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dc.creatorAthanasiadou, A.en
dc.creatorStamatopoulos, K.en
dc.creatorTsompanakou, A.en
dc.creatorFoutsitsakis, D.en
dc.creatorFassas, A.en
dc.creatorAnagnostopoulos, A.en
dc.creatorTsezou, A.en
dc.date.accessioned2015-11-23T10:23:11Z
dc.date.available2015-11-23T10:23:11Z
dc.date.issued2005
dc.identifier10.1080/10428190400011591
dc.identifier.issn1042-8194
dc.identifier.urihttp://hdl.handle.net/11615/25978
dc.description.abstractTwo novel chromosomal translocations were identified in 2 patients with chronic lymphocytic leukemia (CLL). Case 1: 60 year-old male, stage Rai 0/Binet A, with mutated immunoglobulin heavy (IgH) and lambda (Iglambda) light chain genes; karyotype: 46, XY, t(9;12)(q12;p11) [3]/ 46, XY [22]. Case 2: 56 year-old male, stage Rai 2/Binet B, with mutated IgH and unmutated Iglambda genes; karyotype: 46, XY, add(10)(q26), t(13;18)(q14;q21) [8]/ 46, XY [27]. Although both translocations are novel, the involved breakpoints (especially 13q14 and 18q21) have been reported to participate in various aberrations in CLL patients. Aberrations affecting bands 9q12 and 12p11, as in case 1, are generally rare.en
dc.sourceLeukemia & Lymphomaen
dc.source.uri<Go to ISI>://WOS:000225877700017
dc.subjectGENOMIC ABERRATIONSen
dc.subjectGENESen
dc.subjectOncologyen
dc.subjectHematologyen
dc.titleReport of two novel chromosomal translocations in chronic lymphocytic leukemiaen
dc.typejournalArticleen


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