The first case report of distal 16p12.1p11.2 trisomy and proximal 16p11.2 tetrasomy inherited from both parents

por Morožin Pohovski, Leona, Sansović, Ivona, Vulin, Katarina, Odak, Ljubica
Publicado 2023

Neurodevelopmental disorder caused by an inherited novel KMT5B variant: case report

por Odak, Ljubica, Vulin, Katarina, Meašić, Ana-Maria, Šamadan, Lara, Batoš, Ana Tripalo
Publicado 2023

Visual impairment in children with cerebral palsy: Croatian population-based study for birth years 2003-2008

por Striber, Neda, Vulin, Katarina, Đaković, Ivana, Prvčić, Iva, Đuranović, Vlasta, Cerovski, Branimir, Pejić Roško, Sanja, Čokolić Petrović, Dunja, Martinec, Sunčica, Dawidowsky, Barbara, Mejaški Bošnjak, Vlatka
Publicado 2019