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Rare and potentially fatal - Cytogenetically cryptic TNIP1::PDGFRB and PCM1::FGFR1 fusion leading to myeloid/lymphoid neoplasms with eosinophilia in children.
Berking AC, Flaadt T, Behrens YL, Yoshimi A, Leipold A, Holzer U, Lang P, Quintanilla-Martinez L, Schlegelberger B, Reiter A, Niemeyer C, Strahm B, Göhring G. Berking AC, et al. Among authors: gohring g. Cancer Genet. 2023 Apr;272-273:29-34. doi: 10.1016/j.cancergen.2023.01.002. Epub 2023 Jan 7. Cancer Genet. 2023. PMID: 36657267
Cryptic t(15;17) in a patient with AML M3 and a complex karyotype.
Göhring G, Lange K, Atta J, Krauter J, Hölzer D, Schlegelberger B. Göhring G, et al. Cancer Genet Cytogenet. 2007 May;175(1):77-80. doi: 10.1016/j.cancergencyto.2007.01.004. Cancer Genet Cytogenet. 2007. PMID: 17498564 No abstract available.
Copy number alterations in childhood acute lymphoblastic leukemia and their association with minimal residual disease.
Steinemann D, Cario G, Stanulla M, Karawajew L, Tauscher M, Weigmann A, Göhring G, Ludwig WD, Harbott J, Radlwimmer B, Bartram C, Lichter P, Schrappe M, Schlegelberger B. Steinemann D, et al. Among authors: gohring g. Genes Chromosomes Cancer. 2008 Jun;47(6):471-80. doi: 10.1002/gcc.20557. Genes Chromosomes Cancer. 2008. PMID: 18311775
Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome.
Steinemann D, Praulich I, Otto N, Göhring G, Niemeyer CM, Schlegelberger B. Steinemann D, et al. Among authors: gohring g. Br J Haematol. 2009 May;145(4):533-4. doi: 10.1111/j.1365-2141.2009.07634.x. Br J Haematol. 2009. PMID: 19298594 Free article. No abstract available.
252 results