No Sib Pair Concordance for Breast or Ovarian Cancer in BRCA1 Mutation Carriers

Por Møller, Pål, Mæhle, Lovise, Clark, Neal, Apold, Jaran
Publicado em 2007

Haplotype Analysis of Norwegian and Swedish Patients with Acute Intermittent Porphyria (AIP): Extreme Haplotype Heterogeneity for the Mutation R116W

Por Tjensvoll, Kjersti, Bruland, Ove, Floderus, Ylva, Skadberg, Øyvind, Sandberg, Sverre, Apold, Jaran
Publicado em 2003

Survival in Norwegian BRCA1 mutation carriers with breast cancer

Por Hagen, Anne Irene, Tretli, Steinar, Mæhle, Lovise, Apold, Jaran, Vedå, Nina, Møller, Pål
Publicado em 2009

Germline PTEN mutations are rare and highly penetrant

Por Rustad Cecilie F, Bjørnslett Merete, Heimdal Ketil R, Mæhle Lovise, Apold Jaran, Møller Pål
Publicado em 2006-12-01

Germline PTEN mutations are rare and highly penetrant

Por Rustad, Cecilie F, Bjørnslett, Merete, Heimdal, Ketil R, Mæhle, Lovise, Apold, Jaran, Møller, Pål
Publicado em 2006

High penetrances of <it>BRCA1 </it>and <it>BRCA2 </it>mutations confirmed in a prospective series

Por Møller Pål, Mæhle Lovise, Engebretsen Lars F, Ludvigsen Trond, Jonsrud Christoffer, Apold Jaran, Vabø Anita, Clark Neal
Publicado em 2010-01-01

High penetrances of BRCA1 and BRCA2 mutations confirmed in a prospective series

Por Møller, Pål, Mæhle, Lovise, Engebretsen, Lars F, Ludvigsen, Trond, Jonsrud, Christoffer, Apold, Jaran, Vabø, Anita, Clark, Neal
Publicado em 2010

The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations

Por Rudkin, Teresa M, Hamel, Nancy, Galvez, Maria, Hogervorst, Frans, Gille, Johan JP, Møller, Pål, Apold, Jaran, Foulkes, William D
Publicado em 2006

Complete Mutation Screening and Haplotype Characterization of the BRCA1 Gene in 61 Familial Breast Cancer Patients from Norway

Por Frost, Petter, Jugessur, Astanand, Apold, Jaran, Heimdal, Ketil, Aloysius, Thomas, Eliassen, Aud K., Fauske, Lars, Matre, Guri, Eiken, Hans Geir
Publicado em 2005

Efficacy of Early Diagnosis and Treatment in Women with a Family History of Breast Cancer

Por Møller, Pål, Reis, Marta M., Evans, Gareth, Vasen, Hans, Haites, Neva, Anderson, Elaine, Steel, C. Michael, Apold, Jaran, Lalloo, Fiona, Mæhle, Lovise, Preece, Paul, Gregory, Helen, Heimdal, Ketil, European Familial Breast Cancer Collaborative Group
Publicado em 1999

Recurrence of the R408W Mutation in the Phenylalanine Hydroxylase Locus in Europeans

Por Eisensmith, Randy C., Goltsov, Alexei A., O'Neill, Charles, Tyfield, Linda A., Schwartz, Eugene I., Kuzmin, Alexei I., Baranovskaya, Svetlana S., Tsukerman, Gennady L., Treacy, Eileen, Scriver, Charles R., Güttler, Flemming, Guldberg, Per, Eiken, Hans G., Apold, Jaran, Svensson, Elisabeth, Naughten, Eileen, Cahalane, Seamus F., Croke, David T., Cockburn, Forrester, Woo, Savio L. C.
Publicado em 1995