The clinical significance of small copy number variants in neurodevelopmental disorders von 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, André, 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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Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disability von Asadollahi, Reza, Oneda, Beatrice, Sheth, Frenny, Azzarello-Burri, Silvia, Baldinger, Rosa, Joset, Pascal, Latal, Beatrice, Knirsch, Walter, Desai, Soaham, Baumer, Alessandra, Houge, Gunnar, Andrieux, Joris, Rauch, Anita

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The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study von Papuc, Sorina M, Abela, Lucia, Steindl, Katharina, Begemann, Anaïs, Simmons, Thomas L, Schmitt, Bernhard, Zweier, Markus, Oneda, Beatrice, Socher, Eileen, Crowther, Lisa M, Wohlrab, Gabriele, Gogoll, Laura, Poms, Martin, Seiler, Michelle, Papik, Michael, Baldinger, Rosa, Baumer, Alessandra, Asadollahi, Reza, Kroell-Seger, Judith, Schmid, Regula, Iff, Tobias, Schmitt-Mechelke, Thomas, Otten, Karoline, Hackenberg, Annette, Addor, Marie-Claude, Klein, Andrea, Azzarello-Burri, Silvia, Sticht, Heinrich, Joset, Pascal, Plecko, Barbara, Rauch, Anita

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Genome-wide non-invasive prenatal testing in single- and multiple-pregnancies at any risk: Identification of maternal polymorphisms to reduce the number of unnecessary invasive con... von Oneda, Beatrice, Sirleto, Pietro, Baldinger, Rosa, Taralczak, Malgorzata, Joset, Pascal, Zweier, Markus, Niedrist, Dunja, Azzarello-Burri, Silvia, Britschgi, Christian, Breymann, Christian, Ochsenbein-Kölble, Nicole, Burkhardt, Tilo, Wisser, Josef, Zimmermann, Roland, Steindl, Katharina, Rauch, Anita

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High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power von Oneda, Beatrice, Baldinger, Rosa, Reissmann, Regina, Reshetnikova, Irina, Krejci, Pavel, Masood, Rahim, Ochsenbein-Kölble, Nicole, Bartholdi, Deborah, Steindl, Katharina, Morotti, Denise, Faranda, Marzia, Baumer, Alessandra, Asadollahi, Reza, Joset, Pascal, Niedrist, Dunja, Breymann, Christian, Hebisch, Gundula, Hüsler, Margaret, Mueller, René, Prentl, Elke, Wisser, Josef, Zimmermann, Roland, Rauch, Anita

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Noninvasive prenatal testing: more caution in counseling is needed in high risk pregnancies with ultrasound abnormalities von Oneda, Beatrice, Steindl, Katharina, Masood, Rahim, Reshetnikova, Irina, Krejci, Pavel, Baldinger, Rosa, Reissmann, Regina, Taralczak, Malgorzata, Guetg, Adriano, Wisser, Josef, Fauchère, Jean-Claude, Rauch, Anita

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The role of recessive inheritance in early-onset epileptic encephalopathies: a combined whole-exome sequencing and copy number study von Papuc, Sorina M, Abela, Lucia, Steindl, Katharina, Begemann, Anaïs, Simmons, Thomas L, Schmitt, Bernhard, Zweier, Markus, Oneda, Beatrice, Socher, Eileen, Crowther, Lisa M, Wohlrab, Gabriele, Gogoll, Laura, Poms, Martin, Seiler, Michelle, Papik, Michael, Baldinger, Rosa, Baumer, Alessandra, Asadollahi, Reza, Kroell-Seger, Judith, Schmid, Regula, Iff, Tobias, Schmitt-Mechelke, Thomas, Otten, Karoline, Hackenberg, Annette, Addor, Marie-Claude, Klein, Andrea, Azzarello-Burri, Silvia, Sticht, Heinrich, Joset, Pascal, Plecko, Barbara, Rauch, Anita

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Noninvasive prenatal testing: more caution in counseling is needed in high risk pregnancies with ultrasound abnormalities von Oneda, Beatrice, Steindl, Katharina, Masood, Rahim, Reshetnikova, Irina, Krejci, Pavel, Baldinger, Rosa, Reissmann, Regina, Taralczak, Malgorzata, Guetg, Adriano, Wisser, Josef, Fauchère, Jean-Claude, Rauch, Anita

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Low-Level Chromosomal Mosaicism in Neurodevelopmental Disorders von Oneda, Beatrice, Asadollahi, Reza, Azzarello-Burri, Silvia, Niedrist, Dunja, Baldinger, Rosa, Masood, Rahim, Schinzel, Albert, Latal, Bea, Jenni, Oskar G., Rauch, Anita

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Low-Level Chromosomal Mosaicism in Neurodevelopmental Disorders von Oneda, Beatrice, Asadollahi, Reza, Azzarello-Burri, Silvia, Niedrist, Dunja, Baldinger, Rosa, Masood, Rahim, Schinzel, Albert, Latal, Bea, Jenni, Oskar G, Rauch, Anita

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The clinical significance of small copy number variants in neurodevelopmental disorders von 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, André, 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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Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disability von Asadollahi, Reza, Oneda, Beatrice, Sheth, Frenny, Azzarello-Burri, Silvia, Baldinger, Rosa, Joset, Pascal, Latal, Beatrice, Knirsch, Walter, Desai, Soaham, Baumer, Alessandra, Houge, Gunnar, Andrieux, Joris, Rauch, Anita

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High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power von Oneda, Beatrice, Baldinger, Rosa, Reissmann, Regina, Reshetnikova, Irina, Krejci, Pavel, Masood, Rahim, Ochsenbein-Kölble, Nicole, Bartholdi, Deborah, Steindl, Katharina, Morotti, Denise, Faranda, Marzia, Baumer, Alessandra, Asadollahi, Reza, Joset, Pascal, Niedrist, Dunja, Breymann, Christian, Hebisch, Gundula, Hüsler, Margaret, Mueller, René, Prentl, Elke, Wisser, Josef, Zimmermann, Roland, Rauch, Anita

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Pre- and postnatal findings in trisomy 17 mosaicism von Utermann, Barbara, Riegel, Mariluce, Leistritz, Dru, Karall, Thomas, Wisser, Josef, Meisner, Lorraine, Fauth, Christine, Baldinger, Rosa, Johnson, Julie, Erdel, Martin, Taralczak, Malgorzata, Pauli, Richard M., Baumer, Alessandra, Schinzel, Albert, Kotzot, Dieter

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Pre- and postnatal findings in trisomy 17 mosaicism von Utermann, Barbara, Riegel, Mariluce, Leistritz, Dru, Karall, Thomas, Wisser, Josef, Meisner, Lorraine, Fauth, Christine, Baldinger, Rosa, Johnson, Julie, Erdel, Martin, Taralczak, Malgorzata, Pauli, Richard M, Baumer Wolz, Alessandra, Schinzel, Albert, Kotzot, Dieter

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Theœ clinical significance of small copy number variants in neurodevelopmental disorders von Asadollahi, Reza

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