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Cleynen, I.Hestand, M.S.Swillen, A.Vermeesch, J.R.Demaerel, W.Breckpot, J.Devriendt, K.Vogels, A.Engchuan, W.Merico, D.Heung, T.Chow, E.W.C.Butcher, N.J.Costain, G.A.Lowther, C.Fiksinski, A.Bassett, A.S.Boot, E.Holleman, A.M.Johnston, H.R.Warren, S.T.Chopra, P.Cutler, D.J.Duncan, R.Kotlar, A.V.Mulle, J.G.Voss, A.J.Zwick, M.E.Coleman, K.Cubells, J.F.Epstein, M.P.Monfeuga, T.van den Bree, M.Owen, M.J.Holmans, P.Pardinas, A.Walters, J.T.R.Moss, H.Niarchou, M.Williams, N.M.McDonald-McGinn, D.M.Zackai, E.H.Emanuel, B.S.Jin, A.Lilley, B.Salmons, H.I.Tran, O.Crowley, T.B.McGinn, D.E.Moss, E.M.Sharkus, R.J.Unolt, M.Gur, R.E.Calkins, M.E.Gallagher, R.S.Gur, R.C.Tang, S.X.Morrow, B.E.Diacou, A.Golden, A.Guo, T.Lin, J.-R.Zhang, Z.Zhao, Y.Vergaelen, E.Vorstman, J.A.S.Breetvelt, E.Bearden, C.E.Kushan, L.Wang, T.Marshall, C.Evers, R.van Amelsvoort, T.A.M.J.van Duin, E.Vingerhoets, C.Fritsch, R.Ornstein, C.Repetto, G.M.Duijff, S.N.Murphy, K.C.Prasad, S.E.Daly, E.M.Gudbrandsen, M.Murphy, C.M.Murphy, D.G.Buzzanca, A.Fabio, F.D.Digilio, M.C.Pontillo, M.Vicari, S.Marino, B.Ousley, O.Y.Carmel, M.Michaelovsky, E.Weizman, A.Gothelf, D.Mekori-Domachevsky, E.Weinberger, R.Jalbrzikowski, M.Armando, M.Eliez, S.Sandini, C.Schneider, M.Béna, F.S.Antshel, K.M.Fremont, W.Kates, W.R.Belzeaux, R.Busa, T.Philip, N.Campbell, L.E.McCabe, K.L.Hooper, S.R.Schoch, K.Shashi, V.Simon, T.J.Tassone, F.Arango, C.Fraguas, D.García-Miñaúr, S.Morey-Canyelles, J.Rosell, J.Raventos-Simic, J.Suñer, D.H.
In: Molecular Psychiatry. (Molecular Psychiatry, August 2021, 26(8):4496-4510)
Academic Journal
In: American Journal of Human Genetics. (American Journal of Human Genetics, 4 February 2021, 108(2):346-356)
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Hoed, J. denBoer, E. deVoisin, N.Dingemans, A.J.M.Guex, N.Wiel, L.J.M. van deNellaker, C.Amudhavalli, S.M.Banka, S.Bena, F.S.Ben-Zeev, B.Bonagura, V.R.Bruel, A.L.Brunet, T.Brunner, H.G.Chew, H.B.Chrast, J.Cimbalistienė, L.Coon, H.Délot, E.C.Démurger, F.Denommé-Pichon, A.S.Depienne, C.Donnai, D.Dyment, D.A.Elpeleg, O.Faivre, L.Gilissen, C.F.Granger, L.Haber, B.Hachiya, Y.Abedi, Y.H.Hanebeck, J.Hehir-Kwa, J.Y.Horist, B.Itai, T.Jackson, A.Jewell, R.Jones, K.L.Joss, S.Kashii, H.Kato, M.Kattentidt-Mouravieva, A.A.Kok, F.Kotzaeridou, U.Krishnamurthy, V.Kučinskas, V.Kuechler, A.Lavillaureix, A.Liu, PManwaring, L.Matsumoto, N.Mazel, B.McWalter, K.Meiner, V.Mikati, M.A.Miyatake, S.Mizuguchi, T.Moey, L.H.Mohammed, SMor-Shaked, H.Mountford, H.Newbury-Ecob, R.Odent, S.Orec, L.Osmond, M.Palculict, T.B.Parker, M.Petersen, A.K.Pfundt, R.P.Preikšaitienė, E.Radtke, K.Ranza, E.Rosenfeld, J.A.Santiago-Sim, T.Schwager, C.Sinnema, M.Snijders Blok, L.Spillmann, R.C.Stegmann, A.P.A.Thiffault, I.Tran, L.Vaknin-Dembinsky, A.Vedovato-Dos-Santos, J.H.Schrier Vergano, S.A.Vilain, E.Vitobello, A.Wagner, M.Waheeb, A.Willing, M.Zuccarelli, B.Kini, U.Newbury, D.F.Kleefstra, T.Reymond, A.Fisher, S.E.Vissers, L.E.L.M.
American Journal of Human Genetics; 346; 356; 0002-9297; 2; 108; ~American Journal of Human Genetics~346~356~~~0002-9297~2~108~~
Electronic Resource
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction; [preprint] Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
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[AR] Bena, F.S.
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