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Multigene Panel Testing Provides a New Perspective on Lynch Syndrome
PURPOSE: Most existing literature describes Lynch syndrome (LS) as a hereditary syndrome leading to high risks of colorectal cancer (CRC) and endometrial cancer mainly as a result of mutations in MLH1 and MSH2. Most of these studies were performed on cohorts with disease suggestive of hereditary CRC...
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| Publicat a: | J Clin Oncol |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society of Clinical Oncology
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7186580/ https://ncbi.nlm.nih.gov/pubmed/28514183 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1200/JCO.2016.71.9260 |
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