BASAL CELL NEVUS (GORLIN) SYNDROME WITH A NOVEL HETEROZYGOUS DELETION FRAMESHIFT MUTATION (C.959DELC, P.VAL322 PHE FSX2) IN THE PTCH1 GENE ASSOCIATED WITH EPIRETINAL MEMBRANE, ODONTOGENIC KERATOCYSTS AND WITHOUT SKIN LESIONS AND FALX CEREBRI CALCIFICATION

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dc.contributor.authorAkaltun, A.
dc.contributor.authorEröz, Recep
dc.contributor.authorDoğan, Mustafa
dc.contributor.authorBolu, Semih
dc.contributor.authorÖnder, Halil İbrahim
dc.contributor.authorOnbaş, O.
dc.contributor.authorKocabay, Kenan
dc.date.accessioned2020-04-30T22:40:03Z
dc.date.available2020-04-30T22:40:03Z
dc.date.issued2016
dc.departmentDÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.descriptionWOS: 000380178500017en_US
dc.descriptionPubMed: 29485834en_US
dc.description.abstract…en_US
dc.identifier.endpage262en_US
dc.identifier.issn1015-8146
dc.identifier.issue2en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage259en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12684/2894
dc.identifier.volume27en_US
dc.identifier.wosWOS:000380178500017en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherMedecine Et Hygieneen_US
dc.relation.ispartofGenetic Counselingen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleBASAL CELL NEVUS (GORLIN) SYNDROME WITH A NOVEL HETEROZYGOUS DELETION FRAMESHIFT MUTATION (C.959DELC, P.VAL322 PHE FSX2) IN THE PTCH1 GENE ASSOCIATED WITH EPIRETINAL MEMBRANE, ODONTOGENIC KERATOCYSTS AND WITHOUT SKIN LESIONS AND FALX CEREBRI CALCIFICATIONen_US
dc.typeLetteren_US

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