A Rare Abnormal Male Karyotype with 46,X,DER(Y)(YQTER›P11.3
dc.contributor.author | Oral, Diclehan | |
dc.contributor.author | Balkan, Mahmut | |
dc.contributor.author | Tekeş, Selahattin | |
dc.contributor.author | Yücel, İlyas | |
dc.contributor.author | Erdal, Gülbahar Güzel | |
dc.contributor.author | Binici, Mahir | |
dc.contributor.author | Kavak, Fikriye Fulya | |
dc.date.accessioned | 2025-03-08T18:27:45Z | |
dc.date.available | 2025-03-08T18:27:45Z | |
dc.date.issued | 2021 | |
dc.department | Dicle Üniversitesi | |
dc.description.abstract | Objective: Structural chromosomal abnormalities such as translocation in males and y deletions in the molecular missile cause infertility and related azoospermia. The aim of this study was to perform the karyotype analysis of a 51-year-old male patient who was referred to Dicle University Faculty of Medicine, Department of Medical Biology and Genetics for karyotype analysis due to primary infertility. Methods: Chromosome analysis was performed in peripheral blood culture by applying the conventional cytogenetic method and GTG banding technique. Results: Chromosome analysis a rare abnormal karyotype with 46, X, der(Y) (Yqter›p11.3 | |
dc.identifier.endpage | 46 | |
dc.identifier.issn | 2146-6033 | |
dc.identifier.issn | 2146-6033 | |
dc.identifier.issue | 1 | |
dc.identifier.startpage | 42 | |
dc.identifier.uri | https://hdl.handle.net/11468/31197 | |
dc.identifier.volume | 13 | |
dc.language.iso | en | |
dc.publisher | Veysi AKPOLAT | |
dc.relation.ispartof | International Archives of Medical Research | |
dc.relation.publicationcategory | Makale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.snmz | KA_DergiPark_21250205 | |
dc.subject | balanced translocation | |
dc.subject | chromosome anomalies | |
dc.subject | infertility | |
dc.title | A Rare Abnormal Male Karyotype with 46,X,DER(Y)(YQTER›P11.3 | |
dc.type | Article |