A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3
Hsiao‐Tuan Chao(Baylor College of Medicine), Laurel A. Donnell‐Fink(Brigham and Women's Hospital), David R. Adams(National Human Genome Research Institute), Camilo Toro(National Human Genome Research Institute), Elizabeth A. Burke, Ashok Balasubramanyam, Hugo J. Bellen(Baylor College of Medicine), Hayk Barseghyan(Children's National), John Pappas(New York University), Thomas C. Markello(National Human Genome Research Institute), Fan Xia(Baylor Genetics), Lindsay C. Burrage(Baylor College of Medicine), Katherine R. Chao(Broad Institute), Travis K. Johnson(Monash University), Cynthia J. Tifft(Children's National), Mariska Davids, Shinya Yamamoto, May Christine V. Malicdan(National Institutes of Health), Matthew Brush(Oregon Health & Science University), David Bick(Medical College of Wisconsin), Jill A. Rosenfeld(Baylor College of Medicine), Alan H. Beggs(Boston Children's Hospital), Alexandra J. McCarty(National Human Genome Research Institute), Patrick Allard, Nicholas Stong(New York Genome Center), Cynthia M. Cooper, Lynne A. Wolfe(National Institutes of Health), Euan A. Ashley(Stanford University), Shweta U. Dhar, William A. Gahl(National Institute of Child Health), Coral G. Warr(Monash University), Camille L. Birch, Jyoti G. Dayal, Michael F. Wangler(Baylor College of Medicine), Donna M. Brown, Jonathan A. Bernstein(Stanford Medicine), Mercedes E. Alejandro, Lauren C. Briere(Duke Medical Center), Taylor Davis(National Human Genome Research Institute), Braden Boone(HudsonAlpha Institute for Biotechnology), Katrina M. Dipple(Seattle Children's Hospital), Gary Clark, Esteban C. Dell’Angelica, Joy D. Cogan(Vanderbilt University Medical Center), William J. Craigen(Baylor College of Medicine), Carlos A. Bacino(Baylor College of Medicine)
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