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dc.contributor.authorSoysal, Teoman
dc.contributor.authorEskazan, Ahmet Emre
dc.contributor.authorArguden, Yelda Tarkan
dc.contributor.authorUlku, Birsen
dc.contributor.authorHacihanefioglu, Seniha
dc.contributor.authorDeviren, Ayhan
dc.contributor.authorAr, Muhlis Cem
dc.contributor.authorYilmaz, Sukriye
dc.contributor.authorKuru, Dilhan
dc.contributor.authorCirakoglu, Ayse
dc.contributor.authorOngoren, Seniz
dc.date.accessioned2021-03-05T09:06:36Z
dc.date.available2021-03-05T09:06:36Z
dc.date.issued2011
dc.identifier.citationKuru D., Arguden Y. T. , Ar M. C. , Cirakoglu A., Ongoren S., Yilmaz S., Eskazan A. E. , Deviren A., Soysal T., Hacihanefioglu S., et al., "Variant Philadelphia translocations with different breakpoints in six chronic myeloid leukemia patients", TURKISH JOURNAL OF HEMATOLOGY, cilt.28, ss.186-192, 2011
dc.identifier.issn1300-7777
dc.identifier.othervv_1032021
dc.identifier.otherav_9c5b67a6-7568-4a05-93e3-6da86d2f8633
dc.identifier.urihttp://hdl.handle.net/20.500.12627/105066
dc.identifier.urihttps://doi.org/10.5152/tjh.2011.52
dc.description.abstractObjective: The Philadelphia (Ph) chromosome, consisting of the t(9;22)(q34;q11) translocation, is observed in similar to 90% of patients with chronic myeloid leukemia (CML). Variant Ph translocations are observed in 5%-40% of CML patients. In variant translocations 3 and possibly more chromosomes are involved. Herein we report 6 CML patients with variant Ph translocations.
dc.language.isoeng
dc.subjectHematoloji
dc.subjectİç Hastalıkları
dc.subjectHEMATOLOJİ
dc.subjectTıp
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.titleVariant Philadelphia translocations with different breakpoints in six chronic myeloid leukemia patients
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF HEMATOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume28
dc.identifier.issue3
dc.identifier.startpage186
dc.identifier.endpage192
dc.contributor.firstauthorID43611


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