Medicine and Dentistry
Patient
100%
Diagnosis
37%
Disease
25%
Age
24%
Gene
21%
Muscular Dystrophy
20%
Family
19%
Childhood
19%
Inpatient
17%
Phenotype
16%
Experience
15%
Girl
13%
Muscle
13%
Electrical Brain Stimulation
13%
Epilepsy
13%
Magnetic Resonance Imaging
12%
Early Diagnosis
9%
Myopathy
9%
Follow up
9%
Lesion
9%
Muscle Disease
8%
Limb
8%
Creatine Kinase
8%
Mutant
8%
Sanger Sequencing
8%
Weakness
7%
Neuromuscular Disease
7%
Development
7%
Symptom
7%
Epileptic Seizure
7%
Hypotonia
7%
Clinical Feature
6%
Moyamoya Disease
6%
Kidney Cancer
6%
Next Generation Sequencing
6%
Leiomyomatosis
6%
Adolescence
6%
Missense Mutation
6%
Cancer Cell
6%
Meningioma
6%
Hypertrophic Cardiomyopathy
6%
Onasemnogene Abeparvovec
6%
Surveillance
6%
Case Report
6%
Postnatal Growth
6%
Spinal Muscular Atrophy
6%
Tonic-Clonic Seizure
6%
Lid Margin Neovascularized Area
6%
Mobile Health
6%
Enterovirus A71
6%
Biochemistry, Genetics and Molecular Biology
Mutation
62%
Nested Gene
47%
Next Generation Sequencing
26%
Experience
26%
Phenotype
22%
Spectrum
20%
Dystrophin
15%
Childhood
13%
Sequencing
11%
Exome Sequencing
10%
Multiplex Ligation-Dependent Probe Amplification
9%
Exon
9%
Transcriptome
8%
Phenotypic Heterogeneity
8%
Taxonomy
8%
Collagen VI
8%
Age
7%
Magnetic Resonance Imaging
7%
Screening
7%
Missense Mutation
7%
Sialic Acid
7%
Lysozyme
7%
Stem Cell
6%
Genetic Screening
6%
Genetic Heterogeneity
6%
Nerve Cell Differentiation
6%
Development
6%
RNA Sequence
6%
Glycosylation
6%
Comprehension
6%
Inheritance
6%
Data Base
6%
Messenger RNA
6%
Genetic Trait
6%
Mouse Model
6%
GNE (Gene)
6%
Dystroglycan
6%
Candidate Gene
6%
SYNGAP1
6%
Allele
6%
Mouse
5%
Proband
5%
