Localization of a Novel Autosomal Recessive Non‐syndromic Hearing Impairment Locus DFNB63 to Chromosome 11q13.3‐q13.4 von Tlili, A., Masmoudi, S., Dhouib, H., Bouaziz, S., Rebeh, I. Ben, Chouchen, J., Turki, K., Benzina, Z., Charfedine, I., Drira, M., Ayadi, H.

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Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers von Masmoudi, S, Charfedine, I, Rebeh, IB, Rebai, A, Tlili, A, Ghorbel, AM, Belguith, H, Petit, C, Drira, M, Ayadi, H

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Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness von Ben Rebeh, Imen, Morinière, Madeleine, Ayadi, Leila, Benzina, Zeineb, Charfedine, Ilhem, Feki, Jamel, Ayadi, Hammadi, Ghorbel, Abdelmonem, Baklouti, Faouzi, Masmoudi, Saber

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Pendred syndrome: Phenotypic variability in two families carrying the same PDS missense mutation von Masmoudi, Saber, Charfedine, Ilhem, Hmani, Mounira, Grati, M'hamed, Ghorbel, Abdel Monem, Elgaied-Boulila, Amel, Drira, Mohamed, Hardelin, Jean-Pierre, Ayadi, Hammadi

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Intelligent supervision approach based on multilayer neural PCA and nonlinear gain scheduling von Chaouch, H., Charfedine, S., Ouni, K., Jerbi, H., Nabli, L.

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Echocardiographic analysis in Hypertrophic Cardiomyopathy von Abid, L., Charfedine, S., Hammami, R., Kammoun, S.

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Mutations of LRTOMT , a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans von Riazuddin, S Amer, Ayadi, Leila, Tlili, Abdelaziz, Masmoudi, Saber, Ahmed, Zubair M, Oostrik, Jaap, Ghorbel, Abdelmonem, Riazuddin, Sheikh, Charfedine, Ilhem, Griffith, Andrew J, Hmani-Aifa, Mounira, Kawar, Mayya N, Kalay, Ersan, Belyantseva, Inna A, Karaguzel, Ahmet, Venselaar, Hanka, Morell, Robert J, Mosrati, Mohamed Ali, Riazuddin, Saima, Khan, Shahid Y, Çaylan, Refik, Friedman, Thomas B, Kremer, Hannie, Ayadi, Hammadi, van der Zwaag, Bert, Collin, Rob W J

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SPECT and MRI fusion for an extended bilateral osteoneocrosis von Chtourou, Khalil, Maloul, Mohamed, Kallel, Faouzi, Charfedine, Salma, Hamza, Fatma, Guermazi, Fadhel

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TMC1 but Not TMC2 Is Responsible for Autosomal Recessive Nonsyndromic Hearing Impairment in Tunisian Families von Tlili, Abdelaziz, Rebeh, Imen Ben, Aifa-Hmani, Mounira, Dhouib, Houria, Moalla, Jihen, Tlili-Chouchène, Jihen, Said, Mariem Ben, Lahmar, Imed, Benzina, Zeineb, Charfedine, Ilhem, Driss, Nabil, Ghorbel, Abdelmonem, Ayadi, Hammadi, Masmoudi, Saber

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Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non-syndromic recessive hearing loss von Tlili, Abdelaziz, Charfedine, Ilhem, Lahmar, Imed, Benzina, Zaineb, Amor Mohamed, Ben, Weil, Dominique, Idriss, Nabil, Drira, Mohamed, Masmoudi, Saber, Ayadi, Hammadi

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Genetic variants in RELN are associated with otosclerosis in a non‐European population from Tunisia von Khalfallah, Ayda, Schrauwen, Isabelle, Mnaja, Malek, Fransen, Erik, Lahmar, Imed, Ealy, Megan, Dhouib, Leila, Ayadi, Hammadi, Charfedine, Ilhem, Driss, Nabil, Ghorbel, Abdelmonem, Smith, Richard J.H., Masmoudi, Saber, Van Camp, Guy

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A Novel Autosomal Recessive Non-Syndromic Deafness Locus, DFNB66, Maps to Chromosome 6p21.2-22.3 in a Large Tunisian Consanguineous Family von Tlili, Abdelaziz, Männikkö, Minna, Charfedine, Ilhem, Lahmar, Imed, Benzina, Zeineb, Amor, Mohamed Ben, Driss, Nabil, Ala-Kokko, Leena, Drira, Mohamed, Masmoudi, Saber, Ayadi, Hammadi

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

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SPECT and MRI fusion for an extended bilateral osteonecrosis von Chtourou, Khalil, Maloul, Mohamed, Kallel, Faouzi, Charfedine, Salma, Hamza, Fatma, Guermazi, Fadhel

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Pendred syndrome: Phenotypic variability in two families carrying the samePDS missense mutation von Masmoudi, Saber, Charfedine, Ilhem, Hmani, Mounira, Grati, M'hamed, Ghorbel, Abdel Monem, Elgaied-Boulila, Amel, Drira, Mohamed, Hardelin, Jean-Pierre, Ayadi, Hammadi

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