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dc.contributor.authorCiavarella, N
dc.contributor.authorJohnson, KM
dc.contributor.authorTerry, VH
dc.contributor.authorWheatley, MA
dc.contributor.authorYang, A
dc.contributor.authorZivelin, A
dc.contributor.authorStefanile, C
dc.contributor.authorMatsushita, T
dc.contributor.authorSaito, H
dc.contributor.authorde Bosch, NB
dc.contributor.authorRuiz-Saez, A
dc.contributor.authorTorres, A
dc.contributor.authorThompson, AR
dc.contributor.authorFeinstein, DI
dc.contributor.authorWhite, GC
dc.contributor.authorNegrier, C
dc.contributor.authorTrzeciak, MC
dc.contributor.authorAktan, M
dc.contributor.authorKaufman, RJ
dc.contributor.authorMorris, MA
dc.contributor.authorMcVey, JH
dc.contributor.authorPeyvandi, F
dc.contributor.authorRossier, C
dc.contributor.authorAntonarakis, SE
dc.contributor.authorTuddenham, EGD
dc.contributor.authorGinsburg, D
dc.contributor.authorSeligsohn, U
dc.contributor.authorNichols, WC
dc.contributor.authorNeerman-Arbez, M
dc.date.accessioned2021-03-05T09:06:13Z
dc.date.available2021-03-05T09:06:13Z
dc.date.issued1998
dc.identifier.citationNichols W., Neerman-Arbez M., Johnson K., Terry V., Wheatley M., Yang A., Zivelin A., Ciavarella N., Stefanile C., Matsushita T., et al., "ERGIC-9 gene mutation analysis in combined factors V and VIII deficiency: Evidence for a second locus.", BLOOD, cilt.92, 1998
dc.identifier.issn0006-4971
dc.identifier.othervv_1032021
dc.identifier.otherav_9c52593d-9de1-4372-a824-c1c4ac02b563
dc.identifier.urihttp://hdl.handle.net/20.500.12627/105041
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectHEMATOLOJİ
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectHematoloji
dc.titleERGIC-9 gene mutation analysis in combined factors V and VIII deficiency: Evidence for a second locus.
dc.typeMakale
dc.relation.journalBLOOD
dc.contributor.department, ,
dc.identifier.volume92
dc.identifier.issue10
dc.contributor.firstauthorID121747


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