Medicine & Life Sciences
Registries
100%
Mutation
75%
Mothers
69%
Pregnancy
65%
Phenotype
56%
Intellectual Disability
46%
Incontinentia Pigmenti
46%
Genes
45%
Microtia-Anotia
40%
Population
34%
Microcephaly
33%
Parturition
33%
Live Birth
31%
Child
29%
Epidemiology
27%
Pregnancy Outcome
27%
Confidence Intervals
26%
Prenatal Diagnosis
25%
Congenital Microtia
25%
Acculturation
23%
Chromosome Deletion
23%
Achondroplasia
23%
Hispanic Americans
23%
Odds Ratio
22%
Trisomy
21%
Undiagnosed Diseases
21%
Muscle Hypotonia
21%
Congenital Disorders of Glycosylation
20%
Epilepsy
19%
Comparative Genomic Hybridization
19%
Cri-du-Chat Syndrome
19%
Cakut
19%
First Pregnancy Trimester
19%
Plagiocephaly
19%
Craniosynostoses
18%
Certolizumab Pegol
18%
De Lange Syndrome
18%
Gastroschisis
18%
Inborn Genetic Diseases
18%
Whole Exome Sequencing
18%
Ventricular Heart Septal Defects
17%
Loss of Function Mutation
17%
Pediatrics
17%
VACTERL association
17%
Omalizumab
16%
Hypermethioninemia
16%
Neurodevelopmental Disorders
16%
Manufacturing and Industrial Facilities
16%
Heart
16%
Williams Syndrome
16%
Chromosomes
16%
Gene Dosage
16%
Language Development Disorders
16%
Genetic Databases
15%
Exome
15%
Extremities
15%
Pharmacovigilance
15%
Atrial Heart Septal Defects
15%
Hyperammonemia
15%
Hypospadias
14%
Genetic Association Studies
14%
Databases
14%
Folic Acid
14%
Neurofibromatosis 1
14%
Mucopolysaccharidosis III
14%
Microphthalmos
13%
Colombia
13%
Mosaicism
13%
Lactic Acidosis
13%
Complementation Group B Fanconi Anemia
12%
Down Syndrome
12%
Proteins
12%
Maternal Age
12%
X-Linked Genes
12%
COOH-terminal signal transamidase
12%
Partial 6q+ Syndrome
12%
Hypertelorism
12%
carglumic acid
12%
Neural Tube Defects
12%
Neural tube defects X-linked
12%
Delivery of Health Care
12%
Trisomy 6q Chromosome 6
12%
Lujan Fryns syndrome
12%
Raine syndrome
11%
methionyl-tRNA formyltransferase
11%
Education
11%
Zidovudine
11%
Missense Mutation
11%
Mitochondrial Diseases
11%
12p trisomy Chromosome 12
11%
Inborn Urea Cycle Disorder
11%
signal sequence receptor
11%
Anophthalmos
11%
Brain Diseases
11%
Capillary Malformation-Arteriovenous Malformation
11%
Heterogeneous-Nuclear Ribonucleoprotein Group C
11%
Mandibulofacial Dysostosis
11%
Genitalia
10%
Trisomy 13 Syndrome
10%
Autism Spectrum Disorder
10%