Misplaced Pages

The following pages link to ALX3

• (link count
• transclusion count
• sorted list) · See help page for transcluding these entries

Showing 16 items.

• Homeobox (links | edit)
• SCARF syndrome (links | edit)
• ALX4 (links | edit)
• Ciliopathy (links | edit)
• List of OMIM disorder codes (links | edit)
• ALX3 (gene) (redirect page) (links | edit)
  • Frontonasal dysplasia (links | edit)
  • Talk:ALX3 (gene) (transclusion) (links | edit)
  • User:Jamesmcmahon0/checkwiki (links | edit)
  • User:KadaneBot/Task3/R from unnecessary disambiguation (links | edit)
  • User:KadaneBot/Task3/Case 1/1 (links | edit)
  • User:KadaneBot/Task3/Edits/gene/Case 1/3 (links | edit)
  • User talk:Elizabeth.obrien (links | edit)
  • Misplaced Pages:CHECKWIKI/111 dump (links | edit)
• List of human transcription factors (links | edit)
• List of human protein-coding genes 1 (links | edit)
• Syndromic microphthalmia (links | edit)
• Talk:ALX3 (transclusion) (links | edit)
• User:Boghog/Sandbox3/tf (links | edit)
• User:KadaneBot/Task3/Edits/gene/Case 1/3 (links | edit)
• User:Seppi333/GeneListNLP (links | edit)
• User:Iolejniczak/sandbox (links | edit)
• Misplaced Pages:Wiki Ed/MTSU/Genetics 3250-18B (Fall) (links | edit)
• Draft:ALX3 Gene (redirect page) (links | edit)
  • User:WordSeventeen/afc (links | edit)
  • User talk:Elizabeth.obrien (links | edit)