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Results: 1-6 |
Results: 6

Authors: Masmoudi, S Antonarakis, SE Schwede, T Ghorbel, AM Gratri, M Pappasavas, MP Drira, M Elgaied-Boutila, A Wattenhofer, M Rossier, C Scott, HS Ayadi, H Guipponi, M
Citation: S. Masmoudi et al., Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness, HUM MUTAT, 18(2), 2001, pp. 101-108

Authors: Ben Zina, Z Masmoudi, S Ayadi, H Chaker, F Ghorbel, AM Drira, M Petit, C
Citation: Z. Ben Zina et al., From DFNB2 to Usher syndrome: Variable expressivity of the same disease, AM J MED G, 101(2), 2001, pp. 181-183

Authors: Henry, S Sacaze, C Berrajah, L Karray, H Drira, M Hammami, A Icart, J Mariame, B
Citation: S. Henry et al., In nasopharyngeal carcinoma-bearing patients, tumors and lymphocytes are infected by different Epstein-Barr virus strains, INT J CANC, 91(5), 2001, pp. 698-704

Authors: Masmoudi, S Charfedine, I Hmani, M Grati, M Ghorbel, AM Elgaied-Boulila, A Drira, M Hardelin, JP Ayadi, H
Citation: S. Masmoudi et al., Pendred syndrome: Phenotypic variability in two families carrying the samePDS missense mutation, AM J MED G, 90(1), 2000, pp. 38-44

Authors: Hmani, M Ghorbel, A Boulila-Elgaied, A Ben Zina, Z Kammoun, W Drira, M Chaabouni, M Petit, C Ayadi, H
Citation: M. Hmani et al., A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2, EUR J HUM G, 7(3), 1999, pp. 363-367

Authors: Khabir, A Boudawara, T Charfeddine, I Drira, M Jlidi, R
Citation: A. Khabir et al., Granular cell tumor of the larynx. Report of a case, SEM HOP PAR, 75(35-36), 1999, pp. 1388-1390
Risultati: 1-6 |