Search Results - Asadollahi, Reza

Genome-wide analysis in neurodevelopmental disorders: in depth approach to decipher the etiological cause

by Asadollahi, Reza 1980-

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Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes

by Begemann, Anaïs, Acuña, Mario A., Zweier, Markus, Vincent, Marie, Steindl, Katharina, Bachmann-Gagescu, Ruxandra, Hackenberg, Annette, Abela, Lucia, Plecko, Barbara, Kroell-Seger, Judith, Baumer, Alessandra, Yamakawa, Kazuhiro, Inoue, Yushi, Asadollahi, Reza, Sticht, Heinrich, Zeilhofer, Hanns Ulrich, Rauch, Anita

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The clinical significance of small copy number variants in neurodevelopmental disorders

by Asadollahi, Reza, Oneda, Beatrice, Joset, Pascal, Azzarello-Burri, Silvia, Bartholdi, Deborah, Steindl, Katharina, Vincent, Marie, Cobilanschi, Joana, Sticht, Heinrich, Baldinger, Rosa, Reissmann, Regina, Sudholt, Irene, Thiel, Christian T., Ekici, Arif B., Reis, Andre, Bijlsma, Emilia K., Andrieux, Joris, Dieux, Anne, Fitzpatrick, David, Ritter, Susanne, Baumer, Alessandra, Latal, Beatrice, Plecko, Barbara, Jenni, Oskar G., Rauch, Anita

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