How to Cite this Article: Crepel A, Steyaert J, De la Marche W, De Wolf V, Fryns J-P, Noens I, Devriendt K, Peeters H. 2011. Narrowing the Critical Deletion Region for Autism Spectrum Disorders on 16p11.2. Am J Med Genet Part B 156:243–245.
Letter to the Editor
Narrowing the critical deletion region for autism spectrum disorders on 16p11.2†
Article first published online: 11 JAN 2011
Copyright © 2011 Wiley-Liss, Inc.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Volume 156, Issue 2, pages 243–245, March 2011
How to Cite
Crepel, A., Steyaert, J., De la Marche, W., De Wolf, V., Fryns, J.-P., Noens, I., Devriendt, K. and Peeters, H. (2011), Narrowing the critical deletion region for autism spectrum disorders on 16p11.2. Am. J. Med. Genet., 156: 243–245. doi: 10.1002/ajmg.b.31163
- Issue published online: 8 FEB 2011
- Article first published online: 11 JAN 2011
- Manuscript Accepted: 30 NOV 2010
- Manuscript Received: 10 MAR 2010
- Interuniversity Attraction Poles (Belgian State). Grant Number: GOA 2006/12
- Cure Autism Now (USA)
Additional Supporting Information may be found in the online version of this article.
|AJMB_31163_suppl_Table-S1.doc||75K||Supplementary Table I: qRT-PCR primersets and results for discovery and confirmation of the size of the ∼118kb deletion|
|AJMB_31163_suppl_Table-S2.doc||39K||Supplementary Table II: Phenotypic data of the individuals. All individuals had a negative medical history regarding epilepsy and the neurological examination was normal in all of them.|
|AJMB_31163_suppl_Table-S3.doc||29K||Supplementary Table III: variants detected in deletion carriers|
|AJMB_31163_suppl_Table-S4.doc||62K||Supplementary Table IV: Endeavour prioritization of the recurrent 16p11.2 deletion region.|
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