CBP-HSF2 structural and functional interplay in Rubinstein-Taybi neurodevelopmental disorder

Rubinstein-Taybi Syndrome 1

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

Chromosome 16p13.3 Contiguous Gene Deletion Syndrome including the SLX4, DNASE1, TRAP1, and CREBBP Genes Presenting as a Relatively Mild Rubinstein- Taybi Syndrome Phenotype: A Case Report of a Saudi Boy. - Document

Microdeletions and mutations of CREBBP (CBP) gene can cause

Main clinical findings of the 16 Brazilian patients with

Rubinstein-Taybi 2 associated to novel EP300 mutations: deepening the clinical and genetic spectrum, BMC Medical Genetics

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

High frequency of copy number imbalances in Rubinstein–Taybi

Expanding the phenotype associated to KMT2A variants: overlapping

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