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Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
Chubb D, Weinhold N, Broderick P, Chen B, Johnson DC, Försti A, Vijayakrishnan J, Migliorini G, Dobbins SE, Holroyd A, Hose D, Walker BA, Davies FE, Gregory WA, Jackson GH, Irving JA, Pratt G, Fegan C, Fenton JA, Neben K, Hoffmann P, Nöthen MM, Mühleisen TW, Eisele L, Ross FM, Straka C, Einsele H, Langer C, Dörner E, Allan JM, Jauch A, Morgan GJ, Hemminki K, Houlston RS, Goldschmidt H. Chubb D, et al. Among authors: pratt g. Nat Genet. 2013 Oct;45(10):1221-1225. doi: 10.1038/ng.2733. Epub 2013 Aug 18. Nat Genet. 2013. PMID: 23955597 Free PMC article.
True spectrum of 14q32 translocations in multiple myeloma.
Pratt G, Fenton JA, Proffitt JA, Rawstron AC, Davies FE, Child JA, Morgan GJ. Pratt G, et al. Br J Haematol. 1998 Dec;103(4):1209-10. doi: 10.1046/j.1365-2141.1998.1161d.x. Br J Haematol. 1998. PMID: 9886346 Free article. No abstract available.
Positive and negative selection to reduce tumour contamination in peripheral blood stem cell harvests.
Davies FE, Rawstron AC, Pratt G, Coupe R, Clarke D, Lubenko A, Short K, Perren TJ, Selby PJ, Maclennan S, Major K, Woodhead V, Robinson F, Child JA, Smith GM, Johnson PW, Morgan GJ. Davies FE, et al. Among authors: pratt g. Hematol Oncol. 2000 Sep;18(3):111-20. doi: 10.1002/1099-1069(200009)18:3<111::aid-hon657>3.0.co;2-#. Hematol Oncol. 2000. PMID: 11027980
590 results