Medicine & Life Sciences
Genetic Databases
100%
Phenotype
99%
Genes
89%
Cystic Fibrosis
64%
Mutation
53%
Genetic Association Studies
52%
Information Dissemination
46%
Genomics
43%
Exome
35%
Medical Genetics
35%
Cystic Fibrosis Transmembrane Conductance Regulator
34%
Databases
34%
Nonketotic Hyperglycinemia
29%
Genome
28%
Genotype
26%
Inborn Genetic Diseases
24%
Inborn Errors Metabolism
24%
Benzoates
24%
Intellectual Disability
23%
Knowledge Bases
22%
Meconium Ileus
21%
Chromosome Deletion
21%
Phenylketonurias
21%
Regulator Genes
21%
Newborn Infant
20%
Human Genome
20%
Research Personnel
20%
Propionic Acidemia
19%
Genetic Testing
19%
Seizures
19%
Human Genetics
19%
Inborn Urea Cycle Disorder
18%
Proteins
18%
Haploinsufficiency
18%
Karyotype
18%
Glycine
16%
Whole Exome Sequencing
16%
Muscle Hypotonia
16%
Missense Mutation
15%
Dextromethorphan
15%
High-Throughput Nucleotide Sequencing
15%
Twins
14%
Microcephaly
14%
Marfan Syndrome
14%
Alleles
13%
Karyotyping
13%
Catalogs
13%
Comparative Genomic Hybridization
13%
Medicine
13%