Torthaí cuardaigh - Adegbola, Abidemi

Concise Review: Induced Pluripotent Stem Cell Models for Neuropsychiatric Diseases de réir Adegbola, Abidemi, Bury, Luke A., Fu, Chen, Zhang, Meixiang, Wynshaw‐Boris, Anthony

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Disruption of CTNND2, encoding delta-catenin, causes a penetrant attention deficit disorder and myopia de réir Adegbola, Abidemi, Lutz, Richard, Nikkola, Elina, Strom, Samuel P., Picker, Jonathan, Wynshaw-Boris, Anthony

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Monoallelic expression of the human FOXP2 speech gene de réir Adegbola, Abidemi A., Cox, Gerald F., Bradshaw, Elizabeth M., Hafler, David A., Gimelbrant, Alexander, Chess, Andrew

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PTPN4 germline variants result in aberrant neurodevelopment and growth de réir Chmielewska, Joanna J., Burkardt, Deepika, Granadillo, Jorge Luis, Slaugh, Rachel, Morgan, Shamile, Rotenberg, Joshua, Keren, Boris, Mignot, Cyril, Escobar, Luis, Turnpenny, Peter, Zuteck, Melissa, Seaver, Laurie H., Ploski, Rafal, Dziembowska, Magdalena, Wynshaw-Boris, Anthony, Adegbola, Abidemi

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Redefining the MED13L syndrome de réir Adegbola, Abidemi, Musante, Luciana, Callewaert, Bert, Maciel, Patricia, Hu, Hao, Isidor, Bertrand, Picker-Minh, Sylvie, Le Caignec, Cedric, Delle Chiaie, Barbara, Vanakker, Olivier, Menten, Björn, Dheedene, Annelies, Bockaert, Nele, Roelens, Filip, Decaestecker, Karin, Silva, João, Soares, Gabriela, Lopes, Fátima, Najmabadi, Hossein, Kahrizi, Kimia, Cox, Gerald F, Angus, Steven P, Staropoli, John F, Fischer, Ute, Suckow, Vanessa, Bartsch, Oliver, Chess, Andrew, Ropers, Hans-Hilger, Wienker, Thomas F, Hübner, Christoph, Kaindl, Angela M, Kalscheuer, Vera M

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