De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype

Author:

Shashi Vandana,Pena Loren D.M.,Kim Katherine,Burton Barbara,Hempel Maja,Schoch Kelly,Walkiewicz Magdalena,McLaughlin Heather M.,Cho Megan,Stong Nicholas,Hickey Scott E.,Shuss Christine M.,Freemark Michael S.,Bellet Jane S.,Keels Martha Ann,Bonner Melanie J.,El-Dairi Maysantoine,Butler Megan,Kranz Peter G.,Stumpel Constance T.R.M.,Klinkenberg Sylvia,Oberndorff Karin,Alawi Malik,Santer Rene,Petrovski Slavé,Kuismin Outi,Korpi-Heikkilä Satu,Pietilainen Olli,Aarno Palotie,Kurki Mitja I.,Hoischen Alexander,Need Anna C.,Goldstein David B.,Kortüm Fanny,Bacino A.,Lee Brendan H.,Balasubramanyam Ashok,Burrage Lindsay C.,Clark Gary D.,Craigen William J.,Dhar Shweta U.,Emrick Lisa T.,Graham Brett H.,Jain Mahim,Lalani Seema R.,Lewis Richard A.,Moretti Paolo M.,Nicholas Sarah K.,Orange Jordan S.,Posey Jennifer E.,Potocki Lorraine,Rosenfeld Jill A.,Scott Daryl A.,Hanchard Neil A.,Alyssa Tran A.,Mercedes Alejandro E.,Mashid Azamian S.,Bellen Hugo J.,Yamamoto Shinya,Wangler Michael F.,Westerfield Monte,Postlethwait John H.,Eng Christine M.,Yang Yaping,Muzny Donna M.,Ward Patricia A.,Ramoni Rachel B.,McCray Alexa T.,Kohane Issac S.,Holm Ingrid A.,Might Matthew,Mazur Paul,Splinter Kimberly,Esteves Cecilia,Shashi Vandana,Jiang Yong-hui,Pena Loren D.M.,McConkie-Rosell Allyn,Schoch Kelly,Spillmann Rebecca C.,Sullivan Jennifer A.,Walley Nicole M.,Goldstein David B.,Stong Nicholas,Beggs Alan H.,Loscalzo Joseph,MacRae Calum A.,Silverman Edwin K.,Stoler Joan M.,Sweetser David A.,Maas Richard L.,Krier Joel B.,Rodan Lance H.,Walsh Chris A.,Cooper Cynthia M.,Pallais Juan C.,Donnell-Fink Laurel A.,Krieg Elizabeth L.,Lincoln Sharyn A.,Briere Lauren C.,Jacob Howard J.,Worthey Elizabeth A.,Lazar Joe,Strong Kim A.,Handley Lori H.,Newberry J. Scott,Bick David P.,Schroeder Molly C.,Brown Donna M.,Birch Camille L.,Levy Shawn E.,Boone Braden E.,Dorset Dan C.,Jones Angela L.,Manolio Teri A.,Mulvihill John J.,Wise Anastasia L.,Dayal Jyoti G.,Eckstein David J.,Krasnewich Donna M.,Loomis Carson R.,Mamounas Laura A.,Iglesias Brenda,Martin Casey,Koeller David M.,Metz Thomas O.,Ashley Euan A.,Fisher Paul G.,Bernstein Jonathan A.,Wheeler Matt T.,Zornio Patricia A.,Waggott Daryl M.,Dries Annika M.,Kohler Jennefer N.,Dipple Katrina M.,Nelson Stan F.,Palmer Christina G.S.,Vilain Eric,Allard Patrick,Dell Angelica Esteban C.,Lee Hane,Sinsheimer Janet S.,Papp Jeanette C.,Dorrani Naghmeh,Herzog Matthew R.,Barseghyan Hayk,Adams David R.,Adams Christopher J.,Burke Elizabeth A.,Chao Katherine R.,Davids Mariska,Draper David D.,Estwick Tyra,Frisby Trevor S.,Frost Kate,Gahl William A.,Gartner Valerie,Godfrey Rena A.,Goheen Mitchell,Golas Gretchen A.,Gordon Mary G.,Groden Catherine A.,Gropman Andrea L.,Hackbarth Mary E.,Hardee Isabel,Johnston Jean M.,Koehler Alanna E.,Latham Lea,Latour Yvonne L.,Lau Chyau Yueh C.,Lee Paul R.,Levy Denise J.,Liebendorder Adam P.,Macnamara Ellen F.,Maduro Valerie V.,Malicdan May V.,Markello Thomas C.,McCarty Alexandra J.,Murphy Jennifer L.,Nehrebecky Michele E.,Novacic Donna,Pusey Barbara N.,Sadozai Sarah,Schaffer Katherine E.,Sharma Prashant,Soldatos Ariane G.,Thomas Sara P.,Tifft Cynthia J.,Tolman Nathanial J.,Toro Camilo,Valivullah Zaheer M.,Wahl Colleen E.,Warburton Mike,Weech Alec A.,Wolfe Lynne A.,Yu Guoyun,Hamid Rizwan,Newman John H.,Phillips John A.,Cogan Joy D.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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