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Browsing by Author Toljic, Mina
Showing results 1 to 6 of 6
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | A rare case of prenatal Stuve-Wiedemann syndrome presenting with asymmetric femoral involvement | Joksic, Ivana D; Toljic, Mina; Stankovic, Andjela; Karadzov-Orlic, Natasa T | Conference Paper | Mp. category will be shown later |
| 2024 | Expanding the phenotypic spectrum of MPDZ gene variants: A case report with prenatally detected Dandy-Walker malformation and single ventricle heart | Stankovic, Andjela; Toljic, Mina; Karadzov-Orlic, Natasa T; Mikovic, Zeljko M; Joksic, Ivana D | Article | 21M21 |
| 2025 | Novel likely pathogenic variant in SHH gene causing holoprosencephaly | Toljic, Mina; Stankovic, Andjela; Karadzov-Orlic, Natasa T; Joksic, Ivana D | Conference Paper | Mp. category will be shown later |
| 2024 | Prenatal diagnosis of Zellweger spectrum disorder caused by novel variant in PEX6 gene | Joksic, Ivana D; Toljic, Mina; Stankovic, Andjela; Milovanovic, Zagorka M | Conference Paper | Mp. category will be shown later |
| 2024 | Rare case of androgenetic-biparental mosacism causing placental mesenchymal dysplasia | Joksic, Ivana D; Toljic, Mina; Milovanovic, Zagorka M; Dzuverovic, Marko; Stankovic, Andjela S; Mikovic, Zeljko M | Conference Paper | Mp. category will be shown later |
| 2024 | Small supernumerary marker chromosomes in prenatal diagnosis-molecular characterization and clinical outcomes | Joksic, Ivana D; Toljic, Mina; Milacic, Iva; Stankovic, Andjela; Karadzov-Orlic, Natasa T; Mikovic, Zeljko M | Article | 21M21 |