Biochemistry, Genetics and Molecular Biology
Allele
49%
BRCA1
10%
BRCA2
10%
CAG Repeat
18%
Carnitine O-Palmitoyltransferase
14%
Cystic Fibrosis
49%
Cytogenetics
11%
Decision Making
16%
Denaturing High Performance Liquid Chromatography
15%
DNA Mismatch Repair
10%
DNA Sequence
13%
Dystrophin
38%
Exome Sequencing
24%
Exome Sequencing
14%
Exon
26%
Fluorescence in Situ Hybridization
14%
Fructose
14%
Gene Deletion
13%
Genetic Screening
100%
Genetic Test
13%
Genetic Variation
16%
Genetics
70%
Genome Sequencing
54%
Genotyping
23%
Glucagon
15%
Hepatocyte
15%
Homozygosity
14%
Human Genetics
26%
Human Genome
19%
Laboratory Test
13%
Lifespan
12%
Major Histocompatibility Complex
14%
Mass Screening
14%
Medical Genetics
67%
Medical Genomics
60%
Molecular Genetics
24%
Mosaicism
10%
Mouse
21%
MSH2
9%
MSH6
14%
Next Generation Sequencing
11%
Oligonucleotide
11%
Phosphofructokinase
14%
Population
10%
Prevalence
15%
Proband
17%
Quality Control
12%
Skewed X-Inactivation
14%
Trinucleotide Repeat Expansion
17%
X Chromosome
31%
Medicine and Dentistry
Allele
7%
BRCA1
8%
Breast Cancer
9%
Carcinogenicity
7%
Carrier Testing
15%
Clinical Genetics
10%
Clinical Health
7%
Clinician
24%
Codon
12%
Colorectal Cancer
20%
Consumer
10%
Cystic Fibrosis
42%
Decision Making
17%
Diagnosis
12%
Disease
55%
DNA Mismatch Repair
11%
DNA Sequence
11%
Dystrophin
7%
Epidermal Growth Factor Receptor
7%
Exome
8%
Exome Sequencing
23%
Family History
24%
FMR1
7%
Gene Repair
7%
Genetic Disorder
9%
Genetic Screening
56%
Genome Sequencing
32%
Health Care Cost
28%
Health Outcomes
25%
Health System
10%
Hereditary Nonpolyposis Colorectal Cancer
19%
Human Genetics
17%
Human Genome
8%
Laboratory Test
13%
Malignant Neoplasm
27%
Mammography
7%
Maturity Onset Diabetes of the Young
7%
Medicine
21%
Metastatic Colorectal Cancer
14%
Neoplasm
18%
Neurofibromatosis Type I
7%
Pathologist
12%
Prenatal Screening
14%
Prevalence
9%
Public Health
8%
Randomized Controlled Trial
7%
Sensitivity and Specificity
8%
Thyroid Medullary Carcinoma
7%
Venous Thromboembolism
7%
Whole Genome Sequencing
14%
Keyphrases
6-P2
14%
American College of Medical Genetics
18%
Analytic Validity
10%
Application in Practice
14%
Becker muscular Dystrophy
8%
CAG Repeat
7%
CAG Repeat Expansion
7%
Clinical Genetic Testing
8%
Clinical Presentation
7%
Clinical Sequencing
18%
Cystic Fibrosis
14%
Denaturing High-performance Liquid Chromatography (DHPLC)
20%
Duchenne muscular Dystrophy
21%
Dystrophin
15%
Dystrophin Gene
16%
EGAPP
10%
Exon
20%
Female Carrier
17%
Fluorescence in Situ Hybridization
14%
Fructose
14%
Gene Deletion
10%
Genetic Testing
11%
Genome Sequencing
11%
Genomic Applications
14%
Genomic Medicine
9%
Glucagon
10%
Health Care Costs
9%
Hepatocytes
14%
Hereditary Colorectal Cancer Syndromes
10%
Homozygosity
14%
Homozygous mutation
7%
Human Genetics
13%
Human Variome Project
21%
Isolated Hepatocytes
8%
Kindred
8%
Major Histocompatibility Complex
10%
Medical Genomics
11%
MLH1
8%
MSH2
8%
MSH6
14%
Mutation Screening
8%
Mutation Testing
9%
Patient Phenotype
8%
Practice Method
9%
Prenatal Diagnosis
8%
Project Meeting
14%
Research Consortium
11%
Sequence Variation
14%
X Chromosome
14%
X-linked
10%
