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SHR Neuro Krebs Kardio Lipid Stoffw 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)
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Führende Autor*innen der Med Uni Graz
Robier Christoph
Co-Autor*innen der 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

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