CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder

Exon deletions of the EP300 and CREBBP genes in two children with

Facial features of Rubinstein-Taybi syndrome

PDF) Rubinstein–Taybi syndrome (CREBBP, EP300) Martine van Belzen and Oliver Bartsch

PDF) CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome

Subclass IgG levels of patients with Rubinstein-Taybi syndrome compared

Mosaic CREBBP mutation causes overlapping clinical features of

Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library

A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics

A novel CREBBP mutation and its phenotype in a case of Rubinstein

Rubinstein-Taybi syndrome: clinical features, genetic basis