eNauka - pregled
Pregled prema Autor Stankovic, Andjela
Prikaz rezultata 1 do 5 od 5
| Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
|---|---|---|---|---|
| 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 | 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 |