A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States
Journal Article
Overview
publication date
- December 1, 2004
has subject area
- Behavior and Behavior Mechanisms - Siblings
- Carrier Proteins - Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
- Cellular Structures - Chromosomes, Human, Pair 6
- Chromosome Mapping
- Colorado
- Genetic Structures - Chromosomes, Human, Pair 6
- Genotype
- Haplotypes
- Humans
- Linkage Disequilibrium
- Nervous System Diseases - Dyslexia
- Nervous System Diseases - Dyslexia
- Neurodevelopmental Disorders - Dyslexia
- Peptides - Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
- Persons - Siblings
- Phenotype
- Polymorphism, Genetic
- Proteins - Tumor Necrosis Factor Receptor-Associated Peptides and Proteins
- Quantitative Trait Loci
- Signs and Symptoms - Dyslexia
- Signs and Symptoms - Dyslexia
- Sociological Factors - Siblings
- United Kingdom
has restriction
- hybrid
Date in CU Experts
- September 9, 2013 10:08 AM
Full Author List
- Francks C; Paracchini S; Smith SD; Richardson AJ; Scerri TS; Cardon LR; Marlow AJ; MacPhie IL; Walter J; Pennington BF
author count
- 15
citation count
- 198
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
- 1046
end page
- 1058
volume
- 75
issue
- 6