Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders

Siblings of those with autism spectrum disorder (ASD) have increased likelihood of ASD or related subclinical traits. Here, studying 253 ASD families, D’Abate et al. test the predictive value of genomic copy number variation involving ASD-associated loci, with confirmation in a second cohort.

Saved in:

Bibliographic Details
Main Authors:	L. D’Abate, S. Walker, R. K. C. Yuen, K. Tammimies, J. A. Buchanan, R. W. Davies, B. Thiruvahindrapuram, J. Wei, J. Brian, S. E. Bryson, K. Dobkins, J. Howe, R. Landa, J. Leef, D. Messinger, S. Ozonoff, I. M. Smith, W. L. Stone, Z. E. Warren, G. Young, L. Zwaigenbaum, S. W. Scherer
Format:	article
Language:	EN
Published:	Nature Portfolio 2019
Subjects:	Science Q
Online Access:	https://doaj.org/article/7940f1b2c2924eec84eda8740660d6c8
Tags:	Add Tag No Tags, Be the first to tag this record!

Be the first to leave a comment!

Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders

Similar Items