Prenatal Ultrasonographic Features Associated With ARSL and X-Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series.
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| Title: | Prenatal Ultrasonographic Features Associated With ARSL and X-Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series. |
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| Authors: | Broeren E; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA., Stover S; Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, Tennessee, USA., Bennett K; Liverpool Centre for Genomic Medicine, Liverpool Women's Hospital, Liverpool, UK., Giordano J; Department of Obstetrics and Gynecology, Columbia University, New York, New York, USA., Galloway S; Department of Obstetrics and Gynecology, Columbia University, New York, New York, USA., Lauzon J; Department of Medical Genetics, Alberta Children's Hospital, Calgary, Canada., Rust L; Department of Clinical Genetics, Mayo Clinic, Rochester, Minnesota, USA., Suerink M; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands., van Haeringen A; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands., Reimers R; Departments of Genetics/Dysmorphology and Perinatology, Rady Children's Hospital, San Diego, California, USA.; Scripps Research, Scripps Research Translational Institute, San Diego, California, USA.; Department of Reproductive Sciences, University of California, San Diego, California, USA. |
| Corporate Authors: | Australian Genomic Autopsy Study Team |
| Source: | Prenatal diagnosis [Prenat Diagn] 2024 Dec; Vol. 44 (13), pp. 1663-1670. Date of Electronic Publication: 2024 Sep 23. |
| Publication Type: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Systematic Review |
| 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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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 39313411 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Prenatal Ultrasonographic Features Associated With ARSL and X-Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Broeren+E%22">Broeren E</searchLink>; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.<br /><searchLink fieldCode="AU" term="%22Stover+S%22">Stover S</searchLink>; Department of Obstetrics and Gynecology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.<br /><searchLink fieldCode="AU" term="%22Bennett+K%22">Bennett K</searchLink>; Liverpool Centre for Genomic Medicine, Liverpool Women's Hospital, Liverpool, UK.<br /><searchLink fieldCode="AU" term="%22Giordano+J%22">Giordano J</searchLink>; Department of Obstetrics and Gynecology, Columbia University, New York, New York, USA.<br /><searchLink fieldCode="AU" term="%22Galloway+S%22">Galloway S</searchLink>; Department of Obstetrics and Gynecology, Columbia University, New York, New York, USA.<br /><searchLink fieldCode="AU" term="%22Lauzon+J%22">Lauzon J</searchLink>; Department of Medical Genetics, Alberta Children's Hospital, Calgary, Canada.<br /><searchLink fieldCode="AU" term="%22Rust+L%22">Rust L</searchLink>; Department of Clinical Genetics, Mayo Clinic, Rochester, Minnesota, USA.<br /><searchLink fieldCode="AU" term="%22Suerink+M%22">Suerink M</searchLink>; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+Haeringen+A%22">van Haeringen A</searchLink>; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Reimers+R%22">Reimers R</searchLink>; Departments of Genetics/Dysmorphology and Perinatology, Rady Children's Hospital, San Diego, California, USA.; Scripps Research, Scripps Research Translational Institute, San Diego, California, USA.; Department of Reproductive Sciences, University of California, San Diego, California, USA. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22Australian+Genomic+Autopsy+Study+Team%22">Australian Genomic Autopsy Study Team</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%228106540%22">Prenatal diagnosis</searchLink> [Prenat Diagn] 2024 Dec; Vol. 44 (13), pp. 1663-1670. <i>Date of Electronic Publication: </i>2024 Sep 23. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Systematic Review – 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=39313411 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/pd.6649 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1663 Titles: – TitleFull: Prenatal Ultrasonographic Features Associated With ARSL and X-Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Broeren E – PersonEntity: Name: NameFull: Stover S – PersonEntity: Name: NameFull: Bennett K – PersonEntity: Name: NameFull: Giordano J – PersonEntity: Name: NameFull: Galloway S – PersonEntity: Name: NameFull: Lauzon J – PersonEntity: Name: NameFull: Rust L – PersonEntity: Name: NameFull: Suerink M – PersonEntity: Name: NameFull: van Haeringen A – PersonEntity: Name: NameFull: Reimers R IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: 2024 Dec Type: published Y: 2024 Identifiers: – Type: issn-electronic Value: 1097-0223 Numbering: – Type: volume Value: 44 – Type: issue Value: 13 Titles: – TitleFull: Prenatal diagnosis Type: main |
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