Craniosynostosis
Premature fusion of bones in the skull
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Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations
Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis
Scalp fibroblasts have a shared expression profile in monogenic craniosynostosis
Clinical dividends from the molecular genetic diagnosis of craniosynostosis
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases
