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Identification of genetic variants for clinical management of familial colorectal tumors
BACKGROUND: The genetic mechanisms for families who meet the clinical criteria for Lynch syndrome (LS) but do not carry pathogenic variants in the mismatch repair (MMR) genes are still undetermined. We aimed to study the potential contribution of genes other than MMR genes to the biological and clin...
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| Publicado no: | BMC Med Genet |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5819082/ https://ncbi.nlm.nih.gov/pubmed/29458332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-018-0533-9 |
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