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COMPLEX GENOTYPE SARCOMAS DISPLAY FAMILIAL INHERITANCE INDEPENDENT OF KNOWN CANCER PREDISPOSITION SYNDROMES
BACKGROUND: The low incidence of sarcomas in the general population makes heritable contribution to disease risk difficult to discern beyond highly penetrant Mendelian syndromes. METHODS: The Utah Cancer Registry (UCR) and Utah Population Database (UPBD) were interrogated for sarcoma diagnostic code...
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| Glavni autori: | , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2011
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3085094/ https://ncbi.nlm.nih.gov/pubmed/21242332 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/1055-9965.EPI-10-1174 |
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