Growth charts for individuals with Rubinstein–Taybi syndrome

IJMS, Free Full-Text

First case report of inherited Rubinstein-Taybi syndrome associated with a novel EP300 variant, BMC Medical Genetics

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

OMIM diseases as a function of associated HPO phenotypes. Data include

Clinical and molecular findings of the six patients with Rubinstein

Genes involved in histone acetylation known to cause rare diseases

Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine

Expanding the phenotype associated to KMT2A variants: overlapping clinical signs between Wiedemann–Steiner and Rubinstein–Taybi syndromes

Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics

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