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Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield: Results from a nationwide prospective cohort.
Svensson, Sara; Zagoras, Theofanis; Aravidis, Christos; Askmalm, Marie Stenmark; Björck, Erik; Borg, Åke; Kuchinskaya, Ekaterina; Nilbert, Mef; Nordling, Margareta; Rohlin, Anna; Silander, Gustav; Lagerstedt-Robinson, Kristina; Gebre-Medhin, Samuel.
Afiliação
  • Svensson S; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
  • Zagoras T; Department of Clinical Genetics and Pathology, Office for Medical Service, Lund, Sweden.
  • Aravidis C; Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Askmalm MS; Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Björck E; Department of Clinical Genetics, Akademiska University Hospital, Uppsala, Sweden.
  • Borg Å; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
  • Kuchinskaya E; Department of Clinical Genetics and Pathology, Office for Medical Service, Lund, Sweden.
  • Nilbert M; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Nordling M; Department of Clinical Genetics, Karolinska University Laboratory, Karolinska University Hospital, Stockholm, Sweden.
  • Rohlin A; Institute of Clinical Sciences, Division of Oncology, Lund University, Lund, Sweden.
  • Silander G; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Lagerstedt-Robinson K; Department of Clinical Genetics, Karolinska University Laboratory, Karolinska University Hospital, Stockholm, Sweden.
  • Gebre-Medhin S; Institute of Clinical Sciences, Division of Oncology, Lund University, Lund, Sweden.
Genes Chromosomes Cancer ; 61(10): 585-591, 2022 10.
Article em En | MEDLINE | ID: mdl-35430768
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Humans Idioma: En Revista: Genes Chromosomes Cancer Assunto da revista: BIOLOGIA MOLECULAR / NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suécia
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Neoplasias Colorretais Hereditárias sem Polipose Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Humans Idioma: En Revista: Genes Chromosomes Cancer Assunto da revista: BIOLOGIA MOLECULAR / NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Suécia