• A Rare Case of Gorlin-Goltz Syndrome Presented to the Emergency Department as Facial Swelling
• Alagille syndrome: Oral manifestations-A case report
• Apert syndrome: craniofacial challenges and clinical implications
• Clinical assessment and FGFR2 mutation analysis in a Chinese family with Crouzon syndrome: A case report
• Crouzon syndrome - A rare case report
• Crouzon syndrome in a fraternal twin: A case report and review of the literature
• Delayed Diagnosis of Gorlin-Goltz Syndrome: The Importance of the Multidisciplinary Approach
• Is the "Habsburg jaw" related to inbreeding?
• Myhre Syndrome
• Nance-Horan Syndrome: A Rare Case Report
• Osteoglophonic Dysplasia
• Potential interactions among single nucleotide polymorphisms in bone- and cartilage-related genes in skeletal malocclusions
• Reproductive losses caused by the ingestion of Poincianella pyramidalis in sheep
• Three novel genes tied to mandibular prognathism in eastern Mediterranean families
• Treatment of the Patient With Crouzon Syndrome With Orthognathic Surgery
• Trichodentoosseous syndrome: a case report and review of literature
• What to Expect of Feeding Abilities and Nutritional Aspects in Achondroplasia Patients: A Narrative Review