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Molecular alterations in a patient with Turcot's syndrome.
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...
Autores principales: | Rochlitz, C. F., Heide, I., de Kant, E., Neubauer, A., Schmidt, C. A., Neuhaus, P., Huhn, D., Herrmann, R. |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1993
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968408/ https://www.ncbi.nlm.nih.gov/pubmed/8394730 |
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