The following pages link to Familial Amyloidosis, Finnish Type
External toolsShowing 9 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- FAF (links | edit)
- Lattice corneal dystrophy (links | edit)
- Meretoja syndrome (redirect page) (links | edit)
- Hereditary gelsolin amyloidosis (redirect page) (links | edit)
- List of skin conditions (links | edit)
- Finnish heritage disease (links | edit)
- Plasma gelsolin (links | edit)
- Talk:Hereditary gelsolin amyloidosis (transclusion) (links | edit)
- User:AlexNewArtBot/MedicineSearchResult/archive31 (links | edit)
- User:AlexNewArtBot/ReferencesSearchResult/archive84 (links | edit)
- User:MastCell/Ignored medical articles (links | edit)
- User:Gavivz/Books/Inborn errors of metabolism (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- User:Sun Creator/A to An files (links | edit)
- User:Seppi333/List sandbox (links | edit)
- Misplaced Pages:WikiProject Medicine/Dermatology task force/Articles created (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Mid-importance medicine articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Popular pages En 2013b (links | edit)
- Talk:Familial Amyloidosis, Finnish Type (transclusion) (links | edit)
- User:JAAqqO/List of WikiProject Finland articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Misplaced Pages:Arbitration Committee/Requests for comment/Article creation at scale (links | edit)
- Misplaced Pages:WikiProject Medicine/The ICD-11 coding challenge/5800–5899 (links | edit)