About - DECIPHER v11.23

Genes, Free Full-Text

Facial features of Rubinstein-Taybi syndrome

IJMS, Free Full-Text

First case of Rubinstein–Taybi syndrome with desquamation associated with a novel mutation in the bromodomain of the CREBBP gene - Wang - 2019 - Clinical and Experimental Dermatology - Wiley Online Library

Ocular symptoms in patients with Rubinstein-Taybi syndrome; 117 out of

PDF) Rubinstein–Taybi syndrome (CREBBP, EP300) Martine van Belzen and Oliver Bartsch

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

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

High frequency of copy number imbalances in Rubinstein–Taybi

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