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The frequency of C609T polymorphism in the NQO1 gene and its relation to cytogenetic abnormalities in patients with myelodysplastic syndrome.

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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