Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.
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| Title: | Currarino syndrome: a comprehensive genetic review of a rare congenital disorder. |
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| Authors: | Dworschak GC; Institute of Human Genetics, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127, Bonn, Germany. gabriel.dworschak@uni-bonn.de.; Institute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, 53115, Bonn, Germany. gabriel.dworschak@uni-bonn.de.; Department of Pediatrics, University Hospital Bonn, 53127, Bonn, Germany. gabriel.dworschak@uni-bonn.de., Reutter HM; Institute of Human Genetics, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.; Department of Neonatology and Pediatric Intensive Care, University Hospital Bonn, 53127, Bonn, Germany., Ludwig M; Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, 53127, Bonn, Germany. |
| Source: | Orphanet journal of rare diseases [Orphanet J Rare Dis] 2021 Apr 09; Vol. 16 (1), pp. 167. Date of Electronic Publication: 2021 Apr 09. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't; Review |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 33836786 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Currarino syndrome: a comprehensive genetic review of a rare congenital disorder. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Dworschak+GC%22">Dworschak GC</searchLink>; Institute of Human Genetics, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127, Bonn, Germany. gabriel.dworschak@uni-bonn.de.; Institute of Anatomy and Cell Biology, Medical Faculty, University of Bonn, 53115, Bonn, Germany. gabriel.dworschak@uni-bonn.de.; Department of Pediatrics, University Hospital Bonn, 53127, Bonn, Germany. gabriel.dworschak@uni-bonn.de.<br /><searchLink fieldCode="AU" term="%22Reutter+HM%22">Reutter HM</searchLink>; Institute of Human Genetics, Medical Faculty, University of Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.; Department of Neonatology and Pediatric Intensive Care, University Hospital Bonn, 53127, Bonn, Germany.<br /><searchLink fieldCode="AU" term="%22Ludwig+M%22">Ludwig M</searchLink>; Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, 53127, Bonn, Germany. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101266602%22">Orphanet journal of rare diseases</searchLink> [Orphanet J Rare Dis] 2021 Apr 09; Vol. 16 (1), pp. 167. <i>Date of Electronic Publication: </i>2021 Apr 09. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't; Review – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22BioMed+Central%22">BioMed Central </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>101266602 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1750-1172 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217501172%22">17501172 </searchLink><i>NLM ISO Abbreviation: </i>Orphanet J Rare Dis <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=33836786 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-021-01799-0 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 167 Titles: – TitleFull: Currarino syndrome: a comprehensive genetic review of a rare congenital disorder. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Dworschak GC – PersonEntity: Name: NameFull: Reutter HM – PersonEntity: Name: NameFull: Ludwig M IsPartOfRelationships: – BibEntity: Dates: – D: 09 M: 04 Text: 2021 Apr 09 Type: published Y: 2021 Identifiers: – Type: issn-electronic Value: 1750-1172 Numbering: – Type: volume Value: 16 – Type: issue Value: 1 Titles: – TitleFull: Orphanet journal of rare diseases Type: main |
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