Misplaced Pages

The following pages link to PHF8

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Showing 50 items.

• P53 (links | edit)
• Transcription factor (links | edit)
• Diabetes insipidus (links | edit)
• Androgen insensitivity syndrome (links | edit)
• Adrenoleukodystrophy (links | edit)
• Fragile X syndrome (links | edit)
• Pelizaeus–Merzbacher disease (links | edit)
• Rett syndrome (links | edit)
• List of genetic disorders (links | edit)
• Homeobox (links | edit)
• FOXP2 (links | edit)
• Haemophilia A (links | edit)
• Haemophilia B (links | edit)
• Barth syndrome (links | edit)
• Zinc finger (links | edit)
• Cleft lip and cleft palate (links | edit)
• FOX proteins (links | edit)
• Glucose-6-phosphate dehydrogenase deficiency (links | edit)
• Occipital horn syndrome (links | edit)
• Rho factor (links | edit)
• Sigma factor (links | edit)
• Hormone receptor (links | edit)
• Receptor (biochemistry) (links | edit)
• Peroxisome proliferator-activated receptor (links | edit)
• Chronic granulomatous disease (links | edit)
• Alport syndrome (links | edit)
• CREB (links | edit)
• MASA syndrome (links | edit)
• Aicardi syndrome (links | edit)
• Duchenne muscular dystrophy (links | edit)
• Becker muscular dystrophy (links | edit)
• Steroid hormone receptor (links | edit)
• Ornithine transcarbamylase deficiency (links | edit)
• Helix-turn-helix (links | edit)
• Kallmann syndrome (links | edit)
• MyoD (links | edit)
• Lesch–Nyhan syndrome (links | edit)
• Menkes disease (links | edit)
• Oct-4 (links | edit)
• Wiskott–Aldrich syndrome (links | edit)
• Incontinentia pigmenti (links | edit)
• X-linked recessive inheritance (links | edit)
• EGR1 (links | edit)
• Sex linkage (links | edit)
• Sex-determining region Y protein (links | edit)
• Coffin–Lowry syndrome (links | edit)
• Zinc finger inhibitor (links | edit)
• Estrogen receptor (links | edit)
• X-linked ichthyosis (links | edit)
• FOXP3 (links | edit)