Biochemistry, Genetics and Molecular Biology
Phenotype
100%
Mutation
78%
Nested Gene
70%
Mental Retardation
55%
Protein
40%
Spectrum
39%
Genetics
32%
Haploinsufficiency
31%
Exome Sequencing
20%
Fibroblast
18%
G6PC3
17%
Growth
17%
Chromosome
16%
Development
15%
Zebra Fish
15%
Electric Potential
15%
Introspection
15%
Autosomal Recessive Inheritance
14%
MLL2
13%
Genotyping
12%
Proband
12%
Exome
11%
DNA Methylation
10%
Mouse
10%
RAC1
10%
Amino Acids
10%
Human
10%
Computer Model
9%
Germline
9%
Learning
9%
Lysozyme
8%
Lysine
8%
SATB1
8%
Health
8%
Age
7%
Body Height
7%
Helicase
7%
Thiamine
7%
Eukaryotic Initiation Factor
7%
Aging
7%
Chromatin
7%
RNA Sequence
7%
Nerve Cell Differentiation
7%
Methylation
7%
Epigenetics
7%
Drosophila
7%
Metabolic Pathway
7%
Sex
6%
EZH2
6%
Hearing
6%
Medicine and Dentistry
Patient
51%
Syndrome
37%
Family
34%
Diseases
31%
Phenotype
27%
Diagnosis
24%
Gene
22%
Kabuki Syndrome
22%
Intellectual Disability
19%
Epilepsy
14%
Child
13%
Severe Congenital Neutropenia
13%
Congenital Malformation
12%
Next Generation Sequencing
10%
Epileptic Seizure
10%
Base
10%
Introspection
9%
Exome Sequencing
9%
Clinical Feature
9%
Developmental Delay
9%
Therapeutic Procedure
9%
Glucose 6 Phosphatase
9%
DNA Methylation
8%
Inpatient
8%
Enzyme Active Site
7%
Muscle
7%
Age
7%
Fibroblast
7%
Protein
7%
Exon
6%
Analysis
6%
Human Genetics
6%
Pernicious Anemia
5%
Arthrogryposis
5%
Blood
5%
In Silico
5%
Infant
5%
Childhood
5%
Kidney Malformation
5%