Familial Cancer, 1389-9600

Journal

More filtering options
  1. Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries

    Anne Brédart, Jean Luc Kop, Antonis C. Antoniou, Alex P. Cunningham, Antoine de Pauw, Marc Tischkowitz, Hans Ehrencrona, Sylvie Dolbeault, Léonore Robieux, Kerstin Rhiem, Douglas F. Easton, Peter Devilee, Dominique Stoppa-Lyonnet & Rita Schmutlzer, 2018, In: Familial Cancer. 17, 1, p. 31-41

    Research output: Contribution to journalArticle

  2. 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, In: Familial Cancer. 10, 4, p. 641-647

    Research output: Contribution to journalArticle

  3. Can a phenotype for recessive inheritance in breast cancer be defined?

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

    Research output: Contribution to journalArticle

  4. 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, In: Familial Cancer. 5, 4, p. 353-358

    Research output: Contribution to journalArticle

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

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

    Research output: Contribution to journalArticle

  6. 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, In: Familial Cancer. 10, 2, p. 173-185

    Research output: Contribution to journalArticle

  7. 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, In: Familial Cancer. 6, 4, p. 445-452

    Research output: Contribution to journalArticle

  8. Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer.

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

    Research output: Contribution to journalArticle

Previous 1 2 3 Next