• A case of the orocraniodigital (Juberg-Hayward) syndrome
• A new familial syndrome of oral, cranial, and digital anomalies
• A novel chromosomal aberration in a child with suspected Juberg-Hayward syndrome
• An atypical case suggesting the possibility of overlap between Malpuech and Juberg-Hayward syndromes
• Further case of aminopterin syndrome sine aminopterin in a Spanish child
• Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2
• Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2
• Juberg-Hayward syndrome: a new case report and clinical delineation of the syndrome
• Juberg-Hayward syndrome: report of a case with cleft palate, distally placed thumbs and vertebral anomalies
• Juberg-Hayward syndrome: report of a new patient with severe phenotype and novel clinical features
• Orocraniodigital (Juberg-Hayward) syndrome with growth hormone deficiency
• Prenatal diagnosis of Juberg-Hayward syndrome
• Pseudoaminopterin syndrome
• Simple febrile seizure, complex seizure, generalized epilepsy with febrile seizure plus, FIRES and new syndromes
• The orocraniodigital syndrome of Juberg and Hayward