Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome

Rubinstein-Taybi Syndrome OMIM# 180849 - FDNA™

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

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

Clinical and molecular findings of the six patients with Rubinstein

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

Microdeletions and mutations of CREBBP (CBP) gene can cause

IJMS, Free Full-Text

CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein–Taybi syndrome - Wincent - 2016 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics

Chemical and genetic rescue of an ep300 knockdown model for Rubinstein Taybi Syndrome in zebrafish - ScienceDirect