31. Flecked retina associated with ring 17 chromosome. Issue 2 (February 1991) Authors: Charles, S J; Moore, A T; Davison, B C; Dyson, H M; Willatt, L Journal: British journal of ophthalmology Issue: Volume 75:Issue 2(1991) Page Start: 125 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
32. Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone–rod dystrophy. Issue 1 (25th October 2007) Authors: Robson, A G; Michaelides, M; Luong, V A; Holder, G E; Bird, A C; Webster, A R; Moore, A T; Fitzke, F W Journal: British journal of ophthalmology Issue: Volume 92:Issue 1(2008) Page Start: 95 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
33. Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing loss. Issue 7 (1st July 2003) Authors: Francis, P J; Johnson, S; Edmunds, B; Kelsell, R E; Sheridan, E; Garrett, C; Holder, G E; Hunt, D M; Moore, A T Journal: British journal of ophthalmology Issue: Volume 87:Issue 7(2003) Page Start: 893 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
34. Genetic mapping of the Kallmann syndrome and X linked ocular albinism gene loci. Issue 11 (November 1993) Authors: Zhang, Y; McMahon, R; Charles, S J; Green, J S; Moore, A T; Barton, D E; Yates, J R Journal: Journal of medical genetics Issue: Volume 30:Issue 11(1993) Page Start: 923 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
35. Genetic mapping of X linked ocular albinism: linkage analysis in British families. Issue 8 (August 1992) Authors: Charles, S J; Moore, A T; Yates, J R Journal: Journal of medical genetics Issue: Volume 29:Issue 8(1992) Page Start: 552 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
36. Genetic refinement of dominant optic atrophy (OPA1) locus to within a 2 cM interval of chromosome 3q. Issue 2 (February 1997) Authors: Votruba, M; Moore, A T; Bhattacharya, S S Journal: Journal of medical genetics Issue: Volume 34:Issue 2(1997) Page Start: 117 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
37. Genotype-phenotype correlation in British families with X linked congenital stationary night blindness. Issue 11 (10th November 2003) Authors: Allen, L E; Zito, I; Bradshaw, K; Patel, R J; Bird, A C; Fitzke, F; Yates, J R; Trump, D; Hardcastle, A J; Moore, A T Journal: British journal of ophthalmology Issue: Volume 87:Issue 11(2003) Page Start: 1413 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
38. Histiocytosis X: an ophthalmological review. Issue 1 (January 1985) Authors: Moore, A T; Pritchard, J; Taylor, D S Journal: British journal of ophthalmology Issue: Volume 69:Issue 1(1985) Page Start: 7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
39. Identification of the gene for Nance-Horan syndrome (NHS). Issue 10 (1st October 2004) Authors: Brooks, S P; Ebenezer, N D; Poopalasundaram, S; Lehmann, O J; Moore, A T; Hardcastle, A J Journal: Journal of medical genetics Issue: Volume 41:Issue 10(2004) Page Start: 768 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
40. Improved genetic mapping of X linked retinoschisis. Issue 11 (November 1996) Authors: George, N D; Payne, S J; Bill, R M; Barton, D E; Moore, A T; Yates, J R Journal: Journal of medical genetics Issue: Volume 33:Issue 11(1996) Page Start: 919 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗