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Author/Creator Müller, Amelie J.

1. A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies. (20th May 2022)

Authors:
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,...
Other Names:
Van den Veyver Igna guestEditor.
Journal:
Prenatal diagnosis
Issue:
Volume 42:Number 7(2022)
Page Start:
901
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. Issue 2 (8th June 2022)

Authors:
Christensen, Maria B.; Levy, Amanda M.; Mohammadi, Nazanin A.; Niceta, Marcello; Kaiyrzhanov, Rauan; Dentici, Maria Lisa; Al Alam, Chadi; Alesi, Viola; Benoit, Valérie; Bhatia, Kailash P.; Bierhals, Tatjana; Boßelmann, Christian M.; Buratti, Julien; Callewaert, Bert; Ceulemans, Berten; Charles, P...
Journal:
Clinical genetics
Issue:
Volume 102:Issue 2(2022)
Page Start:
98
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗