Misplaced Pages

The following pages link to BCS1L

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Showing 26 items.

• List of genetic disorders (links | edit)
• Coenzyme Q – cytochrome c reductase (links | edit)
• Iron overload (links | edit)
• Leigh syndrome (links | edit)
• AAA proteins (links | edit)
• Mitochondrial myopathy (links | edit)
• Chromosome 2 (links | edit)
• UQCRFS1 (links | edit)
• Björnstad syndrome (links | edit)
• GRACILE syndrome (links | edit)
• List of OMIM disorder codes (links | edit)
• Gracility (links | edit)
• BCS1L (gene) (redirect page) (links | edit)
  • User:KadaneBot/Task3/R from unnecessary disambiguation (links | edit)
  • User:KadaneBot/Task3/Case 1/2 (links | edit)
  • User:KadaneBot/Task3/Edits/gene/Case 1/1 (links | edit)
• List of human protein-coding genes 1 (links | edit)
• Talk:BCS1L (transclusion) (links | edit)
• User:Boghog/Sandbox3/ec3 (links | edit)
• User:ProteinBoxBot/PBB Log Wiki 12-20-2007-A-15 (links | edit)
• User:AlexNewArtBot/MedicineSearchResult/archive5 (links | edit)
• User:ProteinBoxBot/Protein Directory links (links | edit)
• User:Cboursnell/Sandbox/B (links | edit)
• User:Jimw338/Books/Disorganized Biochemistry (links | edit)
• User:Lothar buchmann/Books/My Body mitochondrion (links | edit)
• User:KadaneBot/Task3/Edits/gene/Case 1/1 (links | edit)
• User:Seppi333/GeneListNLP (links | edit)
• User:Eteceterally/Mitochondrial Genetic Disorders (links | edit)
• Misplaced Pages:WikiProject Spam/LinkReports/amino.heartproteome.org (links | edit)