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Molecular alterations in a patient with Turcot's syndrome
C F Rochlitz1, I Heide, E de Kant
1Department Innere Medizin, Kantonsspital Basel.
British Journal of Cancer
|September 1, 1993
Abstract:
Cells of a patient with Turcot's syndrome and of her parents were evaluated for the presence of molecular alterations in the p53 and the Ki-ras gene. Deletions on chromosome 17p, overexpression and point mutations of the p53 gene as well as mutations of the Ki-ras gene were detected in primary and metastatic tumour but not in the germline of the patient nor in her parents.