Sfoglia per Rivista FAMILIAL CANCER
A PALB2 germline mutation associated with hereditary breast cancer in Italy.
2009 L. Papi;A. L. Putignano;C. Congregati;I. Piaceri;I. Zanna;F. Sera;D. Morrone;M. Genuardi;D. Palli
Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism.
2016 Gigante, L; Paganini, I; Frontali, M; Ciabattoni, S; Sangiuolo, Fc; Papi, L
Ventricular fibrillation resulting from electrolyte imbalance reveals vipoma in MEN1 syndrome.
2016 Cavalli, T; Giudici, F; Santi, R; Nesi, G; Brandi, Ml; Tonelli, F
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
A PALB2 germline mutation associated with hereditary breast cancer in Italy. | 2009 | L. Papi;A. L. Putignano;C. Congregati;I. Piaceri;I. Zanna;F. Sera;D. Morrone;M. Genuardi;D. Palli | |
Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism. | 2016 | Gigante, L; Paganini, I; Frontali, M; Ciabattoni, S; Sangiuolo, Fc; Papi, L | |
Ventricular fibrillation resulting from electrolyte imbalance reveals vipoma in MEN1 syndrome. | 2016 | Cavalli, T; Giudici, F; Santi, R; Nesi, G; Brandi, Ml; Tonelli, F |
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