Frontiers Case report: A preterm infant with rubinstein-taybi

Epigenetics modifiers: potential hub for understanding and treating neurodevelopmental disorders from hypoxic injury, Journal of Neurodevelopmental Disorders

Frontiers Case report: Fatal lung hyperinflammation in a preterm newborn with SARS-CoV-2 infection

of skull anomalies in Pfeiffer syndrome

Frontiers in Pediatrics Genetics of Common and Rare Diseases

Low bone mineral density on DXA and slipped capital femoral epiphysis as rare presentation in a child with Rubinstein-Taybi syndrome

PDF] Chromosome 16p13.3 Contiguous Gene Deletion Syndrome including the SLX4, DNASE1, TRAP1, and CREBBP Genes Presenting as a Relatively Mild Rubinstein–Taybi Syndrome Phenotype: A Case Report of a Saudi Boy

Frontiers The effects of early combined training on the physical development of preterm infants with different gestational ages

Exome Sequencing: Most Up-to-Date Encyclopedia, News & Reviews

Mutation spectrum of CREBBP and EP300 in RSTS individuals referenced in

Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant

Calaméo - Embryo and Fetal Pathology