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Molecular alterations in a patient with Turcot's syndrome.
Rochlitz, C F; Heide, I; de Kant, E; Neubauer, A; Schmidt, C A; Neuhaus, P; Huhn, D; Herrmann, R.
Afiliación
  • Rochlitz CF; Department Innere Medizin, Kantonsspital Basel.
Br J Cancer ; 68(3): 519-23, 1993 Sep.
Article en En | MEDLINE | ID: mdl-8394730
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Genes p53 / Genes ras / Poliposis Adenomatosa del Colon Límite: Adolescent / Humans Idioma: En Revista: Br J Cancer Año: 1993 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Genes p53 / Genes ras / Poliposis Adenomatosa del Colon Límite: Adolescent / Humans Idioma: En Revista: Br J Cancer Año: 1993 Tipo del documento: Article