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Costs and benefits of diagnosing familial breast cancer.
Heimdal K, Maehle L, Møller P. Heimdal K, et al. Among authors: moller p. Dis Markers. 1999 Oct;15(1-3):167-73. doi: 10.1155/1999/751892. Dis Markers. 1999. PMID: 10595273 Free PMC article.
Genetic epidemiology of BRCA1 mutations in Norway.
Møller P, Heimdal K, Apold J, Fredriksen A, Borg A, Hovig E, Hagen A, Hagen B, Pedersen JC, Maehle L; Norwegian Inherited Breast Cancer Group; Norwegian Inherited Ovarian Cancer Group. Møller P, et al. Eur J Cancer. 2001 Dec;37(18):2428-34. doi: 10.1016/s0959-8049(01)00299-4. Eur J Cancer. 2001. PMID: 11720839
Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study.
Phelan CM, Iqbal J, Lynch HT, Lubinski J, Gronwald J, Moller P, Ghadirian P, Foulkes WD, Armel S, Eisen A, Neuhausen SL, Senter L, Singer CF, Ainsworth P, Kim-Sing C, Tung N, Llacuachaqui M, Chornokur G, Ping S, Narod SA; Hereditary Breast Cancer Study Group. Phelan CM, et al. Among authors: moller p. Br J Cancer. 2014 Jan 21;110(2):530-4. doi: 10.1038/bjc.2013.741. Epub 2013 Nov 28. Br J Cancer. 2014. PMID: 24292448 Free PMC article.
[Hereditary breast cancer in Norway].
Heimdal K, Apold J, Maehle L, Dørum A, Møller P. Heimdal K, et al. Among authors: moller p. Tidsskr Nor Laegeforen. 1999 Oct 30;119(26):3929-32. Tidsskr Nor Laegeforen. 1999. PMID: 10592755 Review. Norwegian.
Screening for familial ovarian cancer: poor survival of BRCA1/2 related cancers.
Evans DG, Gaarenstroom KN, Stirling D, Shenton A, Maehle L, Dørum A, Steel M, Lalloo F, Apold J, Porteous ME, Vasen HF, van Asperen CJ, Moller P. Evans DG, et al. Among authors: moller p. J Med Genet. 2009 Sep;46(9):593-7. doi: 10.1136/jmg.2008.058248. Epub 2008 Apr 15. J Med Genet. 2009. PMID: 18413372
1,948 results