Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy.
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| Title: | Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy. |
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| Authors: | Santoro SL; Division of Molecular and Human Genetics, Columbus, OH, USA., Hashimoto S, McKinney A, Mihalic Mosher T, Pyatt R, Reshmi SC, Astbury C, Hickey SE |
| Source: | Cytogenetic and genome research [Cytogenet Genome Res] 2017; Vol. 152 (2), pp. 105-109. Date of Electronic Publication: 2017 Jul 27. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101142708 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1424-859X (Electronic) Linking ISSN: 14248581 NLM ISO Abbreviation: Cytogenet Genome Res 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: 28746920 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Santoro+SL%22">Santoro SL</searchLink>; Division of Molecular and Human Genetics, Columbus, OH, USA.<br /><searchLink fieldCode="AU" term="%22Hashimoto+S%22">Hashimoto S</searchLink><br /><searchLink fieldCode="AU" term="%22McKinney+A%22">McKinney A</searchLink><br /><searchLink fieldCode="AU" term="%22Mihalic+Mosher+T%22">Mihalic Mosher T</searchLink><br /><searchLink fieldCode="AU" term="%22Pyatt+R%22">Pyatt R</searchLink><br /><searchLink fieldCode="AU" term="%22Reshmi+SC%22">Reshmi SC</searchLink><br /><searchLink fieldCode="AU" term="%22Astbury+C%22">Astbury C</searchLink><br /><searchLink fieldCode="AU" term="%22Hickey+SE%22">Hickey SE</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101142708%22">Cytogenetic and genome research</searchLink> [Cytogenet Genome Res] 2017; Vol. 152 (2), pp. 105-109. <i>Date of Electronic Publication: </i>2017 Jul 27. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22S%2E+Karger%22">S. Karger </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101142708 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1424-859X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2214248581%22">14248581 </searchLink><i>NLM ISO Abbreviation: </i>Cytogenet Genome Res <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=28746920 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1159/000478921 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 105 Titles: – TitleFull: Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Santoro SL – PersonEntity: Name: NameFull: Hashimoto S – PersonEntity: Name: NameFull: McKinney A – PersonEntity: Name: NameFull: Mihalic Mosher T – PersonEntity: Name: NameFull: Pyatt R – PersonEntity: Name: NameFull: Reshmi SC – PersonEntity: Name: NameFull: Astbury C – PersonEntity: Name: NameFull: Hickey SE IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: 2017 Type: published Y: 2017 Identifiers: – Type: issn-electronic Value: 1424-859X Numbering: – Type: volume Value: 152 – Type: issue Value: 2 Titles: – TitleFull: Cytogenetic and genome research Type: main |
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