Lack of association between signaling lymphocytic activation molecule family member 1 gene and rheumatoid arthritis in the French and Tunisian populations

Por G Chabchoub, Petit‐Teixeira, E, Maalej, A, Pierlot, C, Bahloul, Z, Cornélis, F, Ayadi, H
Publicado em 2006

Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse origins.

Por Adato, A, Weil, D, Kalinski, H, Pel-Or, Y, Ayadi, H, Petit, C, Korostishevsky, M, Bonne-Tamir, B
Publicado em 1997

Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome

Por Hmani-Aifa, M, Arab, S, Kharrat, K, Orten, D, Boulila-Elgaied, A, Drira, M, Hachicha, S, Kimberling, W, Ayadi, H
Publicado em 2002

Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE

Por MASMOUDI, S., ELGAIED-BOULILA, A., KASSAB, I., ARAB, S. B., BLANCHARD, S., BOUZOUITA, J., DRIRA, M., KASSAB, A., HACHICHA, S., PETIT, C., AYADI, H.
Publicado em 2000