Article
Detecting rare mutations associated with cancer risk.
American journal of pharmacogenomics : genomics-related research in drug development and clinical practice - 1 Jan 2001
Wilson V L
Abstract excerpt
For more than a decade, investigators have been searching for a means of determining the risk of individuals developing cancer by detecting rare oncogenic mutations. The accumulation of mutations and the clonal evolvement of tumors provide opportunities for monitoring disease development and intervening prior to the presentation of clinical symptoms, or determining the risk of disease relapse during remission. A...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
