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
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
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