Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in
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A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics

Genetics and therapy for pediatric eye diseases - eBioMedicine

New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients - Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Inheritance and variable expression in Rubinstein–Taybi syndrome - Bartsch - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library

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

PDF) Epigenetic Mechanisms of Rubinstein–Taybi Syndrome

Rubinstein-Taybi Syndrome: A case report

Rubinstein-Taybi Syndrome – New Indian Journal of Pediatrics

Psychiatric Profile in Rubinstein-Taybi Syndrome

Localisation of nine CREBBP mutations (six of them of novel

Dysmorphic and skeletal features of Rubinstein‐Taybi syndrome patients.
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