Skip to content
CCFR
  • Home
  • For Participants
    • Your Contribution
    • Research Discoveries
    • Protecting Your Privacy
    • FAQs
    • Site Newsletters
      • Cleveland Clinic – Cleveland
        Ohio, USA
      • Fred Hutch Cancer Center
      • Mayo Clinic – Phoenix, Arizona, USA
      • Ontario Familial Colorectal
        Cancer Registry
  • For Researchers
    • The CCFR Resource
    • Data Dictionaries
    • Questionnaires & Forms
    • Data Access
      • dbGaP
      • Collaborate
    • Publications Policy
  • News & Events
  • Publications
  • About Us
    • Who We Are
    • Our Team
    • Our Sites

Familial Colorectal Cancer Type X: the other half of hereditary nonpolyposis colon cancer syndrome.

Authors Lindor NM.
Citation Surg Oncol Clin N Am. 2009 Oct;18(4):637-45.
PubMedLink https://pubmed.ncbi.nlm.nih.gov/19793571/
PMCID PMC3454516

Posted in PublicationsTagged 2009
Read this next

Germline EPHB2 receptor variants in familial colorectal cancer.

© 2025 CCFR • Slightly Theme by Nick Ciliak.
Funded by the National Cancer
Institute (NCI), U01 CA167551, NIH USA
© 2023