The - The Rubinstein-Taybi Syndrome Children's Foundation

Patient Stories Rubinstein-Taybi Syndrome

Rubinstein Taybi Syndrome in an Indian Child due to EP300 Gene Mutation

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

Dermatologic Manifestations of Rubinstein-Taybi Syndrome Clinical Presentation: History, Physical Examination, Complications

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

Rubinstein-Taybi Syndrome

Rubinstein-Taybi Syndrome Support Group

CBP Histone Acetyltransferase Activity Regulates Embryonic Neural Differentiation in the Normal and Rubinstein-Taybi Syndrome Brain: Developmental Cell

22 Rubenstein-Taybi Syndrome ideas

The Rubinstein-Taybi Syndrome Children's Foundation

PDF) CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome

Rubinstein-Taybi Syndrome • RTS Support Group

Rubinstein-Taybi Syndrome • RTS Support Group

Genes, Free Full-Text