i(22)(q10) in myeloid malignancies

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dc.contributor.author Zamecnikova, Adriana -
dc.date.accessioned 2019-05-16T09:22:35Z
dc.date.available 2019-05-16T09:22:35Z
dc.date.issued 2019 -
dc.identifier.citation Adriana, Zamecnikova. i(22)(q10) in myeloid malignancies. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2019, 4, p. 95-97 -
dc.identifier.issn 1768-3262 -
dc.identifier.uri http://hdl.handle.net/2042/70185
dc.description.abstract Isochromosome i(22)(q10) is a rare but non-random karyotypic change in hematologic malignancies, often associated with complex karyotypes and with partial or complete loss of chromosomes 5 and/or 7. en
dc.language.iso en -
dc.publisher ARMGHM - Atlas Génétique des Cancers -
dc.relation Atlas of Genetics and Cytogenetics in Oncology and Haematology ; http://AtlasGeneticsOncology.org/Anomalies/iso22qMyeloID1819.html -
dc.relation.ispartofseries Atlas of Genetics and Cytogenetics in Oncology and Haematology en
dc.rights Open access resource - terms and conditions : http://irevues.inist.fr/utilisation -
dc.subject Isochromosome en
dc.subject chromosome 22 en
dc.subject.classification Leukaemia Section en
dc.title i(22)(q10) in myeloid malignancies en
dc.type Article -
dc.contributor.affiliation Kuwait Cancer Control Center, Kuwait -
dc.identifier.doi https://doi.org/10.4267/2042/70185

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