Moore AT - Search Results

1

The genetics of inherited macular dystrophies.

Michaelides M, Hunt DM, Moore AT. Michaelides M, et al. Among authors: moore at. J Med Genet. 2003 Sep;40(9):641-50. doi: 10.1136/jmg.40.9.641. J Med Genet. 2003. PMID: 12960208 Free PMC article. Review.

2

Localization of the gene for progressive bifocal chorioretinal atrophy (PBCRA) to chromosome 6q.

Kelsell RE, Godley BF, Evans K, Tiffin PA, Gregory CY, Plant C, Moore AT, Bird AC, Hunt DM. Kelsell RE, et al. Among authors: moore at. Hum Mol Genet. 1995 Sep;4(9):1653-6. doi: 10.1093/hmg/4.9.1653. Hum Mol Genet. 1995. PMID: 8541856

3

Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p.

Kelsell RE, Evans K, Gregory CY, Moore AT, Bird AC, Hunt DM. Kelsell RE, et al. Among authors: moore at. Hum Mol Genet. 1997 Apr;6(4):597-600. doi: 10.1093/hmg/6.4.597. Hum Mol Genet. 1997. PMID: 9097965

4

Mapping of a novel locus for achromatopsia (ACHM4) to 1p and identification of a germline mutation in the alpha subunit of cone transducin (GNAT2).

Aligianis IA, Forshew T, Johnson S, Michaelides M, Johnson CA, Trembath RC, Hunt DM, Moore AT, Maher ER. Aligianis IA, et al. Among authors: moore at. J Med Genet. 2002 Sep;39(9):656-60. doi: 10.1136/jmg.39.9.656. J Med Genet. 2002. PMID: 12205108 Free PMC article.

5

Genetic linkage analysis of a novel syndrome comprising North Carolina-like macular dystrophy and progressive sensorineural hearing loss.

Francis PJ, Johnson S, Edmunds B, Kelsell RE, Sheridan E, Garrett C, Holder GE, Hunt DM, Moore AT. Francis PJ, et al. Among authors: moore at. Br J Ophthalmol. 2003 Jul;87(7):893-8. doi: 10.1136/bjo.87.7.893. Br J Ophthalmol. 2003. PMID: 12812894 Free PMC article.

6

The cone dysfunction syndromes.

Michaelides M, Hunt DM, Moore AT. Michaelides M, et al. Among authors: moore at. Br J Ophthalmol. 2004 Feb;88(2):291-7. doi: 10.1136/bjo.2003.027102. Br J Ophthalmol. 2004. PMID: 14736794 Free PMC article. Review.

7

Achromatopsia caused by novel mutations in both CNGA3 and CNGB3.

Johnson S, Michaelides M, Aligianis IA, Ainsworth JR, Mollon JD, Maher ER, Moore AT, Hunt DM. Johnson S, et al. Among authors: moore at. J Med Genet. 2004 Feb;41(2):e20. doi: 10.1136/jmg.2003.011437. J Med Genet. 2004. PMID: 14757870 Free PMC article. No abstract available.

8

The genetics of strabismus.

Michaelides M, Moore AT. Michaelides M, et al. Among authors: moore at. J Med Genet. 2004 Sep;41(9):641-6. doi: 10.1136/jmg.2004.021667. J Med Genet. 2004. PMID: 15342692 Free PMC article. Review.

9

A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts.

Arora A, Minogue PJ, Liu X, Addison PK, Russel-Eggitt I, Webster AR, Hunt DM, Ebihara L, Beyer EC, Berthoud VM, Moore AT. Arora A, et al. Among authors: moore at. J Med Genet. 2008 Mar;45(3):155-60. doi: 10.1136/jmg.2007.051029. Epub 2007 Nov 15. J Med Genet. 2008. PMID: 18006672 Free PMC article.

10

Advanced diagnostic genetic testing in inherited retinal disease: experience from a single tertiary referral centre in the UK National Health Service.

Khan KN, Chana R, Ali N, Wright G, Webster AR, Moore AT, Michaelides M. Khan KN, et al. Among authors: moore at. Clin Genet. 2017 Jan;91(1):38-45. doi: 10.1111/cge.12798. Epub 2016 Jun 30. Clin Genet. 2017. PMID: 27160483

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