Publication:
A rare combination of 45,X/46,XY mosaicism and Y chromosome microdeletion in an infertile man with azoospermia

dc.contributor.authorAydemir, Hüseyin
dc.contributor.authorKarkucak, Mutlu
dc.contributor.authorCimen, Hacı İbrahim
dc.contributor.authorHalis, Fikret
dc.contributor.authorKumsar, Şükrü
dc.contributor.authorSonbahar, Adil E.
dc.contributor.buuauthorYakut, Tahsin
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Genetik Ana Bilim Dalı
dc.contributor.scopusid6602802424tr_TR
dc.date.accessioned2023-06-07T12:24:16Z
dc.date.available2023-06-07T12:24:16Z
dc.date.issued2016
dc.identifier.citationAydemir, H. vd. (2016). "A rare combination of 45,X/46,XY mosaicism and Y chromosome microdeletion in an infertile man with azoospermia". Genetic Counseling, 27(1), 95-98.en_US
dc.identifier.endpage98tr_TR
dc.identifier.issn1015-8146
dc.identifier.issue1tr_TR
dc.identifier.pubmed27192898tr_TR
dc.identifier.scopus2-s2.0-85001740534tr_TR
dc.identifier.startpage95tr_TR
dc.identifier.urihttp://hdl.handle.net/11452/32963
dc.identifier.volume27tr_TR
dc.identifier.wos000385210500012
dc.indexed.pubmedPubMeden_US
dc.indexed.scopusScopusen_US
dc.indexed.wosSCIEen_US
dc.language.isoenen_US
dc.publisherMedecine et Hygieneen_US
dc.relation.collaborationYurt içitr_TR
dc.relation.journalGenetic Counselingen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.rightsinfo:eu-repo/semantics/closedAccesstr_TR
dc.subjectBiotechnology & applied microbiologyen_US
dc.subjectGenetics & heredityen_US
dc.subjectMedical ethicsen_US
dc.subjectResearch & experimental medicineen_US
dc.subjectDeletionsen_US
dc.subject.emtree45,X/46,XY mosaicismen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAzoospermiaen_US
dc.subject.emtreeBlood samplingen_US
dc.subject.emtreeCase reporten_US
dc.subject.emtreeCentromereen_US
dc.subject.emtreeChromosome analysisen_US
dc.subject.emtreeChromosome deletion Yen_US
dc.subject.emtreeClinical articleen_US
dc.subject.emtreeDNA isolationen_US
dc.subject.emtreeDoppler ultrasonographyen_US
dc.subject.emtreeEchocardiographyen_US
dc.subject.emtreeGenetic variationen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeKaryotypeen_US
dc.subject.emtreeLetteren_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeMale infertilityen_US
dc.subject.emtreeMultiplex polymerase chain reactionen_US
dc.subject.emtreePhenotypeen_US
dc.subject.emtreeSemen analysisen_US
dc.subject.emtreeX chromosomeen_US
dc.subject.emtreeY chromosomeen_US
dc.subject.emtreeY chromosome microdeletionen_US
dc.subject.emtreeAzoospermiaen_US
dc.subject.emtreeChromosome deletionen_US
dc.subject.emtreeDisorder of sex developmenten_US
dc.subject.emtreeGeneticsen_US
dc.subject.emtreeMosaicismen_US
dc.subject.emtreeSex chromosome aberrationen_US
dc.subject.meshAdulten_US
dc.subject.meshAzoospermiaen_US
dc.subject.meshChromosome deletionen_US
dc.subject.meshChromosomes, human, Yen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshMosaicismen_US
dc.subject.meshSex chromosome aberrationsen_US
dc.subject.meshSex chromosome disorders of sex developmenten_US
dc.subject.wosBiotechnology & applied microbiologyen_US
dc.subject.wosGenetics & heredityen_US
dc.subject.wosMedical ethicsen_US
dc.subject.wosMedicine, research & experimentalen_US
dc.titleA rare combination of 45,X/46,XY mosaicism and Y chromosome microdeletion in an infertile man with azoospermiaen_US
dc.typeLetter
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Genetik Ana Bilim Dalıtr_TR

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