A Rare Abnormal Male Karyotype with 46,X,DER(Y)(YQTER›P11.3

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dc.contributor.authorOral, Diclehan
dc.contributor.authorBalkan, Mahmut
dc.contributor.authorTekeş, Selahattin
dc.contributor.authorYücel, İlyas
dc.contributor.authorErdal, Gülbahar Güzel
dc.contributor.authorBinici, Mahir
dc.contributor.authorKavak, Fikriye Fulya
dc.date.accessioned2025-03-08T18:27:45Z
dc.date.available2025-03-08T18:27:45Z
dc.date.issued2021
dc.departmentDicle Üniversitesi
dc.description.abstractObjective: 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.endpage46
dc.identifier.issn2146-6033
dc.identifier.issn2146-6033
dc.identifier.issue1
dc.identifier.startpage42
dc.identifier.urihttps://hdl.handle.net/11468/31197
dc.identifier.volume13
dc.language.isoen
dc.publisherVeysi AKPOLAT
dc.relation.ispartofInternational Archives of Medical Research
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_DergiPark_21250205
dc.subjectbalanced translocation
dc.subjectchromosome anomalies
dc.subjectinfertility
dc.titleA Rare Abnormal Male Karyotype with 46,X,DER(Y)(YQTER›P11.3
dc.typeArticle

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