
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
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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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