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dc.contributor.authorAral, O
dc.contributor.authorInanc, Murat
dc.contributor.authorKonice, M
dc.contributor.authorOcal, L
dc.contributor.authorGul, A
dc.date.accessioned2021-03-03T15:58:41Z
dc.date.available2021-03-03T15:58:41Z
dc.date.issued2000
dc.identifier.citationGul A., Inanc M., Ocal L., Aral O., Konice M., "Familial aggregation of Behcet's disease in Turkey", ANNALS OF THE RHEUMATIC DISEASES, cilt.59, sa.8, ss.622-625, 2000
dc.identifier.issn0003-4967
dc.identifier.otherav_41c9f54d-8e1e-49fa-87a3-8d2afc06eed5
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/47952
dc.identifier.urihttps://doi.org/10.1136/ard.59.8.622
dc.description.abstractObjective-Familial aggregation of Behcet's disease has been reported previously. The current study aimed at investigating the sibling recurrence risk ratio (lambda s) for Behcet's disease, which is of value in the estimation of the magnitude of genetic factors in the pathogenesis of Behcet's disease. Methods-170 consecutive unrelated index cases (98 male, 72 female) were interviewed with a detailed questionnaire to ascertain their family trees and the manifestations of Behcet's disease in their relatives, Subsequently, the immediately older sibling, or if an older sibling was not available, the immediately younger sibling, was selected as the second sibling for the evaluation. These siblings were contacted by telephone, and all subjects with recurrent oral ulcers were invited for examination.
dc.language.isoeng
dc.subjectİç Hastalıkları
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleFamilial aggregation of Behcet's disease in Turkey
dc.typeMakale
dc.relation.journalANNALS OF THE RHEUMATIC DISEASES
dc.contributor.department, ,
dc.identifier.volume59
dc.identifier.issue8
dc.identifier.startpage622
dc.identifier.endpage625
dc.contributor.firstauthorID126129


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