Rubinstein-Taybi Syndrome - an overview

Rubinstein–Taybi syndrome - Wikipedia

Forgotten Diseases Research Foundation

Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire

First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant – topic of research paper in Clinical medicine. Download scholarly article PDF and read for free on CyberLeninka open

OMIM diseases as a function of associated HPO phenotypes. Data include

PDF) Rubinstein–Taybi syndrome (CREBBP, EP300) Martine van Belzen and Oliver Bartsch

Frontiers Case Report: Low-Level Maternal Mosaicism of a Novel CREBBP Variant Causes Recurrent Rubinstein-Taybi Syndrome in Two Siblings of a Chinese Family

Mosaic CREBBP mutation causes overlapping clinical features of

Rubinstein–Taybi syndrome: clinical and molecular overview