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dc.contributor.authorYılmaz, M
dc.contributor.authorPEHLİVAN, Sacide
dc.contributor.authorÇağırgan, S
dc.contributor.authorOmay, Bedii S
dc.contributor.authorTombuloğlu, M
dc.contributor.authorKavaklı, K
dc.contributor.authorPehlivan, Mustafa
dc.contributor.authorBüyükkeçeci, F
dc.date.accessioned2021-03-06T10:10:58Z
dc.date.available2021-03-06T10:10:58Z
dc.date.issued2007
dc.identifier.citationPehlivan M., PEHLİVAN S., Büyükkeçeci F., Çağırgan S., Yılmaz M., Omay B. S. , Tombuloğlu M., Kavaklı K., "Factor VIII-intron 1 inversion of Hemophilia A patients in West Anatolia", BALKAN JOURNAL OF MEDICAL GENETICS, cilt.10, ss.49-50, 2007
dc.identifier.issn1311-0160
dc.identifier.otherav_e928b980-fa39-4bcd-97f4-3d73ebe00335
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/153208
dc.identifier.urihttps://doi.org/10.2478/v10034-007-0009-2
dc.description.abstractHemophilia A (HA) is a hereditary, life-threatening and disabling disorder. In this study, we have examined 61 unrelated HA patients in order to identify the incidence of the intron 1 factor VIII (FVIII) gene inversion in the West Anatolian population. According to the results of DNA analyses of the 61 HA patients, no intron 1 inversion of the FVIII gene was found.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titleFactor VIII-intron 1 inversion of Hemophilia A patients in West Anatolia
dc.typeMakale
dc.relation.journalBALKAN JOURNAL OF MEDICAL GENETICS
dc.contributor.departmentEge Üniversitesi , ,
dc.identifier.volume10
dc.identifier.issue1
dc.identifier.startpage49
dc.identifier.endpage50
dc.contributor.firstauthorID464388


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