Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma.
Loss of heterozygosity on chromosome 16 is a common genetic alteration in human hepatocellular carcinoma (HCC). To clarify the pathogenetic significance of allele loss on chromosome 16, we performed restriction fragment length polymorphism analysis of 70 surgically resected tumors by using 15 polymo...
Guardat en:
| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1990
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC54623/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2168560/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.17.6791 |
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