Medizinische Universität Graz - Research portal
Selected Publication:
SHR Neuro Cancer Cardio Lipid Metab Microb
Robier, C; Hoefler, G; Aubell, K; Hubmann, E.
Acquired elliptocytosis as presenting sign of a myelodysplastic syndrome associated with deletion of chromosome 20 and mutations in TET2, DNMT3A, and U2AF1.
Ann Hematol. 2021; 100(8):2111-2112
Doi: 10.1007/s00277-020-04368-w
(- Case Report)
Web of Science
PubMed
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- Leading authors Med Uni Graz
- Robier Christoph
- Co-authors Med Uni Graz
- Aubell Kristina
- Höfler Gerald
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- Find related publications in this database (using NLM MeSH Indexing)
- Aged - administration & dosage
- Chromosome Deletion - administration & dosage
- Chromosomes, Human, Pair 20 - administration & dosage
- DNA Methyltransferase 3A - genetics
- DNA-Binding Proteins - genetics
- Dioxygenases - genetics
- Elliptocytosis, Hereditary - diagnosis, genetics
- Humans - administration & dosage
- Male - administration & dosage
- Myelodysplastic Syndromes - diagnosis, genetics
- Splicing Factor U2AF - genetics