Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders
Thygesen, Johan H., Wolfe, Kate, McQuillin, Andrew, Viñas-Jornet, Marina, Baena, Neus, Brison, Nathalie, D'Haenens, Greet, Esteba-Castillo, Susanna, Gabau, Elisabeth, Ribas-Vidal, Núria, Ruiz, Anna, Vermeesch, Joris, Weyts, Eddy, Novell, Ramon, Buggenhout, Griet Van, Strydom, André, Bass, Nick, Guitart, Miriam, Vogels, Annick
Published in British journal of psychiatry (01.05.2018)
Published in British journal of psychiatry (01.05.2018)
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Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor
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Published in European journal of medical genetics (01.09.2016)
Published in European journal of medical genetics (01.09.2016)
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Presenting symptoms in adults with the 22q11 deletion syndrome
Vogels, Annick, Schevenels, Sara, Cayenberghs, Richard, Weyts, Eddy, Van Buggenhout, Griet, Swillen, Ann, Van Esch, Hilde, de Ravel, Thomy, Corveleyn, Pieter, Devriendt, Koen
Published in European journal of medical genetics (01.03.2014)
Published in European journal of medical genetics (01.03.2014)
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