Biochemistry, Genetics and Molecular Biology
Familial Hypercholesterolemia
100%
Sequencing
82%
Gene
62%
Calcium
50%
PMS2
50%
Colon
50%
Exon
50%
Mental Retardation
50%
Case Report
50%
Proband
34%
DNA Extraction
32%
Exome Sequencing
32%
Optics
25%
Molecular Genetics
25%
Missense
25%
Haplotype
25%
Vascular Endothelial Growth Factor
25%
Spectrum
25%
DNA
25%
Protein
25%
Gene Repair
10%
Loss of Heterozygosity
7%
Consanguinity
7%
Saturated Fatty Acids
7%
Lipoprotein
7%
Case-Control Study
6%
MLH1
5%
Next Generation Sequencing
5%
Medicine and Dentistry
Patient
63%
Familial Hypercholesterolemia
50%
Syndrome
50%
Drusen
50%
Isotopes of Calcium
50%
Adult
50%
Inpatient
50%
Atherosclerosis
50%
Autosomal Dominant Inheritance
50%
Visual Impairment
30%
Pierre Robin Syndrome
18%
Gene
16%
Diagnosis
12%
Exon
12%
Atrial Septal Defect
12%
Male
12%
Intellectual Disability
12%
Exome Sequencing
10%
Family History
10%
Haplotype
10%
Vasculotropin
10%
Hyperpigmentation
10%
Woman
10%
Retina
10%
Retinal Disease
10%
Odds Ratio
6%
Carrier Testing
6%
Diseases
6%
Esotropia
6%
Cardiac Shunt
6%
Persistent Left Superior Vena Cava
6%
Scoliosis
6%
Family Planning
6%
Foot Malformation
6%
Cleft Palate
6%
Protein
6%
Tooth
6%
Micrognathism
6%
Lethality
6%
Nose
6%
DNA
6%
