Biochemistry, Genetics and Molecular Biology
Phenotype
87%
Mental Retardation
79%
Mutation
66%
Dysplasia
54%
Nested Gene
50%
Protein
46%
Alternative Splicing
37%
BCL11A
37%
Kinase
37%
Allele
35%
FLNA
32%
Exome Sequencing
28%
Age
26%
Electric Potential
25%
Nerve Cell Plasticity
21%
Haploinsufficiency
17%
HBG1
16%
Genetics
16%
FBN1
16%
Spectrum
15%
Pregnancy
14%
Western Blot
12%
Contrast
12%
Promoter Region
12%
Fetal Hemoglobin
12%
Orthology
12%
Locomotion
12%
Cell Membrane
12%
Aptitude
12%
Fibroblast
12%
Drosophila
12%
GenBank
12%
Reduction (Chemistry)
12%
Lifespan
12%
Neurotransmission
12%
mRNA Expression Level
10%
Cellular Respiration
10%
Expression Analysis
10%
Splicing Factor
9%
Genetic Transcription
9%
Nerve Cell Differentiation
9%
Regulatory Mechanism
9%
Mutant
9%
Chromosome
9%
Proband
9%
Genotype Phenotype Correlation
8%
Erythropoiesis
8%
Chromatin
8%
Electrophysiology
6%
Pediatrics
6%
Medicine and Dentistry
Patient
100%
Phenotype
62%
Dysplasia
54%
Gene
45%
Alternative RNA Splicing
37%
Mitogen Activated Protein Kinase 3
33%
Neurodevelopmental Disorder
28%
Age
26%
Syndrome
25%
Cells
21%
Embryonic Hemoglobin
20%
Skin
18%
Energy-Dispersive X-Ray Spectroscopy
18%
Brain Abnormalities
18%
Neuron
18%
Cardiomyopathy
18%
Dissection
17%
Haploinsufficiency
17%
Diseases
14%
Diagnosis
14%
Pregnancy
14%
Connective Tissue Disease
13%
Aortic Dissection
12%
Vascular Disease
12%
Male
12%
Family
12%
Promoter Region
12%
Exome Sequencing
9%
Complementary DNA
9%
Clinical Feature
9%
Attention Deficit Disorder
9%
Apraxia
9%
Regulatory Mechanism
9%
Skin Defect
9%
Clubfoot
9%
Genetic Transcription
9%
Female
9%
Chromosome
9%
Cell Type
9%
Disease Course
9%
Facies
9%
Mutant
9%
Nerve Cell Differentiation
9%
Hypotonia
9%
Protein
8%
Tissues
8%
Analysis
8%
Differential Diagnosis
8%
Noonan Syndrome
8%
Adult
8%
Neuroscience
Alternative Splicing
37%
Synapse
37%
Psychopathology
37%
Epilepsy
37%
Intellectual Disability
37%
Exome Sequencing
28%
Phenotype
28%
Neurodevelopmental Disorder
28%
Neuron
25%
Dependent Personality Disorder
18%
Aneurysm
16%
Single-Pass Transmembrane Proteins
12%
Reference Memory
12%
X Chromosome
12%
Long-Term Memory
12%
Gait
12%
Cognition
12%
Neurite Outgrowth
12%
Receptor Tyrosine Kinase
12%
Membrane Transport
12%
Apraxia
9%
Attention Deficit Hyperactivity Disorder
9%
Nerve Cell Differentiation
9%
Complementary DNA
9%
Genetic Transcription
9%
Hypotonia
9%
CRISPR
6%
Channel Gating
6%
Electrophysiology
6%
Seizure
6%
Electroencephalography
6%
Gain of Function Mutation
6%
In Vivo
6%
Pediatrics
6%
Language Delay
6%
Protein Expression
5%
Gene
5%
Vascular Smooth Muscle
5%
RNA Sequence
5%
Proteomics
5%
