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The primary site of the acrocephalic feature in Apert syndrome is a dwarf cranial base with accelerated chondrocytic differentiation due to aberrant activation of the FGFR2 signaling

Developmental AnomalyDevelopmental BiologyDwarf Cranial BaseGeneticsPathologyCraniofacial DevelopmentMorphogenesisApert SyndromeMedicineCraniofacial DisorderFgfr2 Signaling