Apert Syndrome: Report of a rare congenital malformation
Title: | Apert Syndrome: Report of a rare congenital malformation |
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Authors: | Rathore, Ehsan, Rathore, Altaf Hussain |
Source: | Pakistan journal of medical sciences. 33(3):773-775 |
Availability: | http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCRN612028691&indx=1&recIds=ETOCRN612028691 |
Database: | British Library Document Supply Centre Inside Serials & Conference Proceedings |
FullText | Links: – Type: pdflink Text: Availability: 0 CustomLinks: – Url: https://resolver.ebsco.com/c/xy5jbn/result?sid=EBSCO:edsbl&genre=article&issn=1682024X&ISBN=&volume=33&issue=3&date=20170101&spage=773&pages=773-775&title=Pakistan journal of medical sciences&atitle=Apert%20Syndrome%3A%20Report%20of%20a%20rare%20congenital%20malformation&aulast=Rathore%2C%20Ehsan&id=DOI: Name: Full Text Finder (for New FTF UI) (s8985755) Category: fullText Text: Find It @ SCU Libraries MouseOverText: Find It @ SCU Libraries |
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RecordInfo | BibRecord: BibEntity: Languages: – Text: English PhysicalDescription: Pagination: PageCount: 3 StartPage: 773 Titles: – TitleFull: Apert Syndrome: Report of a rare congenital malformation Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Rathore, Ehsan – PersonEntity: Name: NameFull: Rathore, Altaf Hussain IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Type: published Y: 2017 Identifiers: – Type: issn-print Value: 1682024X – Type: issn-locals Value: edsbl.Periodical Numbering: – Type: volume Value: 33 – Type: issue Value: 3 Titles: – TitleFull: Pakistan journal of medical sciences Type: main |
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