Search Results - Dhouib, Houria

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  1. 1
    Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family

    Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family by Hmani-Aifa, Mounira, Benzina, Zeineb, Zulfiqar, Fareeha, Dhouib, Houria, Shahzadi, Amber, Ghorbel, Abdelmonem, Rebaï, Ahmed, Söderkvist, Peter, Riazuddin, Sheikh, Kimberling, William J, Ayadi, Hammadi

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  2. 2
    Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome

    Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome by Said, Mariem Ben, Dhouib, Houria, BenZina, Zeineb, Ghorbel, AbdelMoneem, Moreno, Felipe, Masmoudi, Saber, Ayadi, Hammadi, Hmani-Aifa, Mounira

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  3. 3
    Mutation in gap and tight junctions in patients with non-syndromic hearing loss

    Mutation in gap and tight junctions in patients with non-syndromic hearing loss by Belguith, Hanen, Tlili, Abedelaziz, Dhouib, Houria, Rebeh, Imen Ben, Lahmar, Imed, Charfeddine, Ilhem, Driss, Nabil, Ghorbel, Abdelmonem, Ayadi, Hammadi, Masmoudi, Saber

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  4. 4
    Identification of candidate regions for a novel Usher syndrome type II locus

    Identification of candidate regions for a novel Usher syndrome type II locus by Ben Rebeh, Imen, Benzina, Zeineb, Dhouib, Houria, Hadjamor, Imen, Amyere, Mustapha, Ayadi, Leila, Turki, Khalil, Hammami, Bouthaina, Kmiha, Noureddine, Kammoun, Hassen, Hakim, Bochra, Charfedine, Ilhem, Vikkula, Miikka, Ghorbel, Abdelmonem, Ayadi, Hammadi, Masmoudi, Saber

    Published in Molecular vision
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