Rubinstein-Taybi Syndrome Images — DermNet

What Is Rubinstein-Taybi Syndrome? - StoryMD

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

Loving Leanne: Living with Rubinstein-Taybi Syndrome: Roome

Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in

a,b: Patient A at 3 weeks; c,d: Patient B at 6 weeks, note the

Long-term results following osteotomy of the thumb delta phalanx

Rubinstein-Taybi syndrome 2 with cerebellar abnormality and neural

Molecular studies in 10 cases of Rubinstein-Taybi syndrome, including a mild variant showing a missense mutation in codon 1175 of CREBBP

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library

Rubinstein–Taybi syndrome: clinical and molecular overview