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Results: 1-6 |
Results: 6

Authors: Moller, P Borg, A Heimdal, K Apold, J Vallon-Christersson, J Hovig, E Maehle, L
Citation: P. Moller et al., The BRCA1 syndrome and other inherited breast or breast-ovarian cancers ina Norwegian prospective series, EUR J CANC, 37(8), 2001, pp. 1027-1032

Authors: Moller, P Heimdal, K Apold, J Fredriksen, A Borg, A Hovig, E Hagen, A Hagen, B Pedersen, JC Maehle, L
Citation: P. Moller et al., Genetic epidemiology of BRCA1 mutations in Norway, EUR J CANC, 37(18), 2001, pp. 2428-2434

Authors: Moller, P Reis, MM Evans, G Vasen, H Haites, N Anderson, E Steel, CM Apold, J Lalloo, F Maehle, L Preece, P Gregory, H Heimdal, K
Citation: P. Moller et al., Efficacy of early diagnosis and treatment in women with a family history of breast cancer, DIS MARKER, 15(1-3), 1999, pp. 179-186

Authors: Moller, P Borg, A Evans, G Haites, N Steel, CM Vasen, H Gregory, H Hodgson, S Apold, J Lalloo, F Maehle, L Anderson, E Heimdal, K
Citation: P. Moller et al., Mutation-specific survival of inherited breast cancer, DIS MARKER, 15(1-3), 1999, pp. 205-205

Authors: Moller, P Evans, G Haites, N Vasen, H Reis, MM Anderson, E Apold, J Hodgson, S Eccles, D Olsson, H Stoppa-Lyonnet, D Chang-Claude, J Morrison, PJ Bevilacqua, G Heimdal, K Maehle, L Lalloo, F Gregory, H Preece, P Borg, A Nevin, NC Caligo, M Steel, CM
Citation: P. Moller et al., Guidelines for follow-up of women at high risk for inherited breast cancer: Consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer, DIS MARKER, 15(1-3), 1999, pp. 207-211

Authors: Ellingsen, S Knappskog, PM Apold, J Eiken, HG
Citation: S. Ellingsen et al., Diverse PAH transcripts in lymphocytes of PKU patients with putative nonsense (G272X, Y356X) and missense (P281L, R408Q) mutations, FEBS LETTER, 457(3), 1999, pp. 505-508
Risultati: 1-6 |