Rubinstein‐Taybi syndrome in Chinese population with four novel

Ocular features in Rubinstein-Taybi syndrome: investigation of 24

Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™

Rubinstein-Taybi Syndrome: Symptoms, Causes, Treatment

Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP

Clinical photos of the patients. (a) Case 1: Dysmorphic facial

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

SciELO - Brasil - Multiple pilomatricomas in twins with Rubinstein

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

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300

Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics