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The Clinical Relevance of Frequent Germline Genetic Variants Detected by Targeted Sequencing in Patients With Rectal Adenocarcinoma (READ)
Background: The progression of colorectal cancer (CRC) mainly stems from the occurrence of somatic mutation. However, there is little information that can be used to comprehensively analyse the importance of germline variants in CRC patients. Patients and Methods: The candidate germline variants bet...
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| Publicado no: | Cancer Genomics Proteomics |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
International Institute of Anticancer Research
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7259889/ https://ncbi.nlm.nih.gov/pubmed/32345670 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21873/cgp.20189 |
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