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

Miletić, Aleksandra; Cuturilo, Goran; Ruml Stojanović, Jelena; Drakulić, Danijela; Mijović, Marija; Bosankić, Brankica; Petrović, Hristina; Stevanović, Milena

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eNauka > Results > 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:	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
Publisher:	Springer Nature
Type:	Conference Paper
Collation:	vol. 31 br. S1 str. 91-344
DOI :	10.1038/s41431-023-01339-3
WoS-ID:	001050507000345
URI:	https://imagine.imgge.bg.ac.rs/handle/123456789/2180 https://enauka.gov.rs/handle/123456789/836443
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)
M-category:	Mp. category will be shown later

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