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Analysis of IgH translocations, chromosome 13q14 and 17p13.1(p53) deletions by fluorescence in situ hybridization in Waldenstrom's macroglobulinemia: a single center study of 22 cases

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A Corrigendum to this article was published on 23 August 2004

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Authors and Affiliations

  1. Department of Laboratory Hematology, Princess Margaret Hospital, University Health Network, University of Toronto, Toronto, Canada

    H Chang, D Li & B Patterson

  2. Department of Medical Oncology and Hematology, Princess Margaret Hospital, University Health Network, University of Toronto, Toronto, Canada

    S Samiee, C I Chen & A Keith Stewart

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  1. H Chang
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  2. S Samiee
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  3. D Li
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  4. B Patterson
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  5. C I Chen
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  6. A Keith Stewart
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Correspondence to H Chang.

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Chang, H., Samiee, S., Li, D. et al. Analysis of IgH translocations, chromosome 13q14 and 17p13.1(p53) deletions by fluorescence in situ hybridization in Waldenstrom's macroglobulinemia: a single center study of 22 cases. Leukemia 18, 1160–1162 (2004). https://doi.org/10.1038/sj.leu.2403369

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  • DOI: https://doi.org/10.1038/sj.leu.2403369

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