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Relationship of lower uterine segment cancer with Lynch syndrome: A novel case with an hMLH1 germline mutation
Lynch syndrome is a genetic disease that often develops in patients with endometrial cancer and is caused by abnormal DNA mismatch repair (MMR) genes. In the United States, it was recently reported that the prevalence of Lynch syndrome with an hMSH2 mutation in patients with endometrial cancer in th...
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| Main Authors: | , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3583565/ https://ncbi.nlm.nih.gov/pubmed/22940821 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/or.2012.2008 |
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