Rubinstein–Taybi syndrome: clinical and molecular overview

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) FISH studies in 45 patients with Rubinstein-Taybi syndrome: Deletions associated with polysplenia, hypoplastic left heart and death in infancy

Rubinstein-Taybi Syndrome: A Rare Case Report

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Microdeletions and mutations of CREBBP (CBP) gene can cause

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Main clinical findings of the 16 Brazilian patients with

Rubinstein–Taybi syndrome in diverse populations - Tekendo

Expanding the phenotype associated to KMT2A variants: overlapping

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