The - The Rubinstein-Taybi Syndrome Children's Foundation

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

The - The Rubinstein-Taybi Syndrome Children's Foundation

Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library

22 Rubenstein-Taybi Syndrome ideas

The Rubinstein-Taybi Syndrome Children's Foundation - So very lucky to spend time with Dr. R.C.M. (Raoul) Hennekam We hope to build stronger ties to the good doctor and other RTS researchers

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

The Rubinstein-Taybi Syndrome Children's Foundation

Born with Rubinstein-Taybi Syndrome (RTS), Braxton and Family are Full of Hope - Global Genes

Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect

Patient Stories Rubinstein-Taybi Syndrome

Rubinstein–Taybi syndrome - Wikipedia

Rubinstein-Taybi Syndrome: Neurosurgery

The Rubinstein-Taybi Syndrome Children's Foundation