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Importance of PCR-Based Tumor Testing in the Evaluation of Lynch Syndrome-Associated Endometrial Cancer
Lynch Syndrome is a hereditary cancer syndrome caused by a germline mutation in a DNA mismatch repair gene, usually MLH1, MSH2, MSH6, or PMS2. The most common cancers associated with Lynch Syndrome are colorectal adenocarcinoma and endometrial carcinoma. Identification of women with Lynch Syndrome-a...
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| Publicado no: | Adv Anat Pathol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5657565/ https://ncbi.nlm.nih.gov/pubmed/28820751 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/PAP.0000000000000169 |
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