Naziv |
Akcije |
Petrović, Davor ; Čulić, Vida ; Swinderek-Alsayed, Zofia
Three Cases of Joubert Syndrome in a Consanguineous Syrian Family and a Interesting Case of Multinational Collaboration // Journal of pediatric genetics, eFirst (2021), 1-4. doi: 10.1055/s-0040-1721826 |
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Tumienė, B. ; Maver, A. ; Writzl, K. ; Hodžić, A. ; Čuturilo, G. ; Kuzmanić-Šamija, R. ; Čulić, V. ; Peterlin, B.
Diagnostic exome sequencing of syndromic epilepsy patients in clinical practice // Clinical genetics, 93 (2018), 5; 1057-1062. doi: 10.1111/cge.13203 |
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Čulić, Vida ; Lasan-Trcić, Ružica ; Liehr, Thomas ; Lebedev, Igor N. ; Pivić, Maja ; Pavelić, Jasminka ; Vulić, Robert
A Familial Small Supernumerary Marker Chromosome 15 Associated with Cryptic Mosaicism with Two Different Additional Marker Chromosomes Derived de novo from Chromosome 9: Detailed Case Study and Implications for Recurrent Pregnancy Loss // Cytogenetic and genome research, 156 (2018), 4; 179-184. doi: 10.1159/000494822 |
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Saraga, Marijan ; Fridl, Vesna ; Tomas, Sandra Zekic ; Arapovic, Adela ; Prgomet, Sandra ; Culic, Vida
The new mutation in PKD2 for early onset of ADPKD // Pediatric Nephrology, 32 (2017), 9; 1759-1759 |
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Vulic, Robert ; Culic, Vida ; Miskovic, Silvana ; Gunjaca, Ivana ; Roje, Damir ; Lasan, Ruzica ; Pavelic, Jasminka
PRENATAL DIAGNOSIS WITH GENETIC COUNSELING IN UHC SPLIT, CROATIA // International journal of advanced research (Indore), 5 (2017), 3; 1272-1276. doi: 10.21474/ijar01/3632 |
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Čulić, Vida ; Polić, Branka: Mišković, Silvana ; Dragišić Ivulić, Slavica ; Žitko, Vanda ; Sipalo, Tatjana ; Pavelić, Jasminka
Sindrom Patau // Paediatria Croatica, 60 (2016), 1; 27-30 |
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Kristina Crkvenac Gornik
Primjena analize mikrosatelitskih lokusa u prenatalnoj i postnatalnoj dijagnostici // Genetičko informiranje u praksi / Čulić, Vida; Pavelić, Jasminka; Radman, Maja) (ur.). Zagreb: Medicinska naklada, 2016. str. 285-286 |
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Čulić, Vida ; Miyake, Noriko ; Janković, Sunčana ; Petrović, Davor ; Šimunović, Marko ; Đapić, Tomislav ; Shiina, Masaaki ; Ogata, Kazuhiro ; Matsumoto, Naomichi ;
Distal arthrogryposis with variable clinical expression caused by TNNI2 mutation // Human genome variation, 3 (2016), 16035, 4. doi: 10.1038/hgv.2016.35 |
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Delaš, Tina
Rascjepi usne i nepca / Čulić, Vida (mentor); Čulić, Vida (neposredni voditelj).
Split, Medicinski fakultet u Splitu, . 2014 |
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Sučić, Matilda
Tumori središnjeg živčanog sustava u djece tijekom petogodišnjeg razdoblja u Splitu / Čulić, Vida (mentor); Čulić, Vida (neposredni voditelj).
Split, Medicinski fakultet u Splitu, . 2014 |
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