• A variant of Fine-Lubinsky syndrome: a Japanese boy with profound deafness, cataracts, mental retardation, and brachycephaly without craniosynostosis
• Atypical retinitis pigmentosa with hypophosphatasia
• Craniosynostosis associated with ocular and distal limb defects is very likely caused by mutations in a gene different from FGFR, TWIST, and MSX2
• Elective procedures and anesthesia in children: pediatric surgeons enter the dialogue on neurotoxicity questions, surgical options, and parental concerns
• Hallermann-Streiff Syndrome and Psychosis: A Case Report
• Multiple sutural synostosis and congenital cataracts
• Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta
• Oculo-facio-cardio-dental syndrome with craniosynostosis, temporal hypertrichosis, and deafness
• Ophthalmic disorders in a referral population of seven breeds of brachycephalic dogs: 970 cases (2008-2017)
• Prevention of cranial reossification after surgical craniectomy
• Previously undescribed spondyloepiphyseal dysplasia associated with craniosynostosis, cataracts, cleft palate, and mental retardation: report of four sibs
• Retrospective investigation of perioperative risk factors for immediate postoperative corneal erosions in dogs undergoing phacoemulsification
• Self-Induced Bilateral Retinal Detachments and Traumatic Cataracts in a Patient With Bohring-Opitz Syndrome
• Spondylo-epiphyseal dysplasia associated with craniosynostosis, cleft palate and mental retardation. A case report
• The association of nausea and vomiting of pregnancy, its treatments, and select birth defects: Findings from the National Birth Defect Prevention Study