Rubinstein-Taybi Syndrome - an overview

Exon deletions of the EP300 and CREBBP genes in two children with

Facial features of Rubinstein-Taybi syndrome

Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™

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

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

PDF) CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome

Rubinstein-Taybi Syndrome: A Rare Case Report

Microdeletions and mutations of CREBBP (CBP) gene can cause

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

Rubinstein‐Taybi syndrome in Chinese population with four novel