Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
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Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
Cornelia de Lange Syndrome: What Is It, Causes, Signs, Symptoms, and More
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
Cornelia de Lange syndrome-associated mutations cause a DNA damage signalling and repair defect
Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
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
STAG2 promotes the myelination transcriptional program in oligodendrocytes
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Cornelia de Lange Syndrome (CdLS) is a cohesinopathy (changes in
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por adulto (o preço varia de acordo com o tamanho do grupo)
