Familial Cancer

, Volume 9, Issue 4, pp 705–711 | Cite as

Report of the Combined Meeting of the International Society for Gastrointestinal Hereditary Tumours, the Human Variome Project and the National Cancer Institute Colon Cancer Family Registry, Duesseldorf, Germany, 24 June 2009

  • Maija Kohonen-Corish
  • Thomas K. Weber
  • Annika Lindblom
  • Finlay Macrae
  • the Meeting Participants


Lynch Syndrome Colonoscopic Surveillance Serrate Polyp Unclassified Variant Genome Wide Association Study Study 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


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    Plon et al (2008) Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results. Hum Mutat 29:1282–1291CrossRefPubMedGoogle Scholar
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    Barnetson et al (2006) Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer. New Engl J Med 354:2751–2763CrossRefPubMedGoogle Scholar
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    Couch et al (2008) Assessment of functional effects of unclassified genetic variants. Hum Mutat 29:1314–1326CrossRefPubMedGoogle Scholar

Copyright information

© Springer Science+Business Media B.V. 2010

Authors and Affiliations

  • Maija Kohonen-Corish
    • 1
  • Thomas K. Weber
    • 2
  • Annika Lindblom
    • 3
  • Finlay Macrae
    • 4
  • the Meeting Participants
  1. 1.Cancer Research Program, Garvan Institute of Medical ResearchDarlinghurst, SydneyAustralia
  2. 2.State University of New York at DownstateBrooklynUSA
  3. 3.Karolinska InstitutetStockholmSweden
  4. 4.Department of Medicine, and Colorectal Medicine and Genetics, The Royal Melbourne HospitalUniversity of MelbourneParkvilleAustralia

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