Ingrid Paine, Jennifer E. Posey, Christopher M. Grochowski, Shalini N. Jhangiani, Sarah Rosenheck, Robert Kleyner, Taylor Marmorale, Margaret Yoon, Kai Wang, Reid Robison, Gerarda Cappuccio, Michele Pinelli, Adriano Magli, Zeynep Coban Akdemir, Joannie Hui, Wai Lan Yeung, Bibiana K.Y. Wong, Lucia Ortega, Mir Reza Bekheirnia, Tatjana Bierhals, Maja Hempel, Jessika Johannsen, René Santer, Dilek Aktas, Mehmet Alikasifoglu, Sevcan Bozdogan, Hatip Aydin, Ender Karaca, Yavuz Bayram, Hadas Ityel, Michael Dorschner, Janson J. White, Ekkehard Wilichowski, Saskia B. Wortmann, Erasmo B. Casella, Joao Paulo Kitajima, Fernando Kok, Fabiola Monteiro, Donna M. Muzny, Michael Bamshad, Richard A. Gibbs, V. Reid Sutton, University of Washington Center for Mendelian Genomics, Baylor-Hopkins Center for Mendelian Genomics, Telethon Undiagnosed Diseases Program, Hilde Van Esch, Nicola Brunetti-Pierri, Friedhelm Hildebrandt, Ariel Brautbar, Ignatia B. Van den Veyver, Ian Glass, Davor Lessel, Gholson J. Lyon, James R. Lupski
Am J Hum Genet. 2019 Aug 1; 105(2): 302–316. Published online 2019 Jun 27. doi: 10.1016/j.ajhg.2019.06.001