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

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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.scopusid6602802424
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.
dc.identifier.endpage98
dc.identifier.issn1015-8146
dc.identifier.issue1
dc.identifier.pubmed27192898
dc.identifier.scopus2-s2.0-85001740534
dc.identifier.startpage95
dc.identifier.urihttp://hdl.handle.net/11452/32963
dc.identifier.volume27
dc.identifier.wos000385210500012
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherMedecine et Hygiene
dc.relation.collaborationYurt içi
dc.relation.journalGenetic Counseling
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectBiotechnology & applied microbiology
dc.subjectGenetics & heredity
dc.subjectMedical ethics
dc.subjectResearch & experimental medicine
dc.subjectDeletions
dc.subject.emtree45,X/46,XY mosaicism
dc.subject.emtreeAdult
dc.subject.emtreeAzoospermia
dc.subject.emtreeBlood sampling
dc.subject.emtreeCase report
dc.subject.emtreeCentromere
dc.subject.emtreeChromosome analysis
dc.subject.emtreeChromosome deletion Y
dc.subject.emtreeClinical article
dc.subject.emtreeDNA isolation
dc.subject.emtreeDoppler ultrasonography
dc.subject.emtreeEchocardiography
dc.subject.emtreeGenetic variation
dc.subject.emtreeHuman
dc.subject.emtreeKaryotype
dc.subject.emtreeLetter
dc.subject.emtreeMale
dc.subject.emtreeMale infertility
dc.subject.emtreeMultiplex polymerase chain reaction
dc.subject.emtreePhenotype
dc.subject.emtreeSemen analysis
dc.subject.emtreeX chromosome
dc.subject.emtreeY chromosome
dc.subject.emtreeY chromosome microdeletion
dc.subject.emtreeAzoospermia
dc.subject.emtreeChromosome deletion
dc.subject.emtreeDisorder of sex development
dc.subject.emtreeGenetics
dc.subject.emtreeMosaicism
dc.subject.emtreeSex chromosome aberration
dc.subject.meshAdult
dc.subject.meshAzoospermia
dc.subject.meshChromosome deletion
dc.subject.meshChromosomes, human, Y
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMosaicism
dc.subject.meshSex chromosome aberrations
dc.subject.meshSex chromosome disorders of sex development
dc.subject.wosBiotechnology & applied microbiology
dc.subject.wosGenetics & heredity
dc.subject.wosMedical ethics
dc.subject.wosMedicine, research & experimental
dc.titleA rare combination of 45,X/46,XY mosaicism and Y chromosome microdeletion in an infertile man with azoospermia
dc.typeLetter
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Genetik Ana Bilim Dalı
local.indexed.atPubMed
local.indexed.atWOS

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