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Identification of OTX1 and OTX2 As Two Possible Molecular Markers for Sinonasal Carcinomas and Olfactory Neuroblastomas
Published on: February 28, 2019
G Ierardo1, V Luzzi, F Panetta
1Sapienza University of Rome, Italy, Department of Paediatric Dentistry.
Noonan syndrome, a genetic disorder on chromosome 12, presents with various systemic issues. Early orthodontic intervention with functional appliances can address dental and facial asymmetry in affected children.
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