Diagnostic value of partial exome sequencing in developmental disorders von Gieldon, Laura, Mackenroth, Luisa, Kahlert, Anne-Karin, Lemke, Johannes R, Porrmann, Joseph, Schallner, Jens, von der Hagen, Maja, Markus, Susanne, Weidensee, Sabine, Novotna, Barbara, Soerensen, Charlotte, Klink, Barbara, Wagner, Johannes, Tzschach, Andreas, Jahn, Arne, Kuhlee, Franziska, Hackmann, Karl, Schrock, Evelin, Di Donato, Nataliya, Rump, Andreas

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Correction: Diagnostic value of partial exome sequencing in developmental disorders von Gieldon, Laura, Mackenroth, Luisa, Kahlert, Anne-Karin, Lemke, Johannes R, Porrmann, Joseph, Schallner, Jens, von der Hagen, Maja, Markus, Susanne, Weidensee, Sabine, Novotna, Barbara, Soerensen, Charlotte, Klink, Barbara, Wagner, Johannes, Tzschach, Andreas, Jahn, Arne, Kuhlee, Franziska, Hackmann, Karl, Schrock, Evelin, Di Donato, Nataliya, Rump, Andreas

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Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons von Bolze, Alexandre, Boisson, Bertrand, Bosch, Barbara, Antipenko, Alexander, Bouaziz, Matthieu, Sackstein, Paul, Chaker-Margot, Malik, Barlogis, Vincent, Briggs, Tracy, Colino, Elena, Elmore, Aurora C., Fischer, Alain, Genel, Ferah, Hewlett, Angela, Jedidi, Maher, Kelecic, Jadranka, Krüger, Renate, Ku, Cheng-Lung, Kumararatne, Dinakantha, Lefevre-Utile, Alain, Loughlin, Sam, Mahlaoui, Nizar, Markus, Susanne, Garcia, Juan-Miguel, Nizon, Mathilde, Oleastro, Matias, Pac, Malgorzata, Picard, Capucine, Pollard, Andrew J., Rodriguez-Gallego, Carlos, Thomas, Caroline, Von Bernuth, Horst, Worth, Austen, Meyts, Isabelle, Risolino, Maurizio, Selleri, Licia, Puel, Anne, Klinge, Sebastian, Abel, Laurent, Casanova, Jean-Laurent

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Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis von Hotz, Alrun, Oji, Vinzenz, Bourrat, Emmanuelle, Jonca, Nathalie, Mazereeuw-Hautier, Juliette, Betz, Regina C, Blume-Peytavi, Ulrike, Stieler, Karola, Morice-Picard, Fanny, Schönbuchner, Ines, Markus, Susanne, Schlipf, Nina, Fischer, Judith

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Genome sequencing in families with congenital limb malformations von Elsner, Jonas, Mensah, Martin A., Holtgrewe, Manuel, Hertzberg, Jakob, Bigoni, Stefania, Busche, Andreas, Coutelier, Marie, de Silva, Deepthi C., Elçioglu, Nursel, Filges, Isabel, Gerkes, Erica, Girisha, Katta M., Graul-Neumann, Luitgard, Jamsheer, Aleksander, Krawitz, Peter, Kurth, Ingo, Markus, Susanne, Megarbane, Andre, Reis, André, Reuter, Miriam S., Svoboda, Daniel, Teller, Christopher, Tuysuz, Beyhan, Türkmen, Seval, Wilson, Meredith, Woitschach, Rixa, Vater, Inga, Caliebe, Almuth, Hülsemann, Wiebke, Horn, Denise, Mundlos, Stefan, Spielmann, Malte

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Next‐generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read... von Neuhaus, Christine, Eisenberger, Tobias, Decker, Christian, Nagl, Sandra, Blank, Cornelia, Pfister, Markus, Kennerknecht, Ingo, Müller‐Hofstede, Cornelie, Charbel Issa, Peter, Heller, Raoul, Beck, Bodo, Rüther, Klaus, Mitter, Diana, Rohrschneider, Klaus, Steinhauer, Ute, Korbmacher, Heike M., Huhle, Dagmar, Elsayed, Solaf M., Taha, Hesham M., Baig, Shahid M., Stöhr, Heidi, Preising, Markus, Markus, Susanne, Moeller, Fabian, Lorenz, Birgit, Nagel‐Wolfrum, Kerstin, Khan, Arif O., Bolz, Hanno J.

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Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons von Bolze, Alexandre, Boisson, Bertrand, Bosch, Barbara, Antipenko, Alexander, Bouaziz, Matthieu, Sackstein, Paul, Chaker-Margot, Malik, Barlogis, Vincent, Briggs, Tracy, Colino, Elena, Elmore, Aurora C, Fischer, Alain, Genel, Ferah, Hewlett, Angela, Jedidi, Maher, Kelecic, Jadranka, Krueger, Renate, Ku, Cheng-Lung, Kumararatne, Dinakantha, Lefevre-Utile, Alain, Loughlin, Sam, Mahlaoui, Nizar, Markus, Susanne, Garcia, Juan-Miguel, Nizon, Mathilde, Oleastro, Matias, Pac, Malgorzata, Picard, Capucine, Pollard, Andrew J, Rodriguez-Gallego, Carlos, Thomas, Caroline, Von Bernuth, Horst, Worth, Austen, Meyts, Isabelle, Risolino, Maurizio, Selleri, Licia, Puel, Anne, Klinge, Sebastian, Abel, Laurent, Casanova, Jean-Laurent

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Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing von Chen, Wei, Ullmann, Reinhard, Langnick, Claudia, Menzel, Corinna, Wotschofsky, Zofia, Hu, Hao, Döring, Andreas, Hu, Yuhui, Kang, Hui, Tzschach, Andreas, Hoeltzenbein, Maria, Neitzel, Heidemarie, Markus, Susanne, Wiedersberg, Eberhard, Kistner, Gerd, van Ravenswaaij-Arts, Conny MA, Kleefstra, Tjitske, Kalscheuer, Vera M, Ropers, Hans-Hilger

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Next‐generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read... von Neuhaus, Christine, Eisenberger, Tobias, Decker, Christian, Nagl, Sandra, Blank, Cornelia, Pfister, Markus, Kennerknecht, Ingo, Cornelie Müller‐Hofstede, Issa, Peter Charbel, Heller, Raoul, Beck, Bodo, Rüther, Klaus, Mitter, Diana, Rohrschneider, Klaus, Steinhauer, Ute, Korbmacher, Heike M, Huhle, Dagmar, Elsayed, Solaf M, Taha, Hesham M, Baig, Shahid M, Stöhr, Heidi, Preising, Markus, Markus, Susanne, Moeller, Fabian, Lorenz, Birgit, Kerstin Nagel‐Wolfrum, Khan, Arif O, Bolz, Hanno J

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Device for testing the quality of microstructurization von MARKUS SUSANNE, MEYER UDO, DIECKHOFF STEFAN

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Low Urethral Pressure Profile - Clinical Implications von E. Dahms, Daniela Schultz Lampel, Susanne Kloeppel, Markus Hohenfellner, Sebastian W. Melchior, Stefan C. Müller, Joachim W. Thüroff, Stefan

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DEVICE FOR TESTING THE QUALITY OF MICROSTRUCTURIZATION von MARKUS SUSANNE, MEYER UDO, DIECKHOFF STEFAN

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Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis von Hotz, Alrun, Oji, Vmzenz, Bourrat, Emmanuelle, Jonca, Nathalie, Mazereeuw-Hautier, Juliette, Betz, Regina C, Blume-Peytavi, Ulrike, Stieler, Karola, Morice-Picard, Fanny, Schoenbuchner, Ines, Markus, Susanne, Schlipf, Nina, Fischer, Judith

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Continuous respiratory monitoring for sleep apnea screening by ambulatory hemodynamic monitor von Dillier, Roger, Baumann, Markus, Young, Mabelle, Erne, Susanne, Schwizer, Bernhard, Zuber, Michel, Erne, Paul

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Diagnostic value of partial exome sequencing in developmental disorders von Gieldon, Laura, Mackenroth, Luisa, Kahlert, Anne-Karin, Lemke, Johannes R, Porrmann, Joseph, Schallner, Jens, von der Hagen, Maja, Markus, Susanne, Weidensee, Sabine, Novotna, Barbara, Soerensen, Charlotte, Klink, Barbara, Wagner, Johannes, Tzschach, Andreas, Jahn, Arne, Kuhlee, Franziska, Hackmann, Karl, Schrock, Evelin, Di Donato, Nataliya, Rump, Andreas

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APPARATUS FOR CHECKING MICROSTRUCTURING QUALITY von MEYER, UDO, MARKUS, SUSANNE, DIECKHOFF, STEFAN

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Vorrichtung zur Prüfung von Mikrostrukturierungsqualität von MEYER, UDO, MARKUS, SUSANNE, DIECKHOFF, STEFAN

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VERFAHREN UND VORRICHTUNG ZUM PRÜFEN EINER OBERFLÄCHENGÜTE von TORNOW, CHRISTIAN, MEYER, UDO, SEILER, ANDREAS, MARKUS, SUSANNE, DIECKHOFF, STEFAN, WILKEN, RALPH, AMKREUTZ, MARC

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METHOD AND DEVICE FOR TESTING A SURFACE QUALITY von TORNOW, CHRISTIAN, MEYER, UDO, SEILER, ANDREAS, MARKUS, SUSANNE, DIECKHOFF, STEFAN, WILKEN, RALPH, AMKREUTZ, MARC

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METHOD AND DEVICE FOR TESTING A SURFACE QUALITY von TORNOW, CHRISTIAN, MEYER, UDO, SEILER, ANDREAS, MARKUS, SUSANNE, DIECKHOFF, STEFAN, WILKEN, RALPH, AMKREUTZ, MARC

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