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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

✍ Scribed by Monika M. Pichler; Claudia Bodner; Carina Fischer; Alexander J. Deutsch; Karin Hiden; Christine Beham-Schmid; Werner Linkesch; Christian Guelly; Heinz Sill; Albert Wölfler


Book ID
108676989
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
157 KB
Volume
152
Category
Article
ISSN
0007-1048

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