@misc
{TN_libero_mab2,
author = {
Shashi, Vandana
AND
Pena, Loren D.M.
AND
Kim, Katherine
AND
Burton, Barbara
AND
Hempel, Maja
AND
Schoch, Kelly
AND
Walkiewicz, Magdalena
AND
McLaughlin, Heather M.
AND
Cho, Megan
AND
Stong, Nicholas
AND
Hickey, Scott E.
AND
Shuss, Christine M.
AND
Freemark, Michael S.
AND
Bellet, Jane S.
AND
Keels, Martha Ann
AND
Bonner, Melanie J.
AND
El-Dairi, Maysantoine
AND
Butler, Megan
AND
Kranz, Peter G.
AND
Stumpel, Constance T.R.M.
AND
Klinkenberg, Sylvia
AND
Oberndorff, Karin
AND
Alawi, Malik
AND
Santer, Rene
AND
Petrovski, Slavé
AND
Kuismin, Outi
AND
Korpi-Heikkilä, Satu
AND
Pietilainen, Olli
AND
Aarno, Palotie
AND
Kurki, Mitja I.
AND
Hoischen, Alexander
AND
Need, Anna C.
AND
Goldstein, David B.
AND
Kortüm, Fanny
},
title = {
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype
},
publisher = {Elsevier BV},
isbn = {0002-9297},
keywords = {
Genetics (clinical)
,
Genetics
},
year = {2017},
url = {
http://slubdd.de/katalog?TN_libero_mab2
}
}