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Browsing by Author Joksić, Ivana
Showing results 1 to 17 of 17
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2015 | Assessment of Single Nucleotide Polymorphisms in Screening 52 DNA Repair and Cell Cycle Control Genes in Fanconi Anemia Patients![]() | Petrović, Sandra | Article | 23M23 |
| 2015 | BAC-Probes Applied for Characterization of Fragile Sites (FS)![]() | Mrasek, Kristin; Wilhelm, Kathleen; Quintana, Luciana; Theuss, Luise; Liehr, Thomas; Leskovac, Andreja | Book parts | Mp. category will be shown later |
| 2020 | Combined presence of coagulation factor XIII V34L and plasminogen activator inhibitor 1 4G/5G gene polymorphisms significantly contribute to recurrent pregnancy loss in serbian population![]() | Joksić, Ivana | Article | 22M22 |
| 2020 | Corrigendum to “Placenta-specific plasma miR518b is a potential biomarker for preeclampsia” [Clin. Biochem. 79 (2020) 28–33]![]() | Munjas, Jelena | Other | Mp. category will be shown later |
| 2024 | Expression of miRNAs and proinflammatory cytokines in pregnant women with gestational diabetes mellitus![]() | Toljić, Mina | Article | 21M21 |
| 2024 | EXPRESSION OF PROINFLAMATORY CYTOKINES IN GESTATIONAL HYPERTENSION![]() | Carkic, Jelena | Conference Paper | Mp. category will be shown later |
| 2019 | Expression of proinflammatory cytokines in pregnant women with gestational diabetes mellitus![]() | Carkic, Jelena | Conference Paper | Mp. category will be shown later |
| 2016 | First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease![]() | Filipović, Jelena G. | Article | 22M22 |
| 2017 | Genetic study of Achondroplasia in Serbian population![]() | Radunović, Sara; Dobričić, Valerija | Conference Paper | Mp. category will be shown later |
| 2017 | Genotyping Fanconi Anemia Patients from Serbia Reveals Three Novel Fancd2 Variants![]() | Filipović Tričković, Jelena G. | Article | 23M23 |
| 2014 | Methylenetetrahydrofolate reductase and glutathione s-tranferase gene polymorphisms in secondary mixed phenotype acute leukemia: A case report![]() | Škorić, Dejan | Article | 22M22 |
| 2015 | Molecular genetic study of congenital adrenal hyperplasia in Serbia: novel p.Leu129Pro and p.Ser165Pro CYP21A2 gene mutations![]() | Milačić, I.; Barać, M.; Milenković, Tatjana; Ugrin, Milena | Article | 22M22 |
| 2019 | Otopalatodigital Syndrome Type I: Novel Characteristics and Prenatal Manifestations in Two Siblings![]() | Joksić, Ivana | Article | 23M23 |
| 2020 | Placenta-specific plasma miR518b is a potential biomarker for preeclampsia![]() | Munjas, Jelena | Article | 21M21 |
| 2023 | Prenatal diagnosis of Saethre-Chotzen syndrome caused by TWIST1 microdeletion and complex chromosomal rearrangement involving chromosomes 5, 7 and 11![]() | Joksić, Ivana | Conference Paper | Mp. category will be shown later |
| 2020 | Prenatal ultrasonographic manifestations of partial trisomy 12q(12q24.2→qter) and partial monosomy 2q (2q37.3→qter)![]() | Joksić, Ivana | Article | 23M23 |
| 2016 | Substitution rate and natural selection in parvovirus B19![]() | Stamenković, Gorana | Article | 21aM21a |
