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A case of partial trisomy 13 findings with 46, XX, der (7)t(7;13)(p22;q31)mat karyotype

dc.contributor.authorE. Ferda Perçin
dc.contributor.authorY. Selma Sungu
dc.contributor.authorIlgın Hatice Ruhi
dc.contributor.authorTörel Ayça Ergür
dc.contributor.authorFüsun Duzcan
dc.contributor.authorİlhan Sezgin
dc.date.accessioned23.07.201910:49:13
dc.date.accessioned2019-07-23T16:19:54Z
dc.date.available23.07.201910:49:13
dc.date.available2019-07-23T16:19:54Z
dc.date.issued2000
dc.identifier.issn1300-0144
dc.identifier.urihttp://www.trdizin.gov.tr/publication/paper/detail/TVRJMk9UQXc=
dc.identifier.urihttps://hdl.handle.net/20.500.12418/1071
dc.description.abstract…en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCerrahien_US
dc.titleA case of partial trisomy 13 findings with 46, XX, der (7)t(7;13)(p22;q31)mat karyotypeen_US
dc.typeotheren_US
dc.relation.journalTurkish Journal of Medical Sciencesen_US
dc.contributor.departmentSivas Cumhuriyet Üniversitesien_US
dc.identifier.volume30en_US
dc.identifier.issue4en_US
dc.identifier.endpage380en_US
dc.identifier.startpage377en_US
dc.relation.publicationcategoryDiğeren_US]


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