Pages that link to "C20orf42"
← C20orf42
The following pages link to C20orf42:
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Charcot–Marie–Tooth disease (← links)
- HFE hereditary haemochromatosis (← links)
- Cleft lip and palate (← links)
- Distal muscular dystrophy (← links)
- Arrhythmogenic right ventricular dysplasia (← links)
- Kindler syndrome (← links)
- Kindlin-1 (redirect page) (← links)
- Integrin (← links)
- Kindler syndrome (← links)
- KIND1 (redirect page) (← links)
- Pleckstrin homology domain (← links)
- Familial exudative vitreoretinopathy (← links)
- Oguchi disease (← links)
- Limb-girdle muscular dystrophy (← links)
- X-linked intellectual disability (← links)