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dc.contributor.authorKumbasar, Gokce
dc.contributor.authorToksoy, Guven
dc.contributor.authorBasaran, Seher
dc.contributor.authorKaraman, Birsen
dc.date.accessioned2021-03-04T13:16:10Z
dc.date.available2021-03-04T13:16:10Z
dc.date.issued2019
dc.identifier.citationKumbasar G., Toksoy G., Basaran S., Karaman B., "Clinical Genetic Approach to De Novo Changes Identified in Array-CGH Analysis", GAZI MEDICAL JOURNAL, cilt.30, sa.4, ss.361-364, 2019
dc.identifier.othervv_1032021
dc.identifier.otherav_7b7e489a-e3ba-4b53-bb90-1c43bb39d1bc
dc.identifier.urihttp://hdl.handle.net/20.500.12627/84539
dc.identifier.urihttps://doi.org/10.12996/gmj.2019.93
dc.description.abstractObjective: In this study, it is planned to work with fluorescent in situ hybridization (FISH), quantitative polymerase chain reaction (Real-Time qPCR) or with another a-CGH platform to verify genomic imbalances detected in a-CGH examination. It is aimed to determine whether the change is clinically relevant, so that genotype-phenotype relationship can be established and contribute effective genetic counseling.
dc.language.isoeng
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectTIP, GENEL & İÇECEK
dc.subjectKlinik Tıp
dc.titleClinical Genetic Approach to De Novo Changes Identified in Array-CGH Analysis
dc.typeMakale
dc.relation.journalGAZI MEDICAL JOURNAL
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume30
dc.identifier.issue4
dc.identifier.startpage361
dc.identifier.endpage364
dc.contributor.firstauthorID260024


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