Pages that link to "Template:WS"
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The following pages link to Template:WS:
Displaying 50 items.
- Agenesis of the corpus callosum (← links)
- Potter syndrome (← links)
- Interrupted aortic arch (← links)
- DNA virus (← links)
- Intron (← links)
- Regulation of gene expression (← links)
- 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)
- Disaccharidase (transclusion) (← links)
- Distal Trisomy 10q (transclusion) (← links)
- Dk phocomelia syndrome (transclusion) (← links)
- Duane-radial ray syndrome (transclusion) (← links)
- Dubowitz syndrome (transclusion) (← links)
- Episodic ataxia (transclusion) (← links)
- Estrogen insensitivity syndrome (transclusion) (← links)
- Ethylmalonic encephalopathy (transclusion) (← links)
- Exinct (transclusion) (← links)
- Familial dysautonomia (transclusion) (← links)
- Fibrous dysplasia (transclusion) (← links)
- Fragile X syndrome (transclusion) (← links)
- Fraser syndrome (transclusion) (← links)
- Frontotemporal dementia and parkinsonism linked to chromosome 17 (transclusion) (← links)
- Fructose malabsorption (transclusion) (← links)
- Gardner's syndrome (transclusion) (← links)
- Glutathione synthetase deficiency (transclusion) (← links)
- Greig cephalopolysyndactyly syndrome (transclusion) (← 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)