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dc.contributor.authorOgur, Gonul
dc.contributor.authorDuru, Feride
dc.contributor.authorOzyurek, Emel
dc.contributor.authorFisgin, Tunc
dc.date.accessioned2020-06-21T14:18:28Z
dc.date.available2020-06-21T14:18:28Z
dc.date.issued2012
dc.identifier.issn1077-4114
dc.identifier.issn1536-3678
dc.identifier.urihttps://doi.org/10.1097/MPH.0b013e318238866f
dc.identifier.urihttps://hdl.handle.net/20.500.12712/16430
dc.descriptionWOS: 000308353000005en_US
dc.descriptionPubMed: 22278197en_US
dc.description.abstractDevelopment of leukemia in patients with sexual chromosome abnormalities is relatively rare and mostly involves cases of monosomy X, Turner syndrome. Here, we report on a child having a 45,X/46,X,derY [?t(Yp;Yq)] chromosomal constitution (variant Turner syndrome) presenting with concordant acute myeloid leukemia and a rarely seen clonal neoplasic cell lineage-related karyotype, t(6;9)(p23;q34).en_US
dc.language.isoengen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.relation.isversionof10.1097/MPH.0b013e318238866fen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject45,X/46,X,derYen_US
dc.subjectacute myeloid leukemiaen_US
dc.subjectt(6;9)(p23;q34)en_US
dc.subjectvariant Turner syndromeen_US
dc.titlet(6;9)(p23;q34) Presenting Acute Myeloid Leukemia in a Child With an Unsuspected 45,X/46,X,derY [?t(Yp;Yq)] Chromosomal Constitution: Yet Another Y Chromosome Overdosage and Malignancy Associationen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume34en_US
dc.identifier.issue6en_US
dc.identifier.startpageE237en_US
dc.identifier.endpageE240en_US
dc.relation.journalJournal of Pediatric Hematology Oncologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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