VALUE OF OPTICAL GENOME MAPPING (OGM) FOR DIAGNOSTICS OF RARE DISEASES: A FAMILY CASE REPORT
Kovanda A1,2, Miljanović O3, Lovrečić L1,2, Maver A1,2, Hodžić A1,2, Peterlin B1,2,*
*Corresponding Author: *Corresponding Author: Prof. Borut Peterlin, Clinical Institute of Genomic Medicine, University Medical Centre Ljubljana, Šlajmerjeva 4, 1000 Ljubljana, Slovenia. borut.peterlin@kclj.si
page: 87

ACKNOWLEDGMENTS

We would like to profoundly thank the patients and their family members for participating in the study. This work presents the results of studies funded by UMCL tertiary project 20210031, Slovenian Research and In- novation Agency (ARIS) Programme P3-0326, Project J3-4517 Advanced genomic diagnostics for discovering the mechanisms of congenital anomalies, and Bilateral project Slovenija – Montenegro: Genetic epidemiology of congenital anomalies in Slovenia and Montenegro; 02/1- 053/20-2152 (2021 – 2023). Declaration of interest The authors report no conflicts of interest. Supplement Gene panels included in the exome sequencing analysis.



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