Pages that link to "Template:National Library of Medicine reference"
Showing 48 items.
- Von Hippel–Lindau disease (transclusion) (links | edit)
- Tay–Sachs disease (transclusion) (links | edit)
- Wilson's disease (transclusion) (links | edit)
- Abetalipoproteinemia (transclusion) (links | edit)
- Hereditary coproporphyria (transclusion) (links | edit)
- Erythropoietic protoporphyria (transclusion) (links | edit)
- Propionic acidemia (transclusion) (links | edit)
- Perforin-1 (transclusion) (links | edit)
- Glycogen storage disease type II (transclusion) (links | edit)
- Familial adenomatous polyposis (transclusion) (links | edit)
- Bloom syndrome (transclusion) (links | edit)
- Thanatophoric dysplasia (transclusion) (links | edit)
- Isovaleric acidemia (transclusion) (links | edit)
- Maple syrup urine disease (transclusion) (links | edit)
- Cystinosis (transclusion) (links | edit)
- Klippel–Feil syndrome (transclusion) (links | edit)
- Glutaric aciduria type 1 (transclusion) (links | edit)
- Giant axonal neuropathy (transclusion) (links | edit)
- Spondyloperipheral dysplasia (transclusion) (links | edit)
- Sideroblastic anemia (transclusion) (links | edit)
- Pseudoxanthoma elasticum (transclusion) (links | edit)
- MELAS syndrome (transclusion) (links | edit)
- Malonic aciduria (transclusion) (links | edit)
- 3-Methylglutaconic aciduria (transclusion) (links | edit)
- Methylmalonyl-CoA mutase deficiency (transclusion) (links | edit)
- Greig cephalopolysyndactyly syndrome (transclusion) (links | edit)
- Vitelliform macular dystrophy (transclusion) (links | edit)
- Pallister–Hall syndrome (transclusion) (links | edit)
- Tangier disease (transclusion) (links | edit)
- Duane-radial ray syndrome (transclusion) (links | edit)
- Isobutyryl-coenzyme A dehydrogenase deficiency (transclusion) (links | edit)
- Loeys–Dietz syndrome (transclusion) (links | edit)
- Carbamoyl phosphate synthetase I deficiency (transclusion) (links | edit)
- Ethylmalonic encephalopathy (transclusion) (links | edit)
- Hepatoerythropoietic porphyria (transclusion) (links | edit)
- Hypohidrotic ectodermal dysplasia (transclusion) (links | edit)
- Pyruvate carboxylase deficiency (transclusion) (links | edit)
- Glutathione synthetase deficiency (transclusion) (links | edit)
- Ornithine translocase deficiency (transclusion) (links | edit)
- Neuropathy, ataxia, and retinitis pigmentosa (transclusion) (links | edit)
- Galactosemic cataract (transclusion) (links | edit)
- User:Ricov53/sandbox (transclusion) (links | edit)
- User:Jcrank07/sandbox (transclusion) (links | edit)
- User:Hganev/sandbox (transclusion) (links | edit)
- User:Aherrera09/sandbox (transclusion) (links | edit)
- Template:NIH-Genetics (redirect page) (links | edit)
- Template:NLM (redirect page) (links | edit)
- Von Hippel–Lindau disease (transclusion) (links | edit)
- Tay–Sachs disease (transclusion) (links | edit)
- Wilson's disease (transclusion) (links | edit)
- Abetalipoproteinemia (transclusion) (links | edit)
- Hereditary coproporphyria (transclusion) (links | edit)
- Erythropoietic protoporphyria (transclusion) (links | edit)
- Propionic acidemia (transclusion) (links | edit)
- Perforin-1 (transclusion) (links | edit)
- Glycogen storage disease type II (transclusion) (links | edit)
- Familial adenomatous polyposis (transclusion) (links | edit)
- Bloom syndrome (transclusion) (links | edit)
- Thanatophoric dysplasia (transclusion) (links | edit)
- Isovaleric acidemia (transclusion) (links | edit)
- Maple syrup urine disease (transclusion) (links | edit)
- Cystinosis (transclusion) (links | edit)
- Klippel–Feil syndrome (transclusion) (links | edit)
- Glutaric aciduria type 1 (transclusion) (links | edit)
- Giant axonal neuropathy (transclusion) (links | edit)
- Spondyloperipheral dysplasia (transclusion) (links | edit)
- Sideroblastic anemia (transclusion) (links | edit)
- Pseudoxanthoma elasticum (transclusion) (links | edit)
- MELAS syndrome (transclusion) (links | edit)
- Malonic aciduria (transclusion) (links | edit)
- 3-Methylglutaconic aciduria (transclusion) (links | edit)
- Methylmalonyl-CoA mutase deficiency (transclusion) (links | edit)
- Greig cephalopolysyndactyly syndrome (transclusion) (links | edit)
- Vitelliform macular dystrophy (transclusion) (links | edit)
- Pallister–Hall syndrome (transclusion) (links | edit)
- Tangier disease (transclusion) (links | edit)
- Duane-radial ray syndrome (transclusion) (links | edit)
- Isobutyryl-coenzyme A dehydrogenase deficiency (transclusion) (links | edit)
- Loeys–Dietz syndrome (transclusion) (links | edit)
- Carbamoyl phosphate synthetase I deficiency (transclusion) (links | edit)
- Ethylmalonic encephalopathy (transclusion) (links | edit)
- Hepatoerythropoietic porphyria (transclusion) (links | edit)
- Hypohidrotic ectodermal dysplasia (transclusion) (links | edit)
- Pyruvate carboxylase deficiency (transclusion) (links | edit)
- Glutathione synthetase deficiency (transclusion) (links | edit)
- Ornithine translocase deficiency (transclusion) (links | edit)
- Neuropathy, ataxia, and retinitis pigmentosa (transclusion) (links | edit)
- Galactosemic cataract (transclusion) (links | edit)
- User:Ricov53/sandbox (transclusion) (links | edit)
- User:Jcrank07/sandbox (transclusion) (links | edit)
- User:Hganev/sandbox (transclusion) (links | edit)
- User:Aherrera09/sandbox (transclusion) (links | edit)
- Wikipedia:WikiProject Medicine/Lists of pages/Templates (links | edit)
- Wikipedia:WikiProject Medicine/Lists of pages/Non-articles (links | edit)
- Wikipedia:Bot requests/Archive 81 (links | edit)
- Wikipedia:Link rot/Templates (links | edit)
- Wikipedia talk:WikiProject Medicine/Archive 35 (links | edit)
- Template:National Library of Medicine reference (links | edit)
- Template:NLM catalog (links | edit)
- Template talk:National Library of Medicine reference (transclusion) (links | edit)