Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Por um escritor misterioso
Last updated 12 janeiro 2025
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
DNA repair pathway implicated in Cornelia de Lange syndrome
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
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
STAG2 promotes the myelination transcriptional program in oligodendrocytes
NIPBL rearrangements in Cornelia de Lange syndrome: evidence for replicative mechanism and genotype–phenotype correlation
Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
Cornelia de Lange syndrome: from molecular diagnosis to therapeutic approach
Frontiers Cornelia de Lange Syndrome as Paradigm of Chromatinopathies
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
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