Medicine and Dentistry
Patient
100%
Syndrome
73%
Familial Hypercholesterolemia
73%
Hearing Impairment
62%
Family
49%
Drusen
43%
Visual Impairment
43%
Hereditary Nonpolyposis Colorectal Cancer
43%
Coronary Artery
43%
Isotopes of Calcium
43%
Gene
41%
Autosomal Dominant Inheritance
36%
Retinal Disease
29%
Gene Repair
29%
Pierre Robin Syndrome
27%
Heterozygosity
25%
Exome Sequencing
25%
Association
24%
Adulthood
23%
DNA Mismatch Repair
21%
Carrier Testing
19%
Diagnosis
18%
Exon
18%
Intellectual Disability
18%
Atrial Septal Defect
18%
Adult
18%
Male
18%
Family History
14%
Haplotype
14%
Vasculotropin
14%
Hyperpigmentation
14%
Polymerase Chain Reaction
14%
Screening
14%
Next Generation Sequencing
14%
Woman
14%
Assay
14%
Inpatient
14%
Age
14%
Laboratory
12%
Consanguinity
10%
Autosomal Recessive Inheritance
10%
Chromosome 11
10%
Sensorineural Hearing Loss
10%
Parent
10%
Odds Ratio
9%
Diseases
9%
Esotropia
9%
Cardiac Shunt
9%
Persistent Left Superior Vena Cava
9%
Scoliosis
9%
Biochemistry, Genetics and Molecular Biology
Familial Hypercholesterolemia
73%
Calcium
43%
Mutation
37%
Nested Gene
34%
Sequencing
34%
Vision
29%
Autosomal Dominant Inheritance
29%
Association
24%
Adulthood
23%
Case Report
18%
Exon
18%
Optics
14%
Molecular Genetics
14%
Multiplex Ligation-Dependent Probe Amplification
14%
Heterozygosity
14%
Haplotype
14%
DNA Extraction
14%
Vascular Endothelial Growth Factor
14%
Age
14%
Contrast
10%
Autosomal Recessive Inheritance
10%
Chromosome 11
10%
Loss of Heterozygosity
10%
Consanguinity
10%
Turkey (Bird)
10%
Case-Control Study
9%
Mosaicism
9%
Coding
9%
Spectrum
9%
Agricultural and Biological Sciences
PMS2
73%
Hearing
73%
Colon
29%
Genes
17%
Mutation
14%
Polymerase Chain Reaction
14%
Screening
14%
Assays
14%
Exome Sequencing
10%
Boys
10%
Europeans
10%
Testing
10%
Wild Turkey
10%
Area
10%
Sequencing
10%
History
10%
Parents
10%
MSH2
7%
MLH1
7%
Laboratories
7%
Detection
7%
Materials
7%
