Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.
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| Title: | Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation. |
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| 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 |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 38593251 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| 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 |
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