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A chromosomal abnormality (21q-) in primary thrombocytosis

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Summary

A patient with primary thrombocytosis was found to present an acquired deletion of the long arm of chromosome 21 (21q-). A similar observation reported in the literature is hereby confirmed.

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Reference

  • Zaccaria, A., Tura, S.: A chromosomal abnormality in primary thrombocythemia. N. Engl. J. Med. 298, 1422–1423 (1978)

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Authors and Affiliations

  1. Centre de Diagnostic Hormonal, 196, Ch. d'Alsemberg, B-1180, Bruxelles, Belgium

    P. Petit

  2. Division of Human Genetics, Department of Human Biology, University of Leuven, Minderbroedersstraat, 12, B-3000, Leuven, Belgium

    H. Van den Berghe

Authors
  1. P. Petit
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  2. H. Van den Berghe
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Petit, P., Van den Berghe, H. A chromosomal abnormality (21q-) in primary thrombocytosis. Hum Genet 50, 105–106 (1979). https://doi.org/10.1007/BF00295597

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  • DOI: https://doi.org/10.1007/BF00295597

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