Vetrini, FrancescoMcKee, ShaneRosenfeld, Jill A.Suri, MohnishLewis, Andrea M.Nugent, Kimberly MargaretRoeder, ElizabethLittlejohn, Rebecca O.Holder, SueZhu, WenmiaoAlaimo, Joseph T.Graham, BrettHarris, Jill M.Gibson, James B.Pastore, MatthewMcBride, Kim L.Komara, MakankoAl-Gazali, LihadhAl Shamsi, AishaFanning, Elizabeth A.Wierenga, Klaas J.Scott, Daryl A.Ben-Neriah, ZivaMeiner, VardiellaCassuto, HanochElpeleg, OrlyLloyd Holder Jr, J.Burrage, Lindsay C.Seaver, Laurie H.Van Maldergem, LionelMahida, SonalSoul, Janet S.Marlatt, MargaretMatyakhina, LudmilaVogt, JulieGold, June-AnnePark, Soo-MiVarghese, VinodLampe, Anne K.Kumar, AjithLees, MelissaHolder-Espinasse, MurielMcConnell, VivienneBernhard, BirgittaBlair, EdHarrison, VictoriaMuzny, Donna M.Gibbs, Richard A.Elsea, Sarah H.Posey, Jennifer E.Bi, WeiminLalani, SeemaXia, FanYang, YapingEng, Christine M.Lupski, James R.Liu, Pengfei2019-08-072019-08-072019-03-25Vetrini, F., McKee, S., Rosenfeld, J. A., Suri, M., Lewis, A. M., Nugent, K. M., … Liu, P. (2019). Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. Genome medicine, 11(1), 16. doi:10.1186/s13073-019-0630-1https://hdl.handle.net/1805/20236It was highlighted that the original article [1] contained a typographical error in the Results section. Subject 17 was incorrectly cited as Subject 1. This Correction article shows the revised statement. The original article has been updated.en-USAttribution-NonCommercial-NoDerivs 3.0 United StatesCorrectionsArticle