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Association of the I1307K APC mutation with hereditary and sporadic breast/ovarian cancer: more questions than answers
The frequency of the APC I1307K mutation and its association with disease pattern was examined in 996 Ashkenazi women consisting of individuals with either sporadic (n = 382) or hereditary (n = 143) breast and/or ovarian cancer; asymptomatic BRCA1/2 mutation carriers (185delAG, 5382insC and 6174delT...
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| Hauptverfasser: | , , , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Nature Publishing Group
2000
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2363478/ https://ncbi.nlm.nih.gov/pubmed/10901363 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1054/bjoc.2000.1248 |
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