Guo, Yiran https://orcid.org/0000-0002-6549-8589
Hwang, Liang-Dar
Li, Jiankang
Eades, Jason
Yu, Chung Wen
Mansfield, Corrine
Burdick-Will, Alexis
Chang, Xiao
Chen, Yulan
Duke, Fujiko F.
Zhang, Jianguo
Fakharzadeh, Steven
Fennessey, Paul
Keating, Brendan J.
Jiang, Hui
Hakonarson, Hakon
Reed, Danielle R.
Preti, George
Funding for this research was provided by:
Children's Hospital of Philadelphia Research Institute (Institutional Development Fund)
National Organization for Rare Disorders
Monell Chemical Senses Center (Monell Institutional Funds, Monell Institutional Funds)
Shenzhen Municipal Government of China (CXZZ20130517144604091)
Shenzhen Key Laboratory of Genomics (CXB200903110066A)
Guangdong Enterprise Key Laboratory of Human Disease Genomics (2011A060906007)
National Institute on Deafness and Other Communication Disorders (P30DC011735)
Article History
Received: 27 July 2016
Accepted: 17 January 2017
First Online: 15 February 2017