3' UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay.
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| Title: | 3' UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay. |
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| Authors: | Bi X; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA., Mulhern MS; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.; Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA., Spiegel E; Department of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, NY 10032, USA., Wapner RJ; Department of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, NY 10032, USA., Levy B; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA., Bain JM; Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY 10032, USA., Liao J; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA. |
| Source: | Genes [Genes (Basel)] 2023 Aug 25; Vol. 14 (9). Date of Electronic Publication: 2023 Aug 25. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) 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: 37761828 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: 3' UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Bi+X%22">Bi X</searchLink>; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.<br /><searchLink fieldCode="AU" term="%22Mulhern+MS%22">Mulhern MS</searchLink>; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.; Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.<br /><searchLink fieldCode="AU" term="%22Spiegel+E%22">Spiegel E</searchLink>; Department of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, NY 10032, USA.<br /><searchLink fieldCode="AU" term="%22Wapner+RJ%22">Wapner RJ</searchLink>; Department of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, NY 10032, USA.<br /><searchLink fieldCode="AU" term="%22Levy+B%22">Levy B</searchLink>; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA.<br /><searchLink fieldCode="AU" term="%22Bain+JM%22">Bain JM</searchLink>; Department of Neurology, Columbia University Irving Medical Center, New York, NY 10032, USA.; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY 10032, USA.<br /><searchLink fieldCode="AU" term="%22Liao+J%22">Liao J</searchLink>; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY 10032, USA. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101551097%22">Genes</searchLink> [Genes (Basel)] 2023 Aug 25; Vol. 14 (9). <i>Date of Electronic Publication: </i>2023 Aug 25. – 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="%22MDPI%22">MDPI </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101551097 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2073-4425 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2220734425%22">20734425 </searchLink><i>NLM ISO Abbreviation: </i>Genes (Basel) <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=37761828 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.3390/genes14091687 Languages: – Code: eng Text: English Titles: – TitleFull: 3' UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Bi X – PersonEntity: Name: NameFull: Mulhern MS – PersonEntity: Name: NameFull: Spiegel E – PersonEntity: Name: NameFull: Wapner RJ – PersonEntity: Name: NameFull: Levy B – PersonEntity: Name: NameFull: Bain JM – PersonEntity: Name: NameFull: Liao J IsPartOfRelationships: – BibEntity: Dates: – D: 25 M: 08 Text: 2023 Aug 25 Type: published Y: 2023 Identifiers: – Type: issn-electronic Value: 2073-4425 Numbering: – Type: volume Value: 14 – Type: issue Value: 9 Titles: – TitleFull: Genes Type: main |
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