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Results: 1-5 |
Results: 5

Authors: Driessen, CAGG Janssen, BPM Winkens, HJ Kuhlmann, LD Van Vugt, AHM Pinckers, AJLG Deutman, AF Janssen, JJM
Citation: Cagg. Driessen et al., Null mutation in the human 11-cis retinol dehydrogenase gene associated with fundus albipunctatus, OPHTHALMOL, 108(8), 2001, pp. 1479-1484

Authors: Tilanus, MAD Cuypers, MHM Bemelmans, NAM Pinckers, AJLG Deutman, AF
Citation: Mad. Tilanus et al., Predictive value of pattern VEP, pattern ERG and hole size in macular holesurgery, GR ARCH CL, 237(8), 1999, pp. 629-635

Authors: den Hollander, A van der Velde-Visser, SD Pinckers, AJLG Hoyng, CB Brunner, HG Cremers, FPM
Citation: A. Den Hollander et al., Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22, HUM GENET, 104(1), 1999, pp. 73-76

Authors: Klevering, BJ van Driel, M van de Pol, DJR Pinckers, AJLG Cremers, FPM Hoyng, CB
Citation: Bj. Klevering et al., Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene, BR J OPHTH, 83(8), 1999, pp. 914-918

Authors: Maugeri, A van Driel, MA van de Pol, DJR Klevering, BJ van Haren, FJJ Tijmes, N Bergen, AAB Rohrschneider, K Blankenagel, A Pinckers, AJLG Dahl, N Brunner, HG Deutman, AF Hoyng, CB Cremers, FPM
Citation: A. Maugeri et al., The 2588G -> C mutation in the ABCR gene is a mild frequent founder mutation in the western European population and allows the classification of ABCRmutations in patients with Stargardt disease, AM J HU GEN, 64(4), 1999, pp. 1024-1035
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