Exon deletions of the EP300 and CREBBP genes in two children with
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Last updated 26 abril 2025


Novel heterozygous variants in the EP300 gene cause Rubinstein–Taybi syndrome 2: Reports from two Chinese children - Du - 2023 - Molecular Genetics & Genomic Medicine - Wiley Online Library

Cancers, Free Full-Text

NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain

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

PDF) Rubinstein–Taybi syndrome (CREBBP, EP300) Martine van Belzen and Oliver Bartsch

Fusion proteins detected in TCGA cohort with genes relevant to this

Characterization of 14 novel deletions underlying Rubinstein–Taybi syndrome: an update of the CREBBP deletion repertoire

CREBBP (CREB binding protein)

Genomic Profiling of Adult and Pediatric B-cell Acute Lymphoblastic Leukemia - eBioMedicine

Unique and Shared Epigenetic Programs of the CREBBP and EP300 Acetyltransferases in Germinal Center B Cells Reveal Targetable Dependencies in Lymphoma. - Abstract - Europe PMC

Chromosome 16p13.3 Deletion Syndrome, Proximal disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
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