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Two novel colorectal cancer risk loci in the region on chromosome 9q22.32
Highly penetrant cancer syndromes account for less than 5% of all cases with familial colorectal cancer (CRC), and other genetic contribution explains the majority of the genetic contribution to CRC. A CRC susceptibility locus on chromosome 9q has been suggested. In this study, families where risk o...
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| Publicado no: | Oncotarget |
|---|---|
| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Impact Journals LLC
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5834248/ https://ncbi.nlm.nih.gov/pubmed/29541405 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.24340 |
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