Acute pre-B lymphoblastic leukemia and congenital anomalies in a child with a de novo 22q11.1q11.22 duplication by Vaisvilas M, Dirse V, Aleksiuniene B, Tamuliene I, Cimbalistiene L, Utkus A, Rascon J

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Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction by den Hoed, J, de Boer, E, Voisin, N, Dingemans, AJM, Guex, N, Wiel, L, Nellaker, C, Amudhavalli, SM, Banka, S, Bena, FS, Ben-Zeev, B, Bonagura, VR, Bruel, A-L, Brunet, T, Brunner, HG, Chew, HB, Chrast, J, Cimbalistienė, L, Coon, H, DDD Study, Délot, EC, Démurger, F, Denommé-Pichon, A-S, Depienne, C, Donnai, D, Dyment, DA, Elpeleg, O, Faivre, L, Gilissen, C, Granger, L, Haber, B, Hachiya, Y, Abedi, YH, Hanebeck, J, Hehir-Kwa, JY, Horist, B, Itai, T, Jackson, A, Jewell, R, Jones, KL, Joss, S, Kashii, H, Kato, M, Kattentidt-Mouravieva, AA, Kok, F, Kotzaeridou, U, Krishnamurthy, V, Kučinskas, V, Kuechler, A, Lavillaureix, A