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