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Authors
Chong, Jessica X.
Yu, Joon-Ho
Lorentzen, Peter
Park, Karen M.
Jamal, Seema M.
Tabor, Holly K.
Rauch, Anita
Saenz, Margarita Sifuentes
Boltshauser, Eugen
Patterson, Karynne E.
Nickerson, Deborah A.
Bamshad, Michael J.
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This article is maintained by: Elsevier
Article Title: Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2015.161
Content Type: article
Copyright: © 2016, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics
