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Lyon G, Jiang T, Wijk RV et al. Whole exome sequencing reveals the genetic basis of a case of idiopathic hemolytic anemia and suggests candidate rare variants for ADHD in a Utah pedigree. F1000Posters 2012, 3:25 (poster)

Whole exome sequencing reveals the genetic basis of a case of idiopathic hemolytic anemia and suggests candidate rare variants for ADHD in a Utah pedigree

Gholson Lyon1, Gholson Lyon2, Gholson Lyon3, Tao Jiang, Richard Van Wijk, Wei Wang, Paul Bodily, Jinchuan Xing, Lifeng Tian, Reid Robison, Mark Clement, Lin Yang, Peng Zhang, Ying Liu, Barry Moore, Wouter van Solinge, Mark Yandell, Hakon Hakonarson, Jun Wang, W Evan Johnson, Zhi Wei, Kai Wang
Published 16 Jan 2012
Author Affiliations
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Published 16 Jan 2012

Whole exome sequencing reveals the genetic basis of a case of idiopathic hemolytic anemia and suggests candidate rare variants for ADHD in a Utah pedigree

[version 1; not peer reviewed]

Gholson Lyon1, Gholson Lyon2, Gholson Lyon3, Tao Jiang, Richard Van Wijk, Wei Wang, Paul Bodily, Jinchuan Xing, Lifeng Tian, Reid Robison, Mark Clement, Lin Yang, Peng Zhang, Ying Liu, Barry Moore, Wouter van Solinge, Mark Yandell, Hakon Hakonarson, Jun Wang, W Evan Johnson, Zhi Wei, Kai Wang
Author Affiliations
1 Department of Psychiatry, University of Utah, USA
2 Center for Applied Genomics, Children's Hospital of Philadelphia, USA
3 New York University Child Study Center, USA
Presented at
29th World Congress of Psychiatric Genetics 2011
Abstract
Competing Interests

No competing interests were disclosed

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