Biesecker, Leslie G.Adam, Margaret P.Alkuraya, Fowzan S.Amemiya, Anne R.Bamshad, Michael J.Beck, Anita E.Bennett, James T.Bird, Lynne M.Carey, John C.Chung, BrianClark, Robin D.Cox, Timothy C.Curry, CynthiaDinulos, Mary Beth PalkoDobyns, William B.Giampietro, Philip F.Girisha, Katta M.Glass, Ian A.Graham, John M., Jr.Gripp, Karen W.Haldeman-Englert, Chad R.Hall, Bryan D.Innes, A. MicheilKalish, Jennifer M.Keppler-Noreuil, Kim M.Kosaki, KenjiroKozel, Beth A.Mirzaa, Ghayda M.Mulvihill, John J.Nowaczyk, Malgorzata J.M.Pagon, Roberta A.Retterer, KyleRope, Alan F.Sanchez-Lara, Pedro A.Seaver, Laurie H.Shieh, Joseph T.Slavotinek, Anne M.Sobering, Andrew K.Stevens, Cathy A.Stevenson, David A.Tan, Tiong YangTan, Wen-HannTsai, Anne C.Weaver, David D.Williams, Marc S.Zackai, ElaineZarate, Yuri A.2023-05-192023-05-192021Biesecker LG, Adam MP, Alkuraya FS, et al. Response to Hamosh et al. Am J Hum Genet. 2021;108(9):1809-1810. doi:10.1016/j.ajhg.2021.07.006https://hdl.handle.net/1805/33149en-USPublisher PolicyMendelian genetic disordersPhenotypeDyadArticle