Forgotten Diseases Research Foundation

Rubinstein-Taybi syndrome: MedlinePlus Genetics

A Case of Rubinstein-Taybi Syndrome with Tetralogy of Fallot

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

Rubinstein-Taybi syndrome: Treatments and life expectancy

Keloids in Rubinstein–Taybi syndrome: a clinical study - Kar

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

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

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

A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics

Rubinstein‐Taybi syndrome in Chinese population with four novel