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Comprehensive mismatch repair gene panel identifies variants in patients with Lynch-like syndrome.
Xavier, Alexandre; Olsen, Maren Fridtjofsen; Lavik, Liss A; Johansen, Jostein; Singh, Ashish Kumar; Sjursen, Wenche; Scott, Rodney J; Talseth-Palmer, Bente A.
Afiliação
  • Xavier A; University of Newcastle Hunter Medical Research Institute, New Lambton Heights, New South Wales, Australia.
  • Olsen MF; Faculty of Medicine and Health Sciences, Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
  • Lavik LA; Department of Medical Genetics, Saint Olavs Hospital University Hospital, Trondheim, Norway.
  • Johansen J; Department of Medical Genetics, Saint Olavs Hospital University Hospital, Trondheim, Norway.
  • Singh AK; Faculty of Medicine and Health Sciences, Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
  • Sjursen W; Department of Medical Genetics, Saint Olavs Hospital University Hospital, Trondheim, Norway.
  • Scott RJ; Faculty of Medicine and Health Sciences, Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
  • Talseth-Palmer BA; Department of Medical Genetics, Saint Olavs Hospital University Hospital, Trondheim, Norway.
Mol Genet Genomic Med ; 7(8): e850, 2019 08.
Article em En | MEDLINE | ID: mdl-31297992
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Testes Genéticos / Predisposição Genética para Doença / Reparo de Erro de Pareamento de DNA Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Testes Genéticos / Predisposição Genética para Doença / Reparo de Erro de Pareamento de DNA Idioma: En Ano de publicação: 2019 Tipo de documento: Article