Biochemistry, Genetics and Molecular Biology
Exon
56%
Screening
52%
Gene Linkage
50%
Genetics
39%
Allele
31%
Prevalence
31%
Genetic Heterogeneity
28%
USH2A
26%
DNA Sequence
26%
Autosomal Dominant Inheritance
25%
Genetic Disorder
25%
Gene Mapping
25%
Gene Mutation
23%
GJB2
22%
DNA Extraction
22%
MYO7A
22%
Genotype Phenotype Correlation
22%
Autosomal Recessive Inheritance
19%
Visual Acuity
18%
Vision
18%
Aminoacyl tRNA Synthetase
18%
Genetic Counseling
18%
Newborn Screening
18%
LDL Receptor
18%
Factor H
18%
Genetic Association
18%
Ranibizumab
18%
Receptor Gene
18%
Evoked Otoacoustic Emission
18%
Epidemiological Data
18%
Familial Hypercholesterolemia
18%
Amino Acids
18%
Phenylketonuria
18%
Frameshift Mutation
18%
Minor Allele Frequency
18%
Retrospective Study
18%
Maternal Age
18%
Genotyping
17%
Nonsyndromic Deafness
15%
Retinitis pigmentosa
14%
Hemoglobin Variant
14%
Isoform
14%
Age-Related Maculopathy Susceptibility 2
14%
Chromosome 10
12%
Autosomal Recessive Disorder
10%
Linkage Analysis
10%
Glucose-6-Phosphate Dehydrogenase
9%
Obligate Carrier
9%
Cell Function
9%
Intraocular Pressure
9%
Medicine and Dentistry
Hearing Impairment
100%
Neonatal Infant
58%
Disease
40%
Screening
36%
Retina Dystrophy
28%
Waardenburg Syndrome
23%
Public Health
22%
Retrospective Study
20%
Genetic Counseling
18%
Brain Malformation
18%
Clinical Health
18%
Opitz Syndrome
18%
Magnetic Resonance Imaging
18%
Fundus (Eye)
18%
Newborn Screening
18%
Providencia
18%
Institutionalized Population
18%
Familial Hypercholesterolemia
18%
Rubella
18%
Evoked Otoacoustic Emission
18%
Genotype Phenotype Correlation
18%
Retinoschisis
18%
Retinol Dehydrogenase
18%
Congenital Disorder
18%
Diagnosis
18%
Retinitis pigmentosa
18%
Odds Ratio
18%
Congenital Malformation
18%
Hypoplasia
15%
Auditory Screening
14%
Hemoglobin Variant
14%
Usher Syndrome
13%
Molecular Diagnosis
13%
Retinopathy
12%
Septum Pellucidum
12%
Genetic Disorder
12%
Leber Congenital Amaurosis
11%
Screening Test
11%
Clinical Finding
10%
Glucose-6-Phosphate Dehydrogenase Deficiency
9%
Bruch's Membrane
9%
Autosomal Dominant Inheritance
9%
Exon
9%
Retinal Pigment Epithelium
9%
Drusen
9%
Macular Degeneration
9%
Low Vision
9%
Pediatrician
9%
DNA Extraction
9%
Table Salt
9%
Pharmacology, Toxicology and Pharmaceutical Science
Hearing Impairment
56%
Congenital Malformation
28%
Disease
22%
Prevalence
18%
Serine Protease HTRA1
18%
Complement Factor H
18%
Wet Macular Degeneration
18%
Congenital Disorder
18%
Ranibizumab
18%
Usher Syndrome
18%
Rubella
18%
Hemoglobin Variant
18%
Retrospective Study
18%
Waardenburg Syndrome
18%
Clinical Feature
18%
Retina Maculopathy
14%
Retinopathy
12%
Glucose 6 Phosphate Dehydrogenase Deficiency
12%
Antiangiogenic Therapy
9%
Microtia
9%
Population Study
9%
Table Salt
9%
Prematurity
6%
Bipolar Disorder
6%
Gait Disorder
6%
Coordination Disorder
6%
Congenital Hypothyroidism
6%
Inborn Error of Metabolism
6%
Monogenic Disorder
6%
Newborn Disease
6%
