Medicine & Life Sciences
Reading
100%
Dyslexia
72%
Genes
44%
Quantitative Trait Loci
34%
Language
34%
Chromosomes
34%
Hearing Loss
34%
Attention Deficit Disorder with Hyperactivity
27%
Nonsyndromic Deafness
21%
Speech Sound Disorder
20%
Specific Language Disorder
19%
Language Disorders
18%
Phenotype
16%
Genetic Association Studies
12%
Deafness
12%
Genetic Linkage
12%
Mutation
12%
Genome
10%
Twin Studies
10%
Single Nucleotide Polymorphism
9%
Chromosomes, Human, Pair 15
9%
Chromosomes, Human, Pair 18
9%
Pedigree
9%
Gene-Environment Interaction
9%
Language Development Disorders
8%
Alleles
8%
Child
8%
Functional Laterality
8%
Genome-Wide Association Study
8%
Learning Disabilities
8%
Literacy
7%
Isochromosomes
7%
Chromosomes, Human, Pair 6
7%
Autosomal Dominant 13 Deafness
7%
Inner Ear
7%
Immune System Diseases
7%
Speech Disorders
6%
Lod Score
6%
Trisomy 7p Chromosome 7
6%
Connexin 26
6%
Behavioral Genetics
6%
Nervous System Diseases
6%
Chromosome 18p deletion syndrome
6%
Schmid-Fraccaro syndrome
6%
Brain
6%
Haplotypes
6%
Connexin 30
5%
Genetic Markers
5%
Molecular Biology
5%
Aptitude
5%
Microsatellite Repeats
5%
Intervertebral Disc Chemolysis
5%
Communication Disorders
5%
Chromosomes, Human, Pair 7
5%
Adrenergic alpha-2 Receptors
5%
Neurodevelopmental Disorders
5%
Cauda Equina Syndrome
5%
Social Sciences
etiology
19%
disability
18%
ADHD
10%
dyslexia
8%
twin studies
5%
developmental disorder
5%
planning of studies
5%