Growth charts for individuals with Rubinstein–Taybi syndrome

Rubinstein-Taybi syndrome: MedlinePlus Genetics

Forgotten Diseases Research Foundation

PDF) Rubinstein-Taybi syndrome: Dental manifestations and management

Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTS

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

PDF) Identification of a novel de novo mutation of CREBBP in a patient with Rubinstein-Taybi syndrome by targeted next-generation sequencing: A case report

Genes involved in histone acetylation known to cause rare diseases

Mosaic CREBBP mutation causes overlapping clinical features of Rubinstein– Taybi and Filippi syndromes

Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library

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