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Elisabeth Sirch
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Journal Articles

Mutations In SETBP1 Occur In 3.1% Of De Novo AML and Show a Distinct Genetic Pattern That Highly Resembles Atypical CML

Manja Meggendorfer, PhD, Tamara Alpermann, Elisabeth Sirch, Claudia Haferlach, MD, Wolfgang Kern, MD, Torsten Haferlach, MD, Susanne Schnittger, PhD
Journal: Blood
Blood (2013) 122 (21): 2560.
https://doi.org/10.1182/blood.V122.21.2560.2560
Published: 2013
Journal Articles

Myeloid Malignancies With Isochromosome 17q Harbor Frequently Mutations In ASXL1 , SETBP1 , and SRSF2 - This Distinct Genotype Presents With Various Morphological Phenotypes

Manja Meggendorfer, PhD, Tamara Alpermann, Claudia Haferlach, MD, Elisabeth Sirch, Wolfgang Kern, MD, Torsten Haferlach, MD, Susanne Schnittger, PhD
Journal: Blood
Blood (2013) 122 (21): 1364.
https://doi.org/10.1182/blood.V122.21.1364.1364
Published: 2013