Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients. by Wang, Z, Churchman, M, Avizienyte, E, McKeown, C, Davies, S, Evans, D, Ferguson, A, Ellis, I, Xu, W, Yan, Z, Aaltonen, L, Tomlinson, I

Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer. by Ylikorkala, A, Avizienyte, E, Tomlinson, I, Tiainen, M, Roth, S, Loukola, A, Hemminki, A, Johansson, M, Sistonen, P, Markie, D, Neale, K, Phillips, R, Zauber, P, Twama, T, Sampson, J, Järvinen, H, Mäkelä, T, Aaltonen, L

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. by Hemminki, A, Markie, D, Tomlinson, I, Avizienyte, E, Roth, S, Loukola, A, Bignell, G, Warren, W, Aminoff, M, Höglund, P, Järvinen, H, Kristo, P, Pelin, K, Ridanpää, M, Salovaara, R, Toro, T, Bodmer, W, Olschwang, S, Olsen, A, Stratton, MR, de la Chapelle, A, Aaltonen, L

Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3. by Olschwang, S, Markie, D, Seal, S, Neale, K, Phillips, R, Cottrell, S, Ellis, I, Hodgson, S, Zauber, P, Spigelman, A, Iwama, T, Loff, S, McKeown, C, Marchese, C, Sampson, J, Davies, S, Talbot, I, Wyke, J, Thomas, G, Bodmer, W, Hemminki, A, Avizienyte, E, de la Chapelle, A, Aaltonen, L, Tomlinson, I