Search Results - Ghorbel, Abdel-Monem

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  1. 1
    Various 30 and 69 bp deletion variants of the Epstein-Barr virus LMP1 may arise by homologous recombination in nasopharyngeal carcinoma of Tunisian patients

    Various 30 and 69 bp deletion variants of the Epstein-Barr virus LMP1 may arise by homologous recombination in nasopharyngeal carcinoma of Tunisian patients by Hadhri-Guiga, Boutheina, Khabir, Abdel-Majid, Mokdad-Gargouri, Raja, Ghorbel, Abdel-Monem, Drira, Mohamed, Daoud, Jamel, Frikha, Mounir, Jlidi, Rachid, Gargouri, Ali

    Published in Virus research
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  2. 2
    Contrasted Frequencies of p53 Accumulation in the Two Age Groups of North African Nasopharyngeal Carcinomas

    Contrasted Frequencies of p53 Accumulation in the Two Age Groups of North African Nasopharyngeal Carcinomas by KHABIR, Ahmed, SELLAMI, Abdelmasid, SAKKA, Mohamed, ABDEL MONEM GHORBEL, DAOUD, Jamel, FRIKHA, Mounir, DRIRA, Mohamed M, BUSSON, Pierre, JLIDI, Rachid

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  3. 3
    Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness

    Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness by Masmoudi, Saber, Antonarakis, Stylianos E., Schwede, Torsten, Ghorbel, Abdel Monem, Gratri, M'hamed, Pappasavas, Marie-Pierre, Drira, Mohamed, Elgaied-Boulila, Amel, Wattenhofer, Marie, Rossier, Colette, Scott, Hamish S., Ayadi, Hammadi, Guipponi, Michel

    Published in Human mutation
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  4. 4
    Various 30 and 69bp deletion variants of the Epstein-Barr virus LMP1 may arise by homologous recombination in nasopharyngeal carcinoma of Tunisian patients

    Various 30 and 69bp deletion variants of the Epstein-Barr virus LMP1 may arise by homologous recombination in nasopharyngeal carcinoma of Tunisian patients by Hadhri-Guiga, Boutheina, Khabir, Abdel-Majid, Mokdad-Gargouri, Raja, Ghorbel, Abdel-Monem, Drira, Mohamed, Daoud, Jamel, Frikha, Mounir, Jlidi, Rachid, Gargouri, Ali

    Published in Virus research
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  5. 5
    Pendred syndrome: Phenotypic variability in two families carrying the same PDS missense mutation

    Pendred syndrome: Phenotypic variability in two families carrying the same PDS missense mutation by 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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  6. 6
    From DFNB2 to Usher syndrome: Variable expressivity of the same disease

    From DFNB2 to Usher syndrome: Variable expressivity of the same disease by Zina, Zeineb Ben, Masmoudi, Saber, Ayadi, Hammadi, Chaker, Fakher, Ghorbel, Abdel Monem, Drira, Mohamed, Petit, Christine

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  7. 7
    Pendred syndrome: Phenotypic variability in two families carrying the samePDS missense mutation

    Pendred syndrome: Phenotypic variability in two families carrying the samePDS missense mutation by 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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