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To determine whether infant cases with craniofacial microsomia (CFM) evidence poorer neurodevelopmental status than demographically similar infants without craniofacial diagnoses (“controls”), and to examine cases' neurodevelopmental outcomes by facial phenotype and hearing status.Multicenter, observational study of 108 cases and 84 controls aged 12-24 months. Participants were assessed by the Bayley...
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