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2017
Mark Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation
Apostolou, P. ; Pertesi, M. ^LU ; Aleporou-Marinou, V. ; Dimitrakakis, C. ; Papadimitriou, C. ; Razis, E. ; Christodoulou, C. ; Fountzilas, G. ; Yannoukakos, D. and Konstantopoulou, I. , et al. (2017) In Clinical Genetics 91(3). p.482-487
- Contribution to journal › Article
2011
Mark A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing
Thomassen, Mads ; Pedersen, Inge Sokilde ; Vogel, Ida ; Hansen, Thomas v. O. ; Brasch-Andersen, Charlotte ; Brasen, Claus L. ; Cruger, Dorthe ; Sunde, Lone ; Nielsen, Finn C. and Jensen, Uffe B. , et al. (2011) In Breast Cancer Research and Treatment 128(1). p.179-185
- Contribution to journal › Article
2001
Mark Genetic epidemiology of BRCA1 mutations in Norway
Moller, P. ; Heimdal, K. ; Apold, J. ; Fredriksen, A. ; Borg, Åke ^LU ; Hovig, E. ; Hagen, A. ; Hagen, B. ; Pedersen, J.C. and Maehle, L. (2001) In European Journal of Cancer 37(18). p.2428-2434
- Contribution to journal › Article
Mark Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families
Barkardottir, Rosa B ; Sarantaus, Laura ; Arason, Adalgeir ; Vehmanen, Paula ; Bendahl, Pär-Ola ^LU ; Kainu, Tommi ; Syrjakoski, Kirsi ; Krahe, Ralf ; Huusko, Pia and Pyrhonen, Seppo , et al. (2001) In European Journal of Human Genetics 9(10). p.773-779
- Contribution to journal › Article

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