The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities

Journal of Neurogenetics

Volumn 22, Issue 4, 2008, Pages 295-313

  Couto, Jillian M ^a   Gomez, Lissette ^a   Wigg, Karen ^a   Cate Carter, Tasha ^b   Archibald, Jennifer ^b   Anderson, Barbara ^b   Tannock, Rosemary ^b   Kerr, Elizabeth N ^b   Lovett, Maureen W ^b   Humphries, Tom ^b   Barr, Cathy L ^a,b  

^a UNIVERSITY HEALTH NETWORK   (Canada)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Association study; Childhood disorder; Complex trait; Developmental dyslexia; QTL

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 1P; CHROMOSOME 6P; DNA EXTRACTION; DYSLEXIA; FEMALE; GENE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC TRAIT; HAPLOTYPE; HUMAN; HUMAN CELL; KIAA0319 LIKE GENE; MALE; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; QUANTITATIVE TRAIT LOCUS; SCHOOL CHILD; SEQUENCE HOMOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM; WORD RECOGNITION;

ADOLESCENT; BASE SEQUENCE; CHI-SQUARE DISTRIBUTION; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; DYSLEXIA; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HAPLOTYPES; HUMANS; MOLECULAR SEQUENCE DATA; NUCLEAR PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; QUANTITATIVE TRAIT, HERITABLE; REGRESSION ANALYSIS;

EID: 57649136416     PISSN: 01677063     EISSN: 15635260     Source Type: Journal    
DOI: 10.1080/01677060802354328     Document Type: Article

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