Search Results - Hasanhodžić, Mensuda

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  1. 1
    Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss

    Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss by Likar, Tina, Hasanhodžić, Mensuda, Teran, Nataša, Maver, Aleš, Peterlin, Borut, Writzl, Karin

    Published in PloS one
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  2. 2
    FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature

    FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature by Cannaerts, Elyssa, Shukla, Anju, Hasanhodzic, Mensuda, Alaerts, Maaike, Schepers, Dorien, Van Laer, Lut, Girisha, Katta M, Hojsak, Iva, Loeys, Bart, Verstraeten, Aline

    Published in BMC medical genetics
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  3. 3
    Down Syndrome and thyroid gland

    Down Syndrome and thyroid gland by Hasanhodzić, Mensuda, Tahirović, Husref, Lukinac, Ljerka

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  4. 4
    Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome

    Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome by Toromanovic, Alma, Tahirovic, Husref, Milenkovic, Tatjana, Koehler, Katrin, Kind, Barbara, Zdravkovic, Dragan, Hasanhodzic, Mensuda, Huebner, Angela

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  5. 5
    Diagnostics of common microdeletion syndromes using fluorescence in situ hybridization: single center experience in a developing country

    Diagnostics of common microdeletion syndromes using fluorescence in situ hybridization: single center experience in a developing country by Kurtovic-Kozaric, Amina, Mehinovic, Lejla, Stomornjak-Vukadin, Meliha, Kurtovic-Basic, Ilvana, Catibusic, Feriha, Kozaric, Mirza, Mesihovic-Dinarevic, Senka, Hasanhodzic, Mensuda, Glamuzina, Darinka

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