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Distinct Gene Expression Signatures in Lynch Syndrome and Familial Colorectal Cancer Type X
INTRODUCTION: Heredity is estimated to cause at least 20% of colorectal cancer. The hereditary nonpolyposis colorectal cancer subset is divided into Lynch syndrome and familial colorectal cancer type X (FCCTX) based on presence of mismatch repair (MMR) gene defects. PURPOSE: We addressed the gene ex...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3741139/ https://ncbi.nlm.nih.gov/pubmed/23951239 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0071755 |
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