Authors: Jameleddine, K Bechir, BH Mustapha, M

Citation: K. Jameleddine et al., Formylation of O-silylated enolates by Vilsmeier's reagent, SYN COMMUN, 30(15), 2000, pp. 2759-2762

Authors: Megarbane, A Mustapha, M Bleik, J Waked, N Delague, V Loiselet, J

Citation: A. Megarbane et al., Exclusion of chromosome 15q21.1 in autosomal-recessive Weill-Marchesani syndrome in an inbred Lebanese family, CLIN GENET, 58(6), 2000, pp. 473-478

Authors: Yasunaga, S Grati, M Cohen-Salmon, M El-Amraoui, A Mustapha, M Salem, N El-Zir, E Loiselet, J Petit, C

Citation: S. Yasunaga et al., A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness, NAT GENET, 21(4), 1999, pp. 363-369

Authors: Mustapha, M Weil, D Chardenoux, S Elias, S El-Zir, E Beckmann, JS Loiselet, J Petit, C

Citation: M. Mustapha et al., An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21, HUM MOL GEN, 8(3), 1999, pp. 409-412

Authors: Mustapha, M Salem, N Weil, D El-Zir, E Loiselet, J Petit, C

Citation: M. Mustapha et al., Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness, EUR J HUM G, 6(6), 1998, pp. 548-551