Order Article Reprints

Gindele R, Kerényi A, Kállai J, Pfliegler G, Schlammadinger Á, Szegedi I, Major T, Szabó Z, Bagoly Z, Kiss C, et al. Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing. Life. 2021; 11(3):202. https://doi.org/10.3390/life11030202

Gindele, Réka, Adrienne Kerényi, Judit Kállai, György Pfliegler, Ágota Schlammadinger, István Szegedi, Tamás Major, Zsuzsanna Szabó, Zsuzsa Bagoly, Csongor Kiss, and et al. 2021. "Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing" Life 11, no. 3: 202. https://doi.org/10.3390/life11030202

Gindele, R., Kerényi, A., Kállai, J., Pfliegler, G., Schlammadinger, Á., Szegedi, I., Major, T., Szabó, Z., Bagoly, Z., Kiss, C., Kappelmayer, J., & Bereczky, Z. (2021). Resolving Differential Diagnostic Problems in von Willebrand Disease, in Fibrinogen Disorders, in Prekallikrein Deficiency and in Hereditary Hemorrhagic Telangiectasia by Next-Generation Sequencing. Life, 11(3), 202. https://doi.org/10.3390/life11030202