A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

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Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

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A Genetic-Pathophysiological Framework for Craniosynostosis

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Msx homeobox gene family and craniofacial development

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Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis

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The role of the msh homeobox gene during Drosophila neurogenesis: implication for the dorsoventral specification of the neuroectoderm

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A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

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Genetic advances in craniosynostosis

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Neural crest cell signaling pathways critical to cranial bone development and pathology

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Ectodermal dysplasias: not only ‘skin’ deep

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Patterning the zebrafish axial skeleton requires early chordin function

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Copy-Number Variations Involving the IHH Locus Are Associated with Syndactyly and Craniosynostosis

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Msx2 −/− transgenic mice develop compound amelogenesis imperfecta, dentinogenesis imperfecta and periodental osteopetrosis

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Msx2 Exerts Bone Anabolism via Canonical Wnt Signaling

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Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop’s classification

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Msx2 mediates the inhibitory action of TNF-α on osteoblast differentiation

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FGFR3 P250R Mutation Increases the Risk of Reoperation in Apparent ‘Nonsyndromic’ Coronal Craniosynostosis

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Initiation of Early Osteoblast Differentiation Events through the Direct Transcriptional Regulation of Msx2 by FOXC1

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Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain

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Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis

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Molecular Mechanisms Involved in Craniosynostosis

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Osteoblast differentiation profiles define sex specific gene expression patterns in craniosynostosis

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Clinical and Genetic Characterization of Craniosynostosis in Saudi Arabia

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Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes

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