Subclass IgG levels of patients with Rubinstein-Taybi syndrome compared

Facial features of Rubinstein-Taybi syndrome

Ocular symptoms in patients with Rubinstein-Taybi syndrome; 117 out of

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

Clinical and molecular findings of the six patients with Rubinstein

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Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly - Yu - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Mosaic CREBBP mutation causes overlapping clinical features of

Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes

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

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP