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Unusual Karyotype 46,XX,inv(8)(p21q24),del(20)(q11q13) in a Case of Acute Leukemia M6 in a Child

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Acute Leukemias VI

Part of the book series: Haematology and Blood Transfusion / Hämatologie und Bluttransfusion ((HAEMATOLOGY,volume 38))

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Abstract

Specific structural chromosome abnormalities are connected with different types of acute myeloid leukemia and have proved to be helpful in establishing the precise diagnosis and the prognosis of disease. For FAB M6 subtype, many karyotype changes have been described and classified as minor and major karyotype abnormalities (MIKA and MAKA) [1]. Here we report the combination of two clonal chromosome changes in a child with M6 AML.

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© 1997 Springer-Verlag Berlin Heidelberg

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Donskaya, S., Andreeva, S., Galantha, A., Sclysarenko, L., Derbenyova, N. (1997). Unusual Karyotype 46,XX,inv(8)(p21q24),del(20)(q11q13) in a Case of Acute Leukemia M6 in a Child. In: Büchner, T., Schellong, G., Ritter, J., Creutzig, U., Hiddemann, W., Wörmann, B. (eds) Acute Leukemias VI. Haematology and Blood Transfusion / Hämatologie und Bluttransfusion, vol 38. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-60377-8_7

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  • DOI: https://doi.org/10.1007/978-3-642-60377-8_7

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-64379-8

  • Online ISBN: 978-3-642-60377-8

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