A Case of Partial Trisomy 13 Findings with 46,XX,der(7)t(7;13)(p22;q31)mat Karyotype

dc.contributor.authorPerçin, E. Ferda
dc.contributor.authorSungu, Y. Selma
dc.contributor.authorRuhi, Hatice Ilgin
dc.contributor.authorErgur, Ayça Törel
dc.contributor.authorDüzcan, Füsun
dc.contributor.authorSezgin, İlhan
dc.date.accessioned2024-10-26T17:53:25Z
dc.date.available2024-10-26T17:53:25Z
dc.date.issued2000
dc.departmentSivas Cumhuriyet Üniversitesi
dc.description.abstract[No abstract available]
dc.identifier.endpage380
dc.identifier.issn1300-0144
dc.identifier.issue4
dc.identifier.scopus2-s2.0-84888037542
dc.identifier.scopusqualityQ3
dc.identifier.startpage377
dc.identifier.urihttps://hdl.handle.net/20.500.12418/26934
dc.identifier.volume30
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherTurkiye Klinikleri
dc.relation.ispartofTurkish Journal of Medical Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectpartial trisomy; translocation; Trisomy 13
dc.titleA Case of Partial Trisomy 13 Findings with 46,XX,der(7)t(7;13)(p22;q31)mat Karyotype
dc.typeArticle

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