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Association between 3'UTR polymorphisms in genes ACVR2A, AGTR1 and RGS2 and preeclampsia. [electronic resource] by
- Mendelova, Andrea
- Holubekova, Veronika
- Grendar, Marian
- Zubor, Pavol
- Svecova, Iveta
- Loderer, Dusan
- Snahnicanova, Zuzana
- Biringer, Kamil
- Danko, Jan
- Lasabova, Zora
Producer: 20180720
In:
General physiology and biophysics vol. 37
Availability: No items available.
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Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop). [electronic resource] by
- Simurda, Tomas
- Caccia, Sonia
- Asselta, Rosanna
- Zolkova, Jana
- Stasko, Jan
- Skornova, Ingrid
- Snahnicanova, Zuzana
- Loderer, Dusan
- Lasabova, Zora
- Kubisz, Peter
Producer: 20210415
In:
Journal of thrombosis and thrombolysis vol. 50
Availability: No items available.
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8.
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Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders. [electronic resource] by
- Simurda, Tomas
- Zolkova, Jana
- Snahnicanova, Zuzana
- Loderer, Dusan
- Skornova, Ingrid
- Sokol, Juraj
- Hudecek, Jan
- Stasko, Jan
- Lasabova, Zora
- Kubisz, Peter
Producer: 20180724
In:
International journal of molecular sciences vol. 19
Availability: No items available.
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Uncertainty of fetal fraction determination in Non-Invasive Prenatal Screening by highly polymorphic SNPs. [electronic resource] by
- Grendár, Marian
- Loderer, Dušan
- Laučeková, Zuzana
- Švecová, Iveta
- Hrtánková, Michaela
- Hornáková, Andrea
- Nagy, Bálint
- Žúbor, Pavol
- Lasabová, Zora
- Danko, Ján
Producer: 20191113
In:
Journal of biotechnology vol. 299
Availability: No items available.
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Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia. [electronic resource] by
- Simurda, Tomas
- Zolkova, Jana
- Kolkova, Zuzana
- Loderer, Dusan
- Dobrotova, Miroslava
- Skornova, Ingrid
- Brunclíkova, Monika
- Grendar, Marian
- Lasabova, Zora
- Stasko, Jan
- Kubisz, Peter
Producer: 20200929
In:
International journal of hematology vol. 111
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Genetic Background of von Willebrand Disease: History, Current State, and Future Perspectives. [electronic resource] by
- Zolkova, Jana
- Sokol, Juraj
- Simurda, Tomas
- Vadelova, Lubica
- Snahnicanova, Zuzana
- Loderer, Dusan
- Dobrotova, Miroslava
- Ivankova, Jela
- Skornova, Ingrid
- Lasabova, Zora
- Kubisz, Peter
- Stasko, Jan
Producer: 20210630
In:
Seminars in thrombosis and hemostasis vol. 46
Availability: No items available.
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