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Clinical and meiotic studies in an infertile man with Y; 13 translocation

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dc.contributor.authorMicic, M. (7005218196)
dc.contributor.authorNikolis, J. (6602309757)
dc.contributor.authorMicic, S. (7006493137)
dc.date.accessioned2025-06-12T11:55:26Z
dc.date.available2025-06-12T11:55:26Z
dc.date.issued1992
dc.description.abstractClinical and meiotic studies were done on an infertile man with a translocation between Yq and 13q, who was identified through the birth of his son with partial trisomy 13q. Seminal plasma transferrin showed preserved Sertoli cell function while lactate dehydrogenase C4 indicated hypospermatogenesis. A quadrivalent in diakinesis and spermatogenic arrest in the second meiotic division was detected. © 1992 Oxford University Press.
dc.identifier.urihttps://doi.org/10.1093/oxfordjournals.humrep.a137804
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-0026630015&doi=10.1093%2foxfordjournals.humrep.a137804&partnerID=40&md5=982e1fbe25db25143d4cabede4905309
dc.identifier.urihttps://remedy.med.bg.ac.rs/handle/123456789/1872
dc.subjectInfertility
dc.subjectMeiosis
dc.subjectTranslocation
dc.titleClinical and meiotic studies in an infertile man with Y; 13 translocation
dspace.entity.typePublication

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