Medicine and Dentistry
Patient
100%
Gene
95%
Analysis
43%
Screening
39%
Base
33%
Single Nucleotide Polymorphism
33%
Prognosis
33%
Adolescent
33%
Somatics
33%
B-Cell Chronic Lymphocytic Leukemia
33%
Atrial Fibrillation
33%
Family
33%
Polycystic Ovary Syndrome
33%
Spinal Muscular Atrophy
33%
DeJerine-Sottas Disease
33%
Inpatient
33%
DNA
21%
Blood
12%
Exon
11%
Laboratory
11%
Cardiomyopathy
11%
Early Diagnosis
11%
Childbirth
11%
Follow up
9%
Diagnosis
9%
Disease
9%
Symptom
9%
Phenotype
7%
Cardiac Dysrhythmia
7%
Prevalence
7%
Heredity
6%
Ensure
5%
Male
5%
DNA Isolation
5%
Tooth
5%
Female
5%
Neurologic Disease
5%
Molecular Diagnostics
5%
Life
5%
Parent
5%
Biochemistry, Genetics and Molecular Biology
Screening
84%
Nested Gene
73%
Genetic Code
73%
Sample
57%
Gene Analysis
42%
GNRHR
33%
Newborn Screening
33%
GJB1
33%
Atrial Fibrillation
33%
Single-Nucleotide Polymorphism
33%
Genotype
27%
Allele
27%
Sanger Sequencing
23%
Phenotype
23%
Multiplex Ligation-Dependent Probe Amplification
19%
Testosterone
13%
Association
13%
Development
13%
SMN1
11%
Birth
11%
Genetic Determinism
10%
Data Base
8%
Genetic Divergence
8%
Chloroform
8%
Mosaicism
8%
Prevalence
7%
Gene Sequence
6%
DNA Analysis
6%
Lysozyme
6%
Experience
6%
Adulthood
6%
Embryology
6%
Age
6%
Cross Sectional Study
6%
Reproduction
6%
Genotyping
6%
Health
6%
Locked Nucleic Acid
5%
Time
5%
DNA Isolation
5%
Life
5%
Real-Time Polymerase Chain Reaction
5%
Nursing and Health Professions
Ovary Polycystic Disease
33%
Nucleotide
33%
Screening
33%
Spinal Muscular Atrophy
33%
Pilot Study
33%
Sample
19%
DNA
16%
Laboratory
11%
Early Diagnosis
11%
Symptom
9%
Ensure
5%
Health Care Personnel
5%
Clinical Outcome
5%
Diseases
5%
Error
5%
Locked Nucleic Acid
5%
Multiplex Ligation Dependent Probe Amplification
5%
DNA Isolation
5%
Time
5%
