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Lookup NU author(s): Emeritus Professor Alan Craft, Professor Archibald Malcolm
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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.
Author(s): King, P., Craft, A. W., Malcolm, A. J.
Publication type: Note
Publication status: Published
Journal: Journal of Clinical Pathology
Year: 1993
Volume: 46
Issue: 7
Pages: 676-677
Print publication date: 01/07/1993
ISSN (print): 0021-9746
ISSN (electronic): 1472-4146
URL: http://dx.doi.org/10.1136/jcp.46.7.676
DOI: 10.1136/jcp.46.7.676
PubMed id: 8157761
