Biochemistry, Genetics and Molecular Biology
Actin
7%
Age
6%
Amino Acids
8%
Autosomal Recessive Inheritance
15%
Body Height
8%
Childhood
10%
Chromosome
18%
Coding
7%
Computer Model
8%
Development
15%
DNA Methylation
9%
Electric Potential
13%
Epigenetics
8%
Exome
9%
Exome Sequencing
25%
Fibroblast
16%
G6PC3
17%
Genetics
34%
Genotype Phenotype Correlation
10%
Genotyping
13%
Germline
9%
Glucose 6-Phosphatase
7%
Growth
14%
Haploinsufficiency
32%
Health
7%
Helicase
6%
Histone
8%
Human
13%
Inborn Error of Metabolism
6%
Introspection
20%
Learning
12%
Lysine
8%
Lysozyme
7%
Mental Retardation
66%
Metabolic Pathway
7%
Missense Mutation
7%
MLL2
11%
Mouse
8%
Mutation
89%
Nerve Cell Differentiation
10%
Nested Gene
72%
Next Generation Sequencing
7%
Phenotype
100%
Proband
13%
Protein
41%
RAC1
8%
SATB1
7%
Spectrum
51%
Thiamine
6%
Zebra Fish
12%
Medicine and Dentistry
Age
6%
Analysis
6%
Arthrogryposis
6%
Base
12%
Child
11%
Childhood
7%
Clinical Feature
8%
Congenital Malformation
13%
Development
8%
Developmental Delay
7%
Diagnosis
17%
Diagnostics
12%
Diseases
32%
DNA Methylation
7%
Enzyme Active Site
6%
Epilepsy
17%
Epileptic Seizure
8%
Exome Sequencing
16%
Exon
5%
Family
31%
Fibroblast
6%
Gene
26%
Genotype
5%
Genotype Phenotype Correlation
7%
Glucose 6 Phosphatase
10%
Hypotonia
5%
Inpatient
12%
Introspection
11%
Kabuki Syndrome
20%
Mosaicism
6%
Muscle
6%
Patient
45%
Pernicious Anemia
6%
Phenotype
32%
Protein
7%
Rare Disease
5%
Severe Congenital Neutropenia
13%
Syndrome
38%
Therapeutic Procedure
10%
Woman
6%
