Biochemistry, Genetics and Molecular Biology
Urea Cycle Disorder
86%
Mutation
73%
Rat
71%
Growth Hormone
70%
Newborn Screening
69%
Messenger RNA
56%
Phenotype
55%
Nested Gene
53%
Age
43%
Glycerol
42%
Regulatory Mechanism
30%
Serine Protease Inhibitor
30%
Growth-Hormone-Releasing Hormone
29%
Protein
28%
Glutamine
22%
Growth
21%
Health
19%
Ornithine Transcarbamylase Deficiency
17%
Pregnancy
16%
Homocysteine
14%
Genetics
14%
Insulin-Like Growth Factor
14%
Inborn Error of Metabolism
14%
Screening
13%
Genetic Counseling
13%
Placental Mammal
12%
Pediatrics
12%
Ontogeny
12%
Contrast
12%
Animal
11%
Chromosome
11%
Homocystinuria
11%
Serpin
11%
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
11%
Case Report
11%
Argininosuccinate Lyase
11%
Methylcrotonyl-CoA Carboxylase
11%
Pyruvate Dehydrogenase
11%
Beta Oxidation
11%
Life
10%
Spectrum
10%
Genetic Screening
10%
Genotyping
9%
Development
9%
Time
9%
Pyruvate Dehydrogenase Complex
9%
Hepatocyte
8%
Growth Hormone Receptor
8%
Incidence
8%
Amino Acids
8%
Medicine and Dentistry
Patient
100%
Newborn Screening
70%
Child
53%
Disease
49%
Therapeutic Procedure
44%
Inborn Error of Metabolism
41%
Neonatal Infant
36%
Inpatient
33%
Urea Cycle Disorder
30%
Symptom
27%
Age
26%
Syndrome
26%
Messenger RNA
25%
Glycerol Phenylbutyrate
24%
Screening
23%
Analysis
18%
Health
18%
Infant
17%
Growth
17%
Neurofibromatosis Type I
17%
Growth Hormone Releasing Factor
17%
Physician
16%
Development
15%
Chromosome
15%
Phenotype
15%
Follow up
15%
Family
14%
Congenital Malformation
14%
Clinician
14%
Testes
13%
Growth Hormone
13%
Blood
13%
Diagnostics
12%
Sibling
11%
Growth Disorder
11%
Diagnosis
11%
Death
10%
Ammonium
10%
Hypoplasia
9%
Liver
9%
Predictor
8%
Exploratory Behavior
8%
Fibroblast
8%
Adult
8%
Glutamine
8%
Primary Health Care
8%
Agenesis
7%
Peptide
7%
Brain Malformation
7%
Male
7%
