Misplaced Pages

The following pages link to FLI1

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Showing 50 items.

• Down syndrome (links | edit)
• Mutation (links | edit)
• P53 (links | edit)
• Transcription factor (links | edit)
• XYY syndrome (links | edit)
• Trisomy (links | edit)
• Turner syndrome (links | edit)
• Fragile X syndrome (links | edit)
• Prader–Willi syndrome (links | edit)
• Homeobox (links | edit)
• Miscarriage (links | edit)
• FOXP2 (links | edit)
• Williams syndrome (links | edit)
• Zinc finger (links | edit)
• TAR syndrome (links | edit)
• Deletion (genetics) (links | edit)
• Sarcoma (links | edit)
• Multiple myeloma (links | edit)
• Aneuploidy (links | edit)
• Birth defect (links | edit)
• FOX proteins (links | edit)
• Uniparental disomy (links | edit)
• Burkitt lymphoma (links | edit)
• Patau syndrome (links | edit)
• Trisomy 18 (links | edit)
• Rho factor (links | edit)
• Sigma factor (links | edit)
• Philadelphia chromosome (links | edit)
• Chromosomal translocation (links | edit)
• Hormone receptor (links | edit)
• Receptor (biochemistry) (links | edit)
• Peroxisome proliferator-activated receptor (links | edit)
• Mosaic (genetics) (links | edit)
• CREB (links | edit)
• Beckwith–Wiedemann syndrome (links | edit)
• Acute lymphoblastic leukemia (links | edit)
• Miller–Dieker syndrome (links | edit)
• Anaplastic large-cell lymphoma (links | edit)
• Steroid hormone receptor (links | edit)
• Helix-turn-helix (links | edit)
• Wolf–Hirschhorn syndrome (links | edit)
• MyoD (links | edit)
• Dermatofibrosarcoma protuberans (links | edit)
• Oct-4 (links | edit)
• Acute promyelocytic leukemia (links | edit)
• EGR1 (links | edit)
• Chromosome 5q deletion syndrome (links | edit)
• Cri du chat syndrome (links | edit)
• Monosomy (links | edit)
• Sex-determining region Y protein (links | edit)