Rubinstein - Taybi Syndrome (Rubinstein syndrome, broad thumb
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a,b: Patient A at 3 weeks; c,d: Patient B at 6 weeks, note the opening
Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature
Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of the phenotype of the first patients carrying mutations in EP300
Rubinstein-Taybi syndrome
Oral and Dental Manifestations in Rubinstein-Taybi Syndrome: Report of a Rare Case
First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant, BMC Medical Genetics
Clinical photos of the patients. (a) Case 1: Dysmorphic facial features
Rubinstein Taybi Syndrome - MEDizzy
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics
Rubinstein–Taybi syndrome - Wikipedia
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
Rubinstein-Taybi Syndrome
