dc.contributor.author | Güney, A.I. | |
dc.contributor.author | Javadova, D. | |
dc.contributor.author | Kirac, D. | |
dc.contributor.author | Ulucan, K. | |
dc.contributor.author | Koc, G. | |
dc.contributor.author | Ergec, D. | |
dc.contributor.author | Tavukcu, H. | |
dc.contributor.author | Tarcan, T. | |
dc.date.accessioned | 2021-12-21T08:41:57Z | |
dc.date.available | 2021-12-21T08:41:57Z | |
dc.date.issued | 2012 | |
dc.identifier.issn | 16765680 | |
dc.identifier.uri | https://doi.org/10.4238/2012.April.27.2 | |
dc.identifier.uri | http://dspace.yeniyuzyil.edu.tr:8080/xmlui/handle/20.500.12629/1558 | |
dc.description.abstract | Infertility affects about 10-15% of all couples attempting pregnancy with infertility attributed to the male partner in approximately half of the cases. Proposed causes of male infertility include sperm motility disturbances, Y chromosome microdeletions, | |
dc.language.iso | English | |
dc.publisher | Fundacao de Pesquisas Cientificas de Ribeirao Preto | |
dc.rights | All Open Access, Bronze, Green | |
dc.title | Detection of Y chromosome microdeletions and mitochondrial DNA mutations in male infertility patients | |
dc.type | Article | |
dc.relation.journal | Genetics and Molecular Research | |
dc.identifier.issue | 2 | |
dc.identifier.startpage | 1039 | |
dc.identifier.endpage | 1048 | |
dc.identifier.volume | 11 | |
dc.identifier.doi | 10.4238/2012.April.27.2 | |
dc.relation.issue | 2 | |
dc.relation.volume | 11 | |