MLH1 and MSH2 mutations in Colombian families with hereditary nonpolyposis colorectal cancer (Lynch syndrome) - Description of four novel mutations

This study searched for mutations in the MLH1 and MSH2 genes in 23 unrelated Colombian families with suspected hereditary nonpolyposis colorectal cancer (HNPCC). The families were grouped according to the fulfillment of the Amsterdam II criteria or the Bethesda guidelines. We screened all probands b...

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Detalles Bibliográficos
Autores Principales: Giraldo A., Gómez A., Salguero G., García H., Aristizábal F., Gutiérrez Ó., Ángel L.A., Padrón J., Martínez C., Martínez H., Malaver O., Flórez L., Barvo R.
Formato: Artículo (Article)
Lenguaje:Inglés (English)
Publicado: 2005
Materias:
DNA
Acceso en línea:https://repository.urosario.edu.co/handle/10336/24054
https://doi.org/10.1007/s10689-005-4523-7