Medicine & Life Sciences
Inborn Urea Cycle Disorder
100%
Neonatal Screening
76%
glycerol phenylbutyrate
61%
Growth Hormone
43%
Inborn Errors Metabolism
35%
Ammonia
28%
Serine Proteinase Inhibitors
25%
Growth Hormone-Releasing Hormone
25%
phenylacetic acid
22%
Mutation
22%
4-phenylbutyric acid
21%
Messenger RNA
20%
Liver
19%
phenylacetylglutamine
19%
Phenotype
18%
Newborn Infant
17%
Genes
15%
Child
15%
Information Systems
14%
Ornithine Carbamoyltransferase Deficiency Disease
13%
Glutamine
13%
Testicular Hormones
13%
Medical Genetics
12%
Homocystinuria
11%
Pediatrics
11%
Phenylketonurias
11%
Pyruvate Dehydrogenase Complex Deficiency Disease
10%
Insulin-Like Growth Factor I
10%
Medium chain acyl CoA dehydrogenase deficiency
10%
3-methylcrotonyl CoA carboxylase 1 deficiency
10%
Neurofibromatoses
10%
Siblings
10%
Partial deletion Chromosome 11p
10%
Therapeutics
9%
Neurofibromatosis 1
9%
Homocysteine
9%
Argininosuccinate Lyase
9%
Systemic carnitine deficiency
9%
Growth
9%
Microcephaly
8%
Hormones
8%
RNA
8%
Genetic Counseling
8%
Biomarkers
8%
Response Elements
8%
Insulin-Like Growth Factor II
7%
Argininosuccinic Aciduria
7%
Databases
7%
Animals
7%
Noonan Syndrome
7%