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OMIM - Congenital disorder
OMIM - Congenital chromosomal disease
L1000 CMAP - Adenocarcinoma of breast MCF7 cells treated with ligand perturbagens
L1000 CMAP - Amelanotic malignant melanoma of skin A375 cells treated with ligand perturbagens
L1000 CMAP - Carcinoma of prostate PC3 cells treated with ligand perturbagens
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Genomic and demographic processes differentially influence genetic variation across the human X chro…
Competition shapes the landscape of X-chromosome-linked genetic diversity.
XIST dampens X chromosome activity in a SPEN-dependent manner during early human development.
Deletion of the XIST promoter from the human inactive X chromosome compromises polycomb heterochroma…
Straight to the X: Modeling Human X Chromosome Inactivation in hESCs by FGF Signal Blockade.
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Implications of Maternal 45,X Mosaicism as a Secondary Genomic Finding Following Cell-Free DNA Seque…
Reversing Epigenetic & Other Markers of Senescence by Transfusing Young Plasma To Older Human Subjec…
Sex Selection of Human Spermatozoa
X-chromosome Inactivation, Epigenetics and the Transcriptome
Immunophenotyping and Xist Gene in AML
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