Carter TC, Kay DM, Pangilinan F, Almli LM, Jenkins MM, Blue EE, Sok P, White JJ, Cunniff CM, Agopian AJ, Bamshad MJ, Botto LD, Brody LC, Gucsavas-Calikoglu M, Chong JX, Gomez-Acevedo H, Lupo PJ, Moore CA, Nembhard WN, Olney RS, Olshan AF, Orloff MS, Reefhuis J, Romitti PA, Shaw GM, Werler MM, Yazdy MM, Browne ML, Howley MM, University of Washington Center for Mendelian Genomics, NISC Comparative Sequencing Program, the National Birth Defects Prevention Study
Verbinnen I, Douzgou Houge S, Hsieh TC, Lesmann H, Kirchhoff A, Geneviève D, Brimble E, Lenaerts L, Haesen D, Levy RJ, Thevenon J, Faivre L, Marco E, Chong JX, Bamshad M, Patterson K, Mirzaa GM, Foss K, Dobyns W, White SM, Pais L, O'Heir E, Itzikowitz R, Donald KA, Van der Merwe C, Mussa A, Cervini R, Giorgio E, Roscioli T, Dias KR, Evans CA, Brown NJ, Ruiz A, Trujillo Quintero JP, Rabin R, Pappas J, Yuan H, Lachlan K, Thomas S, Devlin A, Wright M, Martin R, Karwowska J, Posmyk R, Chatron N, Stark Z, Heath O, Delatycki M, Buchert R, Korenke GC, Ramsey K, Narayanan V, Grange DK, Weisenberg JL, Haack TB, Karch S, Kipkemoi P, Mangi M, Bindels de Heus KGCB, de Wit MY, Barakat TS, Lim D, Van Winckel G, Spillmann RC, Shashi V, Jacob M, Stehr AM, Undiagnosed Diseases Network, Krawitz P, Douzgos Houge G, Janssens V