Exon deletions of the EP300 and CREBBP genes in two children with
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Last updated 30 maio 2024
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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