Frontiers Case report: A preterm infant with rubinstein-taybi

A case with Rubinstein-Taybi syndrome: A novel frameshift mutation in the CREBBP gene.

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

novel frameshift mutation - List of Frontiers' open access articles

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

Frontiers in Pediatrics Genetics of Common and Rare Diseases

PDF) Van Lohuizen Syndrome, a Late-Diagnosed Case in an 18 Years-Old Female

Children May 2022 - Browse Articles

Frontiers in Pediatrics

Patent Ductus Arteriosus: A Contemporary Perspective for the Pediatric and Adult Cardiac Care Provider

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

PDF) The perinatal health challenges of emerging and re-emerging infectious diseases: A narrative review