Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/49110
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dc.contributor.authorÇetin, G. Ozan-
dc.contributor.authorYalçın, Nagihan-
dc.date.accessioned2023-01-09T21:44:27Z-
dc.date.available2023-01-09T21:44:27Z-
dc.date.issued2010-
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/610737-
dc.identifier.urihttps://hdl.handle.net/11499/49110-
dc.language.isotren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleVANGL1 geni heterozigot missens V239I, R274Q, M328T mutasyonlarının nöral tüp defektlerinin etiyolojisindeki rolünün değerlendirilmesien_US
dc.typeProject-
dc.identifier.startpage1en_US
dc.identifier.endpage23en_US
dc.departmentPAUen_US
dc.identifier.trdizinid610737en_US
dc.ownerPamukkale University-
item.languageiso639-1tr-
item.openairetypeProject-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.01. Surgical Medicine-
Appears in Collections:Tıp Fakültesi Koleksiyonu
TR Dizin İndeksli Yayınlar Koleksiyonu / TR Dizin Indexed Publications Collection
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