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

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

PDF) Prevalence of Immunological Defects in a Cohort of 97 Rubinstein–Taybi Syndrome Patients

Subclass IgG levels of patients with Rubinstein-Taybi syndrome compared

Rubinstein-Taybi Syndrome: A Rare Case Report

Novel cAMP binding protein-BP (CREBBP) mutation in a girl with Rubinstein- Taybi syndrome, GH deficiency, Arnold Chiari malformation and pituitary hypoplasia – topic of research paper in Clinical medicine. Download scholarly article PDF

Rubinstein‐Taybi syndrome in Chinese population with four novel mutations - Yu - 2021 - 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

Rubinstein–Taybi syndrome: clinical and molecular overview

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP

Genetic heterogeneity in Rubinstein–Taybi syndrome: delineation of