Rubinstein Taybi Syndrome in an Indian Child due to EP300 Gene

Forgotten Diseases Research Foundation

Rubinstein-Taybi Syndrome

Severe persistent pulmonary hypertension in a neonate with

Learning to Speak at Age 18 with a Sister Who Never Quits

Patient Stories Rubinstein-Taybi Syndrome

Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP

Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine

High frequency of copy number imbalances in Rubinstein–Taybi

Rubinstein–Taybi syndrome: clinical and molecular overview

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of