Biochemistry, Genetics and Molecular Biology
Mutation
100%
Nested Gene
62%
Mental Retardation
38%
Phenotype
35%
BCL11A
32%
Spectrum
28%
Exon
26%
Genotype Phenotype Correlation
24%
Genetics
24%
Regulatory Element
21%
ASCL1
21%
Autosomal Dominant Inheritance
19%
Exome Sequencing
17%
Introspection
17%
Gene Expression
16%
Germline
16%
Missense Mutation
15%
Regulatory Mechanism
14%
Haploinsufficiency
14%
Proband
13%
Pediatrics
13%
Data Base
13%
Childhood
11%
SMARCA2
11%
Chromatin Remodeling
11%
Ambiguity
10%
Chromatin
10%
Enhancer Region
10%
Angelman Syndrome
10%
Transcription
10%
Dysferlin
10%
Helicase
10%
Body Weight
10%
Stem Cell
10%
Development
10%
NIPBL
10%
Cholesterol Synthesis
10%
Phospholipase A2
10%
SMARCA4
10%
Founder Effect
10%
Exon Skipping
10%
Alternative Splicing
10%
Position
8%
Mouse
8%
Transcription Factor
8%
Iron
8%
Association
8%
SLC3A1
8%
Screening
8%
SLC7A9
8%
Medicine and Dentistry
Patient
39%
Gene
32%
Diagnostics
21%
Diagnosis
18%
Analysis
18%
Syndrome
17%
Autosomal Dominant Inheritance
15%
Exon
15%
Exome Sequencing
15%
Limb
13%
Family
12%
Vocal Folds
10%
Childhood
10%
Dentinogenesis Imperfecta
10%
Induced Pluripotent Stem Cell
10%
Pathogenesis
10%
Spastic Paraplegia
10%
Calcification
10%
Outpatient
10%
Sudden Death
10%
Rheumatoid Arthritis
10%
Dysplasia
10%
Muscle Disease
10%
Missense Mutation
10%
Pediatric Neurology
10%
Disease
9%
Sibling
9%
Female
8%
Therapeutic Procedure
7%
Association
7%
Male
7%
Growth
5%
Phenotype
5%
Epileptic Seizure
5%
Exome
5%
Base
5%
Neuroscience
Gene
39%
Neurodegeneration
32%
Phenotype
23%
Genotype
15%
Haploinsufficiency
10%
Dysferlin
10%
Ataxia
10%
Appetite
10%
Phospholipase A2
10%
Intellectual Disability
10%
Angelman Syndrome
10%
Exon Skipping
10%
Alternative Splicing
10%
Exon
10%
BCL11A
10%
Muscle Disorder
8%
Brain Imaging
7%
Exome Sequencing
6%
Neurodegeneration with Brain Iron Accumulation
5%
Morphogen
5%
Brain Development
5%
Nuclear Pore Complex
5%
Energy Expenditure
5%
Central Nervous System
5%
Chromosome 2
5%
Genetic Variation
5%
Human Chromosome
5%
Intergenic Region
5%
Fat
5%
Forebrain
5%
Haplotype
5%
