Medicine and Dentistry
Patient
100%
Newborn Screening
83%
Evaluation Study
66%
Family
55%
Child
53%
Neonatal Infant
52%
Infant
44%
Screening
43%
Diseases
39%
Syndrome
37%
Cells
37%
Follow up
30%
Health
30%
Pediatrician
30%
Public Health
27%
Assessment
26%
Male
26%
Cleft Palate
26%
Congenital Malformation
26%
Quality Improvement
25%
Development
25%
Karyotype
25%
Therapeutic Procedure
24%
Craniofacial Malformation
22%
Hereditary Nonpolyposis Colorectal Cancer
20%
Colorectal Cancer
20%
Skin Fibroblast
20%
Obstetric Delivery
20%
Exercise
20%
Primary Health Care
20%
Arm
19%
Microtia
19%
Goldenhar Syndrome
18%
Age
18%
Pediatrics
18%
Skeleton Malformation
17%
Genetic Screening
17%
Mortality
17%
Analysis
16%
Facies
16%
Adult
16%
Morbidity
15%
Etiology
15%
Chromosome Aberration
15%
Sibling
15%
Diagnosis
15%
Chromosome Analysis
14%
Female
14%
Health Care
13%
Cell Line
13%
Nursing and Health Professions
Newborn Screening
41%
Genetic Service
36%
Child
35%
Patient
30%
Diseases
28%
Woman
24%
Pediatrics
22%
Evaluation Study
22%
Total Quality Management
20%
Follow up
20%
Primary Medical Care
18%
Congenital Malformation
15%
Syndrome
13%
Parent
13%
Advisory Committee
12%
Genetic Screening
12%
Phenylketonuria
11%
Branchiootorenal Syndrome
10%
Etiology
10%
Craniofacial Malformation
10%
Family
10%
Health Care Delivery
10%
Folic Acid
10%
Combination Therapy
10%
Neural Tube Defect
10%
Congenital Hypothyroidism
10%
Classification
10%
Electric Potential
9%
Diagnosis
9%
Client
8%
Screening
7%
Health Care Personnel
7%
Phenylalanine
6%
Indicator
6%
Control
6%
Analysis
5%
Clinical Practice
5%
Thyrotropin
5%
Hypothyroidism
5%
Recurrence Risk
5%
Biochemistry, Genetics and Molecular Biology
Fibroblast
31%
Newborn Screening
31%
Genetics
27%
Health
22%
Chromosome
14%
Karyotype
14%
Proband
13%
Colon
13%
Phenylketonuria
12%
Mental Retardation
12%
Reduction (Chemistry)
11%
Normal Human
11%
Progeny
11%
Karyotype 46,XX
11%
Electric Potential
11%
Tumor Gene
10%
Gangliosidosis
10%
Selective Serotonin Reuptake Inhibitor
10%
Pedigree
10%
Glutathione
10%
Williams Syndrome
10%
Klinefelter Syndrome
10%
Acid Phosphatase
10%
Agent Orange
10%
Pregnancy
10%
Trisomy
10%
Cytochrome P450
10%
Galactosidase
10%
Chromosome 2
10%
Methylmalonic Acidemia
10%
Cystine
10%
Screening
7%
pH
7%
Phenylalanine
6%
Birth
6%
Methylmalonyl-CoA
5%
Thyroid-Stimulating Hormone
5%
Genetic Counseling
5%
Multifactorial Inheritance
5%
Fluorescence in Situ Hybridization
5%
Genotype Phenotype Correlation
5%
Ketosis
5%
Mutase
5%
Metabolic Pathway
5%
Chromosome 7
5%
Thyroid Hormone
5%
Chromosome Abnormality
5%
Age
5%
Drug Megadose
5%
Vitamin B12
5%
