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Exome sequencing to detect rare variants associated with general cognitive ability: a pilot study.
Luciano M, Svinti V, Campbell A, Marioni RE, Hayward C, Wright AF, Taylor MS, Porteous DJ, Thomson P, Prendergast JG, Hastie ND, Farrington SM, Scotland G, Dunlop MG, Deary IJ. Luciano M, et al. Among authors: dunlop mg. Twin Res Hum Genet. 2015 Apr;18(2):117-25. doi: 10.1017/thg.2015.10. Epub 2015 Mar 6. Twin Res Hum Genet. 2015. PMID: 25744449 Free article. Clinical Trial.
Mosaicism and sporadic familial adenomatous polyposis.
Farrington SM, Dunlop MG. Farrington SM, et al. Among authors: dunlop mg. Am J Hum Genet. 1999 Feb;64(2):653-8. doi: 10.1086/302236. Am J Hum Genet. 1999. PMID: 9973305 Free PMC article. No abstract available.
Population carrier frequency of hMSH2 and hMLH1 mutations.
Dunlop MG, Farrington SM, Nicholl I, Aaltonen L, Petersen G, Porteous M, Carothers A. Dunlop MG, et al. Br J Cancer. 2000 Dec;83(12):1643-5. doi: 10.1054/bjoc.2000.1520. Br J Cancer. 2000. PMID: 11104559 Free PMC article.
Hypermutability at a poly(A/T) tract in the human germline.
Bacon AL, Dunlop MG, Farrington SM. Bacon AL, et al. Among authors: dunlop mg. Nucleic Acids Res. 2001 Nov 1;29(21):4405-13. doi: 10.1093/nar/29.21.4405. Nucleic Acids Res. 2001. PMID: 11691928 Free PMC article.
308 results