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Issue DateTitleAuthor(s)
2009The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African populationDieterich, Klaus; Zouari, Raoudha; Harbuz, Radu; Vialard, Franc¸ois; Martinez, Delphine; Bellayou, Hanane; Prisant, Nadia; Zoghmar, Abdelali; Guichaoua, Marie Roberte; Koscinski, Isabelle; Kharouf, Mahmoud; Noruzinia, Mehrdad; Nadifi, Sellama; Sefiani, Abdelaziz; Lornage, Jacqueline; Zahi, Mohamed; Viville, Ste´phane; Se`le, Bernard; Jouk, Pierre-Simon; Jacob, Marie-Christine; Escalier, Denise; Nikas, Yorgos; Hennebicq, Sylviane; Lunardi, Joe¨l; F. Ray, Pierre
2003Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS a protein that associates with the USH1C protein harmoninWeil, Dominique; El-Amraoui, Aziz; Masmoudi, Saber; Mustapha, Mirna; Kikkawa, Yoshiaki; Laine, Sophie; Delmaghani, Sedigheh; Adato, Avital; Nadifi, Sellama; Ben Zina, Zeineb; Hamel, Christian; Gal, Andreas; Ayadi, Hammadi; Yonekawa, Hiromichi; Petit, Christine
2003Population genetic data of eight tetrameric short tandem repeats (STRs) in Casablanca resident population to use in forensic casework.Chbel, Faiza; Nadifi, Sellama; Martinez-Bouzas, Cristina; Louahlia, Said; Azeddoug, Houssine; Martinez De Pancorbo, Marian
2009Duchenne and becker muscular dystrophy: Contribution of a molecular and immunohistochemical analysis in diagnosis in MoroccoBellayou, Hanane; Hamzi, Khalil; Rafai, Mohamed Abdou; Karkouri, Mehdi; Slassi, Ilham; Azeddoug, Houssine; Nadifi, Sellama
2005Autosomal recessive and sporadic deafness in Morocco: High frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variantGazzaz, Bouchaïb; Weil, Dominique; Raïs, Leïla; Akhyat, Omar; Azeddoug, Houssine; Nadifi, Sellama
2003Population genetic data of eight tetrameric short tandem repeats (STRs) in Casablanca resident population to use in forensic casework.Chbel, Faiza; Nadifi, Sellama; Martinez-Bouzas, Cristina; Louahlia, Said; Azeddoug, Houssine; De Pancorbo, Marian Martinez
2009Duchenne and becker muscular dystrophy: Contribution of a molecular and immunohistochemical analysis in diagnosis in MoroccoBellayou, Hanane; Hamzi, Khalil; Abdou Rafai, Mohamed; Karkouri, Mehdi; Slassi, Ilham; Azeddoug, Houssine; Nadifi, Sellama

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