Frontiers Case report: A preterm infant with rubinstein-taybi
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Frontiers in Pediatrics Genetics of Common and Rare Diseases
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
rubinstein-taybi syndrome - List of Frontiers' open access articles
of brain anomalies in Pfeiffer syndrome
Syndromic forms of congenital hyperinsulinism. - Abstract - Europe PMC
novel frameshift mutation - List of Frontiers' open access articles
Rubinstein-Taybi Syndrome: A Pediatric Case Report
Frontiers Tailored treatments in inborn errors of immunity associated with atopy (IEIs-A) with skin involvement
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
Children May 2022 - Browse Articles
PDF) Rubinstein-Taybi Syndrome: A Case Report
Frontiers Syndromic forms of congenital hyperinsulinism
of skull anomalies in Pfeiffer syndrome
Frontiers Risk Factors for Adverse Neurodevelopment in Transient or Persistent Congenital Hyperinsulinism
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