Pages that link to "Template:WS"
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The following pages link to Template:WS:
Displaying 50 items.
- Okazaki fragment (← links)
- Abderhalden-Kaufmann-Lignac syndrome (← links)
- Anticipation (genetics) (← links)
- Autosomal dominant nocturnal frontal lobe epilepsy (← links)
- Birt-Hogg-Dubé syndrome (← links)
- Canavan disease (← links)
- Cardiofaciocutaneous syndrome (← links)
- Carpenter syndrome (← links)
- Channelopathy (← links)
- Charcot-Marie-Tooth disease (← links)
- Cherubism (← links)
- Coffin-Lowry syndrome (← links)
- Cohen syndrome (← links)
- Crouzon syndrome (← links)
- Diastrophic dysplasia (← links)
- Dk phocomelia syndrome (← links)
- Dubowitz syndrome (← links)
- Episodic ataxia (← links)
- Familial dysautonomia (← links)
- Fibrous dysplasia (← links)
- Fragile X syndrome (← links)
- Frontotemporal dementia and parkinsonism linked to chromosome 17 (← links)
- Gardner's syndrome (← links)
- Greig cephalopolysyndactyly syndrome (← links)
- Guanidinoacetate methyltransferase deficiency (transclusion) (← links)
- Health aspects of Down syndrome (transclusion) (← links)
- Hunter syndrome (transclusion) (← links)
- Huntington's disease (transclusion) (← links)
- Hyperlysinemia (transclusion) (← links)
- Hypermethioninemia (transclusion) (← links)
- Hyperprolinemia (transclusion) (← links)
- Hypochondrogenesis (transclusion) (← links)
- Infantile neuroaxonal dystrophy (transclusion) (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (transclusion) (← links)
- Joubert syndrome (transclusion) (← links)
- Leopard syndrome (transclusion) (← links)
- Liddle's syndrome (transclusion) (← links)
- Lipoid congenital adrenal hyperplasia (transclusion) (← links)
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (transclusion) (← links)
- Lysinuric protein intolerance (transclusion) (← links)
- Léri-Weill dyschondrosteosis (transclusion) (← links)
- Malonyl-CoA decarboxylase deficiency (transclusion) (← links)
- Maple syrup urine disease (transclusion) (← links)
- Meckel syndrome (transclusion) (← links)
- Microphthalmia (transclusion) (← links)
- Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (transclusion) (← links)
- Muscular dystrophy (transclusion) (← links)
- Myelokathexis (transclusion) (← links)
- Myeloperoxidase deficiency (transclusion) (← links)
- Myotonia congenita (transclusion) (← links)