Exon deletions of the EP300 and CREBBP genes in two children with
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IJMS, Free Full-Text
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Rubinstein-Taybi syndrome in a Saudi boy with distinct features and variants in both the CREBBP and EP300 genes: a case report, BMC Medical Genetics
![Exon deletions of the EP300 and CREBBP genes in two children with](https://pub.mdpi-res.com/genes/genes-12-00968/article_deploy/html/images/genes-12-00968-g006.png?1626846418)
Genes, Free Full-Text
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CREBBP/EP300 mutations promoted tumor progression in diffuse large B-cell lymphoma through altering tumor-associated macrophage polarization via FBXW7-NOTCH-CCL2/CSF1 axis
![Exon deletions of the EP300 and CREBBP genes in two children with](https://static.cambridge.org/binary/version/id/urn:cambridge.org:id:binary-alt:20160627193219-61475-mediumThumb-S1462399407000415_tab1.jpg?pub-status=live)
Rubinstein–Taybi syndrome: clinical and molecular overview, Expert Reviews in Molecular Medicine
![Exon deletions of the EP300 and CREBBP genes in two children with](https://pub.mdpi-res.com/genes/genes-12-00968/article_deploy/html/images/genes-12-00968-g001.png?1626846418)
Genes, Free Full-Text
![Exon deletions of the EP300 and CREBBP genes in two children with](https://media.springernature.com/m685/springer-static/image/art%3A10.1186%2Fs12920-023-01516-9/MediaObjects/12920_2023_1516_Fig3_HTML.png)
De novo variation in EP300 gene cause Rubinstein-Taybi syndrome 2 in a Chinese family with severe early-onset high myopia, BMC Medical Genomics
![Exon deletions of the EP300 and CREBBP genes in two children with](https://atlasgeneticsoncology.org/img/cards_genes/CREBBPFig3.png)
CREBBP (CREB binding protein)
![Exon deletions of the EP300 and CREBBP genes in two children with](https://www.pnas.org/cms/10.1073/pnas.2218330120/asset/2a6e158e-7479-4fbb-8812-fcd62086e50d/assets/images/large/pnas.2218330120fig07.jpg)
KMT2D acetylation by CREBBP reveals a cooperative functional interaction at enhancers in normal and malignant germinal center B cells
![Exon deletions of the EP300 and CREBBP genes in two children with](https://www.frontiersin.org/files/Articles/848879/fgene-13-848879-HTML-r1/image_m/fgene-13-848879-g005.jpg)
Frontiers Genetic Diagnosis of Rubinstein–Taybi Syndrome With Multiplex Ligation-Dependent Probe Amplification (MLPA) and Whole-Exome Sequencing (WES): Case Series With a Novel CREBBP Variant
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PDF) Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein-Taybi syndrome detected by aCGH
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