A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3

Author:

Chao Hsiao-Tuan,Davids Mariska,Burke Elizabeth,Pappas John G.,Rosenfeld Jill A.,McCarty Alexandra J.,Davis Taylor,Wolfe Lynne,Toro Camilo,Tifft Cynthia,Xia Fan,Stong Nicholas,Johnson Travis K.,Warr Coral G.,Yamamoto Shinya,Adams David R.,Markello Thomas C.,Gahl William A.,Bellen Hugo J.,Wangler Michael F.,Malicdan May Christine V.,Adams David R.,Adams Christopher J.,Alejandro Mercedes E.,Allard Patrick,Ashley Euan A.,Bacino Carlos A.,Balasubramanyam Ashok,Barseghyan Hayk,Beggs Alan H.,Bellen Hugo J.,Bernstein Jonathan A.,Bick David P.,Birch Camille L.,Boone Braden E.,Briere Lauren C.,Brown Donna M.,Brush Matthew,Burrage Lindsay C.,Chao Katherine R.,Clark Gary D.,Cogan Joy D.,Cooper Cynthia M.,Craigen William J.,Davids Mariska,Dayal Jyoti G.,Dell'Angelica Esteban C.,Dhar Shweta U.,Dipple Katrina M.,Donnell-Fink Laurel A.,Dorrani Naghmeh,Dorset Dan C.,Draper David D.,Dries Annika M.,Eckstein David J.,Emrick Lisa T.,Eng Christine M.,Esteves Cecilia,Estwick Tyra,Fisher Paul G.,Frisby Trevor S.,Frost Kate,Gahl William A.,Gartner Valerie,Godfrey Rena A.,Goheen Mitchell,Golas Gretchen A.,Goldstein David B.,Gordon Mary “Gracie” G.,Gould Sarah E.,Gourdine Jean-Philippe F.,Graham Brett H.,Groden Catherine A.,Gropman Andrea L.,Hackbarth Mary E.,Haendel Melissa,Hamid Rizwan,Hanchard Neil A.,Handley Lori H.,Hardee Isabel,Herzog Matthew R.,Holm Ingrid A.,Howerton Ellen M.,Jacob Howard J.,Jain Mahim,Jiang Yong-hui,Johnston Jean M.,Jones Angela L.,Koehler Alanna E.,Koeller David M.,Kohane Isaac S.,Kohler Jennefer N.,Krasnewich Donna M.,Krieg Elizabeth L.,Krier Joel B.,Kyle Jennifer E.,Lalani Seema R.,Latham Lea,Latour Yvonne L.,Lau C. Christopher,Lazar Jozef,Lee Brendan H.,Lee Hane,Lee Paul R.,Levy Shawn E.,Levy Denise J.,Lewis Richard A.,Liebendorder Adam P.,Lincoln Sharyn A.,Loomis Carson R.,Loscalzo Joseph,Maas Richard L.,Macnamara Ellen F.,MacRae Calum A.,Maduro Valerie V.,Malicdan May Christine V.,Mamounas Laura A.,Manolio Teri A.,Markello Thomas C.,Mashid Azamian S.,Mazur Paul,McCarty Alexandra J.,McConkie-Rosell Allyn,McCray Alexa T.,Metz Thomas O.,Might Matthew,Moretti Paolo M.,Mulvihill John J.,Murphy Jennifer L.,Muzny Donna M.,Nehrebecky Michele E.,Nelson Stan F.,Newberry J. Scott,Newman John H.,Nicholas Sarah K.,Novacic Donna,Orange Jordan S.,Pallais J. Carl,Palmer Christina G.S.,Papp Jeanette C.,Pena Loren D.M.,Phillips John A.,Posey Jennifer E.,Postlethwait John H.,Potocki Lorraine,Pusey Barbara N.,Ramoni Rachel B.,Rodan Lance H.,Sadozai Sarah,Schaffer Katherine E.,Schoch Kelly,Schroeder Molly C.,Scott Daryl A.,Sharma Prashant,Shashi Vandana,Silverman Edwin K.,Sinsheimer Janet S.,Soldatos Ariane G.,Spillmann Rebecca C.,Splinter Kimberly,Stoler Joan M.,Stong Nicholas,Strong Kimberly A.,Sullivan Jennifer A.,Sweetser David A.,Thomas Sara P.,Tift Cynthia J.,Tolman Nathanial J.,Toro Camilo,Tran Alyssa A.,Valivullah Zaheer M.,Vilain Eric,Waggott Daryl M.,Wahl Colleen E.,Walley Nicole M.,Walsh Chris A.,Wangler Michael F.,Warburton Mike,Ward Patricia A.,Waters Katrina M.,Webb-Robertson Bobbie-Jo M.,Weech Alec A.,Westerfield Monte,Wheeler Matt T.,Wise Anastasia L.,Worthe Lynne A.,Worthey Elizabeth A.,Yamamoto Shinya,Yang Yaping,Yu Guoyun,Zornio Patricia A.

Funder

NIH

Intramural Research Program of the National Human Genome Research Institute

Common Fund of the NIH Office of the Director

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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