Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
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Frontiers A Chinese Case of Cornelia de Lange Syndrome Caused by a Pathogenic Variant in SMC3 and a Literature Review
PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach
The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes
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
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PDF) Relevance of BET Family Proteins in SARS-CoV-2 Infection
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