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

Clinical relevance of the TECTA c.6183G>T variant identified in a family with autosomal dominant hearing loss: a case report

por Sansović, Ivona, Meašić, Ana-Maria, Odak, Ljubica, Kero, Mijana
Publicado 2023

Chromosomal microarray in clinical diagnosis: a study of 337 patients with congenital anomalies and developmental delays or intellectual disability

por Sansović, Ivona, Ivankov, Ana-Maria, Bobinec, Adriana, Kero, Mijana, Barišić, Ingeborg
Publicado 2017

Trends in the treatment of undescended testes: a pediatric tertiary care center experience from Croatia

por Bašković, Marko, Zaninović, Luca, Sansović, Ivona, Meašić, Ana Maria, Katušić Bojanac, Ana, Ježek, Davor
Publicado 2022