检索结果 - Apold, Jaran

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  1. 1
    No Sib Pair Concordance for Breast or Ovarian Cancer in BRCA1 Mutation Carriers

    No Sib Pair Concordance for Breast or Ovarian Cancer in BRCA1 Mutation Carriers 由 Møller, Pål, Mæhle, Lovise, Clark, Neal, Apold, Jaran

    出版 2007
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  2. 2
    Haplotype Analysis of Norwegian and Swedish Patients with Acute Intermittent Porphyria (AIP): Extreme Haplotype Heterogeneity for the Mutation R116W

    Haplotype Analysis of Norwegian and Swedish Patients with Acute Intermittent Porphyria (AIP): Extreme Haplotype Heterogeneity for the Mutation R116W 由 Tjensvoll, Kjersti, Bruland, Ove, Floderus, Ylva, Skadberg, Øyvind, Sandberg, Sverre, Apold, Jaran

    出版 2003
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  3. 3
    Survival in Norwegian BRCA1 mutation carriers with breast cancer

    Survival in Norwegian BRCA1 mutation carriers with breast cancer 由 Hagen, Anne Irene, Tretli, Steinar, Mæhle, Lovise, Apold, Jaran, Vedå, Nina, Møller, Pål

    出版 2009
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  4. 4
    Germline PTEN mutations are rare and highly penetrant

    Germline PTEN mutations are rare and highly penetrant 由 Rustad, Cecilie F, Bjørnslett, Merete, Heimdal, Ketil R, Mæhle, Lovise, Apold, Jaran, Møller, Pål

    出版 2006
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  5. 5
    High penetrances of BRCA1 and BRCA2 mutations confirmed in a prospective series

    High penetrances of BRCA1 and BRCA2 mutations confirmed in a prospective series 由 Møller, Pål, Mæhle, Lovise, Engebretsen, Lars F, Ludvigsen, Trond, Jonsrud, Christoffer, Apold, Jaran, Vabø, Anita, Clark, Neal

    出版 2010
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  6. 6
    The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations

    The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations 由 Rudkin, Teresa M, Hamel, Nancy, Galvez, Maria, Hogervorst, Frans, Gille, Johan JP, Møller, Pål, Apold, Jaran, Foulkes, William D

    出版 2006
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  7. 7
    Complete Mutation Screening and Haplotype Characterization of the BRCA1 Gene in 61 Familial Breast Cancer Patients from Norway

    Complete Mutation Screening and Haplotype Characterization of the BRCA1 Gene in 61 Familial Breast Cancer Patients from Norway 由 Frost, Petter, Jugessur, Astanand, Apold, Jaran, Heimdal, Ketil, Aloysius, Thomas, Eliassen, Aud K., Fauske, Lars, Matre, Guri, Eiken, Hans Geir

    出版 2005
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  8. 8
    Efficacy of Early Diagnosis and Treatment in Women with a Family History of Breast Cancer

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

    出版 1999
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  9. 9
    Recurrence of the R408W Mutation in the Phenylalanine Hydroxylase Locus in Europeans

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

    出版 1995
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