Pivotal role of Twist in skeletal biology and pathology
Molecular Genetic Advances in Understanding Craniosynostosis
Mutations within or upstream of the basic helix–loop–helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome
Craniosynostosis: genes and mechanisms
Recurrence of Synostosis following Surgical Repair of Craniosynostosis
Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies
Clinical and Genetic Analysis of Patients with Saethre-Chotzen Syndrome
Fronto-orbital re-operation in craniosynostosis
Increased Intracranial Pressure After Coronal Suturectomy in Craniosynostotic Rabbits
Craniosynostosis in <i>Twist</i> heterozygous mice: A model for Saethre‐Chotzen syndrome
Craniofacial Shape Variation in <i>Twist1<sup>+/−</sup></i> Mutant Mice
Craniofacial abnormalities in a murine model of Saethre-Chotzen Syndrome
The pathogenesis of craniosynostosis in the fetus
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases
Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome
Saethre–Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome
Twenty-Year Experience with Early Surgery for Craniosynostosis
twist is required in head mesenchyme for cranial neural tube morphogenesis.
Twist is required for establishment of the mouse coronal suture
The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome
Interrelationship of Cranial Suture Fusion, Basicranial Development, and Resynostosis Following Suturectomy in Twist1+/− Mice, a Murine Model of Saethre-Chotzen Syndrome
Saethre-Chotzen syndrome.
Parallels of craniofacial maldevelopment in down syndrome and Ts65Dn mice
Genetic advances in craniosynostosis
Reoperation for Intracranial Hypertension in TWIST1-Confirmed Saethre-Chotzen Syndrome: A 15-Year Review
Mutations of the TWIST gene in the Saethre-Chotzene syndrome
The Craniofacial Phenotype of the Crouzon Mouse: Analysis of a Model for Syndromic Craniosynostosis Using Three-Dimensional MicroCT
Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndrome
Genetic Heterogeneity of Saethre-Chotzen Syndrome, Due to TWIST and FGFR Mutations
A population‐based study of craniosynostosis in metropolitan Atlanta, 1989–2003
Clinical genetics of craniosynostosis
Craniosynostosis.