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Cost-Benefit Implications in the Surveillance of Lynch Syndrome Subjects

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Part of the book series: ESO Monographs ((ESO MONOGRAPHS))

Abstract

Hereditary diseases, especially tumours of the gastrointestinal (Gl) tract, are gaining interest throughout the world [1,2]. They represent a unique model for the understanding of the aetiology of cancer and its biological behaviour, enabling us to introduce preventive strategies and possibly newer, more sophisticated therapies which are currently being searched for by molecular biologists [3].

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References

  1. Lynch HT, Lanspa SJ, Smyrk TC, Fitzgibbons RJ, Watson P, Boman BM, Lynch JF and Cristofaro G: Historical and natural cancer history facets of the Lynch Syndromes. In: Utsunomiya J and Lynch HT (eds) Hereditary Colon Cancer. Springer Verlag, Tokyo, Berlin, Heidelberg, New York, London, Paris, Hong Kong, Barcelona 1990 pp 17–25

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  2. Cristofaro G, Lynch HT, Caruso ML, Attolini A et al: New phenotypic aspects in a family with Lynch Syndrome II. Cancer 1987 (60):51–58

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  3. Vogelstein B, Fearon ER, Hamilton SR, Bodmer WF, Jass JR, Jeffreys AJ, Lucibello FC, Patel I and Rider SH: Genetic alterations during colorectal tumor development. N Engl J Med 1988 (319):525–532

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  4. Lynch HT: Frequency of hereditary nonpolyposis colorectal cancer. Gastroenterology 1986 (90):486–492

    PubMed  CAS  Google Scholar 

  5. Mecklin JP: Frequency of hereditary colorectal cancer. Gastroenterology 1987 (93):1021–1025

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© 1992 Springer-Verlag Berlin Heidelberg

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Cristofaro, G., Carrozzo, E., Gentile, F., Di Giulio, E. (1992). Cost-Benefit Implications in the Surveillance of Lynch Syndrome Subjects. In: Weber, W. (eds) Familial Cancer Control. ESO Monographs. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-77582-6_11

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  • DOI: https://doi.org/10.1007/978-3-642-77582-6_11

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-77584-0

  • Online ISBN: 978-3-642-77582-6

  • eBook Packages: Springer Book Archive

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