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dc.contributor.authorSezgin, I.
dc.contributor.authorAltuntas, E.
dc.contributor.authorBora, A.
dc.contributor.authorKurtulgan, H.
dc.contributor.authorKoksal, B.
dc.contributor.authorMuderris, S.
dc.contributor.authorOzdemir, O.
dc.date.accessioned2019-07-27T12:10:23Z
dc.date.accessioned2019-07-28T10:14:13Z
dc.date.available2019-07-27T12:10:23Z
dc.date.available2019-07-28T10:14:13Z
dc.date.issued2009
dc.identifier.issn0967-3849
dc.identifier.urihttps://hdl.handle.net/20.500.12418/10108
dc.description7th European Cytogenetics Conference -- JUL 04-07, 2009 -- Stockholm, SWEDENen_US
dc.descriptionWOS: 000267485000105en_US
dc.description.abstracten_US
dc.description.sponsorshipEuropean Cytogeneticists Assocen_US
dc.language.isoengen_US
dc.publisherSPRINGERen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleHeterozygous deletion of exon 8 in WFS1 gene in two Wolfram Syndrome probands with hearing lossen_US
dc.typeconferenceObjecten_US
dc.relation.journalCHROMOSOME RESEARCHen_US
dc.contributor.department[Sezgin, I. -- Altuntas, E. -- Bora, A. -- Kurtulgan, H. -- Koksal, B. -- Muderris, S. -- Ozdemir, O.] Cumhuriyet Univ, Fac Med, Sivas, Turkeyen_US
dc.identifier.volume17en_US
dc.identifier.endpage60en_US
dc.identifier.startpage59en_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US


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