Exon deletions of the EP300 and CREBBP genes in two children with
Por um escritor misterioso
Last updated 22 março 2025


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

Mutation spectrum of CREBBP and EP300 in RSTS individuals referenced in

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

Genes, Free Full-Text

New insights into genetic variant spectrum and genotype–phenotype correlations of Rubinstein‐Taybi syndrome in 39 CREBBP‐positive patients - Pérez‐Grijalba - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library

iPSC-derived neurons of CREBBP- and EP300-mutated Rubinstein-Taybi syndrome patients show morphological alterations and hypoexcitability - ScienceDirect

Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein–Taybi syndrome detected by aCGH

De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia, BMC Medical Genomics

Genes, Free Full-Text
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