Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
Sansović, Ivona; Barišić, Ingeborg; Morožin Pohovski, Leona; Odak, Ljubica; Vulin, Katarina
Nova missense varijanta u genu KIF1A kod bolesnice s NESCAV sindromom // Liječnički vjesnik : glasilo Hrvatskog liječničkog zbora. Suplement, 145, suppl 5. 2023. str. 205-205
Morožin Pohovski, Leona; Sansović, Ivona; Vulin, Katarina; Odak, Ljubica
The first case report of distal 16p12.1p11.2 trisomy and proximal 16p11.2 tetrasomy inherited from both parents // Croatian medical journal, 64 (2023), 5; 339-343. doi: 10.3325/cmj.2023.64.339
Vulin, Katarina ; Odak, Ljubica ; Morožin Pohovski, Leona ; Đaković, Ivana ; Tripalo Batoš, Ana ; Meašić, Ana-Maria ; Kero, Mijana ; Sansović, Ivona ; Bobinec, Adrana ; Barišić, Ingeborg
Chromosomal microarray in clinical diagnosis of cerebral palsy // Journal of bioanthropology / Marjanović, D (ur.). 2022. str. 308-308 doi: 10.54062/jb
Morozin Pohovski, Leona ; Bobinec, Adriana ; Measic, Ana-Maria ; Sansovic, Ivona ; Barisic, Ingeborg
A new case of intragenic deletion of the TCF4 gene without features of Pitt-Hopkins syndrome // Molecular and experimental biology in medicine, 3 (2020), 2; 56-58. doi: 10.33602/mebm.3.2.8
Zergollern-Čupak, Ljiljana ; Barišić, Ingeborg ; Morožin-Pohovski, Leona
Development of genetics in the world and in Croatia – forty years of the Croatian Society of Human Genetics of the Croatian Medical Association // Collegium antropologicum, 38 (2014), 3; 809-818
Morožin Pohovski, L ; Barišić, I
Identification of microdeletion 8q23.3q24.11 by MLPA in patient with multiple hereditary exostoses // European journal of human genetics Supplement 1. Nature publishing group, 2014. str. 447-448
Sansović, I ; Morožin Pohovski, L ; Barišić, I
Microduplication of Xp22.31 region involving the STS gene in two males with intellectual disability // European journal of human genetics. Nature publishing group, 2014. str. 163-164
Kero, Mijana ; Morožin-Pohovski, Leona ; Čače, Neven ; Barišić, Ingeborg
Sindrom Kleefstra: prikaz bolesnika s asimetričnom hipetrofičnom kardiomiopatijom // Pediatria Croatica Supplement. 2014. str. 106-107
Morožin Pohovski, Leona ; Barišić, Ingeborg
Multiplex ligation-dependent probe amplification (MLPA) genetic testing in the diagnostics of children with developmental delay/intellectual disabilities. // Folia medica Facultatis medicinae Universitatis Saraeviensis, 49 (2014), 1; 15-21
