Adults with Rubinstein–Taybi syndrome - Stevens - 2011 - American

a,b: Patient A at 3 weeks; c,d: Patient B at 6 weeks, note the opening

PDF) Rubinstein-Taybi syndrome medical guidelines

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300

Epigenetic Mechanisms of Rubinstein–Taybi Syndrome

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

Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome

Forgotten Diseases Research Foundation

Psychiatric Profile in Rubinstein-Taybi Syndrome

Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature

De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia, BMC Medical Genomics

The natural history of adults with Rubinstein-Taybi syndrome: a families-reported experience

Rubinstein-Taybi Syndrome

Frontiers Behavioral and neuropsychiatric challenges across the lifespan in individuals with Rubinstein-Taybi syndrome