Browsing by Author Bennani, Siham
Showing results 1 to 5 of 5
Issue Date | Title | Author(s) |
2010 | The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: Evidence for a founder effect in the Moroccan population | Naamane, Hamid; El Maataoui, Ouafaa; Ailal, Fatima; Barakat, Abdelhamid; Bennani, Siham; Najib, Jilali; Hassar, Mohammed; Saile, Rachid; Bousfiha, Ahmed Aziz |
2011 | allele associated to behçet's disease and to anterior uveitis in Moroccan patients | Radouane, Asmaa; Oudghiri, Mounia; Chakib, Abdelfettah; Naya, Abdallah; Belhouari, Abderrahman; El Malki, Abdelouhab; Bennani, Siham |
2010 | alleles and haplotypes frequencies in Moroccan patients with leukemia Fréquences des allèles et des haplotypes | Radouane, Asmaa; Oudghiri, Mounia; Chakib, Abdelfettah; Naya, Abdallah; Belhouari, Abderrahman; El Malki, Abdelouhab; Bennani, Siham |
2011 | HLA-B*27 allele associated to behçet's disease and to anterior uveitis in Moroccan patients | Kabbaj, Maria; Oudghiri, Mounia; Naya, Abdellah; Naamane, Hamid; El Turk, Joumana; Bennani, Siham; Hassar, Mohamed |
2012 | Snps in the tnf-α gene promoter associated with behçet's disease in moroccan patients | Radouane, Asmaa; Oudghiri, Mounia; Chakib, Abdelfettah; Bennani, Siham; Touitou, Isabelle; Barat-Houari, Mouna |