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Publikationen 2017

Alisch, Franz; Weichert, Alexander; Kalache, Karim; Paradiso, Viola; Longardt, Ann Carolin; Dame, Christof, Hoffmann, Katrin et al. (2017): Familial Gordon syndrome associated with a PIEZO2 mutation. In: American journal of medical genetics. Part A 173 (1), S. 254–259. DOI: 10.1002/ajmg.a.37997.

Foja, Sabine; Luther, Mirjam; Hoffmann, Katrin; Rupprecht, Andreas; Gruenauer-Kloevekorn, Claudia (2017): CTG18.1 repeat expansion may reduce TCF4 gene expression in corneal endothelial cells of German patients with Fuchs' dystrophy. In: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 255 (8), S. 1621–1631. DOI: 10.1007/s00417-017-3697-7.

Schnipper, Nele; Stassen, Hans H.; Kallinich, Tilmann; Sperling, Karl; Hoffmann, Katrin (2017): Image analysis of neutrophil nuclear morphology: Learning about phenotypic range and its reliable analysis from patients with pelger-Huët-anomaly and treated with colchicine. In: Cytometry. Part B, Clinical cytometry 92 (6), S. 541–549. DOI: 10.1002/cyto.b.21484.