Familial Cancer, 1389-9600

Tidskrift

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  1. 2011
  2. Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.

    Anna Isinger Ekstrand, Christina Therkildsen, Inge Bernstein & Mef Nilbert, 2011, I : Familial Cancer. 10, s. 239-243

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer

    Maria Henningson, Maria Hietala, Therese Törngren, Håkan Olsson & Helena Jernström, 2011, I : Familial Cancer. 10, 2, s. 173-185

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. Limited impact on self-concept in individuals with Lynch syndrome; results from a national cohort study

    Helle Vendel Petersen, Mary Jane Esplen, Steen Ladelund, Inge Bernstein, Lone Sunde, Christina Carlsson & Mef Nilbert, 2011, I : Familial Cancer. 10, 4, s. 633-639

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. 2010
  6. Can a phenotype for recessive inheritance in breast cancer be defined?

    Carolina Ellberg, Göran B Jönsson & Håkan Olsson, 2010, I : Familial Cancer. 9, 4, s. 525-530

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  7. Frequent alterations of the PI3K/AKT/mTOR pathways in hereditary nonpolyposis colorectal cancer.

    Anna Isinger Ekstrand, Mats Jönsson, Annika Lindblom, Åke Borg & Mef Nilbert, 2010, I : Familial Cancer. 9, s. 125-129

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. 2009
  9. Sarcomas associated with hereditary nonpolyposis colorectal cancer: broad anatomical and morphological spectrum

    Mef Nilbert, Christina Therkildsen, Anja Nissen, Måns Åkerman & Inge Bernstein, 2009, I : Familial Cancer. 8, 3, s. 209-213

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. 2008
  11. Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.

    Susanne Magnusson, Åke Borg, Ulf Kristoffersson, Mef Nilbert, Thomas Wiebe & Håkan Olsson, 2008, I : Familial Cancer. 7, s. 331-337

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  12. 2007
  13. Absence of the common IGF1 19 CA-repeat allele is more common among BRCA1 mutation carriers than among non-carriers from BRCA1 families.

    Maria Henningson, Erika Bågeman, Therese Törngren, Åke Borg, Håkan Olsson & Helena Jernström, 2007, I : Familial Cancer. 6, 4, s. 445-452

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. 2006
  15. The added value of PMS2 immunostaining in the diagnosis of hereditary nonpolyposis colorectal cancer.

    Britta Halvarsson, Annika Lindblom, Eva Rambech, Kristina Lagerstedt & Mef Nilbert, 2006, I : Familial Cancer. 5, 4, s. 353-358

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift