RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated
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Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural tube defect. - Abstract - Europe PMC
Facial dysmorphism, skeletal anomalies, congenital glucoma, dysplastic nails: Mild Rubinstein-Taybi Syndrome - ScienceDirect
Clinical photos of the patients. (a) Case 1: Dysmorphic facial features
Rubinstein-Taybi Syndrome 1
Rubinstein-Taybi syndrome: principal oral and dental disorders and literature update : Iberoamerican Journal of Medicine : Free Download, Borrow, and Streaming : Internet Archive
Hyperinsulinism in an individual with an EP300 variant of Rubinstein‐Taybi syndrome - Wild - 2021 - American Journal of Medical Genetics Part A - Wiley Online Library
Rubinstein-Taybi Syndrome: Symptoms, Causes, Treatment
High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis
A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics
Rubinstein-Taybi Syndrome Awareness
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