Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/22404
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dc.contributor.authorErçelen, Nesrin-
dc.contributor.authorAcar, Hasan-
dc.date.accessioned2021-10-19T08:10:49Z-
dc.date.available2021-10-19T08:10:49Z-
dc.date.issued2006-05-15-
dc.identifier.citationYakut, T. vd. (2006). ''Meiotic segregation analysis of reciprocal translocations, both in sperms and blastomeres''. American Journal of Medical Genetics, 140A(10), 1074-1082.en_US
dc.identifier.issn1552-4825-
dc.identifier.urihttps://doi.org/10.1002/ajmg.a.31215-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.31215-
dc.identifier.urihttp://hdl.handle.net/11452/22404-
dc.description.abstractBalanced chromosomal rearrangements could lead to unbalanced segregation gametes during meiosis. In this Study, sperm flourescence ill situ hybridization (FISH) analysis of meiotic segregation products of four reciprocal translocations; 46,XY,t(7;10)(q21;q22), 46:XY,t(15;17)(q11;p12), 46,XY, t(6;13)(p21.1;q32), and 46,XY,t(1;13)(q24;q10) are presented. In three Out Of these four cases with t(15;17), t(6;13), and t(1;13) additional blastomere FISH analyses are also provided. multi-color FISH analysis was applied using diverse probe combinations specific for translocated chromosome segments. The average frequency of sperm nuclei bearing unbalanced products for t(7;10), t(15:17), t(6;13), and t(1;13) were 48.7%, 59.5%, 60.5%, and 62.9%, respectively. Frequencies of blastomeres comprising unbalanced products in Cases with t(15;17), t(6;13), and t(1:13) were 80% (12 of 15), 60% (3 of 5), and 50% (2 of 4), respectively. Chi-square test analysis showed significant differences in the meiotic segregation pattens Clue to the distribution and numbers of the chiasmatas that Could depend oil the size of the translocated segments (P < 0.001). In conclusion, FISH analysis of sperm and blastomere for reciprocal translocation carriers effectively estimates the approximate risk Of unbalanced products and this result might ensure Valuable genetic Counseling.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectGenetics & heredityen_US
dc.subjectSpermen_US
dc.subjectReciprocal translocationen_US
dc.subjectMeiotic segregationen_US
dc.subjectBlastomereen_US
dc.subjectPatternsen_US
dc.subjectDiagnosisen_US
dc.subjectAneuploidyen_US
dc.subjectSpermatozoaen_US
dc.subjectFishen_US
dc.subjectHeterozygotesen_US
dc.subjectCarriersen_US
dc.subjectCytogenetic analysisen_US
dc.subjectChromosome segregationen_US
dc.subjectIn-situ hybridizationen_US
dc.subject.meshTranslocation, geneticen_US
dc.subject.meshSpermatozoaen_US
dc.subject.meshModels, geneticen_US
dc.subject.meshMeiosisen_US
dc.subject.meshMaleen_US
dc.subject.meshKaryotypingen_US
dc.subject.meshInfertility, maleen_US
dc.subject.meshIn situ hybridization, fluorescenceen_US
dc.subject.meshHumansen_US
dc.subject.meshFemaleen_US
dc.subject.meshChromosome segregationen_US
dc.subject.meshBlastomeresen_US
dc.titleMeiotic segregation analysis of reciprocal translocations, both in sperms and blastomeresen_US
dc.typeArticleen_US
dc.identifier.wos000237171100006tr_TR
dc.identifier.scopus2-s2.0-33646230293tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Jinekoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0001-7904-883Xtr_TR
dc.identifier.startpage1074tr_TR
dc.identifier.endpage1082tr_TR
dc.identifier.volume140Atr_TR
dc.identifier.issue10tr_TR
dc.relation.journalAmerican Journal of Medical Geneticsen_US
dc.contributor.buuauthorYakut, Tahsin-
dc.contributor.buuauthorKimya, Yalçın-
dc.contributor.buuauthorEgeli, Ünal-
dc.contributor.researcheridAAH-1420-2021tr_TR
dc.relation.collaborationYurt içitr_TR
dc.relation.collaborationSanayitr_TR
dc.identifier.pubmed16596678tr_TR
dc.subject.wosGenetics & heredityen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ3en_US
dc.contributor.scopusid6602802424tr_TR
dc.contributor.scopusid6603919968tr_TR
dc.contributor.scopusid55665145000tr_TR
dc.subject.scopusRobertsonian Chromosome Translocation; Preimplantation Genetic Diagnosis; Chromosome Aberrationsen_US
dc.subject.emtreeSpermen_US
dc.subject.emtreePriority journalen_US
dc.subject.emtreeMeiosisen_US
dc.subject.emtreeKaryotype 46, XYen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHeterozygoteen_US
dc.subject.emtreeGenetic counselingen_US
dc.subject.emtreeGene probeen_US
dc.subject.emtreeGameteen_US
dc.subject.emtreeFluorescence in situ hybridizationen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeChromosome translocationen_US
dc.subject.emtreeChromosome segregationen_US
dc.subject.emtreeChromosome rearrangementen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBlastomereen_US
dc.subject.emtreeCell nucleusen_US
dc.subject.emtreeChromosome chiasmen_US
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