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Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome)
Causative genetic variants have to date been identified for only a small proportion of familial colorectal cancer (CRC). While conditions such as Familial Adenomatous Polyposis and Lynch syndrome have well defined genetic causes, the search for variants underlying the remainder of familial CRC is pl...
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| Autori principali: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Springer Netherlands
2010
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3100490/ https://ncbi.nlm.nih.gov/pubmed/21165777 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10689-010-9408-8 |
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