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

Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome, Orphanet Journal of Rare Diseases

Emerging roles of BET proteins in transcription and co‐transcriptional RNA processing - Eischer - 2023 - WIREs RNA - Wiley Online Library

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

Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype–phenotype correlations and common mechanisms - Kaur - 2023 - American Journal of Medical Genetics Part A - Wiley Online Library

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Emerging roles of BET proteins in transcription and co‐transcriptional RNA processing - Eischer - 2023 - WIREs RNA - Wiley Online Library

Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect

STAG2 promotes the myelination transcriptional program in oligodendrocytes

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