Competing interests statement: The authors declare no competing financial interests.
Genome-wide copy number scan identifies disruption of PCDH11X in developmental dyslexia
Version of Record online: 20 SEP 2013
© 2013 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Volume 162, Issue 8, pages 889–897, December 2013
How to Cite
2013. Genome-Wide Copy Number Scan Identifies Disruption of PCDH11X in Developmental Dyslexia. Am J Med Genet Part B. 9999:889–897., , , .
- Issue online: 4 NOV 2013
- Version of Record online: 20 SEP 2013
- Manuscript Accepted: 13 AUG 2013
- Manuscript Received: 30 APR 2013
- Department of Science and Technology-Health Science. Grant Number: SR/SO/HS-103/2007
Additional supporting information may be found in the online version of this article at the publisher's web-site.
|ajmgb32199-sm-0001-SuppTab-S1.doc||48K||TABLE SI. The Table Illustrates the Marker Details Which Have Identified the Duplication and Deletion Variants in the DD Subjects|
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