{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,29]],"date-time":"2025-10-29T06:07:06Z","timestamp":1761718026343},"reference-count":32,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2007,2,1]],"date-time":"2007-02-01T00:00:00Z","timestamp":1170288000000},"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":[[2007,2]]},"DOI":"10.1016\/j.cancergencyto.2006.09.003","type":"journal-article","created":{"date-parts":[[2007,2,5]],"date-time":"2007-02-05T12:40:54Z","timestamp":1170679254000},"page":"10-16","source":"Crossref","is-referenced-by-count":14,"title":["Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies"],"prefix":"10.1016","volume":"173","author":[{"given":"Jana","family":"B\u0159ezinov\u00e1","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zuzana","family":"Zemanov\u00e1","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"\u0160\u00e1rka","family":"Ransdorfov\u00e1","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lenka","family":"Pavli\u0161tov\u00e1","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Libu\u0161e","family":"Babick\u00e1","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lucie","family":"Hou\u0161kov\u00e1","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jela","family":"Melicher\u010d\u00edkov\u00e1","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Magda","family":"\u0160i\u0161kov\u00e1","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jaroslav","family":"\u010cerm\u00e1k","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kyra","family":"Michalov\u00e1","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.cancergencyto.2006.09.003_bib1","doi-asserted-by":"crossref","first-page":"325","DOI":"10.1200\/JCO.1986.4.3.325","article-title":"Clinical and cytogenetic correlations in 63 patients with therapy-related myelodysplastic syndrome and acute nonlymphocytic leukemia: further evidence for characteristic abnormalities of chromosomes no. 5 and 7","volume":"4","author":"Le Beau","year":"1986","journal-title":"J Clin Oncol"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib2","first-page":"372","article-title":"Chromosome abnormalities in acute nonlymphocytic leukemia: clinical and biological significance","volume":"14","author":"Bloomfield","year":"1987","journal-title":"Semin Oncol"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib3","doi-asserted-by":"crossref","first-page":"230","DOI":"10.1182\/blood.V73.1.230.230","article-title":"Chromosome 7 long arm deletion in myeloid disorders: a narrow breakpoint region in 7q22 defined by molecular mapping","volume":"73","author":"Kere","year":"1989","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib4","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1046\/j.1365-2141.1996.4841025.x","article-title":"Molecular characterization of the 7q deletion in myeloid disorders","volume":"93","author":"Lewis","year":"1996","journal-title":"Br J Haematol"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib5","doi-asserted-by":"crossref","first-page":"3579","DOI":"10.1182\/blood.V87.9.3579.bloodjournal8793579","article-title":"Molecular definition of a narrow interval at 7q22.1 associated with myelodysplasia","volume":"87","author":"Johnson","year":"1996","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib6","first-page":"1930","article-title":"Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid disorders","volume":"88","author":"Le Beau","year":"1996","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib7","doi-asserted-by":"crossref","first-page":"2036","DOI":"10.1182\/blood.V89.6.2036","article-title":"Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias","volume":"89","author":"Fischer","year":"1997","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib8","doi-asserted-by":"crossref","first-page":"600","DOI":"10.1016\/j.ygeno.2005.01.013","article-title":"Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22","volume":"85","author":"Curtiss","year":"2005","journal-title":"Genomics"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib9","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1006\/geno.2001.6636","article-title":"Candidate gene isolation and comparative analysis of a commonly deleted segment of 7q22 implicated in myeloid malignancies","volume":"77","author":"Kratz","year":"2001","journal-title":"Genomics"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib10","doi-asserted-by":"crossref","first-page":"1501","DOI":"10.1182\/blood.V79.6.1501.1501","article-title":"Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders","volume":"79","author":"Neuman","year":"1992","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib11","doi-asserted-by":"crossref","first-page":"307","DOI":"10.1016\/S0145-2126(98)00159-3","article-title":"Allelotyping of acute myelogenous leukemia: loss of heterozygosity at 7q31.1 (D7S486) and q33-34 (D7S498, D7S505)","volume":"23","author":"Koike","year":"1999","journal-title":"Leuk Res"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib12","doi-asserted-by":"crossref","first-page":"384","DOI":"10.1002\/(SICI)1098-2264(199908)25:4<384::AID-GCC11>3.0.CO;2-D","article-title":"Delineation of multiple deleted regions in 7q in myeloid disorders","volume":"25","author":"Tosi","year":"1999","journal-title":"Genes Chromosomes Cancer"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib13","doi-asserted-by":"crossref","first-page":"2015","DOI":"10.1038\/sj.onc.1202519","article-title":"Refined mapping of the region of loss of heterozygosity on the long arm of chromosome 7 in human breast cancer defines the location of a second tumor suppressor gene at 7q22 in the region of the CUTL1 gene","volume":"18","author":"Zeng","year":"1999","journal-title":"Oncogene"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib14","doi-asserted-by":"crossref","first-page":"4849","DOI":"10.1038\/sj.onc.1205615","article-title":"MLL5, a homolog of Drosophila trithorax located within a segment of chromosome band 7q22 implicated in myeloid leukemia","volume":"21","author":"Emerling","year":"2002","journal-title":"Oncogene"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib15","doi-asserted-by":"crossref","first-page":"95","DOI":"10.1016\/j.cancergencyto.2005.03.017","article-title":"The human Penumbra gene is mapped to a region on chromosome 7 frequently deleted in myeloid malignancies","volume":"162","author":"Chen","year":"2005","journal-title":"Cancer Genet Cytogenet"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib16","unstructured":"Mitelman F, Johansson B, Mertens F, editors. Mitelman database of chromosome aberrations in cancer [Internet]. Updated May 2005. Available at: http:\/\/cgap.nci.nih.gov\/Chromosomes\/Mitelman. Accessed May 2005."},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib17","doi-asserted-by":"crossref","unstructured":"Heerema NA, Nachman JB, Sather HN, La MK, Hutchinson R, Lange BJ, Bostrom B, Steinherz PG, Gaynon PS, Uckun FM; Children's Cancer Group. Deletion of 7p or monosomy 7 in pediatric acute lymphoblastic leukemia is an adverse prognostic factor: a report from the Children's Cancer Group. Leukemia 2004;18:939\u201347.","DOI":"10.1038\/sj.leu.2403327"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib18","first-page":"644","article-title":"Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH)","volume":"10","author":"Tosi","year":"1996","journal-title":"Leukemia"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib19","doi-asserted-by":"crossref","first-page":"136","DOI":"10.1016\/j.cancergencyto.2003.08.019","article-title":"Heterogeneity of structural abnormalities in the 7q31-q34 region in myeloid malignancies","volume":"150","author":"Gonzalez","year":"2004","journal-title":"Cancer Genet Cytogenet"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib20","article-title":"ISCN 1995: an international system for human cytogenetic nomenclature (1995)","year":"1995"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib21","article-title":"ISCN 2005: an international system for human cytogenetic nomenclature (2005)","year":"2005"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib22","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1002\/hon.744","article-title":"Gains, losses and complex karyotypes in myeloid disorders: a light at the end of the tunnel","volume":"23","author":"Alvarez","year":"2005","journal-title":"Hematol Oncol"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib23","doi-asserted-by":"crossref","first-page":"156","DOI":"10.1159\/000015245","article-title":"High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes","volume":"84","author":"Chudoba","year":"1999","journal-title":"Cytogenet Cell Genet"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib24","doi-asserted-by":"crossref","first-page":"118","DOI":"10.1046\/j.1365-2141.2001.02511.x","article-title":"German AML Cooperative Study Group. Patients with de novo acute myeloid leukaemia and complex karyotype aberrations show a poor prognosis despite intensive treatment: a study of 90 patients","volume":"112","author":"Schoch","year":"2001","journal-title":"Br J Haematol"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib25","doi-asserted-by":"crossref","first-page":"1083","DOI":"10.1182\/blood.V76.6.1083.1083","article-title":"Chromosome aberrations and prognostic factors in therapy-related myelodysplasia and acute nonlymphocytic leukaemia","volume":"76","author":"Pedersen-Bjergaard","year":"1990","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib26","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1046\/j.1365-2141.2001.02713.x","article-title":"Molecular characterization of myelodysplasia-associated chromosome 7 inversion","volume":"113","author":"Todd","year":"2001","journal-title":"Br J Haematol"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib27","doi-asserted-by":"crossref","first-page":"4031","DOI":"10.1182\/blood.V92.11.4031","article-title":"Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders","volume":"92","author":"D\u00f6hner","year":"1998","journal-title":"Blood"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib28","doi-asserted-by":"crossref","first-page":"869","DOI":"10.1038\/sj.leu.2401430","article-title":"Deletions and losses in chromosomes 5 and 7 in adult acute lymphocytic leukemia: incidence, associations and implications","volume":"13","author":"Dabaja","year":"1999","journal-title":"Leukemia"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib29","doi-asserted-by":"crossref","first-page":"939","DOI":"10.1038\/sj.leu.2403327","article-title":"Deletion of 7p or monosomy 7 in pediatric acute lymphoblastic leukaemia is an adverse prognostic factor: a report from the Children's Cancer Group","volume":"18","author":"Heerema","year":"2004","journal-title":"Leukemia"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib30","first-page":"401","article-title":"Cytogenetic analysis and clinical significance of chromosome 7 aberrations in acute leukaemia","volume":"44","author":"Brozek","year":"2003","journal-title":"J Appl Genet"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib31","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1016\/j.canlet.2005.04.011","article-title":"Cytogenetic aspects of adult primary myelodysplastic syndromes: clinical implications","volume":"235","author":"Panani","year":"2006","journal-title":"Cancer Lett"},{"key":"10.1016\/j.cancergencyto.2006.09.003_bib32","doi-asserted-by":"crossref","first-page":"287","DOI":"10.1002\/gcc.20154","article-title":"Analysis of myelodysplastic syndromes with complex karyotypes by high-resolution comparative genomic hybridization and subtelomeric CGH array","volume":"42","author":"Martinez-Ram\u00edrez","year":"2005","journal-title":"Genes Chromosomes Cancer"}],"container-title":["Cancer Genetics and Cytogenetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0165460806006054?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0165460806006054?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2020,4,20]],"date-time":"2020-04-20T00:34:56Z","timestamp":1587342896000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0165460806006054"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,2]]},"references-count":32,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2007,2]]}},"alternative-id":["S0165460806006054"],"URL":"https:\/\/doi.org\/10.1016\/j.cancergencyto.2006.09.003","relation":{},"ISSN":["0165-4608"],"issn-type":[{"value":"0165-4608","type":"print"}],"subject":[],"published":{"date-parts":[[2007,2]]}}}