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dc.contributor.authorNasioulas, G.
dc.contributor.authorVenizelos, V.
dc.contributor.authorTansan, S.
dc.contributor.authorKaban, K.
dc.contributor.authorEniu, D. T.
dc.contributor.authorChiorean, A.
dc.contributor.authorAgiannitopoulos, K.
dc.contributor.authorPepe, G.
dc.contributor.authorTsaousis, G.
dc.contributor.authorPapadopoulou, E.
dc.contributor.authorKampouri, S.
dc.contributor.authorMaravelaki, S.
dc.contributor.authorFassas, A.
dc.contributor.authorChristodoulou, C.
dc.contributor.authorIosifidou, R.
dc.contributor.authorKarageorgopoulou, S.
dc.contributor.authorÖZMEN, Vahit
dc.contributor.authorMarkopoulos, C.
dc.contributor.authorNatsiopoulos, I.
dc.contributor.authorPapazisis, K.
dc.contributor.authorVasilaki-Antonatou, M.
dc.date.accessioned2021-12-10T09:50:02Z
dc.date.available2021-12-10T09:50:02Z
dc.date.issued2020
dc.identifier.citationAgiannitopoulos K., Pepe G., Papadopoulou E., Tsaousis G., Kampouri S., Maravelaki S., Fassas A., Christodoulou C., Iosifidou R., Karageorgopoulou S., et al., "Splicing variants in hereditary cancer genes: clinical utility of functional RNA analysis", EUROPEAN JOURNAL OF HUMAN GENETICS, cilt.28, sa.SUPPL 1, ss.538-539, 2020
dc.identifier.issn1018-4813
dc.identifier.othervv_1032021
dc.identifier.otherav_15989c84-2bdf-4d2f-b821-e0e4578f98d5
dc.identifier.urihttp://hdl.handle.net/20.500.12627/168584
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectBiochemistry, Genetics and Molecular Biology (miscellaneous)
dc.subjectGenetics
dc.subjectClinical Biochemistry
dc.subjectCancer Research
dc.subjectMolecular Biology
dc.subjectDrug Discovery
dc.subjectAging
dc.subjectGeneral Biochemistry, Genetics and Molecular Biology
dc.subjectBiochemistry
dc.subjectStructural Biology
dc.subjectGenetics (clinical)
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectYaşam Bilimleri (LIFE)
dc.titleSplicing variants in hereditary cancer genes: clinical utility of functional RNA analysis
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF HUMAN GENETICS
dc.contributor.departmentGenekor MSA , ,
dc.identifier.volume28
dc.identifier.issueSUPPL 1
dc.identifier.startpage538
dc.identifier.endpage539
dc.contributor.firstauthorID2718282


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