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p53 expression in three separate tumours from a patient with Li-Fraumeni's syndrome.
  1. P King,
  2. A W Craft,
  3. A J Malcolm
  1. University Department of Pathology, Royal Victoria Infirmary, Newcastle upon Tyne.

    Abstract

    The Li-Fraumeni cancer syndrome is a rare autosomal dominant syndrome, characterised by the occurrence of diverse mesenchymal and epithelial neoplasms at multiple sites. It has recently been shown that some of these individuals have a germ line mutation of the p53 tumour suppressor gene. The case of one member of such a family who has now developed three separate primary malignant tumours is reported. All three tumours expressed mutant p53 protein.

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