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