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Croatian Medical Journal|November 6, 2023
The first case report of distal 16p12.1p11.2 trisomy and proximal 16p11.2 tetrasomy inherited from both parentsLeona Morožin Pohovski, Ivona Sansović, Katarina Vulin, et al.
Croatian Medical Journal|November 6, 2023
Clinical relevance of the TECTA c.6183G>T variant identified in a family with autosomal dominant hearing loss: a case reportIvona Sansović, Ana-Maria Meašić, Ljubica Odak, et al.
Acta Dermatovenerologica Croatica : ADC|July 14, 2025
Autosomal Recessive Congenital Ichthyosis Due to Heterozygote Variants in the ALOX12B gene Presenting as Mild Nonbullous Congenital Ichthyosiform ErythrodermaIva Hižar Gašpar, Arnes Rešić, Nives Pustišek, et al.
Molecular Cytogenetics|February 7, 2013
Multiplex ligation-dependent probe amplification workflow for the detection of submicroscopic chromosomal abnormalities in patients with developmental delay/intellectual disabilityLeona Morozin Pohovski, Katja K Dumic, Ljubica Odak, et al.
Croatian Medical Journal|June 16, 2011
Novel duplication on chromosome 16 (q12.1-q21) associated with behavioral disorder, mild cognitive impairment, speech delay, and dysmorphic features: case reportLjubica Odak, Ingeborg Barisić, Leona Morozin Pohovski, et al.
Pathology Oncology Research : POR|December 27, 2006
Periacinar Clefting and p63 Immunostaining in Prostatic Intraepithelial Neoplasia and Prostatic CarcinomaBozo Kruslin, Davor Tomas, Aida Cviko, et al.
Croatian Medical Journal|November 6, 2023
Neurodevelopmental disorder caused by an inherited novel KMT5B variant: case reportLjubica Odak, Katarina Vulin, Ana-Maria Meašić, et al.
Croatian Medical Journal|June 13, 2026
Genetic causes of the lissencephaly spectrum: insights from chromosomal microarray and clinical/whole-exome sequencingAna-Maria Meašić, Katarina Vulin, Adriana Bobinec, et al.
Croatian Medical Journal|June 13, 2024
Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from CroatiaIvona Sansović, Ana-Maria Meašić, Adriana Bobinec, et al.
Frontiers in Medicine|April 8, 2021
Sudden Cardiac Death-A New Insight Into Potentially Fatal Genetic MarkersDragan Primorac, Ljubica Odak, Vitorio Perić, et al.
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