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Pichler, MM; Bodner, C; Fischer, C; Deutsch, AJ; Hiden, K; Beham-Schmid, C; Linkesch, W; Guelly, C; Sill, H; Wölfler, A.
Evaluation of mutations in the isocitrate dehydrogenase genes in therapy-related and secondary acute myeloid leukaemia identifies a patient with clonal evolution to IDH2 R172K homozygosity due to uniparental disomy.
Br J Haematol. 2011; 152(5): 669-672.
Doi: 10.1111/j.1365-2141.2010.08404.x
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- Führende Autor*innen der Med Uni Graz
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Pichler Monika
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Wölfler Albert
- Co-Autor*innen der Med Uni Graz
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Beham-Schmid Christine
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Bodner Claudia
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Deutsch Alexander
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Fischer Carina
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Gülly Christian
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Lind Karin
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Linkesch Werner
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Sill Heinz
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Adolescent -
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Adult -
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Aged -
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Aged, 80 and over -
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Female -
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Humans -
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Isocitrate Dehydrogenase - genetics
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Leukemia, Myeloid, Acute - genetics
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Male -
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Middle Aged -
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Mutation -
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Neoplasms, Second Primary - genetics
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Uniparental Disomy -
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Young Adult -
- Find related publications in this database (Keywords)
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acute myeloid leukaemia
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myelodysplastic syndromes
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molecular genetics
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mutation analysis