Search Results - Bobinec, Adriana

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  1. 1
    97 A novel missense mutation in SGSH gene causing Sanfillipo type 3A mucopolysaccharidosis

    97 A novel missense mutation in SGSH gene causing Sanfillipo type 3A mucopolysaccharidosis by Sansović, Ivona, Odak, Ljubica, Bobinec, Adriana, Barišić, Ingeborg

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  2. 2
    96 Homozygous ABCG8 mutation in a 14-year-old boy with sitosterolemia

    96 Homozygous ABCG8 mutation in a 14-year-old boy with sitosterolemia by Meašić, Ana-Maria, Bobinec, Adriana, Sansović, Ivona, Boban, Ljubica, Pavić, Ana Močić, Pušeljić, Silvija, Barišić, Ingeborg

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  3. 3
    98 Clinical exome sequencing in the diagnosis of autism spectrum disorder

    98 Clinical exome sequencing in the diagnosis of autism spectrum disorder by Odak, Ljubica, Meašić, Ana-Marija, Bobinec, Adriana, Kero, Mijana, Sansović, Ivona, Vulin, Katarina, Tomić, Mirko, Barišić, Ingeborg

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  4. 4
    Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia

    Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia by Sansović, Ivona, Meašić, Ana-Maria, Bobinec, Adriana, Morožin Pohovski, Leona, Odak, Ljubica, Vulin, Katarina, Lozić, Bernarda, Kero, Mijana, Huljev Frković, Sanda, Pušeljić, Silvija

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  5. 5
    84 RARE COPY NUMBER VARIANTS IN CONGENITAL HEART DEFECTS

    84 RARE COPY NUMBER VARIANTS IN CONGENITAL HEART DEFECTS by Davidović, Maša, Pohovski, Leona Morožin, Rogulj, Nikolina Vidan, Sansovic, Ivona, Bobinec, Adriana, Meašić, Ana-Maria, Kero, Mijana, Boban, Ljubica, Malčić, Ivan, Barišic, Ingeborg

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  6. 6
    Chromosomal microarray in clinical diagnosis: a study of 337 patients with congenital anomalies and developmental delays or intellectual disability

    Chromosomal microarray in clinical diagnosis: a study of 337 patients with congenital anomalies and developmental delays or intellectual disability by Sansović, Ivona, Ivankov, Ana-Maria, Bobinec, Adriana, Kero, Mijana, Barišić, Ingeborg

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  7. 7
    Clinically relevant copy number variants in children with congenital anomalies

    Clinically relevant copy number variants in children with congenital anomalies by Sansovic, Ivona, Boban, Ljubica, Ivankov, Ana-Maria, Bobinec, Adriana, Barišic, Ingeborg

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  8. 8
    Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia

    Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia by Sansovic, Ivona, Measic, Ana-Maria, Bobinec, Adriana, Pohovski, Leona Morozin, Odak, Ljubica, Vulin, Katarina, Lozic, Bernarda, Kero, Mijana, Frkovic, Sanda Huljev, Puseljic, Silvija

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  9. 9
    Chromosomal microarray in clinical diagnosis: A study of 337 patients with congenital anomalies and developmental delays or intellectual disability

    Chromosomal microarray in clinical diagnosis: A study of 337 patients with congenital anomalies and developmental delays or intellectual disability by Sansovic, Ivona, Ivankov, Ana-Maria, Bobinec, Adriana, Kero, Mijana, Barisic, Ingeborg

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  10. 10
    Chromosomal microarray in clinical diagnosis: A study of 337 patients with congenital anomalies and developmental delays or intellectual disability

    Chromosomal microarray in clinical diagnosis: A study of 337 patients with congenital anomalies and developmental delays or intellectual disability by Sansovic, Ivona, Ivankov, Ana-Maria, Bobinec, Adriana, Kero, Mijana, Barisic, Ingeborg

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