A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies
Dufke, Andreas, Hoopmann, Markus, Waldmüller, Stephan, Prodan, Natalia Carmen, Beck‐Wödl, Stefanie, Grasshoff, Ute, Heinrich, Tilman, Riess, Angelika, Kehrer, Martin, Falb, Ruth J., Liebmann, Alexandra, Roggia, Cristiana, Stampfer, Miriam, Schadeck, Malou, Müller, Amelie J., Grimmel, Mona, Stöbe, Petra, Gauck, Darja, Buchert‐Lo, Rebecca, Baumann, Sarah, Schäferhoff, Karin, Bertrand, Miriam, Menden, Benita, Sturm, Marc, Schütz, Leon, Riess, Olaf, Ossowski, Stephan, Haack, Tobias B., Kagan, Karl Oliver
Published in Prenatal diagnosis (01.06.2022)
Published in Prenatal diagnosis (01.06.2022)
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