Xq27 FRAXA Locus is a Strong Candidate for Dyslexia: Evidence from a Genome-Wide Scan in French Families-Reference-Cited by-同舟云学术

Xq27 FRAXA Locus is a Strong Candidate for Dyslexia: Evidence from a Genome-Wide Scan in French Families

Published:2013-01-11 Issue:2 Volume:43 Page:132-140
ISSN:0001-8244
Container-title:Behavior Genetics
language:en
Short-container-title:Behav Genet

Author:

Huc-Chabrolle M.,Charon C.,Guilmatre A.,Vourc’h P.,Tripi G.,Barthez M. A.,Sizaret E.,Thepault R. A.,Le Gallic S.,Hager J.,Toutain A.,Raynaud M.,Andres C.,Campion D.,Laumonnier F.,Bonnet-Brilhault F.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics,Ecology, Evolution, Behavior and Systematics

Link

http://link.springer.com/content/pdf/10.1007/s10519-012-9575-5.pdf

Reference51 articles.

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4. Bates T, Luciano M, Castles A, Coltheart M, Wright M, Martin N (2007) Replication of reported linkages for dyslexia and spelling and suggestive evidence for novel regions on chromosomes 4 and 17. Eur J Hum Genet 15:194–203

5. Brown WE, Eliez S, Menon V, Rumsey JM, White CD, Reiss AL (2001) Preliminary evidence of widespread morphological variations of the brain in dyslexia. Neurology 56:781–783

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