Cell-free DNA Testing in Routine Practice: Characterisation of a Cohort with Positive Results for Trisomies, Sex Chromosome Anomalies and Microdeletions

por Tekesin, Ismail
Publicado 2021

Prenatal Diagnosis and Clinical Course of a Patent Urachus Associated with an Allantoic Cord Cyst and a Giant Umbilical Cord

por Tekesin, Ismail, Küper-Steffen, Regina
Publicado 2018

Is Fetal Hydrops in Turner Syndrome a Risk Factor for the Development of Maternal Mirror Syndrome?

por Bedei, Ivonne Alexandra, Graf, Alexander, Gloning, Karl-Philipp, Meyer-Wittkopf, Matthias, Willner, Daria, Krapp, Martin, Hentze, Sabine, Scharf, Alexander, Degenhardt, Jan, Heling, Kai-Sven, Kozlowski, Peter, Trautmann, Kathrin, Jahns, Kai, Geipel, Anne, Tekesin, Ismail, Elsässer, Michael, Wilhelm, Lucas, Gottschalk, Ingo, Baumüller, Jan-Erik, Birdir, Cahit, Zöllner, Felix, Wolter, Aline, Schenk, Johanna, Gehrke, Tascha, Keil, Corinna, Espinosa, Jimmy, Axt-Fliedner, Roland
Publicado 2022

Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex

por Falb, Ruth J, Müller, Amelie J, Klein, Wolfram, Grimmel, Mona, Grasshoff, Ute, Spranger, Stephanie, Stöbe, Petra, Gauck, Darja, Kuechler, Alma, Dikow, Nicola, Schwaibold, Eva M C, Schmidt, Christoph, Averdunk, Luisa, Buchert, Rebecca, Heinrich, Tilman, Prodan, Natalia, Park, Joohyun, Kehrer, Martin, Sturm, Marc, Kelemen, Olga, Hartmann, Silke, Horn, Denise, Emmerich, Dirk, Hirt, Nina, Neumann, Armin, Kristiansen, Glen, Gembruch, Ulrich, Haen, Susanne, Siebert, Reiner, Hentze, Sabine, Hoopmann, Markus, Ossowski, Stephan, Waldmüller, Stephan, Beck-Wödl, Stefanie, Gläser, Dieter, Tekesin, Ismail, Distelmaier, Felix, Riess, Olaf, Kagan, Karl-Oliver, Dufke, Andreas, Haack, Tobias B
Publicado 2023