Brunclikova, M.; Simurda, T.; Zolkova, J.; Sterankova, M.; Skornova, I.; Dobrotova, M.; Kolkova, Z.; Loderer, D.; Grendar, M.; Hudecek, J.;
et al. Heterogeneity of Genotype–Phenotype in Congenital Hypofibrinogenemia—A Review of Case Reports Associated with Bleeding and Thrombosis. J. Clin. Med. 2022, 11, 1083.
https://doi.org/10.3390/jcm11041083
AMA Style
Brunclikova M, Simurda T, Zolkova J, Sterankova M, Skornova I, Dobrotova M, Kolkova Z, Loderer D, Grendar M, Hudecek J,
et al. Heterogeneity of Genotype–Phenotype in Congenital Hypofibrinogenemia—A Review of Case Reports Associated with Bleeding and Thrombosis. Journal of Clinical Medicine. 2022; 11(4):1083.
https://doi.org/10.3390/jcm11041083
Chicago/Turabian Style
Brunclikova, Monika, Tomas Simurda, Jana Zolkova, Miroslava Sterankova, Ingrid Skornova, Miroslava Dobrotova, Zuzana Kolkova, Dusan Loderer, Marian Grendar, Jan Hudecek,
and et al. 2022. "Heterogeneity of Genotype–Phenotype in Congenital Hypofibrinogenemia—A Review of Case Reports Associated with Bleeding and Thrombosis" Journal of Clinical Medicine 11, no. 4: 1083.
https://doi.org/10.3390/jcm11041083
APA Style
Brunclikova, M., Simurda, T., Zolkova, J., Sterankova, M., Skornova, I., Dobrotova, M., Kolkova, Z., Loderer, D., Grendar, M., Hudecek, J., Stasko, J., & Kubisz, P.
(2022). Heterogeneity of Genotype–Phenotype in Congenital Hypofibrinogenemia—A Review of Case Reports Associated with Bleeding and Thrombosis. Journal of Clinical Medicine, 11(4), 1083.
https://doi.org/10.3390/jcm11041083
