Yayın:
Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD

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dc.contributor.authorCangül, Hakan
dc.contributor.buuauthorTemel, Şehime Gülsün
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Genetik Ana Bilim Dalı
dc.contributor.orcid0000-0002-9802-0880
dc.contributor.researcheridAAG-8385-2021
dc.contributor.scopusid6507885442
dc.date.accessioned2024-02-06T07:29:22Z
dc.date.available2024-02-06T07:29:22Z
dc.date.issued2013-02
dc.identifier.citationTemel, Ş. G. ve Cangül, H. (2013). “Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD”. Journal of Pediatric Endocrinology and Metabolism, 26(1-2), 191-191.
dc.identifier.doi10.1515/jpem-2012-0280
dc.identifier.endpage191
dc.identifier.issn0334-018X
dc.identifier.issue1-2
dc.identifier.pubmed23457319
dc.identifier.scopus2-s2.0-84878328865
dc.identifier.startpage191
dc.identifier.urihttps://doi.org/10.1515/jpem-2012-0280
dc.identifier.urihttps://hdl.handle.net/11452/39555
dc.identifier.volume26
dc.identifier.wos000316895000033
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherWalter De Gruyter
dc.relation.collaborationYurt içi
dc.relation.journalJournal of Pediatric Endocrinology and Metabolism
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectEndocrinology & metabolism
dc.subjectPediatrics
dc.subjectTrue hermaphroditism
dc.subjectSry
dc.subject.emtreeTranscription factor Sox9
dc.subject.emtreeGene duplication
dc.subject.emtreeHuman
dc.subject.emtreeKaryotype 46,XX
dc.subject.emtreeLetter
dc.subject.emtreeMosaicism
dc.subject.emtreePhenotype
dc.subject.emtreeSex differentiation disorder
dc.subject.emtreeSRY gene
dc.subject.emtreeTestis
dc.subject.mesh46, XX testicular disorders of sex development
dc.subject.meshGene duplication
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshOvotesticular disorders of sex development
dc.subject.meshSOX9 transcription factor
dc.subject.scopusGonads; Disorders of Sex Development; Sex Determination
dc.subject.wosEndocrinology & metabolism
dc.subject.wosPediatrics
dc.titleDuplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD
dc.typeLetter
dc.wos.quartileQ4
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Genetik Ana Bilim Dalı
local.indexed.atWOS
local.indexed.atScopus
local.indexed.atPubMed

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