The following pages link to PCNT
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- CNTRL (links | edit)
- CEP250 (links | edit)
- CEP170 (links | edit)
- CEP68 (links | edit)
- CEP63 (links | edit)
- CEP57 (links | edit)
- CCP110 (links | edit)
- Weill–Marchesani syndrome (links | edit)
- Ninein-like protein (links | edit)
- CEP72 (links | edit)
- CEP70 (links | edit)
- CEP135 (links | edit)
- CNTROB (links | edit)
- Boomerang dysplasia (links | edit)
- Microcephalic osteodysplastic primordial dwarfism type II (links | edit)
- Pericentrin (redirect page) (links | edit)
- Elejalde syndrome (links | edit)
- Ichthyosis bullosa of Siemens (links | edit)
- FG syndrome (links | edit)
- Ichthyosis hystrix (links | edit)
- Reticular pigmented anomaly of the flexures (links | edit)
- Naxos syndrome (links | edit)
- Mandibuloacral dysplasia (links | edit)
- Keratin disease (links | edit)
- Familial cirrhosis (links | edit)
- Dunnigan familial partial lipodystrophy (links | edit)
- Familial partial lipodystrophy (links | edit)
- Pericentriolar material (links | edit)
- Terminal osseous dysplasia with pigmentary defects (links | edit)
- Skin fragility syndrome (links | edit)
- CEP192 (links | edit)
- Kendrin (redirect page) (links | edit)
- CEP164 (links | edit)
- CEP76 (links | edit)
- CEP78 (links | edit)
- CEP97 (links | edit)
- CEP120 (links | edit)
- CEP152 (links | edit)
- Asphyxiating thoracic dysplasia (links | edit)
- Desmin-related myofibrillar myopathy (links | edit)
- List of OMIM disorder codes (links | edit)
- SASS6 (links | edit)
- PCNT (gene) (redirect page) (links | edit)
- CEP104 (links | edit)
- SFI1 (links | edit)
- C21orf58 (links | edit)
- List of human protein-coding genes 3 (links | edit)
- PROSER3 (links | edit)
- Talk:PCNT (transclusion) (links | edit)
- User:AlexNewArtBot/JapanSearchResult/archive4 (links | edit)