Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.

Saved in:
Bibliographic Details
Title: Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.
Authors: Goldmuntz E; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, USA., Bassett AS; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.; Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada., Boot E; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands.; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands., Marino B; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome (Italy), Roma, Italy., Moldenhauer JS; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, Section of Genetic Counseling, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Departments of Obstetrics and Gynecology and Surgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA., Óskarsdóttir S; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Rheumatology and Immunology, Queen Silvia Children's Hospital, Gothenburg, Sweden., Putotto C; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome (Italy), Roma, Italy., Rychik J; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, USA., Schindewolf E; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, Section of Genetic Counseling, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA., McDonald-McGinn DM; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, Section of Genetic Counseling, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Human Biology and Medical Genetics, Sapienza University, Rome, Italy., Blagowidow N; The Harvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, Maryland, USA.
Source: Prenatal diagnosis [Prenat Diagn] 2024 Jun; Vol. 44 (6-7), pp. 804-814. Date of Electronic Publication: 2024 Apr 09.
Publication Type: Journal Article; Review; Research Support, N.I.H., Extramural
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: 38593251
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Goldmuntz+E%22">Goldmuntz E</searchLink>; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Bassett+AS%22">Bassett AS</searchLink>; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.; Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.; Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Boot+E%22">Boot E</searchLink>; The Dalglish Family 22q Clinic, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.; Advisium, 's Heeren Loo Zorggroep, Amersfoort, The Netherlands.; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Marino+B%22">Marino B</searchLink>; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome (Italy), Roma, Italy.<br /><searchLink fieldCode="AU" term="%22Moldenhauer+JS%22">Moldenhauer JS</searchLink>; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, Section of Genetic Counseling, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Departments of Obstetrics and Gynecology and Surgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Óskarsdóttir+S%22">Óskarsdóttir S</searchLink>; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.; Department of Rheumatology and Immunology, Queen Silvia Children's Hospital, Gothenburg, Sweden.<br /><searchLink fieldCode="AU" term="%22Putotto+C%22">Putotto C</searchLink>; Department of Maternal Infantile and Urological Sciences, Sapienza University of Rome (Italy), Roma, Italy.<br /><searchLink fieldCode="AU" term="%22Rychik+J%22">Rychik J</searchLink>; Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Schindewolf+E%22">Schindewolf E</searchLink>; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, Section of Genetic Counseling, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22McDonald-McGinn+DM%22">McDonald-McGinn DM</searchLink>; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.; Division of Human Genetics, 22q and You Center, Clinical Genetics Center, Section of Genetic Counseling, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.; Department of Human Biology and Medical Genetics, Sapienza University, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Blagowidow+N%22">Blagowidow N</searchLink>; The Harvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, Maryland, USA.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%228106540%22">Prenatal diagnosis</searchLink> [Prenat Diagn] 2024 Jun; Vol. 44 (6-7), pp. 804-814. <i>Date of Electronic Publication: </i>2024 Apr 09.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Journal Article; Review; Research Support, N.I.H., Extramural
– 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=38593251
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1002/pd.6566
    Languages:
      – Code: eng
        Text: English
    PhysicalDescription:
      Pagination:
        StartPage: 804
    Titles:
      – TitleFull: Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Goldmuntz E
      – PersonEntity:
          Name:
            NameFull: Bassett AS
      – PersonEntity:
          Name:
            NameFull: Boot E
      – PersonEntity:
          Name:
            NameFull: Marino B
      – PersonEntity:
          Name:
            NameFull: Moldenhauer JS
      – PersonEntity:
          Name:
            NameFull: Óskarsdóttir S
      – PersonEntity:
          Name:
            NameFull: Putotto C
      – PersonEntity:
          Name:
            NameFull: Rychik J
      – PersonEntity:
          Name:
            NameFull: Schindewolf E
      – PersonEntity:
          Name:
            NameFull: McDonald-McGinn DM
      – PersonEntity:
          Name:
            NameFull: Blagowidow N
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 06
              Text: 2024 Jun
              Type: published
              Y: 2024
          Identifiers:
            – Type: issn-electronic
              Value: 1097-0223
          Numbering:
            – Type: volume
              Value: 44
            – Type: issue
              Value: 6-7
          Titles:
            – TitleFull: Prenatal diagnosis
              Type: main
ResultId 1