Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations
Fabian, Julia, Dworschak, Gabriel C, Waffenschmidt, Lea, Schierbaum, Luca, Bendixen, Charlotte, Heilmann-Heimbach, Stefanie, Sivalingam, Sugirthan, Buness, Andreas, Schwarzer, Nicole, Boemers, Thomas M, Schmiedeke, Eberhard, Neser, Jörg, Leonhardt, Johannes, Kosch, Ferdinand, Weih, Sandra, Gielen, Helen Maya, Hosie, Stuart, Kabs, Carmen, Palta, Markus, Märzheuser, Stefanie, Bode, Lena Marie, Lacher, Martin, Schäfer, Frank-Mattias, Stehr, Maximilian, Knorr, Christian, Ure, Benno, Kleine, Katharina, Rolle, Udo, Zaniew, Marcin, Phillip, Grote, Zwink, Nadine, Jenetzky, Ekkehart, Reutter, Heiko, Hilger, Alina C
Published in European journal of human genetics : EJHG (01.01.2023)
Published in European journal of human genetics : EJHG (01.01.2023)
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Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia
Zhang, Rong, Gehlen, Jan, Kawalia, Amit, Melissari, Maria-Theodora, Dakal, Tikam Chand, Menon, Athira M, Höfele, Julia, Riedhammer, Korbinian, Waffenschmidt, Lea, Fabian, Julia, Breuer, Katinka, Kalanithy, Jeshurun, Hilger, Alina Christine, Sharma, Amit, Hölscher, Alice, Boemers, Thomas M, Pauly, Markus, Leutner, Andreas, Fuchs, Jörg, Seitz, Guido, Ludwikowski, Barbara M, Gomez, Barbara, Hubertus, Jochen, Heydweiller, Andreas, Kurz, Ralf, Leonhardt, Johannes, Kosch, Ferdinand, Holland-Cunz, Stefan, Münsterer, Oliver, Ure, Beno, Schmiedeke, Eberhard, Neser, Jörg, Degenhardt, Petra, Märzheuser, Stefanie, Kleine, Katharina, Schäfer, Mattias, Spychalski, Nicole, Deffaa, Oliver J, Gosemann, Jan-Hendrik, Lacher, Martin, Heilmann-Heimbach, Stefanie, Zwink, Nadine, Jenetzky, Ekkehart, Ludwig, Michael, Grote, Phillip, Schumacher, Johannes, Thiele, Holger, Reutter, Heiko, Santos-Cortez, Regie Lyn Pastor
Published in PloS one (05.06.2020)
Published in PloS one (05.06.2020)
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Re‐sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL‐like association, and isolated anorectal malformation
Thiem, Corina E., Stegmann, Jil D., Hilger, Alina C., Waffenschmidt, Lea, Bendixen, Charlotte, Köllges, Ricarda, Schmiedeke, Eberhard, Schäfer, Frank‐Mattias, Lacher, Martin, Kosch, Ferdinand, Grasshoff‐Derr, Sabine, Kabs, Carmen, Neser, Jörg, Jenetzky, Ekkehart, Fazaal, Julia, Schumacher, Johannes, Hoefele, Julia, Ludwig, Kerstin U., Reutter, Heiko
Published in Birth defects research (01.06.2022)
Published in Birth defects research (01.06.2022)
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Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations
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
Published in Birth defects research (17.07.2017)
Published in Birth defects research (17.07.2017)
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A Golgi deimpregnation study of neurons in the rhesus monkey visual cortex (areas 17 and 18)
Werner, L, Winkelmann, E, Koglin, A, Neser, J, Rodewohl, H
Published in Anatomy and embryology (01.01.1989)
Published in Anatomy and embryology (01.01.1989)
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