Evidence for linkage and association with reading disability, on 6p21.3-22
Journal Article
Overview
publication date
- May 1, 2002
has subject area
- Adolescent
- Alleles
- Biochemical Phenomena - Tandem Repeat Sequences
- Biomarkers - Genetic Markers
- Cellular Structures - Chromosomes, Human, Pair 6
- Child
- Chromosome Mapping
- Diseases in Twins
- Genetic Structures - Chromosomes, Human, Pair 6
- Genetic Structures - Tandem Repeat Sequences
- Genome Components - Tandem Repeat Sequences
- Genotype
- Humans
- Linkage Disequilibrium
- Nervous System Diseases - Dyslexia
- Nervous System Diseases - Dyslexia
- Neurodevelopmental Disorders - Dyslexia
- Phenotype - Genetic Markers
- Quantitative Trait, Heritable
- Signs and Symptoms - Dyslexia
- Signs and Symptoms - Dyslexia
has restriction
- bronze
Date in CU Experts
- September 9, 2013 10:08 AM
Full Author List
- Kaplan DE; Gayan J; Ahn J; Won TW; Pauls D; Olson RK; DeFries JC; Wood F; Pennington BF; Page GP
author count
- 12
citation count
- 105
published in
Other Profiles
International Standard Serial Number (ISSN)
- 0002-9297
Electronic International Standard Serial Number (EISSN)
- 1537-6605
Digital Object Identifier (DOI)
Additional Document Info
start page
- 1287
end page
- 1298
volume
- 70
issue
- 5