Medicine & Life Sciences
Mucopolysaccharidosis III
100%
Colombia
99%
Complementation Group B Fanconi Anemia
92%
methionyl-tRNA formyltransferase
84%
Phenotype
79%
glucosidase I
74%
VACTERL association
70%
Congenital Disorders of Glycosylation
64%
Comparative Genomic Hybridization
62%
Exome
60%
Glycogen Storage Disease
59%
Williams Syndrome
58%
DiGeorge Syndrome
57%
Mutation
56%
Genes
55%
Fanconi Anemia
55%
Aortic Coarctation
52%
Gene Dosage
49%
Neurodevelopmental Disorders
48%
Germ-Line Mutation
47%
Demyelinating Diseases
43%
Oligonucleotide Array Sequence Analysis
43%
Molecular Biology
40%
Histones
39%
Inborn Genetic Diseases
38%
Neurodegenerative Diseases
36%
Ellis-Van Creveld Syndrome
35%
Heart Diseases
33%
Post Translational Protein Processing
32%
Esophageal Fistula
29%
Hypoplastic Left Heart Syndrome
28%
Clinical Studies
28%
Multiple Abnormalities
28%
Chromosome Breakage
28%
Incidence
27%
Chromosome Deletion
27%
Education
26%
Family Health
23%
Neurologists
23%
Proteins
23%
Patient Care
22%
Primary Prevention
21%
Liver
21%
Leigh Disease
20%
Secondary Prevention
20%
Chromosome Aberrations
20%
Oligosaccharides
18%
Health Services
18%
Health Personnel
18%
Chromatin Immunoprecipitation Sequencing
17%