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

Rubinstein–Taybi syndrome - Wikipedia

Facial features of Rubinstein-Taybi syndrome

Rubinstein-Taybi syndrome: Dental manifestations and management

PDF) Oro-dental features as useful diagnostic tool in Rubinstein–Taybi syndrome

PDF) Rubinstein-Taybi 2 associated to novel EP300 mutations: Deepening the clinical and genetic spectrum

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

Subclass IgG levels of patients with Rubinstein-Taybi syndrome compared

Rubinstein-Taybi syndrome - wikidoc

IJMS, Free Full-Text

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