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Paper Details

Gene discovery for Mendelian conditions via social networking: de novo variants in KDM1A cause developmental delay and distinctive facial features.
Genet Med
74
2016
Author NameAffiliation
Jessica X ChongUniversity of Washington
Jessica X ChongUniversity of Washington
Joon-Ho YuUniversity of Washington
Seema M JamalUniversity of Washington
Holly K TaborUniversity of Washington
Holly K TaborTreuman Katz Center for Pediatric Bioethics, Seattle Children's Research Institute
Holly K TaborUniversity of Washington
Eugen BoltshauserChildren's Hospital of the University of Zurich
Karynne E PattersonUniversity of Washington
Deborah A NickersonUniversity of Washington
Deborah A NickersonUniversity of Washington
Michael J BamshadUniversity of Washington
Michael J BamshadUniversity of Washington
Michael J BamshadSeattle Children's Hospital
Michael J BamshadUniversity of Washington
Michael J BamshadUniversity of Washington
Michael J BamshadSeattle Children's Hospital
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Release 1.2