Oligoasthenozoospermia with rare karyotype

Basit Öğe Kaydı
dc.contributor.authorÖzbey, Ülkü
dc.contributor.authorYüce, Hüseyin
dc.date.accessioned2026-08-12T16:07:57Z
dc.date.issued2007
dc.departmentFırat Üniversitesi
dc.description.abstractIn a couple who had been investigated because of infertility, oligo-asthenozoospermia was diagnosed in man, by sperm analysis. Cytogenetic analyse, the karyotype of man was exhibited as 46, XY, t(9;15) (pter ?q21.1
dc.identifier.endpage160
dc.identifier.issn1300-526X
dc.identifier.issue4
dc.identifier.scopus2-s2.0-38949199645
dc.identifier.scopusqualityN/A
dc.identifier.startpage158
dc.identifier.trdizinid81149
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/81149
dc.identifier.urihttps://hdl.handle.net/11508/40966
dc.identifier.volume22
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.language.isotr
dc.relation.ispartofGoztepe Tip Dergisi
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20260511
dc.subjectChromosomal translocation; Male infertility; Meiotic pattern; Oligoasthenozoospermia
dc.titleOligoasthenozoospermia with rare karyotype
dc.title.alternativeNadir karyotipli oligoastenozoospermi
dc.typeArticle

Dosyalar

Koleksiyon

Scopus İndeksli Yayınlar Koleksiyonu
TR-Dizin İndeksli Yayınlar Koleksiyonu