Your browser doesn't support javascript.
loading
Use of multigene-panel identifies pathogenic variants in several CRC-predisposing genes in patients previously tested for Lynch Syndrome.
Hansen, Maren F; Johansen, Jostein; Sylvander, Anna E; Bjørnevoll, Inga; Talseth-Palmer, Bente A; Lavik, Liss A S; Xavier, Alexandre; Engebretsen, Lars F; Scott, Rodney J; Drabløs, Finn; Sjursen, Wenche.
Afiliação
  • Hansen MF; Department of Laboratory Medicine, Children's and Women's Health, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
  • Johansen J; Department of Pathology and Medical Genetics, St. Olavs University Hospital, Trondheim, Norway.
  • Sylvander AE; Department of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
  • Bjørnevoll I; Department of Pathology and Medical Genetics, St. Olavs University Hospital, Trondheim, Norway.
  • Talseth-Palmer BA; Department of Pathology and Medical Genetics, St. Olavs University Hospital, Trondheim, Norway.
  • Lavik LAS; Department of Laboratory Medicine, Children's and Women's Health, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
  • Xavier A; School of Biomedical Science and Pharmacy, University of Newcastle and Hunter Medical Research Institute, Newcastle, Australia.
  • Engebretsen LF; Clinic for Medicine, Møre and Romsdal Hospital Trust, Molde, Norway.
  • Scott RJ; Department of Pathology and Medical Genetics, St. Olavs University Hospital, Trondheim, Norway.
  • Drabløs F; School of Biomedical Science and Pharmacy, University of Newcastle and Hunter Medical Research Institute, Newcastle, Australia.
  • Sjursen W; Department of Pathology and Medical Genetics, St. Olavs University Hospital, Trondheim, Norway.
Clin Genet ; 92(4): 405-414, 2017 Oct.
Article em En | MEDLINE | ID: mdl-28195393

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Prevencao_e_fatores_de_risco / Hereditariedade / Tipos_de_cancer / Colon_e_reto Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose / Predisposição Genética para Doença / Proteínas de Neoplasias Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Noruega

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Prevencao_e_fatores_de_risco / Hereditariedade / Tipos_de_cancer / Colon_e_reto Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose / Predisposição Genética para Doença / Proteínas de Neoplasias Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Noruega