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Results: 1-3 |
Results: 3
Deletion in the OA1 gene in a family with congenital X linked nystagmus
Authors: Preising, M de Laak, JPO Lorenz, B
Citation: M. Preising et al., Deletion in the OA1 gene in a family with congenital X linked nystagmus, BR J OPHTH, 85(9), 2001, pp. 1098-1103
A novel missense mutation of the CBFA1 gene in a family with cleidocranialdysplasia (CCD) and variable expressivity
Authors: Golan, L Preising, M Wagener, H Baumert, U Niederdellmann, H Lorenz, S Mussig, D
Citation: L. Golan et al., A novel missense mutation of the CBFA1 gene in a family with cleidocranialdysplasia (CCD) and variable expressivity, J CRAN GENE, 20(3), 2000, pp. 113-120
Early-onset severe rod-cone dystrophy in young children with RPE65 mutations
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
Risultati: 1-3 |