Published in
Elsevier, Genetics in Medicine, 8(18), p. 788-795, 2016
DOI: 10.1038/gim.2015.161
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Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features
Journal article published in 2015 by
Jessica X. Chong 
,
Joon-Ho Yu,
Peter Lorentzen ,
Karen M. Park ,
Seema M. Jamal,
Holly K. Tabor ,
Anita Rauch,
Margarita Sifuentes Saenz ,
Eugen Boltshauser,
Karynne E. Patterson,
Deborah A. Nickerson,
Michael J. Bamshad
,
Joon-Ho Yu,
Peter Lorentzen ,
Karen M. Park ,
Seema M. Jamal,
Holly K. Tabor ,
Anita Rauch,
Margarita Sifuentes Saenz ,
Eugen Boltshauser,
Karynne E. Patterson,
Deborah A. Nickerson,
Michael J. Bamshad
This paper is made freely available by the publisher.
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