Data based on next-generation sequencing (NGS) of colorectal cancers (CRC) clearly show that up to 10% of all cases harbour pathogenic variants. Thus, NGS performed for all patients with CRC under the age of 50 could be a cost-effective strategy, leading to a personalized approach to patients and family members.
Laghi L., Ricciardiello L. (2020). The changing approach for identifying hereditary colorectal cancer syndromes. NATURE REVIEWS. GASTROENTEROLOGY & HEPATOLOGY, 17(10), 593-594 [10.1038/s41575-020-0348-y].
The changing approach for identifying hereditary colorectal cancer syndromes
Ricciardiello L.
Writing – Review & Editing
2020
Abstract
Data based on next-generation sequencing (NGS) of colorectal cancers (CRC) clearly show that up to 10% of all cases harbour pathogenic variants. Thus, NGS performed for all patients with CRC under the age of 50 could be a cost-effective strategy, leading to a personalized approach to patients and family members.File in questo prodotto:
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