Refraction in childhoodMOORE, A. T.Transactions of the Ophthalmological Societies of the United Kingdom. 1985, Vol 104, Num 6, pp 648-652, issn 0078-5334Article

Unique individuality redeemedMOORE, A. T.Contemporary psychoanalysis. 1984, Vol 20, Num 1, pp 1-33, issn 0010-7530Article

The cone dystrophiesSIMUNOVIC, M. P; MOORE, A. T.Eye (London. 1987). 1998, Vol 12, pp 553-565, issn 0950-222X, 3BConference Paper

An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfectaMICHAELIDES, M; BLOCH-ZUPAN, A; HOLDER, G. E et al.Journal of medical genetics. 2004, Vol 41, Num 6, pp 468-473, issn 0022-2593, 6 p.Article

Cognitive functioning in humans with mutations of the PAX6 geneTHOMPSON, P. J; MITCHELL, T. N; FREE, S. L et al.Neurology. 2004, Vol 62, Num 7, pp 1216-1218, issn 0028-3878, 3 p.Article

Identification of the gene for Nance-Horan syndrome (NHS)BROOKS, S. P; EBENEZER, N. D; POOPALASUNDARAM, S et al.Journal of medical genetics. 2004, Vol 41, Num 10, pp 768-771, issn 0022-2593, 4 p.Article

Oligocone trichromacy: a rare and unusual cone dysfunction syndromeMICHGELIDES, M; HOLDER, G. E; BRADSHAW, K et al.British journal of ophthalmology. 2004, Vol 88, Num 4, pp 497-500, issn 0007-1161, 4 p.Article

Genotype-phenotype correlation in British families with X linked congenital stationary night blindnessALLEN, L. E; ZITO, I; BRADSHAW, K et al.British journal of ophthalmology. 2003, Vol 87, Num 11, pp 1413-1420, issn 0007-1161, 8 p.Article

A locus for isolated cataract on human XpFRANCIS, P. J; BERRY, V; HARDCASTLE, A. J et al.Journal of medical genetics. 2002, Vol 39, Num 2, pp 105-109, issn 0022-2593Article

A Clinical and molecular genetic analysis of solitary ocular angiomaWEBSTER, A. R; MAHER, E. R; BIRD, A. C et al.Ophthalmology (Rochester, MN). 1999, Vol 106, Num 3, pp 623-629, issn 0161-6420Article

Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17pKELSELL, R. E; EVANS, K; GREGORY, C. Y et al.Human molecular genetics (Print). 1997, Vol 6, Num 4, pp 597-600, issn 0964-6906Article

Clinial features in affected males with X-linked retinoschisisGEORGE, N. D. L; YATES, J. R. W; MOORE, A. T et al.Archives of ophthalmology (1960). 1996, Vol 114, Num 3, pp 274-280, issn 0003-9950Article

Molecular genetic analysis of the 3p-syndromePHIPPS, M. E; LATIF, F; LERMAN, M. I et al.Human molecular genetics (Print). 1994, Vol 3, Num 6, pp 903-908, issn 0964-6906Article

Flecked retina associated with ring 17 chromosomeCHARLES, S. J; MOORE, A. T; DAVISON, B. C. C et al.British journal of ophthalmology. 1991, Vol 75, Num 2, pp 125-127, issn 0007-1161, 3 p.Article

Choroidal neovascularisation in childrenSIVAPRASAD, S; MOORE, A. T.British journal of ophthalmology. 2008, Vol 92, Num 4, pp 451-454, issn 0007-1161, 4 p.Article

Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataractREDDY, M. A; BATEMAN, O. A; SLINGSBY, C et al.Human molecular genetics (Print). 2004, Vol 13, Num 9, pp 945-953, issn 0964-6906, 9 p.Article

Mapping of a novel locus for achromatopsia (ACHM4) to 1 p and identification of a germline mutation in the α subunit of cone transducin (GNAT2)ALIGIANIS, I. A; FORSHEW, T; JOHNSON, S et al.Journal of medical genetics. 2002, Vol 39, Num 9, pp 656-660, issn 0022-2593Article

Autosomal dominant cone-rod retinal dystrophy (CORD6) from heterozygous mutation of GUCY2D, which encodes retinal guanylate cyclaseGREGORY-EVANS, K; KELSELL, R. E; BIRD, A. C et al.Ophthalmology (Rochester, MN). 2000, Vol 107, Num 1, pp 55-61, issn 0161-6420Article

Demonstration of a founder effect and fine mapping of dominant optic atrophy locus on 3q28-qter by linkage disequilibrium method : A study of 38 British Isles pedigreesVOTRUBA, M; MOORE, A. T; BHATTACHARYA, S. S et al.Human genetics. 1998, Vol 102, Num 1, pp 79-86, issn 0340-6717Article

Mutations in the retinal guanylate cyclase (RETGC-1) gene in dominant cone-rod dystrophyKELSELL, R. E; GREGORY-EVANS, K; PAYNE, A. M et al.Human molecular genetics (Print). 1998, Vol 7, Num 7, pp 1179-1184, issn 0964-6906Article

What is the function of the cone-rich rim of the retina?MOLLON, J. D; REGAN, B. C; BOWMAKER, J. K et al.Eye (London. 1987). 1998, Vol 12, pp 548-552, issn 0950-222X, 3BConference Paper

Bimodal expressivity in dominant retinitis pigmentosa genetically linked to chromosome 19_qEVANS, K; AL-MAGHTHEH, M; FITZKE, F. W et al.British journal of ophthalmology. 1995, Vol 79, Num 9, pp 841-846, issn 0007-1161Article

Infantile presentation of X linked retinoschisisGEORGE, N. D. L; YATES, J. R. W; BRADSHAW, K et al.British journal of ophthalmology. 1995, Vol 79, Num 7, pp 653-657, issn 0007-1161Article

Ischaemic retinopathy occurring in patients receiving bone marrow allografts and campath-1G : a clinicopathological studyWEBSTER, A. R; ANDERSON, J. R; RICHARDS, E. M et al.British journal of ophthalmology. 1995, Vol 79, Num 7, pp 687-691, issn 0007-1161Article

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