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Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome
Scalp fibroblasts have a shared expression profile in monogenic craniosynostosis
Clinical dividends from the molecular genetic diagnosis of craniosynostosis