Ivona Sansović

Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia

Katja K. Dumic, Zorana Grubić, Tony Yuen et al. · The Journal of Steroid Biochemistry and Molecular Biology · 2016 · 42 citations

Life Sciences, Endocrinology, Genetics +16

Beckwith Wiedemann syndrome: A population-based study on prevalence, prenatal diagnosis, associated anomalies and survival in Europe

Ingeborg Barišić, Ljubica Boban, Diana Akhmedzhanova et al. · European Journal of Medical Genetics · 2018 · 42 citations · Full text

Life Sciences, Genetics, Obstetrics +15

Improved Detection of Deletions and Duplications in the DMD Gene Using the Multiplex Ligation-Dependent Probe Amplification (MLPA) Method

Ivona Sansović, Ingeborg Barišić, Katja Dumić · Biochemical Genetics · 2012 · 29 citations

Life Sciences, Genetics, Molecular Genetics +12

<i>GJB2</i> Mutations in Patients with Nonsyndromic Hearing Loss from Croatia

Ivona Sansović, Jelena Knežević, Vesna Musani et al. · Genetic Testing and Molecular Biomarkers · 2009 · 28 citations

Life Sciences, Genetics, Molecular Genetics +17

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

Ivona Sansović, Ana-Maria Ivankov, Adriana Bobinec et al. · Croatian Medical Journal · 2017 · 18 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17