Familial Cancer, 1389-9600

Tidskrift

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  1. 2006
  2. 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

  3. The added value of PMS2 staining for the diagnosis of hereditary nonpolyposis colorectal cancer

    Britta Halvarsson, Mef Nilbert, E. Rambech & A. Lindblom, 2006, I : Familial Cancer. 5, s. 353

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. 2007
  5. 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

  6. 2008
  7. 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

  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. 2010
  11. 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

  12. 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

  13. 2011
  14. Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individuals

    Mev Dominguez, Felipe Carneiro da Silva, Erika Maria Monteiro dos Santos, Bianca Garcia Lisboa, Ligia Petrolini de Oliveira, Fabio de Oliveira Ferreira, Israel Gomy, Wilson Toshihiko Nakagawa, Samuel Aguiar Junior, Mariana Redal, Carlos Vaccaro, Adriana Della Valle, Carlos Sarroca, Dirce Maria Carraro & Benedito Mauro Rossi, 2011, I : Familial Cancer. 10, 4, s. 641-647

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  15. 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

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