Resultats de la cerca - Adegbola, Abidemi

Concise Review: Induced Pluripotent Stem Cell Models for Neuropsychiatric Diseases per 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 per 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 per 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 per 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 per 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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