AAAAAA

   
Results: 1-5 |
Results: 5

Authors: Kramer, F White, K Pauleikhoff, D Gehrig, A Passmore, L Rivera, A Rudolph, G Kellner, U Andrassi, M Lorenz, B Rohrschneider, K Blankenagel, A Jurklies, B Schilling, H Schutt, F Holz, FG Weber, BHF
Citation: F. Kramer et al., Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration, EUR J HUM G, 8(4), 2000, pp. 286-292

Authors: Lorenz, B Gyurus, P Preising, M Bremser, D Gu, SM Andrassi, M Gerth, C Gal, A
Citation: B. Lorenz et al., Early-onset severe rod-cone dystrophy in young children with RPE65 mutations, INV OPHTH V, 41(9), 2000, pp. 2735-2742

Authors: Gehrig, A Weber, BHF Lorenz, B Andrassi, M
Citation: A. Gehrig et al., First molecular evidence for a de novo mutation in RS1 (XLRS1) associated with X linked juvenile retinoschisis, J MED GENET, 36(12), 1999, pp. 932-934

Authors: Bock, M Andrassi, M Belitsky, L Lorenz, B
Citation: M. Bock et al., A comparison of two multifocal ERG systems, DOC OPHTHAL, 97(2), 1999, pp. 157-178

Authors: Gehrig, A White, K Lorenz, B Andrassi, M Clemens, S Weber, BHF
Citation: A. Gehrig et al., Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis, CLIN GENET, 55(6), 1999, pp. 461-465
Risultati: 1-5 |