Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
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STAG2 promotes the myelination transcriptional program in oligodendrocytes
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PDF) Understanding the new BRD4‐related syndrome: Clinical and genomic delineation with an international cohort study
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PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41467-021-23500-6/MediaObjects/41467_2021_23500_Fig1_HTML.png)
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://d16qt3wv6xm098.cloudfront.net/om-NXPG3Tm_DNp_4b-ZmnYO4RrCd1pdP/_.jpg)
Cornelia de Lange Syndrome: What Is It, Causes, Signs, Symptoms, and More
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Genes, Free Full-Text
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-021-23500-6/MediaObjects/41467_2021_23500_Fig3_HTML.png)
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-021-23141-9/MediaObjects/41467_2021_23141_Fig3_HTML.png)
Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
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Frontiers Regulation of Carbohydrate-Responsive Metabolic Genes by Histone Acetylation and the Acetylated Histone Reader BRD4 in the Gene Body Region
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