Showing 1 - 5 results of 5 for search 'Hearle, N', query time: 1.39s
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Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome. by Hearle, N, Tomlinson, I, Lim, W, Murday, V, Swarbrick, E, Lim, G, Phillips, R, Lee, P, O'Donohue, J, Trembath, R, Morrison, P, Norman, A, Taylor, R, Hodgson, S, Lucassen, A, Houlston, R
Published 2005Journal article -
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Variation in the CTLA4/CD28 gene region confers an increased risk of coeliac disease. by Popat, S, Hearle, N, Hogberg, L, Braegger, C, O'Donoghue, D, Falth-Magnusson, K, Holmes, G, Howdle, P, Jenkins, H, Johnston, S, Kennedy, N, Kumar, P, Logan, R, Marsh, M, Mulder, C, Torinsson Naluai, A, Sjoberg, K, Stenhammar, L, Walters, JR, Jewell, D, Houlston, R
Published 2002Journal article -
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Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. by Tomlinson, I, Alam, N, Rowan, A, Barclay, E, Jaeger, E, Kelsell, D, Leigh, I, Gorman, P, Lamlum, H, Rahman, S, Roylance, R, Olpin, S, Bevan, S, Barker, K, Hearle, N, Houlston, R, Kiuru, M, Lehtonen, R, Karhu, A, Vilkki, S, Laiho, P, Eklund, C, Vierimaa, O, Aittomäki, K, Hietala, M
Published 2002Journal article -
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Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome. by Lim, W, Hearle, N, Shah, B, Murday, V, Hodgson, S, Lucassen, A, Eccles, D, Talbot, I, Neale, K, Lim, A, O'Donohue, J, Donaldson, A, Macdonald, R, Young, I, Robinson, M, Lee, P, Stoodley, B, Tomlinson, I, Alderson, D, Holbrook, A, Vyas, S, Swarbrick, E, Lewis, A, Phillips, R, Houlston, R
Published 2003Journal article