Treatment inferred from mutations identified using massive parallel sequencing leads to clinical benefit in some heavily pretreated cancer patients
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| Veröffentlicht in: | Annals of oncology 2016-10, Vol.27, p.vi26-vi26 |
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| container_title | Annals of oncology |
| container_volume | 27 |
| creator | Zick, A. Peretz, T. Lotem, M. Hubert, A. Katz, D. Temper, M. Rottenberg, Y. Uziely, B. Nechushtan, H. Meirovitz, A. Sonnenblick, A. Sapir, E. Edelman, D. Goldberg, Y. Lossos, A. Rosenberg, S. Fried, I. Finklstein, R. Pikarsky, E. Goldshmidt, H. |
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| doi_str_mv | 10.1093/annonc/mdw363.36 |
| format | Article |
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| language | eng |
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| source | EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
| title | Treatment inferred from mutations identified using massive parallel sequencing leads to clinical benefit in some heavily pretreated cancer patients |
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