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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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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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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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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Molecular basis of choroideremia (CHM): Mutations involving the rab escort protein-1 (REP-1) gene von van den Hurk, JAJM, Schwartz, M, van Bokhoven, H, van de Pol, TJR, Bogerd, L, Pinckers, AJLG, Bleeker-Wagemakers, EM, Pawlowitzki, IH, Rüther, K, Ropers, H-H, Cremers, FPM

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Mutation Analysis of Patients with Hermansky-Pudlak Syndrome: A Frameshift Hot Spot in the HPS Gene and Apparent Locus Heterogeneity von Oh, Jangsuk, Ho, Lingling, Ala-Mello, Sirpa, Amato, Dominick, Armstrong, Linda, Bellucci, Sylvia, Carakushansky, Gerson, Ellis, Julia P., Fong, Chin-To, Green, Jane S., Heon, Elise, Legius, Eric, Levin, Alex V., Nieuwenhuis, H. Karel, Pinckers, A., Tamura, Naoaki, Whiteford, Margo L., Yamasaki, Hisato, Spritz, Richard A.

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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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Autosomal Dominant Central Areolar Choroidal Dystrophy Caused by a Mutation in Codon 142 in the Peripherin/RDS Gene von HOYNG, CAREL B., HEUTINK, PETER, TESTERS, LEON, PINCKERS, ALFRED, DEUTMAN, AUGUST F., OOSTRA, BEN A.

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Ocular and Systemic Manifestations of Cerebrotendinous Xanthomatosis von CRUYSBERG, J.R.M., WEVERS, R.A., van ENGELEN, B.G.M., PINCKERS, A., van SPREEKEN, A., TOLBOOM, J.J.M.

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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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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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Ectopia lentis et pupillae syndrome in three generations von Cruysberg, J R, Pinckers, A

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The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein von Meindl, Alfons, Pusch, Carsten M, Zeitz, Christina, Brandau, Oliver, Pesch, Katrin, Achatz, Helene, Feil, Silke, Scharfe, Curt, Maurer, Johannes, Jacobi, Felix K, Pinckers, Alfred, Andreasson, Sten, Hardcastle, Alison, Wissinger, Bernd, Berger, Wolfgang

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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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Reply to Inglehearn von Bergen, A A, Pinckers, A J

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Pathologic scotopization: a shortened Nagel-II anomaloscopic micro-screw method von PINCKERS, A

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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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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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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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