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Mosaicism for copy number variations in the placenta is even more difficult to interpret than mosaicism for whole chromosome aneuploidy.

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Title: Mosaicism for copy number variations in the placenta is even more difficult to interpret than mosaicism for whole chromosome aneuploidy.
Authors: Lund ICB; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.; Department of Biomedicine, Aarhus University, Aarhus, Denmark., Becher N; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.; Department of Biomedicine, Aarhus University, Aarhus, Denmark., Graakjaer J; Department of Clinical Genetics, University Hospital of Southern Denmark, Sygehus Lillebaelt, Vejle, Denmark., Lildballe DL; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.; Department of Clinical Genetics, University Hospital of Southern Denmark, Sygehus Lillebaelt, Vejle, Denmark., Uldbjerg N; Department of Obstetrics and Gynaecology, Aarhus University Hospital, Aarhus, Denmark.; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark., Bogaard P; Department of Pathology, Aalborg University Hospital, Aalborg, Denmark., Petersen A; Department of Pathology, Aalborg University Hospital, Aalborg, Denmark., Vestergaard EM; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark., Vogel I; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Source: Prenatal diagnosis [Prenat Diagn] 2021 May; Vol. 41 (6), pp. 668-680. Date of Electronic Publication: 2021 Apr 24.
Publication Type: Journal Article
Journal Info: Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE
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  Data: Mosaicism for copy number variations in the placenta is even more difficult to interpret than mosaicism for whole chromosome aneuploidy.
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  Data: <searchLink fieldCode="AU" term="%22Lund+ICB%22">Lund ICB</searchLink>; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.; Department of Biomedicine, Aarhus University, Aarhus, Denmark.<br /><searchLink fieldCode="AU" term="%22Becher+N%22">Becher N</searchLink>; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.; Department of Biomedicine, Aarhus University, Aarhus, Denmark.<br /><searchLink fieldCode="AU" term="%22Graakjaer+J%22">Graakjaer J</searchLink>; Department of Clinical Genetics, University Hospital of Southern Denmark, Sygehus Lillebaelt, Vejle, Denmark.<br /><searchLink fieldCode="AU" term="%22Lildballe+DL%22">Lildballe DL</searchLink>; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.; Department of Clinical Genetics, University Hospital of Southern Denmark, Sygehus Lillebaelt, Vejle, Denmark.<br /><searchLink fieldCode="AU" term="%22Uldbjerg+N%22">Uldbjerg N</searchLink>; Department of Obstetrics and Gynaecology, Aarhus University Hospital, Aarhus, Denmark.; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.<br /><searchLink fieldCode="AU" term="%22Bogaard+P%22">Bogaard P</searchLink>; Department of Pathology, Aalborg University Hospital, Aalborg, Denmark.<br /><searchLink fieldCode="AU" term="%22Petersen+A%22">Petersen A</searchLink>; Department of Pathology, Aalborg University Hospital, Aalborg, Denmark.<br /><searchLink fieldCode="AU" term="%22Vestergaard+EM%22">Vestergaard EM</searchLink>; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.<br /><searchLink fieldCode="AU" term="%22Vogel+I%22">Vogel I</searchLink>; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Center for Fetal Diagnostics, Aarhus University Hospital, Aarhus, Denmark.; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
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  Data: <searchLink fieldCode="JN" term="%228106540%22">Prenatal diagnosis</searchLink> [Prenat Diagn] 2021 May; Vol. 41 (6), pp. 668-680. <i>Date of Electronic Publication: </i>2021 Apr 24.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley%22">Wiley </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>8106540 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1097-0223 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2201973851%22">01973851 </searchLink><i>NLM ISO Abbreviation: </i>Prenat Diagn <i>Subsets: </i>MEDLINE
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              Text: 2021 May
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