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dc.contributor.authorOZBEK, UĞUR
dc.contributor.authorSIRMA, Serkan Önder
dc.contributor.authorNALCACI, Meliha
dc.contributor.authorCEFLE, Kıvanç
dc.contributor.authorYENEREL, Mustafa Nuri
dc.contributor.authorOZTURK, S
dc.contributor.authorBAGATIR, G
dc.contributor.authorPalanduz, S
dc.date.accessioned2021-03-06T13:09:01Z
dc.date.available2021-03-06T13:09:01Z
dc.identifier.citationBAGATIR G., SIRMA S. Ö. , Palanduz S., OZTURK S., CEFLE K., OZBEK U., YENEREL M. N. , NALCACI M., "The frequency of C609T polymorphism in the NQO1 gene and its relation to cytogenetic abnormalities in patients with myelodysplastic syndrome.", Cellular and molecular biology (Noisy-le-Grand, France), cilt.62, ss.61-5, 2016
dc.identifier.issn0145-5680
dc.identifier.othervv_1032021
dc.identifier.otherav_f73614e5-64aa-4d6d-9866-db59c45db95c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/161966
dc.identifier.urihttps://doi.org/10.14715/cmb/2016.62.7.11
dc.language.isoeng
dc.titleThe frequency of C609T polymorphism in the NQO1 gene and its relation to cytogenetic abnormalities in patients with myelodysplastic syndrome.
dc.typeMakale
dc.relation.journalCellular and molecular biology (Noisy-le-Grand, France)
dc.contributor.department, ,
dc.identifier.volume62
dc.identifier.startpage61
dc.identifier.endpage5
dc.contributor.firstauthorID124610


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