PCR-RFLP, Sequencing, and Quantification in Molecular Diagnosis of Spinal Muscular Atrophy: Limits and Advantages by Hamzi, K., Bellayou, H., Itri, M., Nadifi, S.

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Ataxia with vitamin E deficiency (AVED); an example of the contribution of research in molecular genetic to counselling in Morocco by Bellayou, H., Dehbi, H., Bourezgui, M., Slassi, I., Nadifi, S.

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The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population by Dieterich, Klaus, Zouari, Raoudha, Harbuz, Radu, Vialard, François, 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, Stéphane, Sèle, Bernard, Jouk, Pierre-Simon, Jacob, Marie-Christine, Escalier, Denise, Nikas, Yorgos, Hennebicq, Sylviane, Lunardi, Joël, Ray, Pierre F.

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The normal distribution of PRNP codon 129 polymorphism in the Moroccan population (Arabs and Casablanca residents) by Nadifi, S., Slassi, I., Hachimi, K.M. El, Gazzaz, B., Bellayou, H., Raddaoui, K., Laplanche, J.L.

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Étude de la corrélation génotype–phénotype dans l’amyotrophie spinale infantile (ASI) dans une famille marocaine by They-They, T.P., Nadifi, S., Dehbi, H., Bellayou, H., Brik, H., Slassi, I., Itri, M.

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Phenotype-genotype correspondence in spinal muscular atrophy in a Moroccan family by They-They, T P, Nadifi, S, Dehbi, H, Bellayou, H, Brik, H, Slassi, I, Itri, M

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