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Publications by Lorenza Pastorino
Clinical Utility Gene Card For: Gorlin Syndrome - Update 2013
European Journal of Human Genetics
Genetics
Correction: Combining Molecular and Immunohistochemical Analyses of Key Drivers in Primary Melanomas: Interplay Between Germline and Somatic Variations
Oncotarget
Oncology
Combining Molecular and Immunohistochemical Analyses of Key Drivers in Primary Melanomas: Interplay Between Germline and Somatic Variations
Oncotarget
Oncology
Novel PTCH1 Mutations in Patients With Keratocystic Odontogenic Tumors Screened for Nevoid Basal Cell Carcinoma (NBCC) Syndrome
PLoS ONE
Multidisciplinary
Skeletal and Cranio-Facial Signs in Gorlin Syndrome From Ancient Egypt to the Modern Age: Sphenoid Asymmetry in a Patient With a novelPTCH1mutation
Future Oncology
Medicine
Cancer Research
Oncology
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