The - The Rubinstein-Taybi Syndrome Children's Foundation
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Rubinstein-Taybi Syndrome: Orthopaedics
Forgotten Diseases Research Foundation
Special Friends Foundation
Rubinstein-Taybi Syndrome Support Group
Rubinstein-Taybi Syndrome: Genetics
Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
Cureus, Rubinstein-Taybi Syndrome Associated with Pituitary Macroadenoma: A Case Report
Rubinstein-Taybi Syndrome: Behavior
The Rubinstein-Taybi Syndrome Children's Foundation
Rubinstein–Taybi syndrome - Wikipedia
Rubinstein-Taybi Syndrome • RTS Support Group
A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics
4 Newborn with Rubinstein-Taybi syndrome showing microcephaly, frontal
The Rubinstein-Taybi Syndrome Children's Foundation