Dense-map genome scan for dyslexia supports loci at 4q13, 16p12, 17q22; suggests novel locus at 7q36
Author:
Affiliation:
1. Department of Medical Genetics; University of British Columbia; Vancouver; BC; Canada
2. Department of Pediatrics; University of Calgary; Calgary; AB; Canada
Publisher
Wiley
Subject
Behavioral Neuroscience,Neurology,Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/gbb.12003/fullpdf
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3. Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11;Arcos-Burgos;Am J Hum Genet,2004
4. A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication;Arcos-Burgos;Mol Psychiatry,2010
5. A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27;Auranen;Am J Hum Genet,2002
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