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- Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype / Simurda T., Brunclikova M., Asselta R. et al. . International journal of molecular sciences . - 2020 Jul; 21(13): 4616 [Dokument nie je vo fonde knižnice]
- Heterogeneity of Genotype-Phenotype in Congenital Hypofibrinogenemia-A Review of Case Reports Associated with Bleeding and Thrombosis / Brunclikova M., Simurda T., Zolkova J. et al. . Journal of clinical medicine . - Vol. 11, no. 4 (2022), s. 1083 [Dokument nie je vo fonde knižnice]