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Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li–Fraumeni syndrome
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  • Regular Article
  • Open access
  • Published: 26 March 1999

Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li–Fraumeni syndrome

  • E C Burt1,
  • G McGown1,
  • M Thorncroft1,
  • L A James1,
  • J M Birch2 &
  • …
  • J M Varley1 

British Journal of Cancer volume 80, pages 9–10 (1999)Cite this article

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Abstract

We have analysed Li–Fraumeni syndrome families, previously shown to be negative for mutations in TP53, for mutations to the tumour suppressor genes PTEN and CDKN2. These genes function in cell cycle progression or are mutated in a variety of tumours. We have detected no mutations in the family members tested.

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Authors and Affiliations

  1. CRC Section of Molecular Genetics, Paterson Institute for Cancer Research, Wilmslow Road, Manchester, M20 4BX, UK

    E C Burt, G McGown, M Thorncroft, L A James & J M Varley

  2. CRC Paediatric and Familial Cancer Research Group, Royal Manchester Children’s Hospital, Manchester, M27 1HA, UK

    J M Birch

Authors
  1. E C Burt
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  2. G McGown
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  3. M Thorncroft
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  4. L A James
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  5. J M Birch
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  6. J M Varley
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Rights and permissions

From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Cite this article

Burt, E., McGown, G., Thorncroft, M. et al. Exclusion of the genes CDKN2 and PTEN as causative gene defects in Li–Fraumeni syndrome. Br J Cancer 80, 9–10 (1999). https://doi.org/10.1038/sj.bjc.6690313

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  • Received: 07 August 1998

  • Revised: 28 October 1998

  • Accepted: 29 October 1998

  • Published: 26 March 1999

  • Issue date: 01 April 1999

  • DOI: https://doi.org/10.1038/sj.bjc.6690313

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Keywords

  • Li–Fraumeni syndrome
  • PTEN
  • CDKN2
  • p16
  • p19ARF

This article is cited by

  • The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype

    • Marielle WG Ruijs
    • Annegien Broeks
    • Senno Verhoef

    Hereditary Cancer in Clinical Practice (2009)

  • Screening for TP53 rearrangements in families with the Li–Fraumeni syndrome reveals a complete deletion of the TP53 gene

    • Gaëlle Bougeard
    • Laurence Brugières
    • Thierry Frébourg

    Oncogene (2003)

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