%0 Journal Article
%T De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype
%A Alexander Hoischen
%A Anna C. Need
%A Barbara Burton
%A Christine M. Shuss
%A Constance T.R.M. Stumpel
%A David B. Goldstein
%A Fanny Kort¨¹m
%A Heather M. McLaughlin
%A Jane S. Bellet
%A Karin Oberndorff
%A Katherine Kim
%A Kelly Schoch
%A Loren D.M. Pena
%A Magdalena Walkiewicz
%A Maja Hempel
%A Malik Alawi
%A Martha Ann Keels
%A Maysantoine El-Dairi
%A Megan Butler
%A Megan Cho
%A Melanie J. Bonner
%A Michael S. Freemark
%A Mitja I. Kurki
%A Nicholas Stong
%A Olli Pietilainen
%A Outi Kuismin
%A Palotie Aarno
%A Peter G. Kranz
%A Rene Santer
%A Satu Korpi-Heikkil£¿
%A Scott E. Hickey
%A Slav¨¦ Petrovski
%A Sylvia Klinkenberg
%A Undiagnosed Diseases Network
%J Archive of "American Journal of Human Genetics".
%D 2017
%R 10.1016/j.ajhg.2016.12.004
%X (The American Journal of Human Genetics 99, 991¨C999; October 6, 2016
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223056/