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Pregled prema Autor Bosankic, Brankica

Prikaz rezultata 1 do 7 od 7
GodinaNaslovAutor(i)Tip rezultataMp-kat.
2024Clinical utility of diagnostic NGS for detection CNV variants in genes associated with skeletal dysplasiaMijovic, Marija; Cuturilo, Goran; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, HristinaKonferencijski rad
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2023Constitutional mismatch repair deficiency syndrome (CMMRD): the significance of customized surveillance protocol for Lynch syndrome-related tumors in relatives at risk-a case reportBosankic, Brankica; Cuturilo, Goran; Petrovic, Hristina; Mijovic, Marija; Ruml-Stojanovic, Jelena; Miletic, AleksandraKonferencijski rad
Mp kategorija će biti prikazana naknadno.
2024Dual molecular diagnosis in patients with skeletal dysplasia - data from tertiary genetic centerMijovic, Marija; Cuturilo, Goran; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, Hristina; Vasic, Bojana; Vukasinovic, NadjaConference Paper
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2023Internal Skeletal Dysplasia Registry within the electronic database of Department of Clinical Genetics University Children's Hospital in Belgrade - basis for a personalised medicine in the futureMijovic, Marija; Cuturilo, Goran; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, HristinaConference Paper
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2022Multiple major anomalies and microcephaly predict the detection of pathogenic copy number variations in patients with moderate and severe global developmental delay/intellectual disabilityRuml-Stojanovic, Jelena; Mijovic, Marija; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, Hristina; Cuturilo, GoranConference Paper
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2020Skeletal dysplasia in the era of genomic testing: first experience of a single genetic outpatient clinic from SerbiaMijovic, Marija; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Janeski, Hristina; Peterlin, Borut; Maver, Ales; Cuturilo, GoranConference Paper
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2022What are key parameters for obtaining the most likely clinical diagnosis from the wide phenotypic spectrum of skeletal dysplasia in patients with previously identified disease-causing gene variantMijovic, Marija; Bukva, Bojan; Ruml-Stojanovic, Jelena; Miletic, Aleksandra; Bosankic, Brankica; Petrovic, Hristina; Cuturilo, GoranConference Paper
Mp. category will be shown later