Key Facts

Ocular features in Rubinstein-Taybi syndrome: investigation of 24

Rubinstein–Taybi syndrome - Wikipedia

Exon deletions of the EP300 and CREBBP genes in two children with

The - The Rubinstein-Taybi Syndrome Children's Foundation

Severe persistent pulmonary hypertension in a neonate with

Rubinstein Taybi Syndrome Awareness RTS Hearts and

High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis

Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library

Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics