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Letter to the Editors

1q triplication as sole cytogenetic abnormality in myelodysplastic syndrome

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Pages 1387-1389 | Received 03 Jan 2011, Accepted 05 Mar 2011, Published online: 23 May 2011

References

  • Park TS, Lee ST, Song JW, A tandem triplication, trp(1)(q21q23), in a patient with follicular lymphoma: a case study and review of the literature. Cancer Genet Cytogenet 2009;189:127–131.
  • Tien HF, Wang CH, Chuang SM, Cytogenetic studies, ras mutation, and clinical characteristics in primary myelodysplastic syndrome: a study on 68 Chinese patients in Taiwan. Cancer Genet Cytogenet 1994;74:40–49.
  • Schindler D, Kubbies M, Hoehn H, Schinzel A, Rabinovitch PS. Confirmation of Fanconi's anemia and detection of a chromosomal aberration (1q12-32 triplication) via BrdU/Hoechst flow cytometry. Am J Pediatr Hematol Oncol 1987;9:172–177.
  • Park TS, Lee SG, Cheong JW, Two case reports of 1q triplication in myeloproliferative neoplasms. Cancer Genet Cytogenet 2009;191:111–112.
  • Swerdlow SH, Campo E, Harris NL, et al, editors. WHO classification of tumours of haematopoietic and lymphoid tissues. Lyon: IARC2008.
  • Alfaro R, Pérez-Granero A, Durán MA, Besalduch J, Rosell J, Bernués M. dup(1)(q21q32) as a sole cytogenetic event is associated to a leukemic transformation in myelodysplastic syndromes. Leuk Res 2008;32:159–161.
  • Siebert R, Rosenwald A, Staudt LM, Morris SW. Molecular features of B-cell lymphoma. Curr Opin Oncol 2001;13:316–324.

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