Disease: Saethre-Chotzen syndrome
- A Twist-Box domain of the C. elegans Twist homolog, HLH-8, plays a complex role in transcriptional regulation
- Apert Syndrome Type III Hand: Prevalence and Outcomes
- Apert syndrome: a rare clinical image
- Apert Syndrome: Selection Rationale for Midface Advancement Technique
- Automated three-dimensional analysis of facial asymmetry in patients with syndromic coronal synostosis: A retrospective study
- Case report: A third variant in the 5' UTR of <em>TWIST1</em> creates a novel upstream translation initiation site in a child with Saethre-Chotzen syndrome
- Clinical and operative risk factors for complications after Apert hand syndactyly reconstruction
- Comparison of Internal and External Distraction in Frontofacial Monobloc Advancement: A Three-Dimensional Quantification
- Discussion of "Does the Mutation Type Affect the Response to Cranial Vault Expansion in Children With Apert Syndrome?"
- Discussion: Two-Center Review of Posterior Vault Expansion following a Staged or Expectant Treatment of Crouzon and Apert Craniosynostosis
- Does the Mutation Type Affect the Response to Cranial Vault Expansion in Children With Apert Syndrome?
- Exosome-mediated small interfering RNA delivery inhibits aberrant osteoblast differentiation in Apert syndrome model mice
- Facial Fat Graft Injection Reduces Asymmetry and Improves Forehead Contour in Early Infancy Apert Syndrome Patients
- Left Ophthalmic Segment Internal Carotid Artery Aneurysm Treated with Flow Diversion in a Child with Apert Syndrome: Technical Note
- Measurement of the Neutrophils Count and Oxidative Burst in Neutrophils of Patients with Sanjad Sakati Syndrome
- Molecular Scalpels: The Future of Pediatric Craniofacial Surgery?
- Patient Tailored Surgery in Saethre-Chotzen Syndrome: Analysis of Reoperation for Intracranial Hypertension
- Pfeiffer Syndrome
- Pfeiffer Syndrome
- Sensitivity, specificity and cutoff identifying optic atrophy by macular ganglion cell layer volume in syndromic craniosynostosis
- Sensitivity, Specificity, and Cutoff Identifying Optic Atrophy by Macular Ganglion Cell Layer Volume in Syndromic Craniosynostosis
- Ser252Trp mutation in fibroblast growth factor receptor 2 promotes branching morphogenesis in mouse salivary glands
- Skull progenitor cell-driven meningeal lymphatic restoration improves neurocognitive functions in craniosynostosis
- Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis
- Syndromic Craniofacial Disorders
- Syndromic Craniosynostosis: A Comprehensive Review
- The influence of orbital architecture on strabismus in craniosynostosis
- The Role of Airway Management on Feeding Difficulties in Children With Pfeiffer Syndrome
- Whole exome sequencing combined with dynamic ultrasound assessments for fetal skeletal dysplasias: 4 case reports