{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T20:42:07Z","timestamp":1786653727747,"version":"build-2736575974"},"reference-count":10,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2015]]},"abstract":"<jats:sec>\n                    <jats:title\/>\n                    <jats:p>The t (9;22)(q34;q11) translocation is found in about 90% of the chronic myeloid leukemia patients. About 5 - 10% of these patients have complex variant translocations involving a third chromosome in addition to chromosomes 9 and 22. We describe five male patients in the chronic myeloid leukemia-chronic phase, with rare variant Philadelphia translocations. All of them had the BCR-ABL fusion gene and responded well to treatment with imatinib mesylate. All the patients are on regular follow-up.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/0973-1482.138036","type":"journal-article","created":{"date-parts":[[2015,10,9]],"date-time":"2015-10-09T11:54:49Z","timestamp":1444391689000},"page":"654","source":"Crossref","is-referenced-by-count":4,"title":["Variant Philadelphia translocations in chronic myeloid leukemia"],"prefix":"10.4103","volume":"11","author":[{"given":"Vijaya V.","family":"Mysorekar","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Murali","family":"Subramanian","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nalini","family":"Kilara","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tambarahalli S.","family":"Sundareshan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-72-20231126","doi-asserted-by":"crossref","first-page":"290","DOI":"10.1038\/243290a0","article-title":"Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining","volume":"243","author":"Rowley","year":"1973","journal-title":"Nature"},{"key":"R2-72-20231126","doi-asserted-by":"crossref","first-page":"1027","DOI":"10.3892\/ol.2012.623","article-title":"A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t (9;22;21)(q34;q11;p12)","volume":"3","author":"Al-Achkar","year":"2012","journal-title":"Oncol Lett"},{"key":"R3-72-20231126","doi-asserted-by":"crossref","first-page":"6793","DOI":"10.1182\/blood-2011-01-328294","article-title":"Variant Philadelphia translocations: Molecular-cytogenetic characterization and 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case report","volume":"2011","author":"Manabe","year":"2011","journal-title":"Leuk Res Treatment"},{"key":"R7-72-20231126","doi-asserted-by":"crossref","first-page":"20","DOI":"10.1186\/1755-8166-5-20","article-title":"A novel five-way translocation t (7;11;9;22;9)(q22;q13;q34;q11.2;q34) involving Ph chromosome in a patient of chronic myeloid leukemia: A case report","volume":"5","author":"Yokota","year":"2012","journal-title":"Mol Cytogenet"},{"key":"R8-72-20231126","first-page":"ECR37","article-title":"Complex variant Philadelphia translocation involving the short arm of chromosome 9 in a case of chronic myeloid leukemia","volume":"89","author":"Cianciulli","year":"2004","journal-title":"Haematologica"},{"key":"R9-72-20231126","doi-asserted-by":"crossref","first-page":"506","DOI":"10.3109\/02841861003660031","article-title":"Influence of complex variant chromosomal translocations in chronic myeloid leukemia patients treated with tyrosine kinase inhibitors","volume":"49","author":"Stagno","year":"2010","journal-title":"Acta Oncol"},{"key":"R10-72-20231126","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1016\/j.cancergencyto.2006.10.006","article-title":"On the genesis and prognosis of variant translocations in chronic myeloid leukemia","volume":"173","author":"Gorusu","year":"2007","journal-title":"Cancer Genet Cytogenet"}],"container-title":["Journal of Cancer Research and Therapeutics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/01363817-201511030-00072","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T19:41:36Z","timestamp":1786650096000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/01363817-201511030-00072"}},"subtitle":["A report of five cases"],"short-title":[],"issued":{"date-parts":[[2015]]},"references-count":10,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2015]]}},"URL":"https:\/\/doi.org\/10.4103\/0973-1482.138036","relation":{},"ISSN":["0973-1482"],"issn-type":[{"value":"0973-1482","type":"print"}],"subject":[],"published":{"date-parts":[[2015]]}}}