Biochemistry, Genetics and Molecular Biology
Genetics
100%
Autoantibodies
50%
Missense Mutation
48%
Autoimmunity
47%
Infancy
43%
Testis Development
40%
Insulin Release
33%
Genomics
32%
Exome Sequencing
30%
Propionic Acidemia
30%
Single-Nucleotide Polymorphism
30%
Autosomal Dominant Inheritance
28%
Body Height
26%
Haplotype
26%
Exon
24%
Haploinsufficiency
24%
Carboxy-Lyases
23%
Allele
20%
Genotyping
20%
Type I Collagen
20%
ALDH7A1
20%
Molecular Systematics
20%
Interspersed Repeat
20%
GC-content
20%
Bone Development
20%
Gene Deletion
20%
KCNQ4
20%
Induced Mutation
20%
Genotype Phenotype Correlation
20%
Pedigree
20%
21-Hydroxylase
20%
Genome-Wide Association Study
20%
ABCC8
20%
Deep Vein Thrombosis
20%
Glycine Cleavage System
20%
Codon
20%
Methionine
20%
Phosphatidylinositol
20%
Vitamin B6
20%
Pyridoxine
20%
Polysaccharides
20%
Gonad Development
20%
Aneuploidy
20%
Titer
20%
Thyroid Peroxidase
20%
Low Copy Repeats
20%
Adenosine Monophosphate
20%
Binding Site
20%
Rare Variant
20%
Indel
20%
Medicine and Dentistry
Insulin Dependent Diabetes Mellitus
80%
Achondroplasia
60%
Glycine Encephalopathy
50%
Infancy
42%
Fulminant
40%
Growth Hormone
37%
Glycine Cleavage System
35%
Diabetes
33%
Hearing Impairment
33%
Neonatal Infant
30%
Insulin Release
30%
Developmental Delay
28%
Hyperglycinemia
25%
Breathing
25%
Insulin Treatment
25%
Hypoglycemia
23%
Short Stature
22%
Osteogenesis Imperfecta
22%
Clinical Feature
22%
Autoantibodies
22%
Diseases
20%
Disorders of Sex Development
20%
Pediatric Endocrinologist
20%
Transitional Care
20%
Cancer in Young Adults
20%
Carbon 13
20%
Prenatal Diagnosis
20%
Glycan
20%
Down Syndrome
20%
Subfornical Organ
20%
Congenital Adrenal Hyperplasia
20%
Pamidronic Acid
20%
Immune Response
20%
Nateglinide
20%
Diabetes Mellitus
20%
Collagen Type 1
20%
Phosphatidylinositol
20%
Medical Record
20%
Methionine
20%
Lipoid Congenital Adrenal Hyperplasia
20%
Codon
20%
Lipopolysaccharide
20%
Cerebrospinal Fluid
20%
Growth Retardation
20%
Aneuploidy
20%
CYP24A1
20%
Acanthosis Nigricans
20%
Paget Bone Disease
20%
Receptor Activator of Nuclear Factor Kappa B
20%
Syndrome CHARGE
20%
