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Non-invasive prenatal testing offered as part of a combined first-trimester screening program identifies tetrasomy 18p in a high-risk pregnancy.

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Title: Non-invasive prenatal testing offered as part of a combined first-trimester screening program identifies tetrasomy 18p in a high-risk pregnancy.
Authors: Lildballe DL; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark., Vogel I; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark., Lund IC; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark., Stornes I; Department of Obstetrics and Gynecology, Regional Hospital Randers, Randers, Denmark., Jørgensen MW; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Department of Pathology Aarhus, University Hospital, Aarhus, Denmark., Vestergaard EM; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
Source: Prenatal diagnosis [Prenat Diagn] 2016 Dec; Vol. 36 (12), pp. 1112-1114. Date of Electronic Publication: 2016 Nov 10.
Publication Type: Case Reports; 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
Database: MEDLINE Ultimate
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  Data: Non-invasive prenatal testing offered as part of a combined first-trimester screening program identifies tetrasomy 18p in a high-risk pregnancy.
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  Data: <searchLink fieldCode="AU" term="%22Lildballe+DL%22">Lildballe DL</searchLink>; Department of Clinical Genetics, 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.<br /><searchLink fieldCode="AU" term="%22Lund+IC%22">Lund IC</searchLink>; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.<br /><searchLink fieldCode="AU" term="%22Stornes+I%22">Stornes I</searchLink>; Department of Obstetrics and Gynecology, Regional Hospital Randers, Randers, Denmark.<br /><searchLink fieldCode="AU" term="%22Jørgensen+MW%22">Jørgensen MW</searchLink>; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.; Department of Pathology Aarhus, University Hospital, Aarhus, Denmark.<br /><searchLink fieldCode="AU" term="%22Vestergaard+EM%22">Vestergaard EM</searchLink>; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
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  Data: <searchLink fieldCode="JN" term="%228106540%22">Prenatal diagnosis</searchLink> [Prenat Diagn] 2016 Dec; Vol. 36 (12), pp. 1112-1114. <i>Date of Electronic Publication: </i>2016 Nov 10.
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  Data: Case Reports; Journal Article
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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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        Value: 10.1002/pd.4943
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              Text: 2016 Dec
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