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Results: 3

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: Ben Arab, S Hmani, M Denoyelle, F Boulila-Elgaied, A Chardenoux, S Hachicha, S Petit, C Ayadi, H
Citation: S. Ben Arab et al., Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates, CLIN GENET, 57(6), 2000, pp. 439-443

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
Risultati: 1-3 |