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Prognostic significance of the TEL-AML1 fusion gene in pediatric acute lymphoblastic leukemia in Turkey

dc.contributor.authorTimur, C
dc.contributor.authorSirma, S
dc.contributor.authorDevecioglu, O
dc.contributor.authorMeral, A
dc.contributor.authorGedikoglu, G
dc.contributor.authorOzbek, U
dc.contributor.authorAgaoglu, L
dc.contributor.authorYuksel, L
dc.contributor.authorAnak, S
dc.contributor.authorYildiz, I
dc.date.accessioned2021-03-02T22:31:30Z
dc.date.available2021-03-02T22:31:30Z
dc.date.issued2003
dc.identifier.citationOzbek U., Sirma S., Agaoglu L., Yuksel L., Anak S., Yildiz I., Devecioglu O., Timur C., Meral A., Gedikoglu G., "Prognostic significance of the TEL-AML1 fusion gene in pediatric acute lymphoblastic leukemia in Turkey", JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, cilt.25, sa.3, ss.204-208, 2003
dc.identifier.issn1077-4114
dc.identifier.othervv_1032021
dc.identifier.otherav_0d2f6cb6-e9ca-494d-bfe6-fb84f99a4cb3
dc.identifier.urihttp://hdl.handle.net/20.500.12627/14475
dc.identifier.urihttps://doi.org/10.1097/00043426-200303000-00005
dc.description.abstractPurpose: The t(12;21) translocation is the most common reciprocal chromosomal rearrangement in pediatric acute lymphoblastic leukemia (ALL). This translocation fuses two genes, TEL and AML1, and results in the production of the TEL-AML1 fusion protein. The authors investigated the incidence and prognostic significance of the TEL-AML1 fusion gene in patients with ALL in Turkey.
dc.language.isoeng
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectİç Hastalıkları
dc.subjectHematoloji
dc.subjectOnkoloji
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectPEDİATRİ
dc.subjectHEMATOLOJİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectONKOLOJİ
dc.titlePrognostic significance of the TEL-AML1 fusion gene in pediatric acute lymphoblastic leukemia in Turkey
dc.typeMakale
dc.relation.journalJOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
dc.contributor.department, ,
dc.identifier.volume25
dc.identifier.issue3
dc.identifier.startpage204
dc.identifier.endpage208
dc.contributor.firstauthorID70138


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