Autori: Stankovic Andjela S
Naslov | Prenatal diagnosis of Zellweger spectrum disorder caused by novel variant in PEX6 gene (Meeting Abstract) |
Autori | Joksic Ivana D ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 950-951 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Prenatal diagnosis of Zellweger spectrum disorder caused by novel variant in PEX6 gene (Meeting Abstract) |
Autori | Joksic Ivana D ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 950-951 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Expanding the phenotypic spectrum of MPDZ gene variants: A case report with prenatally detected Dandy-Walker malformation and single ventricle heart (Article) |
Autori | Stankovic Andjela S Toljic Mina Karadzov-Orlic Natasa T Mikovic Zeljko M Joksic Ivana D ![]() |
Info | PRENATAL DIAGNOSIS, (2024), vol. 44 br. 8, str. 1008-1011 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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Naslov | Small supernumerary marker chromosomes in prenatal diagnosis-molecular characterization and clinical outcomes (Article) |
Autori | Joksic Ivana D ![]() |
Info | FRONTIERS IN GENETICS, (2024), vol. 14 br. , str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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Naslov | Rare case of androgenetic-biparental mosacism causing placental mesenchymal dysplasia (Meeting Abstract) |
Autori | Joksic Ivana D ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 1, str. 108-108 |
Ispravka | Web of Science Elečas Rang časopisa |
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