Medicine & Life Sciences
2-hydroxyglutarate dehydrogenase
39%
2-Hydroxyglutaricaciduria
17%
acylcarnitine
39%
Alleles
25%
Carnitine
35%
Cysteamine
28%
Cystinosis
30%
Denmark
83%
Dermatan Sulfate
27%
Disaccharides
25%
Fatty Acids
18%
Fertility
18%
Fishes
18%
Genes
32%
glutaconic acid
39%
Glutaric Acidemia I
64%
Glutaryl-CoA Dehydrogenase
36%
Greenland
29%
Growth Charts
28%
Heparitin Sulfate
24%
hydroxide ion
22%
Inborn Errors Metabolism
23%
Inborn Genetic Diseases
18%
Isovaleric acidemia
35%
Kidney Transplantation
18%
Leucine
20%
Ligases
21%
Marfan Syndrome
50%
Medium chain acyl CoA dehydrogenase deficiency
32%
Metachromatic Leukodystrophy
29%
Miller-McKusick-Malvaux-Syndrome (3M Syndrome)
38%
Mucopolysaccharidosis I
32%
Mucopolysaccharidosis II
59%
Mucopolysaccharidosis III
31%
Mutation
68%
N-acetylaspartate
25%
N-Methyl-D-Aspartate Receptors
19%
Neonatal Screening
100%
Newborn Infant
33%
Nuchal Translucency Measurement
27%
Odorants
20%
Osteogenesis Imperfecta
52%
Phenotype
32%
Physiologic Monitoring
20%
Protein-Restricted Diet
25%
Rare Diseases
19%
Receptor, Fibroblast Growth Factor, Type 3
30%
Systemic carnitine deficiency
44%
Transferases
20%
Trimethylaminuria
36%