1. A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma. Issue 2 (1st February 2003) Authors: Reddy, M A; Francis, P J; Berry, V; Bradshaw, K; Patel, R J; Maher, E R; Kumar, R; Bhattacharya, S S; Moore, A T Journal: British journal of ophthalmology Issue: Volume 87:Issue 2(2003) Page Start: 197 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A detailed phenotypic study of "cone dystrophy with supernormal rod ERG". Issue 3 (17th February 2005) Authors: Michaelides, M; Holder, G E; Webster, A R; Hunt, D M; Bird, A C; Fitzke, F W; Mollon, J D; Moore, A T Journal: British journal of ophthalmology Issue: Volume 89:Issue 3(2005) Page Start: 332 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1. Issue 2 (21st January 2005) Authors: Michaelides, M; Holder, G E; Hunt, D M; Fitzke, F W; Bird, A C; Moore, A T Journal: British journal of ophthalmology Issue: Volume 89:Issue 2(2005) Page Start: 198 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A locus for isolated cataract on human Xp. Issue 2 (1st February 2002) Authors: Francis, P J; Berry, V; Hardcastle, A J; Maher, E R; Moore, A T; Bhattacharya, S S Journal: Journal of medical genetics Issue: Volume 39:Issue 2(2002) Page Start: 105 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. A new dominant retinitis pigmentosa family mapping to the RP18 locus on chromosome 1q11-21. Issue 9 (September 1998) Authors: Inglehearn, C F; Tarttelin, E E; Keen, T J; Bhattacharya, S S; Moore, A T; Taylor, R; Bird, A C Journal: Journal of medical genetics Issue: Volume 35:Issue 9(1998) Page Start: 788 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts. Issue 3 (15th November 2007) Authors: Arora, A; Minogue, P J; Liu, X; Addison, P K; Russel-Eggitt, I; Webster, A R; Hunt, D M; Ebihara, L; Beyer, E C; Berthoud, V M; Moore, A T Journal: Journal of medical genetics Issue: Volume 45:Issue 3(2008) Page Start: 155 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract. Issue 1 (5th January 2006) Authors: Arora, A; Minogue, P J; Liu, X; Reddy, M A; Ainsworth, J R; Bhattacharya, S S; Webster, A R; Hunt, D M; Ebihara, L; Moore, A T; Beyer, E C; Berthoud, V M Journal: Journal of medical genetics Issue: Volume 43:Issue 1(2006) Page Start: e2 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation. Issue 8 (August 1992) Authors: Moore, A T; Fitzke, F W; Kemp, C M; Arden, G B; Keen, T J; Inglehearn, C F; Bhattacharya, S S; Bird, A C Journal: British journal of ophthalmology Issue: Volume 76:Issue 8(1992) Page Start: 465 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Achromatopsia caused by novel mutations in both CNGA3 and CNGB3. Issue 2 (2nd February 2004) Authors: Johnson, S; Michaelides, M; Aligianis, I A; Ainsworth, J R; Mollon, J D; Maher, E R; Moore, A T; Hunt, D M Journal: Journal of medical genetics Issue: Volume 41:Issue 2(2004) Page Start: e20 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. ADVIRC is caused by distinct mutations in BEST1 that alter pre-mRNA splicing. Issue 9 (8th July 2008) Authors: Burgess, R; MacLaren, R E; Davidson, A E; Urquhart, J E; Holder, G E; Robson, A G; Moore, A T; Keefe, R O'; Black, G C M; Manson, F D C Journal: Journal of medical genetics Issue: Volume 46:Issue 9(2009) Page Start: 620 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗