Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/6643
DC FieldValueLanguage
dc.contributor.authorVesna Škodrić-Trifunovićen_US
dc.contributor.authorMihailo Stjepanovićen_US
dc.contributor.authorŽivorad Savićen_US
dc.contributor.authorMiroslav Ilićen_US
dc.contributor.authorIvana Kavečanen_US
dc.contributor.authorJadranka Jovanović Privrodskien_US
dc.contributor.authorVesna Spasovskien_US
dc.contributor.authorMaja Stojiljkovićen_US
dc.contributor.authorSonja Pavlovićen_US
dc.date.accessioned2019-09-30T08:56:30Z-
dc.date.available2019-09-30T08:56:30Z-
dc.date.issued2015-01-01-
dc.identifier.issn3539504en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/6643-
dc.language.isoenen_US
dc.relation.ispartofCroatian Medical Journalen_US
dc.subjectmutationen_US
dc.subjectGorlin syndromeen_US
dc.subjectMolecular analysisen_US
dc.titleNovel Patched 1 mutations inpatients with nevoid basal cellcarcinoma syndrome - case reporten_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.3325/cmj.2015.56.63-
dc.identifier.pmid56-
dc.identifier.scopus2-s2.0-84924856778-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84924856778-
dc.description.versionPublisheden_US
dc.relation.lastpage67en_US
dc.relation.firstpage63en_US
dc.relation.issue1en_US
dc.relation.volume56en_US
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptMedicinski fakultet, Katedra za stomatologiju sa maksilofacijalnom hirurgijom-
crisitem.author.deptMedicinski fakultet, Katedra za pedijatriju-
crisitem.author.parentorgMedicinski fakultet-
crisitem.author.parentorgMedicinski fakultet-
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