers, Liesbeth M., Bergen, Arthur A. B., Post, Jan, Beck, Alfred, Reinhardt, Richard, Ropers, Hans-Hilger, Cremers, Frans P. M., Berger, Wolfgang

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Genetic fine mapping of the gene for recessive Stargardt disease von HOYNG, C. B, POPPELAARS, F, VAN DE POL, T. J. R, KREMER, H, PINCKERS, A. J. L. G, DEUTMAN, A. F, CREMERS, F. P. M

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Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencing von VAN DEN HURK, J. A. J. M, VAN DE POL, T. J. R, ROPERS, H.-H, CREMERS, F. P. M, MOLLOY, C. M, BRUNSMANN, F, RÜTHER, K, ZRENNER, E, PINCKERS, A. J. L. G, PAWLOWITZKI, I. H, BLEEKER-WAGEMAKERS, E. M, WIERINGA, B

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Localization of a Novel X-Linked Progressive Cone Dystrophy Gene to Xq27: Evidence for Genetic Heterogeneity von Bergen, A.A.B., Pinckers, A.J.L.G.

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The electro-oculogram in uveal melanoma : a prospective study von BRINK, H. M. A, PINCKERS, A. J. L. G, VERBEEK, A. M

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Classification of complete and incomplete autosomal recessive achromatopsia von Pokorny, J, Smith, V C, Pinckers, A J, Cozijnsen, M

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Two sibs with chorioretinal dystrophy, hypogonadotrophic hypogonadism, and cerebellar ataxia: Boucher-Neuhäuser syndrome von Rump, R, Hamel, B C, Pinckers, A J, van Dop, P A

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Anomaloscope examination in macular gliosis, macular holes and central serous choroidopathy von TILANUS, M. A. D, PINCKERS, A. J. L. G, AANDEKERK, A. L

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Predictive value of pattern VEP, pattern ERG and hole size in macular hole surgery von TILANUS, M. A. D, CUYPERS, M. H. M, BEMELMANS, N. A. M, PINCKERS, A. J. L. G, DEUTMAN, A. F

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Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22 von HOLLANDER, A. I. D, VAN DER VELDE-VISSER, S. D, PINCKERS, A. J. L. G, HOYNG, C. B, BRUNNER, H. G, CREMERS, F. P. M

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Immune responsiveness to retinal S-antigen and opsin in serpiginous choroiditis and other retinal diseases von BROEKHUYSE, R. M, VAN HERCK, M, PINCKERS, A. J. L. G, WINKENS, H. J, VAN VUGT, A. H. M, RYCKAERT, S, DEUTMAN, A. F

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Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases von CREMERS, F. P. M, SANKILA, E.-M, DE LA CHAPELLE, A, PAWLOWITZKI, I. H, ROPERS, H.-H, BRUNSMANN, F, JAY, M, JAY, B, WRIGHT, A, PINCKERS, A. J. L. G, SCHWARTZ, M, VAN DE POL, D. J. R, WIERINGA, B

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Pattern-Reversal Visual Evoked Potentials in Patients With Epiretinal Membrane von BEMELMANS, NICOLE A.M., TILANUS, MAURITS A.D., CUYPERS, MARINUS H.M., PINCKERS, ALFRED J.L.G.

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Prognostic value of pattern reversal visual-evoked potentials in idiopathic epiretinal membrane von TILANUS, M. A. D, CUYPERS, M. H, BEMELMANS, N. A. M, PINCKERS, A. J. L. G

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Visual acuity, spectacle blur and slit-lamp biomicroscopy on asymptomatic contact-lens-wearing recruits von ROUWEN, A.-J.P, PINCKERS, A. J. L. G, PAD VOS BOSCH, A. A. I. V. P, PUNT, H, DOESBURG, W. H, LEMMENS, W. A. J. G

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