• A GDF5 point mutation strikes twice--causing BDA1 and SYNS2
• A missense <em>GDF5</em> variant causes brachydactyly type A1 and multiple-synostoses syndrome 2
• A missense GDF5 variant causes brachydactyly type A1 and multiple-synostoses syndrome 2
• Absence of Bilateral Multiple Cyclovertical Muscle Insertions in a Patient With Pfeiffer Syndrome
• Bilateral cryptophthalmos with overlapping features of Manitoba oculo-tricho-anal (MOTA) syndrome and Fraser syndrome 2
• Clinical features and orbital anomalies in Fraser syndrome and a review of management options
• Comparing the Increased Intracranial Volume From Different Surgical Methods for Syndromic Craniosynostosis
• Craniofacial reconstructions in children with craniosynostosis
• Current updates on arrhythmia within Timothy syndrome: genetics, mechanisms and therapeutics
• External-internal cranial expansion to treat patients with craniocerebral disproportion due to post-shunt craniosynostosis: a case series
• Flexible endoscope-assisted suture release and barrel stave osteotomy for the correction of sagittal synostosis
• Frontofacial Monobloc Advancement With Internal Distraction: Surgical Technique and Osteotomy Guide
• Improved bone defect healing by a superagonistic GDF5 variant derived from a patient with multiple synostoses syndrome
• Perioperative management and complication control of Le Fort Ⅲ osteotomy in children with syndromic craniosynostosis
• Practical Algorithm for the Management of Multisutural Craniosynostosis with Associated Chiari Malformation and/or Hydrocephalus
• Reference ranges for standard-echocardiography in pugs and impact of clinical severity of Brachycephalic Obstructive Airway Syndrome (BOAS) on echocardiographic parameters
• Siblings with profound connective tissue disease: First report of biallelic TGFBR1-related Loeys-Dietz syndrome
• The genetic factors contributing to the risk of cleft lip-cleft palate and their clinical utility
• Update in Management of Craniosynostosis