dc.contributor.author | Ogur, Gonul | |
dc.contributor.author | Duru, Feride | |
dc.contributor.author | Ozyurek, Emel | |
dc.contributor.author | Fisgin, Tunc | |
dc.date.accessioned | 2020-06-21T14:18:28Z | |
dc.date.available | 2020-06-21T14:18:28Z | |
dc.date.issued | 2012 | |
dc.identifier.issn | 1077-4114 | |
dc.identifier.issn | 1536-3678 | |
dc.identifier.uri | https://doi.org/10.1097/MPH.0b013e318238866f | |
dc.identifier.uri | https://hdl.handle.net/20.500.12712/16430 | |
dc.description | WOS: 000308353000005 | en_US |
dc.description | PubMed: 22278197 | en_US |
dc.description.abstract | Development 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.iso | eng | en_US |
dc.publisher | Lippincott Williams & Wilkins | en_US |
dc.relation.isversionof | 10.1097/MPH.0b013e318238866f | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | 45,X/46,X,derY | en_US |
dc.subject | acute myeloid leukemia | en_US |
dc.subject | t(6;9)(p23;q34) | en_US |
dc.subject | variant Turner syndrome | en_US |
dc.title | t(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 Association | en_US |
dc.type | article | en_US |
dc.contributor.department | OMÜ | en_US |
dc.identifier.volume | 34 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.startpage | E237 | en_US |
dc.identifier.endpage | E240 | en_US |
dc.relation.journal | Journal of Pediatric Hematology Oncology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |