Rubinstein–Taybi syndrome European Journal of Human Genetics
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Rubinstein-Taybi syndrome: MedlinePlus Genetics
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
PDF) Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein-Taybi syndrome detected by aCGH
Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes
Genes, Free Full-Text
Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS
PDF] Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease.
CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder
Psychiatric Profile in Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients, BMC Medical Genetics
PDF) Genetic heterogeneity in Rubinstein-Taybi syndrome: Delineation of the phenotype of the first patients carrying mutations in EP300
