A single center experience of prenatal parent-fetus trio exome sequencing for pregnancies with congenital anomalies

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A single center experience of prenatal parent-fetus trio exome sequencing for pregnancies with congenital anomalies

Author: Dufke, Andreas; Hoopmann, Markus; Waldmuller, Stephan; Prodan, Natalia Carmen; Beck-Woedl, Stefanie; Grasshoff, Ute; Heinrich, Tilman; Riess, Angelika; Kehrer, Martin; Falb, Ruth J.; Liebmann, Alexandra; Roggia, Cristiana; Stampfer, Miriam; Schadeck, Malou; Mueller, Amelie J.; Grimmel, Mona; Stoebe, Petra; Gauck, Darja; Buchert-Lo, Rebecca; Baumann, Sarah; Schaeferhoff, Karin; Bertrand, Miriam; Menden, Benita; Sturm, Marc; Schuetz, Leon; Riess, Olaf; Ossowski, Stephan; Haack, Tobias B.; Kagan, Karl Oliver
Tübinger Autor(en):
Dufke, Andreas
Hoopmann, Markus
Grasshoff, Ute
Heinrich, Tilman
Riess, Angelika
Kehrer, Martin
Liebmann, Alexandra
Roggia, Cristiana
Stampfer, Miriam
Schadeck, Malou
Grimmel, Mona
Gauck, Darja
Baumann, Sarah
Bertrand, Miriam
Menden, Benita
Sturm, Marc
Schuetz, Leon
Ossowski, Stephan
Kagan, Karl Oliver
Waldmüller, Stephan
Prodan, Natalia
Beck-Wödl, Stefanie
Falb, Ruth
Müller, Amelie Johanna
Stöbe, Petra
Buchert, Rebecca
Schäferhoff, Karin
Rieß, Olaf
Haack, Tobias
Published in: Prenatal Diagnosis (2022), Bd. 42, H. 7, S. 901-910
Verlagsangabe: Wiley
Language: English
Full text: http://dx.doi.org/10.1002/pd.6170
ISSN: 0197-3851
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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