1. Açık Erişim@BUU
  2. İndeksli Yayınlar
  3. Web of Science
Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/34992
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dc.contributor.authorGörükmez, Özlem-
dc.contributor.authorCarrillo, Jaime-
dc.contributor.authorPerona, R.-
dc.date.accessioned2023-11-23T11:24:40Z-
dc.date.available2023-11-23T11:24:40Z-
dc.date.issued2016-
dc.identifier.citationSağ, Ş. Ö. vd. (2016). "Dyskeratosis congenita: A case report". Genetic Counseling, 27(2), 263-267.en_US
dc.identifier.issn1015-8146-
dc.identifier.urihttp://hdl.handle.net/11452/34992-
dc.language.isoenen_US
dc.publisherMedecine et Hygieneen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBiotechnology & applied microbiologyen_US
dc.subjectGenetics & heredityen_US
dc.subjectMedical ethicsen_US
dc.subjectResearch & experimental medicineen_US
dc.subjectTelomerase componenten_US
dc.subjectMutationsen_US
dc.subjectDKC1en_US
dc.subject.meshAdulten_US
dc.subject.meshCell cycle proteinsen_US
dc.subject.meshDyskeratosis congenitaen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshNuclear proteinsen_US
dc.subject.meshYoung adulten_US
dc.titleDyskeratosis congenita: A case reporten_US
dc.typeLetteren_US
dc.identifier.wos000380178500018tr_TR
dc.identifier.scopus2-s2.0-85016206066tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-7612-0055tr_TR
dc.identifier.startpage263tr_TR
dc.identifier.endpage267tr_TR
dc.identifier.volume27tr_TR
dc.identifier.issue2tr_TR
dc.relation.journalGenetic Counselingen_US
dc.contributor.buuauthorSağ, Şebnem Özemri-
dc.contributor.buuauthorTopak, Ali-
dc.contributor.buuauthorTüre, Mehmet-
dc.contributor.buuauthorŞahintürk, Serdar-
dc.contributor.buuauthorGülten, Tuna-
dc.contributor.buuauthorYakut, Tahsin-
dc.contributor.researcheridAAH-8355-2021tr_TR
dc.contributor.researcheridHOQ-5853-2023tr_TR
dc.contributor.researcheridECY-8582-2022tr_TR
dc.contributor.researcheridACQ-9887-2022tr_TR
dc.contributor.researcheridEYU-9227-2022tr_TR
dc.contributor.researcheridGIS-1493-2022tr_TR
dc.relation.collaborationYurt dışıtr_TR
dc.relation.collaborationSanayitr_TR
dc.identifier.pubmed29485835tr_TR
dc.subject.wosBiotechnology & applied microbiologyen_US
dc.subject.wosGenetics & heredityen_US
dc.subject.wosMedical ethicsen_US
dc.subject.wosMedicine, research & experimentalen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ4en_US
dc.contributor.scopusid57193738647tr_TR
dc.contributor.scopusid55313334700tr_TR
dc.contributor.scopusid6602186133tr_TR
dc.contributor.scopusid57214054591tr_TR
dc.contributor.scopusid6505944216tr_TR
dc.contributor.scopusid6602802424tr_TR
dc.subject.emtreeCell cycle proteinen_US
dc.subject.emtreeDKC1 protein, humanen_US
dc.subject.emtreeNuclear proteinen_US
dc.subject.emtreeAdulten_US
dc.subject.emtreeAnemiaen_US
dc.subject.emtreeBone marrow depressionen_US
dc.subject.emtreeCase reporten_US
dc.subject.emtreeDental cariesen_US
dc.subject.emtreeDyskeratosis congenitaen_US
dc.subject.emtreeEsophagus stenosisen_US
dc.subject.emtreeEsophagus varicesen_US
dc.subject.emtreeFinger dermatoglyphicsen_US
dc.subject.emtreeGene mutationen_US
dc.subject.emtreeHeterozygoteen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeLetteren_US
dc.subject.emtreeLeukoplakiaen_US
dc.subject.emtreeLive birthen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeNail dystrophyen_US
dc.subject.emtreePancytopeniaen_US
dc.subject.emtreePeriodontal diseaseen_US
dc.subject.emtreePortal hypertensionen_US
dc.subject.emtreeSkin pigmentationen_US
dc.subject.emtreeSplenomegalyen_US
dc.subject.emtreeYoung adulten_US
dc.subject.emtreeDyskeratosis congenitaen_US
dc.subject.emtreeGeneticsen_US
dc.subject.emtreePathologyen_US
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