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MOLECULAR ANALYSIS OF FGFR1-3, TWIST1, MSX2, POR, FREM1 AND RAB23 GENES IN SYNDROMIC AND NON-SYNDROMIC CRANIOSYNOSTOSIS CASES

dc.contributor.authorKaraman, Birsen
dc.contributor.authorAltunoglu, Umut
dc.contributor.authorBasaran, Seher
dc.contributor.authorToksoy, Guven
dc.contributor.authorKaraman, Volkan
dc.contributor.authorUyguner, Zehra Oya
dc.contributor.authorKayserili Karabey, Hulya
dc.contributor.authorAvci, Sahin
dc.date.accessioned2021-03-05T10:49:22Z
dc.date.available2021-03-05T10:49:22Z
dc.date.issued2019
dc.identifier.citationKaraman V., Toksoy G., Karaman B., Kayserili Karabey H., Basaran S., Altunoglu U., Avci S., Uyguner Z. O. , "MOLECULAR ANALYSIS OF FGFR1-3, TWIST1, MSX2, POR, FREM1 AND RAB23 GENES IN SYNDROMIC AND NON-SYNDROMIC CRANIOSYNOSTOSIS CASES", JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.82, ss.116-122, 2019
dc.identifier.othervv_1032021
dc.identifier.otherav_a5283f6e-c5f0-43a5-b421-0a7e5f217047
dc.identifier.urihttp://hdl.handle.net/20.500.12627/110444
dc.identifier.urihttps://doi.org/10.26650/iuitfd.422258
dc.description.abstractObjective: Craniosynostosis (CS) associated genes (FGFR1-3, TWIST1, MSX2, POR, FREM1 and RAB23) were investigated in order to determine the mutation rates and establish an effective flow chart for molecular genetic diagnosis for syndromic (SCS) and non-syndromic craniosynostosis (NSCS).
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleMOLECULAR ANALYSIS OF FGFR1-3, TWIST1, MSX2, POR, FREM1 AND RAB23 GENES IN SYNDROMIC AND NON-SYNDROMIC CRANIOSYNOSTOSIS CASES
dc.typeMakale
dc.relation.journalJOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Bilimler
dc.identifier.volume82
dc.identifier.issue2
dc.identifier.startpage116
dc.identifier.endpage122
dc.contributor.firstauthorID264655


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