Rare cytogenetic anomalies in two pediatric patients with acute leukemia
dc.authorid | Süreyya Bozkurt / 0000-0002-1765-9894 | en_US |
dc.authorscopusid | Süreyya Bozkurt / 55540860700 | |
dc.authorwosid | Süreyya Bozkurt / AAP-1146-2020 | |
dc.contributor.author | Bozkurt, Süreyya | |
dc.contributor.author | Ünal, Şule | |
dc.contributor.author | Bayhan, Turan | |
dc.contributor.author | Gümrük, Fatma | |
dc.contributor.author | Çetin, Mualla | |
dc.date.accessioned | 2020-08-30T20:06:19Z | |
dc.date.available | 2020-08-30T20:06:19Z | |
dc.date.issued | 2020 | |
dc.department | İstinye Üniversitesi, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü | en_US |
dc.description.abstract | Structural chromosomal abnormalities are frequently seen in both pediatric acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML) cases [1,2,3]. Although some chromosomal abnormalities are common, other abnormalities are rarely seen [4,5]. In this study two relatively rare cytogenetic abnormalities are reported. All procedures were performed in accordance with the Helsinki Declaration and approved by the local ethics committee (Approval No: GO 16/267-45). | en_US |
dc.identifier.citation | Bozkurt, S., Unal, S., Bayhan, T., Gumruk, F., & Cetin, M. (2020). Rare Cytogenetic Anomalies in Two Pediatric Patients with Acute Leukemia. TURKISH JOURNAL OF HEMATOLOGY, 37(2), 132–133. https://doi.org/10.4274/tjh.galenos.2020.2019.0425 | en_US |
dc.identifier.doi | 10.4274/tjh.galenos.2020.2019.0425 | en_US |
dc.identifier.endpage | 133 | en_US |
dc.identifier.issn | 1300-7777 | en_US |
dc.identifier.issn | 1308-5263 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.pmid | 32054260 | en_US |
dc.identifier.scopus | 2-s2.0-85084272002 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 132 | en_US |
dc.identifier.trdizinid | 365987 | en_US |
dc.identifier.uri | https://doi.org/10.4274/tjh.galenos.2020.2019.0425 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12713/473 | |
dc.identifier.volume | 37 | en_US |
dc.identifier.wos | WOS:000531086600012 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | TR-Dizin | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.institutionauthor | Bozkurt, Süreyya | en_US |
dc.language.iso | en | en_US |
dc.publisher | Galenos Yayincilik | en_US |
dc.relation.ispartof | Turkish Journal of Hematology | en_US |
dc.relation.publicationcategory | Diğer | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Acute Myeloid Leukemia | en_US |
dc.subject | Rare Cytogenetic Anomalies | en_US |
dc.subject | Karyotype | en_US |
dc.title | Rare cytogenetic anomalies in two pediatric patients with acute leukemia | en_US |
dc.title.alternative | Akut lösemili iki pediatrik hastada nadir görülen sitogenetik anomaliler | en_US |
dc.type | Letter | en_US |
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