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Unicystic ameloblastoma associated with the novel K729M PTCH1 mutation in a patient with nevoid basal cell carcinoma (Gorlin) syndrome

✍ Scribed by Giovanni Ponti; Annamaria Pollio; Michele Davide Mignogna; Giovanni Pellacani; Lorenza Pastorino; Giovanna Bianchi-Scarrà; Carmela Di Gregorio; Cristina Magnoni; Paola Azzoni; Maurizio Greco; Stefania Seidenari

Book ID: 116332665
Publisher: Elsevier
Year: 2012
Tongue: English
Weight: 781 KB
Volume: 205
Category: Article
ISSN: 2210-7762
DOI: 10.1016/j.cancergen.2012.01.012

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