The following pages link to Usher syndrome
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Hereditary elliptocytosis (links | edit)
- Motor protein (links | edit)
- Usher 1C (links | edit)
- Chromosome 1 (links | edit)
- Chromosome 3 (links | edit)
- Chromosome 5 (links | edit)
- Chromosome 10 (links | edit)
- Chromosome 11 (links | edit)
- Nonsyndromic deafness (links | edit)
- Chromosome 17 (links | edit)
- Hereditary pyropoikilocytosis (links | edit)
- Tauopathy (links | edit)
- Freeman–Sheldon syndrome (links | edit)
- Usher syndromes (redirect page) (links | edit)
- Unterberger test (links | edit)
- Usher syndrome type II (redirect page) (links | edit)
- Chromosome 1 (links | edit)
- User:Nmmuller/sandbox (links | edit)
- Larsen syndrome (links | edit)
- Epidermolysis bullosa simplex (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- Short rib–polydactyly syndrome (links | edit)
- Deafness-retinitis pigmentosa syndrome (redirect page) (links | edit)
- Dystrophia retinae pigmentosa-dysostosis syndrome (redirect page) (links | edit)
- Usher syndrome, type 1C (redirect page) (links | edit)
- Usher syndrome, type IA (redirect page) (links | edit)
- Usher syndrome, type 1E (redirect page) (links | edit)
- Usher syndrome, type 2A (redirect page) (links | edit)
- Usher syndrome, type 2B (redirect page) (links | edit)
- Usher syndrome, type 2C (redirect page) (links | edit)
- Usher syndrome, type 3 (redirect page) (links | edit)
- Usher syndrome, type IB (redirect page) (links | edit)
- Usher syndrome, type 1D (redirect page) (links | edit)
- Dix–Hallpike test (links | edit)
- Type 2 (links | edit)
- White sponge nevus (links | edit)
- MASS syndrome (links | edit)
- John Tracy Clinic (links | edit)
- Müller glia (links | edit)
- Nuclear mitochondrial DNA segment (links | edit)
- Naegeli–Franceschetti–Jadassohn syndrome (links | edit)
- Optic disc drusen (links | edit)
- Laminopathy (links | edit)
- Pure-tone audiometry (links | edit)
- Monilethrix (links | edit)
- Congenital hearing loss (links | edit)
- May–Hegglin anomaly (links | edit)
- MYO7A (links | edit)
- Strongylocentrotus purpuratus (links | edit)
- Congenital contractural arachnodactyly (links | edit)
- List of events in NHGRI history (links | edit)
- Richard Liebreich (links | edit)