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SHR Neuro Krebs Kardio Lipid Stoffw Microb

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 [OPEN ACCESS]
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Führende Autor*innen der Med Uni Graz
Pichler Monika
Wölfler Albert
Co-Autor*innen der Med Uni Graz
Beham-Schmid Christine
Bodner Claudia
Deutsch Alexander
Fischer Carina
Gülly Christian
Lind Karin
Linkesch Werner
Sill Heinz
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Find related publications in this database (using NLM MeSH Indexing)
Adolescent -
Adult -
Aged -
Aged, 80 and over -
Female -
Humans -
Isocitrate Dehydrogenase - genetics
Leukemia, Myeloid, Acute - genetics
Male -
Middle Aged -
Mutation -
Neoplasms, Second Primary - genetics
Uniparental Disomy -
Young Adult -

Find related publications in this database (Keywords)
acute myeloid leukaemia
myelodysplastic syndromes
molecular genetics
mutation analysis
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