Frontiers Case report: A preterm infant with rubinstein-taybi

A) sequence analysis of the genomic DNA of our rubinstein-taybi

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

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

novel frameshift mutation - List of Frontiers' open access articles

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

Mutation spectrum of CREBBP and EP300 in RSTS individuals referenced in

Rubinstein-Taybi Syndrome: A Pediatric Case Report

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

Frontiers Case report: A case of spinal muscular atrophy in a preterm infant: risks and benefits of treatment

Frontiers High-Risk Preterm Infant Born to a Mother With COVID-19: A Case Report