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A missense mutation in both hMSH2 andAPC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening
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| Autors principals: | , , , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Publishing Group
1999
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3622028/ https://ncbi.nlm.nih.gov/pubmed/10528862 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.36.10.792 |
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