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Dissecting developmental disorders caused by CTCF mutation at R567 [ChIP-seq]
PubMed Full text in PMC Similar studies
Illumina NovaSeq 6000 (Mus musculus)
input_lung_homo
SRA Run Selector
input_lung_wt
input_heart_homo
input_heart_wt
input_brain_homo
input_brain_wt
CTCF_ChIP_lung_homo
CTCF_ChIP_lung_wt
CTCF_ChIP_heart_homo
CTCF_ChIP_heart_wt
CTCF_ChIP_brain_homo
CTCF_ChIP_brain_wt
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