The following pages link to SAMHD1
External toolsShowing 29 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- List of genetic disorders (links | edit)
- Encephalopathy (links | edit)
- Ribonuclease H (links | edit)
- Cytarabine (links | edit)
- CUL4A (links | edit)
- Eukaryotic translation elongation factor 1 alpha 1 (links | edit)
- CUL4B (links | edit)
- USP18 (links | edit)
- Lupus (links | edit)
- List of OMIM disorder codes (links | edit)
- SAMHD1 (gene) (redirect page) (links | edit)
- Vpx (links | edit)
- Aicardi–Goutières syndrome (links | edit)
- List of primary immunodeficiencies (links | edit)
- List of human protein-coding genes 3 (links | edit)
- FAM13B (links | edit)
- Childhood-onset systemic lupus erythematosus (links | edit)
- Talk:SAMHD1 (transclusion) (links | edit)
- User:Boghog/Sandbox3/ec3 (links | edit)
- User:Boghog/Sandbox3/im (links | edit)
- User:ProteinBoxBot/Protein Directory links (links | edit)
- User:ProteinBoxBot/ASU 20080409B-4 (links | edit)
- User:Tim.landscheidt/Sandbox/Long stubs (links | edit)
- User:NIMBLatManchester/sandbox (links | edit)
- User:Paulaosu (links | edit)
- User:KadaneBot/Task3/Edits/gene/Case 1/2 (links | edit)
- User:Seppi333/GeneListNLP (links | edit)
- User:Joflaher/sandbox (links | edit)
- Misplaced Pages:CHECKWIKI/WPC 557 dump (links | edit)