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

Forgotten Diseases Research Foundation

Rubinstein–Taybi syndrome European Journal of Human Genetics

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 (CREBBP, EP300) Martine van Belzen and Oliver Bartsch

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

Subclass IgG levels of patients with Rubinstein-Taybi syndrome compared

Microdeletions and mutations of CREBBP (CBP) gene can cause

CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome - Wincent - 2016 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Rubinstein‐Taybi syndrome in Chinese population with four novel

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of