TDT-association analysis of EKN1 and dyslexia in a Colorado twin cohort
Journal Article
Overview
publication date
has subject area
-
Biochemical Phenomena - Base Sequence
-
Cellular Structures - Chromosomes, Human, Pair 15
-
Cellular Structures - Chromosomes, Human, Pair 2
-
Cytoskeletal Proteins
-
Environment and Public Health - Cohort Studies
-
Genetic Structures - Base Sequence
-
Genetic Structures - Chromosomes, Human, Pair 15
-
Genetic Structures - Chromosomes, Human, Pair 2
-
Health Care Evaluation Mechanisms - Cohort Studies
-
Humans
-
Investigative Techniques - Cohort Studies
-
Laboratory Chemicals - DNA Primers
-
Molecular Sequence Data - Base Sequence
-
Mutagenesis - Translocation, Genetic
-
Mutation - Translocation, Genetic
-
Mutation, Missense
-
Nerve Tissue Proteins
-
Nervous System Diseases - Dyslexia
-
Nervous System Diseases - Dyslexia
-
Neurodevelopmental Disorders - Dyslexia
-
Nuclear Proteins
-
Oligodeoxyribonucleotides - DNA Primers
-
Pathologic Processes - Translocation, Genetic
-
Quantitative Trait Loci
-
Signs and Symptoms - Dyslexia
-
Signs and Symptoms - Dyslexia
has restriction
Date in CU Experts
-
September 9, 2013 10:08 AM
Full Author List
-
Meng HY; Hager K; Held M; Page GP; Olson RK; Pennington BF; DeFries JC; Smith SD; Gruen JR
author count
citation count
published in
Other Profiles
International Standard Serial Number (ISSN)
Electronic International Standard Serial Number (EISSN)
Digital Object Identifier (DOI)
Additional Document Info
start page
end page
volume
issue