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Results:
1-7
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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
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