View in EDS HTML Full Text PDF Full Text

A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound.

Saved in:
Bibliographic Details
Title: A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound.
Authors: Corsten-Janssen N; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Bouman K; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Diphoorn JCD; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Scheper AJ; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Kinds R; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., El Mecky J; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.; Clinical Ethics and Law, University of Southampton, Southampton, UK., Breet H; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Verheij JBGM; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Suijkerbuijk R; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Duin LK; Department of Obstetrics, Gynecology and Prenatal Diagnosis, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Manten GTR; Department of Obstetrics and Gynecology, Isala, Zwolle, The Netherlands., van Langen IM; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Sijmons RH; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Sikkema-Raddatz B; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., Westers H; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands., van Diemen CC; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Source: Prenatal diagnosis [Prenat Diagn] 2020 Sep; Vol. 40 (10), pp. 1300-1309. Date of Electronic Publication: 2020 Jul 20.
Publication Type: Evaluation Study; 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
Full text is not displayed to guests.
FullText Links:
  – Type: pdflink
Text:
  Availability: 1
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 32627857
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Corsten-Janssen+N%22">Corsten-Janssen N</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Bouman+K%22">Bouman K</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Diphoorn+JCD%22">Diphoorn JCD</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Scheper+AJ%22">Scheper AJ</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Kinds+R%22">Kinds R</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22El+Mecky+J%22">El Mecky J</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.; Clinical Ethics and Law, University of Southampton, Southampton, UK.<br /><searchLink fieldCode="AU" term="%22Breet+H%22">Breet H</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Verheij+JBGM%22">Verheij JBGM</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Suijkerbuijk+R%22">Suijkerbuijk R</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Duin+LK%22">Duin LK</searchLink>; Department of Obstetrics, Gynecology and Prenatal Diagnosis, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Manten+GTR%22">Manten GTR</searchLink>; Department of Obstetrics and Gynecology, Isala, Zwolle, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+Langen+IM%22">van Langen IM</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Sijmons+RH%22">Sijmons RH</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Sikkema-Raddatz+B%22">Sikkema-Raddatz B</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Westers+H%22">Westers H</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+Diemen+CC%22">van Diemen CC</searchLink>; Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%228106540%22">Prenatal diagnosis</searchLink> [Prenat Diagn] 2020 Sep; Vol. 40 (10), pp. 1300-1309. <i>Date of Electronic Publication: </i>2020 Jul 20.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Evaluation Study; Journal Article
– Name: TitleSource
  Label: Journal Info
  Group: Src
  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
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32627857
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1002/pd.5781
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 1300
    Titles:
      – TitleFull: A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Corsten-Janssen N
      – PersonEntity:
          Name:
            NameFull: Bouman K
      – PersonEntity:
          Name:
            NameFull: Diphoorn JCD
      – PersonEntity:
          Name:
            NameFull: Scheper AJ
      – PersonEntity:
          Name:
            NameFull: Kinds R
      – PersonEntity:
          Name:
            NameFull: El Mecky J
      – PersonEntity:
          Name:
            NameFull: Breet H
      – PersonEntity:
          Name:
            NameFull: Verheij JBGM
      – PersonEntity:
          Name:
            NameFull: Suijkerbuijk R
      – PersonEntity:
          Name:
            NameFull: Duin LK
      – PersonEntity:
          Name:
            NameFull: Manten GTR
      – PersonEntity:
          Name:
            NameFull: van Langen IM
      – PersonEntity:
          Name:
            NameFull: Sijmons RH
      – PersonEntity:
          Name:
            NameFull: Sikkema-Raddatz B
      – PersonEntity:
          Name:
            NameFull: Westers H
      – PersonEntity:
          Name:
            NameFull: van Diemen CC
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 09
              Text: 2020 Sep
              Type: published
              Y: 2020
          Identifiers:
            – Type: issn-electronic
              Value: 1097-0223
          Numbering:
            – Type: volume
              Value: 40
            – Type: issue
              Value: 10
          Titles:
            – TitleFull: Prenatal diagnosis
              Type: main
ResultId 1