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Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome

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Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
STAG2 promotes the myelination transcriptional program in oligodendrocytes
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
PDF) Understanding the new BRD4‐related syndrome: Clinical and genomic delineation with an international cohort study
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
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
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
Cornelia de Lange Syndrome: What Is It, Causes, Signs, Symptoms, and More
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Genes, Free Full-Text
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
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
Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
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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