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

First case of Rubinstein–Taybi syndrome with desquamation associated with a novel mutation in the bromodomain of the CREBBP gene - Wang - 2019 - Clinical and Experimental Dermatology - Wiley Online Library

PDF) Rubinstein-Taybi syndrome medical guidelines

Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients

Rubinstein-Taybi Syndrome: A Rare Case Report

Main clinical findings of the 16 Brazilian patients with

Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome

Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes

Ultra-Rare Syndromes: The Example of Rubinstein-Taybi Syndrome. - Abstract - Europe PMC

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of

Rubinstein-Taybi syndrome in a Saudi boy with distinct features