First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study

DSpace Repository

First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study

Author: Kagan, Karl Oliver; Hoopmann, Markus; Pfaff, Theresa; Prodan, Natalia; Wagner, Philipp; Schmid, Maximilian; Dufke, Andreas; Mau-Holzmann, Ulrike; Brucker, Sara; Marcato, Livia; Malvestiti, Barbara; Grati, Francesca Romana
Tübinger Autor(en):
Kagan, Karl Oliver
Hoopmann, Markus
Pfaff, Theresa
Prodan, Natalia
Dufke, Andreas
Brucker, Sara
Wagner, Philipp Georg
Mau-Holzmann, Ulrike A.
Published in: Fetal Diagnosis and Therapy (2020), Bd. 47, H. 11, S. 841-851
Verlagsangabe: Karger
Language: English
Full text: http://dx.doi.org/10.1159/000510069
ISSN: 1421-9964
DDC Classifikation: 610 - Medicine and health
Dokumentart: Artikel
Show full item record

This item appears in the following Collection(s)