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, 202.
https://doi.org/10.3390/life11030202
AMA Style
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
Chicago/Turabian Style
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
APA Style
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
