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Unicystic ameloblastoma associated with the novel K729M PTCH1 mutation in a patient with nevoid basal cell carcinoma (Gorlin) syndrome. [electronic resource] by
- Ponti, Giovanni
- Pollio, Annamaria
- Mignogna, Michele Davide
- Pellacani, Giovanni
- Pastorino, Lorenza
- Bianchi-Scarrà, Giovanna
- Di Gregorio, Carmela
- Magnoni, Cristina
- Azzoni, Paola
- Greco, Maurizio
- Seidenari, Stefania
Producer: 20120627
In:
Cancer genetics vol. 205
Availability: No items available.
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