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dc.contributor.authorKuskonmaz, Baris
dc.contributor.authorKafalı, Candaş
dc.contributor.authorAkcoren, Zuhal
dc.contributor.authorKarabulut, Halil G
dc.contributor.authorAkalın, İbrahim
dc.contributor.authorTuncer, A Murat
dc.date.accessioned2020-10-21T08:08:29Z
dc.date.available2020-10-21T08:08:29Z
dc.date.issued2007
dc.identifier.issn0145-2126
dc.identifier.urihttp://hdl.handle.net/11655/22987
dc.description.abstractWe read the interesting report by Wong et al. describing 8p11 stem cell syndrome in a 14-year-old Chinese boy [1]. We wish to report our recent observations on a 3-year-old boy with T-cell lymphoma who was referred to the Pediatric Hematology Department with an increased white blood cell count and atypical mononuclear cells on peripheral blood smear. On admission, physical examination revealed cervical, submandibular, axillary and inguinal lymphadenopathies, and hepatosplenomegaly 7 and 8 cm, respectively, below the costal margins.tr_TR
dc.language.isoentr_TR
dc.publisherElseviertr_TR
dc.relation.isversionof10.1016/j.leukres.2007.04.007
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.rights
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject8p11 myeloproliferative syndrometr_TR
dc.titleThe 8p11 Myeloproliferative Syndrome in A 3-year-Old Childtr_TR
dc.typeinfo:eu-repo/semantics/articletr_TR
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalLeukemia Researchtr_TR
dc.contributor.departmentÇocuk Sağlığı ve Hastalıklarıtr_TR
dc.identifier.volume32tr_TR
dc.identifier.issue1tr_TR
dc.description.indexWoStr_TR
dc.fundingYoktr_TR


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