• <em>De novo</em> variants of dominant monogenic disorders in Vietnam detected by a noninvasive prenatal test: a case series
• <em>Drosophila</em> Homolog of the Human Carpenter Syndrome Linked Gene, <em>MEGF8</em>, Is Required for Synapse Development and Function
• 3D Imaging Reveals Changes in the Neurovascular Architecture of the Murine Calvarium with Aging
• A Complex Case of Clino-Syndactyly with Fourth Metacarpal Aplasia
• A European multicenter outcome study on the different perioperative airway management policies following midface surgery in syndromic craniosynostosis: a proposal for a Standard Operating Procedure
• A longitudinal study of the role of fingers in the development of early number and arithmetic skills in children with Apert syndrome
• A Twist-Box domain of the C. elegans Twist homolog, HLH-8, plays a complex role in transcriptional regulation
• Advances in genetic research on Non-syndromic congenital joint synostosis
• Alterations in Sphenoid Anatomy in Craniosynostosis: Implications for Fronto-Orbital Advancement
• Anatomical study of first palmar intermetacarpal flap in cadavers and application for congenital first web contracture in a child with Apert's syndrome
• Apert Syndrome
• Apert Syndrome
• Apert Syndrome - caveats of squint management
• Apert syndrome in a newborn with premature fusion of skull bones, a rostral nose, and cleft palate: A case report
• Apert Syndrome Type III Hand: Prevalence and Outcomes
• Apert syndrome: a rare clinical image
• Apert syndrome: craniofacial challenges and clinical implications
• Apert syndrome: neurosurgical outcomes and complications following posterior vault distraction osteogenesis
• Apert Syndrome: Selection Rationale for Midface Advancement Technique
• Apical expansion of calvarial osteoblasts and suture patency is dependent on fibronectin cues
• Auricles Anomalies in Patients With a TCF12 Gene Mutation
• Automated three-dimensional analysis of facial asymmetry in patients with syndromic coronal synostosis: A retrospective study
• Bacterial Sepsis among Children with Congenital Heart Disease in Tikur Anbessa Specialized Hospital, Addis Ababa, Ethiopia
• Cleft Palate in Apert Syndrome
• Cleft Palate in Apert Syndrome: A Descriptive Study of Incidence and Surgical Outcome
• Clinical and Genetic Studies of the First Monozygotic Twins with Pfeiffer Syndrome
• Clinical and operative risk factors for complications after Apert hand syndactyly reconstruction
• Clinical manifestations of Apert syndrome
• Clinical-Epidemiological Study of a Cohort of 35 Patients with Craniosynostosis
• Coexistence of Two Rare Conditions Complicating the Other's Management: Propionic Acidemia and Apert Syndrome
• Comparison of Internal and External Distraction in Frontofacial Monobloc Advancement: A Three-Dimensional Quantification
• Contemporary Management of the Upper Limb in Apert Syndrome: A Review
• Craniofacial syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis
• Delayed Postnatal Synostosis without Spheno-occipital Synchondrosis Fusion: A Curious Case of Apert Syndrome
• 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?
• Drosophila Homolog of the Human Carpenter Syndrome Linked Gene, MEGF8, Is Required for Synapse Development and Function
• Early Cranioplasty in an Apert's Syndrome Infant With Occipital Encephalocele
• Emphasis on Early Prenatal Diagnosis and Perinatal Outcomes Analysis of Apert Syndrome
• Evaluation of polysomnography findings in children with genetic skeletal disorders
• 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
• Factors Affecting Optic Nerve Damage in Le Fort III Osteotomy: A Retrospective Study
• Genetic Subtypes of Apert Syndrome Are Associated With Differences in Airway Morphology and Early Upper Airway Obstruction
• Humanitarian Facial Recognition for Rare Craniofacial Malformations
• Impact of Anterior and Posterior Vault Distraction Osteogenesis (A-PVDO) and 3D-Printed Positioning/Shaping Templates in Apert Syndrome: A Case Series Study
• Impact of paternal age on assisted reproductive technology outcomes and offspring health: a systematic review
• Introduction of Spring-Assisted Cranioplasty for Bicoronal Synotosis in India: Description of First Case and Our Learning Experience
• Lacrimal Obstruction in Craniosynostosis: Anatomical and Genetic Risk Factors
• Left Ophthalmic Segment Internal Carotid Artery Aneurysm Treated with Flow Diversion in a Child with Apert Syndrome: Technical Note
• Long-Term Follow-Up of Apert Syndrome Following Mid-Face Advancement: More Than 3 Decades Later
• Male reproductive ageing: a radical road to ruin
• Measurement of the Neutrophils Count and Oxidative Burst in Neutrophils of Patients with Sanjad Sakati Syndrome
• Molecular Mechanisms Involved in Craniosynostosis
• Molecular Scalpels: The Future of Pediatric Craniofacial Surgery?
• Mother and Daughter Carrying of the Same Pathogenic Variant in <em>FGFR2</em> with Discordant Phenotype
• Mystery of the Muenke midface: spheno-occipital synchondrosis fusion and craniofacial skeletal patterns
• Noninvasive Ventilation in Pediatric Acute Respiratory Distress Syndrome: "Another Dogma Bites the Dust"
• Orbital and Eyelid Characteristics, Strabismus, and Intracranial Pressure Control in Apert Children Treated by Endoscopic Strip Craniectomy versus Fronto-Orbital Advancement
• Orthognathic Surgery in Patients with Syndromic Craniosynostosis
• Outcome of Bilateral Hand Reconstruction in a Child Presenting Late With Apert Syndrome: A Case Report and Literature Review
• Outcomes of Apert Syndrome Hand Reconstruction With Tilapia Skin: A Prospective Study
• Patient Tailored Surgery in Saethre-Chotzen Syndrome: Analysis of Reoperation for Intracranial Hypertension
• Perinatal imaging findings of a fetus with Pfeiffer syndrome and a heterozygous c.1019A>G, p.Tyr340Cys (Y340C) mutation in FGFR2 presenting a cloverleaf skull, craniosynostosis and short limbs on prenatal ultrasound mimicking thanatophoric dysplasia ty
• Persistent falcine sinus in the newborn: 3 case reports of associated anomalies
• Pfeiffer Syndrome
• Pfeiffer Syndrome
• Plantar intermetatarsal perforator flap for first web skin-graftless syndactyly release: Anatomical study and clinical application
• Posterior Cranial Distraction in Craniosynostosis: A Systematic Review of the Literature
• Prenatal diagnosis and management of Apert syndrome in a low-middle income country: Case report
• Prenatal imaging of a fetus with the rare combination of Pfeiffer syndrome and hypoplastic left heart syndrome
• Preprocedural Electrophysiological Monitoring in Craniofacial Surgery for a Patient with Chiari Malformation
• Presentation and Treatment of a Patient With Jacobs Syndrome and Metopic Craniosynostosis
• 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
• Skeletal changes after midface surgery in patients with craniofacial deformities: a three-dimensional quantification method
• Subcranial Midface Advancement in Patients with Syndromic Craniosynostosis
• Successful reverse total shoulder replacement in a patient with Apert syndrome
• Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis
• Syndactyly
• Syndactyly
• Syndromic Craniofacial Disorders
• Syndromic Craniosynostosis: A Comprehensive Review
• The influence of orbital architecture on strabismus in craniosynostosis
• The Kaleidoscope of Midface Management in Apert Syndrome: A 23-Year Single-Institution Experience
• The phenotype of MEGF8-related Carpenter syndrome (CRPT2) is refined through the identification of eight new patients
• The Role of Airway Management on Feeding Difficulties in Children With Pfeiffer Syndrome
• The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4
• Thirty-year Experience Treating Syndromic Craniosynostosis: Long-term Outcomes Following Cranial Expansions
• Three-Dimensional Evaluation of Dental Arches in Individuals with Syndromic Craniosynostosis
• Three-dimensional quantification of soft tissue changes and its relationship to skeletal changes after Le Fort III, monobloc, and facial bipartition in syndromic craniosynostosis
• TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouse
• Two-Center Review of Posterior Vault Expansion following a Staged or Expectant Treatment of Crouzon and Apert Craniosynostosis
• Two-stage surgical treatment for medially angulated great toes in Apert feet by wedged corrective osteotomy with distraction of the inter-metatarsal space: A case report
• Unraveling the Complexity of Apert Syndrome: Genetics, Clinical Insights, and Future Frontiers
• Virtual Reality and Mixed Reality-Assisted Endoscopic DCR in Extremely Complex Lacrimal Obstructions
• Webplasty using an external fixator for complex syndactyly caused by Apert syndrome
• Whole exome sequencing combined with dynamic ultrasound assessments for fetal skeletal dysplasias: 4 case reports