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Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.
Kayser, Katrin; Degenhardt, Franziska; Holzapfel, Stefanie; Horpaopan, Sukanya; Peters, Sophia; Spier, Isabel; Morak, Monika; Vangala, Deepak; Rahner, Nils; von Knebel-Doeberitz, Magnus; Schackert, Hans K; Engel, Christoph; Büttner, Reinhard; Wijnen, Juul; Doerks, Tobias; Bork, Peer; Moebus, Susanne; Herms, Stefan; Fischer, Sascha; Hoffmann, Per; Aretz, Stefan; Steinke-Lange, Verena.
Afiliação
  • Kayser K; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Degenhardt F; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Holzapfel S; Department of Genomics, Life and Brain Center, University of Bonn, Bonn, Germany.
  • Horpaopan S; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Peters S; Center for Hereditary Tumor Syndromes, University of Bonn, Bonn, Germany.
  • Spier I; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Morak M; Department of Anatomy, Faculty of Medical Science, Naresuan University, Phitsanulok, Thailand.
  • Vangala D; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Rahner N; Department of Genomics, Life and Brain Center, University of Bonn, Bonn, Germany.
  • von Knebel-Doeberitz M; Institute of Human Genetics, University of Bonn, Bonn, Germany.
  • Schackert HK; Center for Hereditary Tumor Syndromes, University of Bonn, Bonn, Germany.
  • Engel C; Medizinische Klinik und Poliklinik IV, Campus Innenstadt, Klinikum der Universität München, Munich, Germany.
  • Büttner R; Medical Genetics Center (MGZ), Munich, Germany.
  • Wijnen J; Department of Internal Medicine, Knappschaftskrankenhaus, Ruhr-University Bochum, Bochum, Germany.
  • Doerks T; Institute of Human Genetics, University of Düsseldorf, Düsseldorf, Germany.
  • Bork P; Department of Applied Tumor Biology, Institute of Pathology, University Hospital of Heidelberg, Heidelberg, Germany.
  • Moebus S; Cooperation Unit Applied Tumor Biology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • Herms S; Department of Surgical Research, Technische Universität Dresden, Dresden, Germany.
  • Fischer S; Institute of Medical Informatics, Statistics, and Epidemiology, University of Leipzig, Leipzig, Germany.
  • Hoffmann P; Institute of Pathology, University of Cologne, Cologne, Germany.
  • Aretz S; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Steinke-Lange V; Structural and Computational Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Int J Cancer ; 143(11): 2800-2813, 2018 12 01.
Article em En | MEDLINE | ID: mdl-29987844
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Variações do Número de Cópias de DNA Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Int J Cancer Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Estados Unidos
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais Hereditárias sem Polipose / Variações do Número de Cópias de DNA Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Int J Cancer Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Estados Unidos