Literature DB >> 1551073

t(2;14)(p13;q32): a recurring abnormality in lymphocytic leukemia. A Pediatric Oncology Group study.

M S Watson1, V J Land, A J Carroll, J Pullen, M J Borowitz, M P Link, M Amylon, F G Behm.   

Abstract

Chromosome banding studies of 1,411 children with newly diagnosed acute lymphocytic leukemia (ALL) identified two patients with the t(2;14)(p13;q32) chromosome abnormality and a third patient with a complex three-way translocation involving the same breakpoints on chromosomes 2 and 14 but also involving chromosome 12 at band q11. The three cases demonstrated variability of immunophenotypes: one was a T-cell ALL, and two were early pre-B ALLs. All three patients achieved complete remissions and have remained in remission for 14-19 months.

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Year:  1992        PMID: 1551073     DOI: 10.1016/0165-4608(92)90096-q

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  2 in total

1.  Translocation t(2;14)(p13;q32) in a case of Ph+ acute lymphoblastic leukemia.

Authors:  Lily Kerketta; Babu Rao Vundinti; Kanjaksha Ghosh
Journal:  Indian J Hum Genet       Date:  2007-09

2.  A Novel Translocation: t(2;14)(p12;q32) in a Case of Precursor B-acute Lymphoblastic Leukemia.

Authors:  Prasannakumari Sampathkumar; Shanthi Velusamy; Namrata Rajkumar; M Padma
Journal:  Indian J Med Paediatr Oncol       Date:  2017 Jul-Sep
  2 in total

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