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

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

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

Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics

Ocular features in Rubinstein-Taybi syndrome: investigation of 24 patients and review of the literature

A case of bilateral elbow dislocation in a patient with Rubinstein-Taybi syndrome - JSES International

Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant

Epigenetic mechanisms of Rubinstein-Taybi syndrome. - Abstract - Europe PMC

PDF) Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literature

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

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

PDF) Rubinstein-Taybi syndrome: Clinical profile of 11 patients and review of literature

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