Skip to main content
SpringerLink
Log in

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

  • Published:
Familial Cancer Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

References

  1. Plon et al (2008) Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results. Hum Mutat 29:1282–1291

    Article  CAS  PubMed  Google Scholar 

  2. Barnetson et al (2006) Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer. New Engl J Med 354:2751–2763

    Article  CAS  PubMed  Google Scholar 

  3. Couch et al (2008) Assessment of functional effects of unclassified genetic variants. Hum Mutat 29:1314–1326

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Cancer Research Program, Garvan Institute of Medical Research, 384 Victoria Street, Darlinghurst, Sydney, NSW, 2010, Australia

    Maija Kohonen-Corish

  2. State University of New York at Downstate, Brooklyn, NY, USA

    Thomas K. Weber

  3. Karolinska Institutet, Stockholm, Sweden

    Annika Lindblom

  4. Department of Medicine, and Colorectal Medicine and Genetics, The Royal Melbourne Hospital, University of Melbourne, Grattan St, Parkville, VIC, 3050, Australia

    Finlay Macrae

Authors
  1. Maija Kohonen-Corish
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Thomas K. Weber
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Annika Lindblom
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Finlay Macrae
    View author publications

    You can also search for this author in PubMed Google Scholar

Consortia

the Meeting Participants

Corresponding author

Correspondence to Maija Kohonen-Corish.

Additional information

This study is conducted for the InSiGHT, HVP and NCI-CCFR Meeting Participants: G. Moeslein, S. Gallinger, R. Cotton, M. Genuardi, S. Tavtigian, G. Byrnes, A. Spurdle, I. Bernstein, N. de Wind, M. Nystrom, R. Hofstra, M. Woods, J. den Dunnen, B. Bhapat, M. Qi, P. Propping, H. Vasen, S. Povey, R. Sijmons, H. Thomas, J. Baron, S. Thibodeau, A. Boussioutas, J. Young, M. Jenkins, M. Dunlop, R. Houlston, I. Tomlinson, U. Peters, D. Ahnen, S. Parry, B. Parry, R. Scott, G. Hannan.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kohonen-Corish, M., Weber, T.K., Lindblom, A. et al. 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. Familial Cancer 9, 705–711 (2010). https://doi.org/10.1007/s10689-010-9347-4

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10689-010-9347-4

Keywords

Search

Navigation