Delayed Detection of a Carcinoid Tumor after Conservative Therapy for Appendicitis in a 13-Year-Old Boy and a 17-Year-Old Girl von Korsch, Leonie Annina, Michael Boemers, Thomas, Zimmermann, Peter, Stenzel, Martin, Wendenburg, Wera

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Surgical Repair of a Superior Sternal Cleft in an Infant von Klein, Tobias, Kellner, Maximilian, Boemers, Thomas Michael, Mack-Detlefsen, Birte

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Delayed Detection of a Carcinoid Tumor after Conservative Therapy for Appendicitis in a 13-Year-Old Boy and a 17-Year-Old Girl von Korsch, Leonie Annina, Michael Boemers, Thomas, Zimmermann, Peter, Stenzel, Martin, Wendenburg, Wera

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Epidemiologic study of the bladder exstrophy-epispadias complex: analysis of 198 families von Lisa GAMBHIR, Heiko REUTTER , Boris UTSCH , Martin MÜLLER , Birte DETLEFSEN , Hannes VOGT, Thomas M. BOEMERS , Wolfgang H. RÖSCH and Michael LUDWIG

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Surgical Repair of a Superior Sternal Cleft in an Infant von Klein, Tobias, Kellner, Maximilian, Boemers, Thomas Michael, Mack-Detlefsen, Birte

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Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy von Draaken, Markus, Knapp, Michael, Pennimpede, Tracie, Schmidt, Johanna M, Ebert, Anne-Karolin, Rösch, Wolfgang, Stein, Raimund, Utsch, Boris, Hirsch, Karin, Boemers, Thomas M, Mangold, Elisabeth, Heilmann, Stefanie, Ludwig, Kerstin U, Jenetzky, Ekkehart, Zwink, Nadine, Moebus, Susanne, Herrmann, Bernhard G, Mattheisen, Manuel, Nöthen, Markus M, Ludwig, Michael, Reutter, Heiko

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Prenatal Diagnosis of Hydro(metro)colpos: A Series of 20 Cases von Mallmann, Michael R., Reutter, Heiko, Mack-Detlefsen, Birte, Gottschalk, Ingo, Geipel, Annegret, Berg, Christoph, Boemers, Thomas M., Gembruch, Ulrich

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Preliminary report on the International Conference for the Development of Standards for the Treatment of Anorectal Malformations von Holschneider, Alexander, Hutson, John, Peña, Albert, Beket, Elhamy, Chatterjee, Subir, Coran, Arnold, Davies, Michael, Georgeson, Keith, Grosfeld, Jay, Gupta, Devendra, Iwai, Naomi, Kluth, Dieter, Martucciello, Giuseppe, Moore, Samuel, Rintala, Risto, Smith, E. Durham, Sripathi, D.V., Stephens, Douglas, Sen, Sudipta, Ure, Benno, Grasshoff, Sabine, Boemers, Thomas, Murphy, Feilin, Söylet, Yunus, Dübbers, Martin, Kunst, Marc

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Isolated bladder exstrophy in prenatal diagnosis von Mallmann, Michael R., Mack-Detlefsen, Birte, Reutter, Heiko, Pohle, Rebecca, Gottschalk, Ingo, Geipel, Annegret, Berg, Christoph, Boemers, Thomas M., Gembruch, Ulrich

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Stapled neoappendicostomy: A novel technique von Kastenberg, Zachary J., Arkin, Cameron, Wallis, M. Chad, Boemers, Thomas, Rollins, Michael D.

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Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula von Brosens, Erwin, Marsch, Florian, de Jong, Elisabeth M, Zaveri, Hitisha P, Hilger, Alina C, Choinitzki, Vera Gisela, Hölscher, Alice, Hoffmann, Per, Herms, Stefan, Boemers, Thomas M, Ure, Benno M, Lacher, Martin, Ludwig, Michael, Eussen, Bert H, van der Helm, Robert M, Douben, Hannie, Van Opstal, Diane, Wijnen, Rene M H, Beverloo, H Berna, van Bever, Yolande, Brooks, Alice S, IJsselstijn, Hanneke, Scott, Daryl A, Schumacher, Johannes, Tibboel, Dick, Reutter, Heiko, de Klein, Annelies

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Prenatal Diagnosis of Covered Cloacal Exstrophy von Mallmann, Michael R., Reutter, Heiko, Müller, Andreas, Boemers, Thomas M., Geipel, Annegret, Berg, Christoph, Gembruch, Ulrich

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Phenotype Severity in the Bladder Exstrophy-Epispadias Complex: Analysis of Genetic and Nongenetic Contributing Factors in 441 Families from North America and Europe von Reutter, Heiko, MD, Boyadjiev, Simeon A., MD, Gambhir, Lisa, MD, Ebert, Anne-Karoline, MD, Rösch, Wolfgang H., MD, Stein, Raimund, MD, Schröder, Annette, MD, Boemers, Thomas M., MD, Bartels, Enrika, MD, Vogt, Hannes, MD, Utsch, Boris, MD, Müller, Martin, MD, Detlefsen, Birte, MD, Zwink, Nadine, Dipl-Inform Med, Rogenhofer, Sebastian, MD, Gobet, Rita, MD, Beckers, Goedele M.A., MD, Bökenkamp, Arend, MD, Kajbafzadeh, Abdol-Mohammad, MD, Jaureguizar, Enrique, MD, Draaken, Markus, Dipl-Oecotroph, Lakshmanan, Yegappan, MD, Gearhart, John P., MD, Ludwig, Michael, PhD, Nöthen, Markus M., MD, Jenetzky, Ekkehart, MD

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Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region von Draaken, Markus, Baudisch, Friederike, Timmermann, Bernd, Kuhl, Heiner, Kerick, Martin, Proske, Judith, Wittler, Lars, Pennimpede, Tracie, Ebert, Anne-Karoline, Rösch, Wolfgang, Stein, Raimund, Bartels, Enrika, von Lowtzow, Catharina, Boemers, Thomas M., Herms, Stefan, Gearhart, John P., Lakshmanan, Yegappan, Kockum, Christina Clementsson, Holmdahl, Gundela, Läckgren, Göran, Nordenskjöld, Agnetha, Boyadjiev, Simeon A., Herrmann, Bernhard G., Nöthen, Markus M., Ludwig, Michael, Reutter, Heiko

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De novo microduplication at 22q11.21 in a patient with VACTERL association von Schramm, Charlotte, Draaken, Markus, Bartels, Enrika, Boemers, Thomas M, Aretz, Stefan, Brockschmidt, Felix F, Nöthen, Markus M, Ludwig, Michael, Reutter, Heiko

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Involvement of the WNT and FGF signaling pathways in non-isolated anorectal malformations: Sequencing analysis of WNT3A, WNT5A, WNT11, DACT1, FGF10, FGFR2 and the T gene von DRAAKEN, MARKUS, PRINS, WIEBKE, ZEIDLER, CLAUDIA, HILGER, ALINA, MUGHAL, SADAF S, LATUS, JEANETTE, BOEMERS, THOMAS M, SCHMIDT, DOMINIK, SCHMIEDEKE, EBERHARD, SPYCHALSKI, NICOLE, BARTELS, ENRIKA, NÖTHEN, MARKUS M, REUTTER, HEIKO, LUDWIG, MICHAEL

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Prenatal Diagnosis of Hydrocolpos: A Series of 20 Cases von Mallmann, Michael R, Reutter, Heiko, Mack-Detlefsen, Birte, Gottschalk, Ingo, Geipel, Annegret, Berg, Christoph, Boemers, Thomas M

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CNV analysis in 169 patients with bladder exstrophy-epispadias complex von von Lowtzow, Catharina, Hofmann, Andrea, Zhang, Rong, Marsch, Florian, Ebert, Anne-Karoline, Rösch, Wolfgang, Stein, Raimund, Boemers, Thomas M, Hirsch, Karin, Marcelis, Carlo, Feitz, Wouter F J, Brusco, Alfredo, Migone, Nicola, Di Grazia, Massimo, Moebus, Susanne, Nöthen, Markus M, Reutter, Heiko, Ludwig, Michael, Draaken, Markus

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Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies von Zeidler, Claudia, Woelfle, Joachim, Draaken, Markus, Mughal, Sadaf S., Große, Greta, Hilger, Alina C., Dworschak, Gabriel C., Boemers, Thomas M., Jenetzky, Ekkehart, Zwink, Nadine, Lacher, Martin, Schmidt, Dominik, Schmiedeke, Eberhard, Grasshoff-Derr, Sabine, Märzheuser, Stefanie, Holland-Cunz, Stefan, Schäfer, Mattias, Bartels, Enrika, Keppler, Kathleen, Palta, Markus, Leonhardt, Johannes, Kujath, Christina, Rißmann, Anke, Nöthen, Markus M., Reutter, Heiko, Ludwig, Michael

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Array‐based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL‐like patients identifies disease‐causing copy number variations von Zhang, Rong, Marsch, Florian, Kause, Franziska, Degenhardt, Franziska, Schmiedeke, Eeberhard, Märzheuser, Stefanie, Hoppe, Bernd, Bachour, Haitham, Boemers, Thomas M., Schäfer, Matthias, Spychalski, Nicole, Neser, Jörg, Leonhardt, Johannes, Kosch, Ferdinand, Ure, Benno, Gómez, Barbara, Lacher, Martin, Deffaa, Oliver J., Palta, Markus, Wittekindt, Boris, Kleine, Katharina, Schmedding, Andrea, Grasshoff‐Derr, Sabine, Ven, Amelie van der, Heilmann‐Heimbach, Stefanie, Zwink, Nadine, Jenetzky, Ekkehart, Ludwig, Michael, Reutter, Heiko

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