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

The Drosophila melanogaster model for Cornelia de Lange syndrome: Implications for etiology and therapeutics - Dorsett - 2016 - American Journal of Medical Genetics Part C: Seminars in Medical Genetics - Wiley Online Library

The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes

PDF) 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

Chung–Jansen syndrome can mimic Cornelia de Lange syndrome: Another player among chromatinopathies? - Conti - 2023 - American Journal of Medical Genetics Part A - Wiley Online Library

Cornelia de Lange Syndrome (CdLS) is a cohesinopathy (changes in

Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin

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The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes