Hyperdiploid Karyotype in a Childhood MDS Patient

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dc.contributor.authorAcar, Hasan
dc.contributor.authorÇalışkan, Ümran
dc.contributor.authorKaynak, Murat
dc.contributor.authorYıldırım, Mahmut Selman
dc.contributor.authorLargaespada, Davıd A.
dc.date.accessioned2020-03-26T16:37:11Z
dc.date.available2020-03-26T16:37:11Z
dc.date.issued2001
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractWe present a rare case of a paediatric myelodysplastic syndrome (MDS) with congenital anomalies (frontal bossing and premature closure of anterior fontanelle). The case showed the clinical and biological features of a refractory anaemia excess blasts (RAEB). Bone marrow (BM) cytogenetics demonstrated a hyperdiploid karyotype, with several numerical abnormalities and unidentified rearrangements. Fluorescence in situ hybridization (FISH) using chromosome specific alpha -satellite and whole chromosome-specific painting probes verified the hyperdiploid karyotype, and confirmed the origin of the unknown markers and rearrangements more reliably than would be possible using conventional cytogenetic techniques.en_US
dc.identifier.citationAcar, H., Çalışkan, Ü., Kaynak, M., Yıldırım, M. S., Largaespada, D. A., (2001). Hyperdiploid Karyotype in a Childhood MDS Patient. Clinical and Laboratory Haematology, 23(4), 255-258. Doi: 10.1046/j.1365-2257.2001.00396.x
dc.identifier.doi10.1046/j.1365-2257.2001.00396.xen_US
dc.identifier.endpage258en_US
dc.identifier.issn0141-9854en_US
dc.identifier.issue4en_US
dc.identifier.pmid11683788en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage255en_US
dc.identifier.urihttps://dx.doi.org/10.1046/j.1365-2257.2001.00396.x
dc.identifier.urihttps://hdl.handle.net/20.500.12395/17559
dc.identifier.volume23en_US
dc.identifier.wosWOS:000171606400007en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.institutionauthorAcar, Hasan
dc.institutionauthorÇalışkan, Ümran
dc.institutionauthorKaynak, Murat
dc.institutionauthorYıldırım, Mahmut Selman
dc.language.isoenen_US
dc.publisherBlackwell Science Ltden_US
dc.relation.ispartofClinical and Laboratory Haematologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectMDS-RAEBen_US
dc.subjecthyperdiploiden_US
dc.titleHyperdiploid Karyotype in a Childhood MDS Patienten_US
dc.typeArticleen_US

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