Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36

Genes, Brain and Behavior

Volumn 12, Issue 1, 2013, Pages 56-69

  Field, L L ^a   Shumansky, K ^a   Ryan, J ^a   Truong, D ^a   Swiergala, E ^a   Kaplan, B J ^b  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b UNIVERSITY OF CALGARY   (Canada)

Author keywords

ADHD; Association analysis; Autism; Dyslexia genetics; Family based studies; Gene mapping; Genome scan; Linkage analysis; Overlapping predisposition; Susceptibility

Indexed keywords

LPHN3 PROTEIN; MEMBRANE PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; ATTENTION DEFICIT DISORDER; AUTISM; BRAIN CORTEX; CELL LINEAGE; CELL PROLIFERATION; CHILD; CHROMOSOME 16P; CHROMOSOME 17Q; CHROMOSOME 4Q; CHROMOSOME 7Q; DYSLEXIA; FAMILY; FEMALE; GENE LOCUS; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; HUMAN; LANGUAGE DISABILITY; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; REPRODUCIBILITY; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

ADOLESCENT; ATTENTION DEFICIT DISORDER WITH HYPERACTIVITY; AUTISTIC DISORDER; CASE-CONTROL STUDIES; CHILD; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 4; CHROMOSOMES, HUMAN, PAIR 7; DYSLEXIA; FEMALE; FIBROBLAST GROWTH FACTORS; GENETIC ASSOCIATION STUDIES; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; HUMANS; MALE; PEDIGREE; PHYSICAL CHROMOSOME MAPPING; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, G-PROTEIN-COUPLED; RECEPTORS, PEPTIDE; RNA-BINDING PROTEINS; TRANSCRIPTOME;

EID: 84872676162     PISSN: 16011848     EISSN: 1601183X     Source Type: Journal    
DOI: 10.1111/gbb.12003     Document Type: Article

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