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dc.contributor.authorWallace, Graham R.
dc.contributor.authorGÜL, Ahmet
dc.date.accessioned2022-02-18T09:22:58Z
dc.date.available2022-02-18T09:22:58Z
dc.identifier.citationGÜL A., Wallace G. R. , "Genetics of Behcet's Disease", BEHCET SYNDROME, 2ND EDITION, ss.223-233, 2020
dc.identifier.otherav_359bee70-535c-4edf-9bbc-1bfd3873171b
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/177096
dc.identifier.urihttps://doi.org/10.1007/978-3-030-24131-5_16
dc.description.abstractBehcet's disease (BD) is a systemic inflammatory disorder of unknown etiology. It is generally accepted as a multifactorial disease with a strong genetic background, and the disease manifestations are considered to be triggered by various environmental agents in genetically susceptible individuals [1, 2].
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectHistology
dc.subjectPathology and Forensic Medicine
dc.subjectFamily Practice
dc.subjectFundamentals and Skills
dc.subjectGeneral Health Professions
dc.subjectPathophysiology
dc.subjectBiochemistry (medical)
dc.subjectAssessment and Diagnosis
dc.subjectMedicine (miscellaneous)
dc.subjectGeneral Medicine
dc.subjectHealth Sciences
dc.subjectInternal Medicine
dc.subjectTIP, GENEL & İÇECEK
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectPATOLOJİ
dc.subjectBiyoloji ve Biyokimya
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectCerrahi Tıp Bilimleri
dc.subjectPatoloji
dc.titleGenetics of Behcet's Disease
dc.typeMakale
dc.relation.journalBEHCET SYNDROME, 2ND EDITION
dc.contributor.departmentİstanbul Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.identifier.startpage223
dc.identifier.endpage233
dc.contributor.firstauthorID3142112


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