Growth charts for individuals with Rubinstein–Taybi syndrome

Rubinstein–Taybi syndrome European Journal of Human Genetics

PDF) FISH studies in 45 patients with Rubinstein-Taybi syndrome: Deletions associated with polysplenia, hypoplastic left heart and death in infancy

Case report: a Chinese girl like atypical Rubinstein–Taybi syndrome caused by a novel heterozygous mutation of the EP300 gene, BMC Medical Genomics

About - DECIPHER v11.23

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

High frequency of copy number imbalances in Rubinstein–Taybi patients negative to CREBBP mutational analysis

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

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of

Rubinstein-Taybi syndrome: clinical features, genetic basis