PDF) Rubinstein-Taybi Syndrome: A Model of Epigenetic Disorder

Exon deletions of the EP300 and CREBBP genes in two children with

Facial features of Rubinstein-Taybi syndrome

Congenital glaucoma as a presenting feature of Rubinstein-Taybi

Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS

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A novel CREBBP mutation and its phenotype in a case of Rubinstein–Taybi syndrome, BMC Medical Genomics

Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics

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

Rubinstein‐Taybi syndrome in Chinese population with four novel

Chemical and genetic rescue of an ep300 knockdown model for