Rubinstein-Taybi syndrome - wikidoc

Rubinstein-Taybi syndrome: MedlinePlus Genetics

PDF) CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome

Rubinstein-Taybi Syndrome: A Rare Case Report

Rubinstein-Taybi 2 associated to novel EP300 mutations: deepening the clinical and genetic spectrum, BMC Medical Genetics

Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly - Yu - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome

Ultra-Rare Syndromes: The Example of Rubinstein-Taybi Syndrome. - Abstract - Europe PMC

Rubinstein–Taybi syndrome in diverse populations - Tekendo

Rubinstein‐Taybi syndrome in Chinese population with four novel

A novel CREBBP mutation and its phenotype in a case of Rubinstein