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Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families
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  • W Friedl aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • R Caspari aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • M Sengteller aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • S Uhlhaas aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • C Lamberti aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • M Jungck aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • M Kadmon aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • M Wolf aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • J Fahnenstich aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • J Gebert aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • G Möslein aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • E Mangold aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  • P Propping aInstitute of Human Genetics, University of Bonn, Germany, bDepartment of Medicine I, University of Bonn, Germany, cDepartment of Surgery, University of Heidelberg, Germany, dDepartment of Human Genetics, University of Ulm, Germany, eDepartment of Surgery, University of Düsseldorf, Germany PubMed articlesGoogle scholar articles
  1. Dr W Friedl, Institute of Human Genetics, University of Bonn, Wilhelmstrasse 31, D-53111 Bonn, Germany. friedlw{at}meb.uni-bonn.de
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Citation

Friedl W, Caspari R, Sengteller M, et al
Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families

Publication history

  • Accepted November 14, 2000
  • First published April 1, 2001.
Online issue publication 
April 01, 2001

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