Medicine and Dentistry
Patient
100%
Family
69%
Gene
65%
Diagnosis
55%
Syndrome
44%
Protein
38%
Child
37%
Developmental Delay
37%
Fluorescence in Situ Hybridization
37%
Intellectual Disability
36%
Phenotype
34%
Hyperthyroidism
31%
Cardiomyopathy
31%
Point Mutation
31%
Probe
31%
Analysis
30%
Genetic Evaluation
29%
Microcephaly
25%
Age
25%
Mosaicism
25%
Evaluation Study
24%
Capillary
23%
Congenital Malformation
23%
Thyrotropin Receptor
22%
Myeloid Malignancy
21%
Exon
21%
Chromosome 13
21%
Karyotype
20%
Pregnancy
19%
Follow up
19%
Chromosome
18%
Mitochondrial DNA
17%
Platelet Disorder
15%
Thrombocytopenia
15%
Epilepsy
15%
RNA Sequence
15%
Brain Disease
15%
Prematurity
15%
Lipid
15%
Developmental Regression
15%
Nonsense Mediated mRNA Decay
15%
Tetraplegia
15%
Donor Site
15%
Stop Codon
15%
Membrane
15%
Pathogenicity
15%
Screening
14%
Association
13%
Receptor Gene
13%
Interphase
12%
Biochemistry, Genetics and Molecular Biology
Nested Gene
49%
Fluorescence in Situ Hybridization
37%
NADH Dehydrogenase
31%
Point Mutation
31%
Mosaicism
30%
Phenotype
29%
Chromosome
23%
Chromosome 13
21%
Karyotype
20%
Mutation
19%
Pregnancy
19%
Mitochondrial DNA
17%
Stop Codon
15%
RNA Sequence
15%
Nonsense-Mediated Decay
15%
Membrane
15%
Screening
14%
Next Generation Sequencing
13%
Ultrasound
12%
Interphase
12%
Amnion Cell
12%
Proband
11%
Mental Retardation
10%
SH2B3
10%
PHF6
10%
Age
10%
Neuroscience
Gene
49%
Protein
38%
Intellectual Disability
36%
Cardiomyopathy
31%
Point Mutation
31%
Mosaicism
30%
Thyrotropin Receptor
22%
Microcephaly
20%
Mitochondrial DNA
17%
Epilepsy
15%
Lipid
15%
RNA Sequence
15%
Stop Codon
15%
Nonsense Mediated mRNA Decay
15%
Encephalopathy
15%
Exon
15%
Phenotype
13%
Receptor Gene
13%
Interphase
12%
Chromosome
12%
PHF6
10%