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Tumour testing to identify Lynch syndrome in two Australian colorectal cancer cohorts
BACKGROUND AND AIM: Tumour testing of colorectal cancers (CRC) for mismatch repair (MMR) deficiency is an effective approach to identify carriers of germline MMR gene mutation (Lynch syndrome). The aim of this study was to identify MMR gene mutation carriers in two cohorts of population-based CRC ut...
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| Vydáno v: | J Gastroenterol Hepatol |
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| Hlavní autoři: | , , , , , , , , , , , , , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5140773/ https://ncbi.nlm.nih.gov/pubmed/27273229 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jgh.13468 |
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