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Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.
Kirin M, Chandra A, Charteris DG, Hayward C, Campbell S, Celap I, Bencic G, Vatavuk Z, Kirac I, Richards AJ, Tenesa A, Snead MP, Fleck BW, Singh J, Harsum S, Maclaren RE, den Hollander AI, Dunlop MG, Hoyng CB, Wright AF, Campbell H, Vitart V, Mitry D. Kirin M, et al. Among authors: campbell h, campbell s. Hum Mol Genet. 2013 Aug 1;22(15):3174-85. doi: 10.1093/hmg/ddt169. Epub 2013 Apr 11. Hum Mol Genet. 2013. PMID: 23585552
Generation Scotland: the Scottish Family Health Study; a new resource for researching genes and heritability.
Smith BH, Campbell H, Blackwood D, Connell J, Connor M, Deary IJ, Dominiczak AF, Fitzpatrick B, Ford I, Jackson C, Haddow G, Kerr S, Lindsay R, McGilchrist M, Morton R, Murray G, Palmer CN, Pell JP, Ralston SH, St Clair D, Sullivan F, Watt G, Wolf R, Wright A, Porteous D, Morris AD. Smith BH, et al. Among authors: campbell h. BMC Med Genet. 2006 Oct 2;7:74. doi: 10.1186/1471-2350-7-74. BMC Med Genet. 2006. PMID: 17014726 Free PMC article.
1,858 results