Ultra-Rare Syndromes: The Example of Rubinstein-Taybi Syndrome
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Rubinstein-Taybi Syndrome: A Rare Case Report
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
Frontiers Rare diseases of epigenetic origin: Challenges and opportunities
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The Problem Of Obesity Is A Great Concern As Children With
Identification of 22q11.2 deletion in a patient with schizophrenia and clinically diagnosed Rubinstein–Taybi syndrome - Nagai - 2022 - Psychiatry and Clinical Neurosciences Reports - Wiley Online Library
IJMS, Free Full-Text
PDF) Thyroid Function in Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics
De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia, BMC Medical Genomics
Rubinstein-Taybi syndrome: MedlinePlus Genetics
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Rubinstein-Taybi syndrome: MedlinePlus Genetics
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