genereviews.org - GeneReviews® - NCBI Bookshelf

Rubinstein-Taybi Syndrome

Cureus Barrett's Esophagus in Rubinstein-Taybi Syndrome

Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome - ScienceDirect

Clinical heterogeneity of Kabuki syndrome in a cohort of Italian patients and review of the literature

PDF) Rubinstein-Taybi syndrome in diverse populations

Rubinstein-Taybi syndrome (RTS)

Full article: Psychomotor, cognitive, and socio-emotional developmental profiles of children with Rubinstein-Taybi Syndrome and a severe intellectual disability

Rubinstein–Taybi syndrome in diverse populations - Tekendo‐Ngongang - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library

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

Identification of de novo EP300 and PLAU variants in a patient with Rubinstein–Taybi syndrome-related arterial vasculopathy and skeletal anomaly