The following pages link to Missense mutations
External toolsShowing 44 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Androgen insensitivity syndrome (links | edit)
- Adrenoleukodystrophy (links | edit)
- Fragile X syndrome (links | edit)
- Gilbert's syndrome (links | edit)
- Single-nucleotide polymorphism (links | edit)
- Point mutation (links | edit)
- Li–Fraumeni syndrome (links | edit)
- Treacher Collins syndrome (links | edit)
- Seymour Benzer (links | edit)
- Cyclic nucleotide–gated ion channel (links | edit)
- Trimethylaminuria (links | edit)
- Androgen receptor (links | edit)
- Hypophosphatasia (links | edit)
- Point accepted mutation (links | edit)
- Adenine phosphoribosyltransferase (links | edit)
- Freeman–Sheldon syndrome (links | edit)
- Larsen syndrome (links | edit)
- Histidinemia (links | edit)
- UDP glucuronosyltransferase 1 family, polypeptide A1 (links | edit)
- Methylmalonyl-CoA mutase (links | edit)
- Folliculin (links | edit)
- BARD1 (links | edit)
- FOXL2 (links | edit)
- HSD17B10 (links | edit)
- ELAC2 (links | edit)
- IDH2 (links | edit)
- BAP1 (links | edit)
- CCDC113 (links | edit)
- Bcr-Abl tyrosine-kinase inhibitor (links | edit)
- Hereditary diffuse leukoencephalopathy with spheroids (links | edit)
- Fast parallel proteolysis (links | edit)
- Hypodysfibrinogenemia (links | edit)
- Okamoto syndrome (links | edit)
- CDK13-related disorder (links | edit)
- Autosomal dominant Charcot–Marie–Tooth disease type 2 with giant axons (links | edit)
- CAPOS syndrome (links | edit)
- User:Emherrington87/sandbox (links | edit)
- User:Bene0143/sandbox (links | edit)
- User:BVervers/sandbox (links | edit)
- User:Umbacgra (links | edit)
- User:Biermannjordan/sandbox (links | edit)
- User talk:Hankwbass/Group 4 (links | edit)
- Misplaced Pages:Picture peer review/Notable mutations (links | edit)
- Misplaced Pages:Picture peer review/Archives/Jul-Sep 2009 (links | edit)