Rare cytogenetic abnormalities and their clinical relevance in pediatric acute leukemia of Saudi Arabian population
Title: | Rare cytogenetic abnormalities and their clinical relevance in pediatric acute leukemia of Saudi Arabian population |
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Authors: | Alkhayat, Nawaf, Elyamany, Ghaleb, Elborai, Yasser, Sedick, Qanita, Alshahrani, Mohammad, Al Sharif, Omar, Alenezy, Abdulmalik, Hammdan, Amjad, Elghezal, Hatem, Alsuhaibani, Omar, Aljabry, Mansour, AlMoshary, May, Mussaed, Eman |
Source: | Molecular cytogenetics. 12(1):1-11 |
Availability: | http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100190430136.0x000001&indx=1&recIds=ETOCvdc_100190430136.0x000001 |
Database: | British Library Document Supply Centre Inside Serials & Conference Proceedings |
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RecordInfo | BibRecord: BibEntity: Languages: – Text: English PhysicalDescription: Pagination: PageCount: 11 StartPage: 1 Titles: – TitleFull: Rare cytogenetic abnormalities and their clinical relevance in pediatric acute leukemia of Saudi Arabian population Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Alkhayat, Nawaf – PersonEntity: Name: NameFull: Elyamany, Ghaleb – PersonEntity: Name: NameFull: Elborai, Yasser – PersonEntity: Name: NameFull: Sedick, Qanita – PersonEntity: Name: NameFull: Alshahrani, Mohammad – PersonEntity: Name: NameFull: Al Sharif, Omar – PersonEntity: Name: NameFull: Alenezy, Abdulmalik – PersonEntity: Name: NameFull: Hammdan, Amjad – PersonEntity: Name: NameFull: Elghezal, Hatem – PersonEntity: Name: NameFull: Alsuhaibani, Omar – PersonEntity: Name: NameFull: Aljabry, Mansour – PersonEntity: Name: NameFull: AlMoshary, May – PersonEntity: Name: NameFull: Mussaed, Eman IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Type: published Y: 2019 Identifiers: – Type: issn-print Value: 17558166 – Type: issn-locals Value: edsbl.Periodical Numbering: – Type: volume Value: 12 – Type: issue Value: 1 Titles: – TitleFull: Molecular cytogenetics Type: main |
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