Medicine & Life Sciences
Adrenoleukodystrophy
100%
Noonan Syndrome
81%
Cardiofaciocutaneous syndrome
76%
Neonatal Screening
32%
UDP-galactose translocator
29%
Child
26%
Congenital Disorders of Glycosylation
23%
Mitogen-Activated Protein Kinases
21%
Genotype
20%
Fragile X Syndrome
19%
Neurofibromatosis 1
19%
Transplants
19%
Mosaicism
18%
Mutation
17%
Language
16%
Seizures
16%
Down Syndrome
15%
Hematopoietic Stem Cell Transplantation
14%
Demyelinating Diseases
13%
Short-Term Memory
13%
Social Skills
13%
Memory
13%
Nervous System
12%
Hypophosphatasia
12%
Siblings
12%
Fragile X Mental Retardation Protein
11%
Hematopoietic Stem Cells
11%
Autistic Disorder
11%
Intellectual Disability
10%
Specific Language Disorder
10%
Mucopolysaccharidosis I
10%
Homologous Transplantation
10%
Language Development
10%
Phenotype
10%
Addison Disease
10%
Genes
10%
Therapeutic Human Experimentation
10%
Child Language
10%
Infantile Spasms
10%
Epilepsy
10%
Biomarkers
9%
Germ-Line Mutation
9%
Epileptic Syndromes
9%
Neurofibromatoses
9%
Benchmarking
9%
Aptitude
9%
Social Behavior
8%
Psychological Adaptation
8%
Parenting
8%