Results: 1-7 |
Results: 7

Authors: Bessant, DAR Payne, AM Plant, C Bird, AC Swaroop, A Bhattacharya, SS
Citation: Dar. Bessant et al., NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies, EUR J HUM G, 8(10), 2000, pp. 783-787

Authors: Bessant, DAR Payne, AM Mitton, KP Wang, QL Swain, PK Plant, C Bird, AC Zack, DJ Swaroop, A Bhattacharya, SS
Citation: Dar. Bessant et al., A mutation in NRL is associated with autosomal dominant retinitis pigmentosa, NAT GENET, 21(4), 1999, pp. 355-356

Authors: Zito, I Thiselton, DL Gorin, MB Stout, JT Plant, C Bird, AC Bhattacharya, SS Hardcastle, AJ
Citation: I. Zito et al., Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating withthe RP3 locus, HUM GENET, 105(1-2), 1999, pp. 57-62

Authors: Kermani, S Gregory-Evans, K Tarttelin, EE Bellingham, J Plant, C Bird, AC Fox, M Bhattacharya, SS Gregory-Evans, CY
Citation: S. Kermani et al., Refined genetic and physical positioning of the gene for Doyne honeycomb retinal dystrophy (DHRD), HUM GENET, 104(1), 1999, pp. 77-82

Authors: Lois, N Holder, GE Fitzke, FW Plant, C Bird, AC
Citation: N. Lois et al., Intrafamilial variation of phenotype in Stargardt macular dystrophy-Fundusflavimaculatus, INV OPHTH V, 40(11), 1999, pp. 2668-2675

Authors: Payne, AM Downes, SM Bessant, DAR Plant, C Moore, T Bird, AC Bhattacharya, SS
Citation: Am. Payne et al., Genetic analysis of the guanylate cyclase activator 1B (GUCA1B) gene in patients with autosomal dominant retinal dystrophies, J MED GENET, 36(9), 1999, pp. 691-693

Authors: Hardcastle, AJ Thiselton, DL Van Maldergem, L Saha, BK Jay, M Plant, C Taylor, R Bird, AC Bhattacharya, S
Citation: Aj. Hardcastle et al., Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study, AM J HU GEN, 64(4), 1999, pp. 1210-1215
Risultati: 1-7 |