The following pages link to SH3BP2
External toolsShowing 38 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- GRB10 (links | edit)
- TRAF2 (links | edit)
- YWHAZ (links | edit)
- TRAF1 (links | edit)
- BIN1 (links | edit)
- TRAF5 (links | edit)
- TRAF3 (links | edit)
- YWHAE (links | edit)
- TRAF4 (links | edit)
- CHML (gene) (links | edit)
- LDB3 (links | edit)
- Lhermitte–Duclos disease (links | edit)
- X-linked lymphoproliferative disease (links | edit)
- Chylomicron retention disease (links | edit)
- X-linked intellectual disability (links | edit)
- Griscelli syndrome type 2 (links | edit)
- Marinesco–Sjögren syndrome (links | edit)
- Congenital generalized lipodystrophy (links | edit)
- X-linked myotubular myopathy (links | edit)
- Watson syndrome (links | edit)
- Parkes Weber syndrome (links | edit)
- Progressive osseous heteroplasia (links | edit)
- Proteus-like syndrome (links | edit)
- Neutrophil immunodeficiency syndrome (links | edit)
- List of OMIM disorder codes (links | edit)
- Legius syndrome (links | edit)
- Stimulator of interferon genes (links | edit)
- List of human protein-coding genes 3 (links | edit)
- Craniofacial regeneration (links | edit)
- Talk:SH3BP2 (transclusion) (links | edit)
- User:NussPoyava/sandbox (links | edit)
- User:2013MMG230E/sandbox/sandbox (links | edit)
- User:Dwghx8/sandbox (links | edit)
- User:Ramya O/sandbox2 (links | edit)
- User:Seppi333/GeneListNLP (links | edit)
- Misplaced Pages:WikiProject Chemistry/Stubs (links | edit)
- Template:Signal transducing adaptor proteins (links | edit)
- Template:Deficiencies of intracellular signaling peptides and proteins (links | edit)