{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,8]],"date-time":"2026-10-08T20:57:02Z","timestamp":1791493022510,"version":"4.3.4"},"reference-count":25,"publisher":"Elsevier BV","issue":"2","license":[{"start":{"date-parts":[[2005,7,1]],"date-time":"2005-07-01T00:00:00Z","timestamp":1120176000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Cancer Genetics and Cytogenetics"],"published-print":{"date-parts":[[2005,7]]},"DOI":"10.1016\/j.cancergencyto.2004.12.019","type":"journal-article","created":{"date-parts":[[2005,7,1]],"date-time":"2005-07-01T13:15:18Z","timestamp":1120223718000},"page":"188-192","source":"Crossref","is-referenced-by-count":28,"title":["Prognostic significance of del(20q) in patients with hematological malignancies"],"prefix":"10.1016","volume":"160","author":[{"given":"Jana","family":"B\u0159ezinov\u00e1","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zuzana","family":"Zemanov\u00e1","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"\u0160\u00e1rka","family":"Ransdorfov\u00e1","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lenka","family":"\u0160indel\u00e1\u0159ov\u00e1","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Magda","family":"\u0160i\u0161kov\u00e1","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Radana","family":"Neuwirtov\u00e1","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jaroslav","family":"\u010cerm\u00e1k","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kyra","family":"Michalov\u00e1","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.cancergencyto.2004.12.019_bib1","doi-asserted-by":"crossref","first-page":"507","DOI":"10.1111\/j.1365-2141.1966.tb00134.x","article-title":"The chromosomes in polycythaemia vera","volume":"12","author":"Kay","year":"1966","journal-title":"Br J Haematol"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib2","first-page":"127","article-title":"Cytogenetics of myelodysplastic syndromes","volume":"33","author":"Fenaux","year":"1996","journal-title":"Semin Hematol"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib3","doi-asserted-by":"crossref","first-page":"1701","DOI":"10.1002\/1097-0142(19920915)70:4+<1701::AID-CNCR2820701609>3.0.CO;2-S","article-title":"Cytogenetic analysis in the diagnosis of acute leukemia","volume":"70","author":"Heim","year":"1992","journal-title":"Cancer"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib4","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1002\/gcc.2870100204","article-title":"Cell lineage involvement of recurrent chromosomal abnormalities in hematologic neoplasms","volume":"10","author":"Knuutila","year":"1994","journal-title":"Genes Chromosomes Cancer"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib5","doi-asserted-by":"crossref","first-page":"2809","DOI":"10.1182\/blood.V83.10.2809.2809","article-title":"Deletion of chromosome 20q in myelodysplasia can occur in a multipotent precursor of both myeloid cells and B cells","volume":"83","author":"White","year":"1994","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib6","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1016\/0165-4608(94)00068-M","article-title":"Deletion 20q in association with Philadelphia chromosome positive acute lymphoblastic leukemia: a report of two cases","volume":"79","author":"Hollings","year":"1995","journal-title":"Cancer Genet Cytogenet"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib7","doi-asserted-by":"crossref","first-page":"3902","DOI":"10.1038\/sj.onc.1203728","article-title":"Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC\/BAC contig and identification of candidate genes","volume":"19","author":"Bench","year":"2000","journal-title":"Oncogene"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib8","doi-asserted-by":"crossref","first-page":"6692","DOI":"10.1073\/pnas.82.19.6692","article-title":"c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders","volume":"82","author":"Le Beau","year":"1985","journal-title":"Proc Natl Acad Sci U S A"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib9","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1016\/0165-4608(94)00150-A","article-title":"Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes","volume":"80","author":"Nacheva","year":"1995","journal-title":"Cancer Genet Cytogenet"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib10","first-page":"3424","article-title":"Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20","volume":"82","author":"Roulston","year":"1993","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib11","doi-asserted-by":"crossref","first-page":"3086","DOI":"10.1182\/blood.V84.9.3086.3086","article-title":"Molecular analysis of chromosome 20q deletion associated with myeloproliferative disorders and myelodysplastic syndromes","volume":"84","author":"Asimakopoulos","year":"1994","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib12","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1002\/gcc.2870110105","article-title":"Molecular heterogeneity at the breakpoints of smaller 20q deletions","volume":"11","author":"Hollings","year":"1994","journal-title":"Genes Chromosomes Cancer"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib13","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1002\/(SICI)1098-2264(199802)21:2<75::AID-GCC1>3.0.CO;2-4","article-title":"Refinement of the commonly deleted segment in myeloid leukemias with a del(20q)","volume":"21","author":"Wang","year":"1998","journal-title":"Genes Chromosomes Cancer"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib14","first-page":"15","article-title":"Abnormalities of the long arm of chromosome 20 in myeloid malignancies","volume":"85","author":"Nacheva","year":"1999","journal-title":"Cytogenet Cell Genet"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib15","doi-asserted-by":"crossref","first-page":"2079","DOI":"10.1182\/blood.V89.6.2079","article-title":"International scoring system for evaluating prognosis in myelodysplastic syndromes","volume":"89","author":"Greenberg","year":"1997","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib16","article-title":"ISCN 1995: an international system for human cytogenetic nomenclature (1995)","year":"1995"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib17","doi-asserted-by":"crossref","first-page":"819","DOI":"10.1016\/S0950-3536(98)80041-3","article-title":"Molecular genetics and cytogenetics of myeloproliferative disorders","volume":"11","author":"Bench","year":"1998","journal-title":"Baillieres Clin Haematol"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib18","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1016\/0165-4608(92)90043-8","article-title":"Clinical significance of the del(20q) chromosome in hematologic disorders","volume":"62","author":"Aatola","year":"1992","journal-title":"Cancer Genet Cytogenet"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib19","doi-asserted-by":"crossref","first-page":"386","DOI":"10.1182\/blood.V72.2.386.386","article-title":"A prospective long-term cytogenetic study in polycythemia vera in relation to treatment and clinical course","volume":"72","author":"Swolin","year":"1988","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib20","doi-asserted-by":"crossref","first-page":"219","DOI":"10.1046\/j.1365-2141.1996.d01-1896.x","article-title":"Deletions of chromosome 20q and the pathogenesis of myeloproliferative disorders","volume":"95","author":"Asimakopoulos","year":"1996","journal-title":"Br J Haematol"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib21","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1016\/S0165-4608(02)00622-2","article-title":"Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myeloid leukemia","volume":"140","author":"Matteucci","year":"2003","journal-title":"Cancer Genet Cytogenet"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib22","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1016\/S0165-4608(99)00142-9","article-title":"Fluorescence in situ hybridization confirmation of 5q deletions in patients with hematological malignancies","volume":"117","author":"B\u0159ezinov\u00e1","year":"2000","journal-title":"Cancer Genet Cytogenet"},{"issue":"Suppl 1","key":"10.1016\/j.cancergencyto.2004.12.019_bib23","first-page":"191","article-title":"Prognostic significance of deletion del(5)(q31) and complex chromosomal rearrangements in patients with myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML)","volume":"3","author":"Michalov\u00e1","year":"2002","journal-title":"Hematol J"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib24","first-page":"67","article-title":"The prognostic significance of deletion of the long arm of chromosome 20 in myeloid disorders","volume":"8","author":"Campbell","year":"1994","journal-title":"Leukemia"},{"key":"10.1016\/j.cancergencyto.2004.12.019_bib25","doi-asserted-by":"crossref","first-page":"347","DOI":"10.1046\/j.1365-2141.2001.02750.x","article-title":"The prognostic impact of karyotypic subgroups in myelodysplastic syndromes is strongly modified by sex","volume":"113","author":"Mauritzson","year":"2001","journal-title":"Br J Haematol"}],"container-title":["Cancer Genetics and Cytogenetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0165460805000166?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0165460805000166?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2020,4,8]],"date-time":"2020-04-08T03:02:46Z","timestamp":1586314966000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0165460805000166"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2005,7]]},"references-count":25,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2005,7]]}},"alternative-id":["S0165460805000166"],"URL":"https:\/\/doi.org\/10.1016\/j.cancergencyto.2004.12.019","relation":{},"ISSN":["0165-4608"],"issn-type":[{"value":"0165-4608","type":"print"}],"subject":[],"published":{"date-parts":[[2005,7]]}}}