Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2.
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| Title: | Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2. |
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| Authors: | Burrill N; Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA., Khalek N; Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA.; Department of Surgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA., Cristancho AG; Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA.; Department of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA., Coleman B; Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA.; Department of Clinical Radiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA., Murrell J; Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA., Moldenhauer JS; Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA.; Department of Surgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA. |
| Source: | Prenatal diagnosis [Prenat Diagn] 2024 May; Vol. 44 (5), pp. 661-664. Date of Electronic Publication: 2024 Mar 28. |
| 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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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 38549198 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Burrill+N%22">Burrill N</searchLink>; Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Khalek+N%22">Khalek N</searchLink>; Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA.; Department of Surgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Cristancho+AG%22">Cristancho AG</searchLink>; Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA.; Department of Neurology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Coleman+B%22">Coleman B</searchLink>; Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA.; Department of Clinical Radiology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Murrell+J%22">Murrell J</searchLink>; Division of Genomic Diagnostics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Moldenhauer+JS%22">Moldenhauer JS</searchLink>; Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA.; Department of Surgery, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania, USA. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%228106540%22">Prenatal diagnosis</searchLink> [Prenat Diagn] 2024 May; Vol. 44 (5), pp. 661-664. <i>Date of Electronic Publication: </i>2024 Mar 28. – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; 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=38549198 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/pd.6560 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 661 Titles: – TitleFull: Fetus with multiple congenital anomaly syndrome caused by novel variant in ATP1A2. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Burrill N – PersonEntity: Name: NameFull: Khalek N – PersonEntity: Name: NameFull: Cristancho AG – PersonEntity: Name: NameFull: Coleman B – PersonEntity: Name: NameFull: Murrell J – PersonEntity: Name: NameFull: Moldenhauer JS IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: 2024 May Type: published Y: 2024 Identifiers: – Type: issn-electronic Value: 1097-0223 Numbering: – Type: volume Value: 44 – Type: issue Value: 5 Titles: – TitleFull: Prenatal diagnosis Type: main |
| ResultId | 1 |
