1. Multicenter clinical experience with non‐invasive cell‐free DNA screening for monosomy X and related X‐chromosome variants. (9th February 2023) Authors: Bedei, Ivonne; Gehrke, Tascha; Gloning, Karl‐Philipp; Meyer‐Wittkopf, Matthias; Willner, Daria; Krapp, Martin; Scharf, Alexander; Degenhardt, Jan; Heling, Kai‐Sven; Kozlowski, Peter; Trautmann, Kathrin; Jahns, Kai M.; Geipel, Annegret; Baumüller, Jan‐Erik; Wilhelm, Lucas; Gottschalk, Ingo; Schröe... Other Names: Hui Lisa guestEditor.; Langlois Sylvie guestEditor. Journal: Prenatal diagnosis Issue: Volume 43:Number 2(2023) Page Start: 192 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Prenatal Diagnosis of Robin Sequence: Sensitivity, Specificity, and Clinical Relevance of an Index for Micrognathia. (August 2021) Authors: Kruse, Teresa; Neuschulz, Julia; Wilhelm, Lucas; Ritgen, Jochen; Braumann, Bert Journal: Cleft palate-craniofacial journal Issue: Volume 58:Number 8(2021) Page Start: 1012 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Turner syndrome‐omphalocele association: Incidence, karyotype, phenotype and fetal outcome. (31st January 2023) Authors: Bedei, Ivonne; Gloning, Karl‐Philipp; Joyeux, Luc; Meyer‐Wittkopf, Matthias; Willner, Daria; Krapp, Martin; Scharf, Alexander; Degenhardt, Jan; Heling, Kai‐Sven; Kozlowski, Peter; Trautmann, Kathrin; Jahns, Kai M.; Geipel, Annegret; Tekesin, Ismail; Elsässer, Michael; Wilhelm, Lucas; Gottschalk, ... Other Names: Hui Lisa guestEditor.; Langlois Sylvie guestEditor. Journal: Prenatal diagnosis Issue: Volume 43:Number 2(2023) Page Start: 183 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗