Misplaced Pages

The following pages link to X-inactivation

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Showing 50 items.

• Histone methylation (links | edit)
• X-linked severe combined immunodeficiency (links | edit)
• Pseudoautosomal region (links | edit)
• Short-stature homeobox gene (links | edit)
• Arthur Riggs (geneticist) (links | edit)
• XXXXY syndrome (links | edit)
• Hunter syndrome (links | edit)
• Polycomb-group proteins (links | edit)
• XIC (links | edit)
• Sex chromosome (links | edit)
• Craniofrontonasal dysplasia (links | edit)
• X-inactivations (redirect page) (links | edit)
  • User:Jbarin/Autoimmunity draft (links | edit)
• Calico cat (links | edit)
• Marsh rice rat (links | edit)
• Chromosome conformation capture (links | edit)
• EZH2 (links | edit)
• DNA (cytosine-5)-methyltransferase 3A (links | edit)
• 40S ribosomal protein S4, X isoform (links | edit)
• USP9X (links | edit)
• XIST (links | edit)
• FANCB (links | edit)
• Cis-natural antisense transcript (links | edit)
• Long non-coding RNA (links | edit)
• CTCFL (links | edit)
• Frontonasal dysplasia (links | edit)
• Obligate carrier (links | edit)
• Ernest Beutler (links | edit)
• Klinefelter syndrome (links | edit)
• Female (links | edit)
• OPN1MW2 (links | edit)
• Inactivation (links | edit)
• Skewed X-inactivation (links | edit)
• Barton Childs (links | edit)
• Lyon Hypothesis (redirect page) (links | edit)
• X-chromosome inactivation (redirect page) (links | edit)
  • Barr body (links | edit)
  • DNA methylation (links | edit)
  • X-linked recessive inheritance (links | edit)
  • Mary F. Lyon (links | edit)
  • Sex differences in human physiology (links | edit)
  • DNMT3L (links | edit)
  • Gail R. Martin (links | edit)
  • Trithorax-group proteins (links | edit)
  • Lupus (links | edit)
  • Edith Heard (links | edit)
  • Monoallelic gene expression (links | edit)
  • Trisomy X (links | edit)
  • X-chromosome reactivation (links | edit)
  • User:Bio561grp3s12/sandbox (links | edit)
  • User:Hetal05/sandbox (links | edit)
  • User:Krildrik/sandbox (links | edit)
• X-linked myotubular myopathy (links | edit)
• Wilson–Turner syndrome (links | edit)
• Tortoiseshell cat (links | edit)
• Meiotic recombination checkpoint (links | edit)
• BRCA mutation (links | edit)
• Cell potency (links | edit)
• Pyruvate dehydrogenase (lipoamide) alpha 2 (links | edit)
• List of OMIM disorder codes (links | edit)
• Microcell-mediated chromosome transfer (links | edit)
• Epilepsy-intellectual disability in females (links | edit)
• Tsix (links | edit)
• Edith Heard (links | edit)
• Epitranscriptome (links | edit)
• Marnie Blewitt (links | edit)
• Epigenetics of neurodegenerative diseases (links | edit)