Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
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Last updated 27 setembro 2024
Frontiers A Chinese Case of Cornelia de Lange Syndrome Caused by a Pathogenic Variant in SMC3 and a Literature Review
STAG2 promotes the myelination transcriptional program in oligodendrocytes
PDF) 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
Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement
Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library
Emerging roles of BET proteins in transcription and co‐transcriptional RNA processing - Eischer - 2023 - WIREs RNA - Wiley Online Library
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Genes, Free Full-Text
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
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
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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