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eNauka >  Results >  EP06.016 22q11.2 microdeletion is the most common genomic abnormality in Serbian newborns with critical congenital heart disease and could be rapidly detected by Multiplex ligation probe amplification analysis
Title: EP06.016 22q11.2 microdeletion is the most common genomic abnormality in Serbian newborns with critical congenital heart disease and could be rapidly detected by Multiplex ligation probe amplification analysis
Authors : Miletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela  ; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena  
Issue Date: 2023
Publication: European Journal of Human Genetics
ISSN: 1018-4813 European Journal of Human Genetics Search Idenfier
1476-5438 European Journal of Human Genetics Search Idenfier
Publisher: Springer Nature
Type: Conference Paper
Collation: vol. 31 br. S1 str. 91-344
DOI : 10.1038/s41431-023-01339-3
URI: https://imagine.imgge.bg.ac.rs/handle/123456789/2180
https://enauka.gov.rs/handle/123456789/866011
Project: Ministarstvo prosvete, nauke i tehnološkog razvoja Republike Srbije, Ugovor br. 200042 (Univerzitet u Beogradu, Institut za molekularnu genetiku i genetičko inženjerstvo)
Serbian Academy of Sciences and Arts (MIKRONEURO_no. 01-2021)
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