Familial Cancer, 1389-9600
Tidskrift
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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. 641-647Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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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. 633-639Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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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. 239-243Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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. 525-530Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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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. 125-129Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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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. 209-213Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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Prolactin levels, breast-feeding and milk production in a cohort of young healthy women from high-risk breast cancer families: implications for breast cancer risk.
Maria Hietala, Håkan Olsson & Helena Jernström, 2008, I: Familial Cancer. 7, 3, s. 221-228Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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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. 331-337Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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. 445-452Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift
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. 353-358Forskningsoutput: Tidskriftsbidrag › Artikel i vetenskaplig tidskrift