Publications by authors named "Hanane Bellayou"

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Evolution of molecular diagnosis of Duchenne muscular dystrophy.
Afaf Ben Itto, Khalil Hamzi, Hanane Bellayou, Mohammed Itri, Ilham Slassi

J Mol Neurosci· June 2013

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Prevalence of angiotensin-converting enzyme, methylenetetrahydrofolate reductase, Factor V Leiden, prothrombin and apolipoprotein E gene polymorphisms in Morocco.
Thierry Paluku They-They, Khalil Hamzi, Mohamed Taha Moutawafik, Hanane Bellayou, Mariame El Messal

Ann Hum Biol· November 2010

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A rapid polymerase chain reaction-based test for screening Steinert's disease (DM1).
Khalil Hamzi, Hanane Bellayou, Ilham Slassi, Sellama Nadifi

Neurol India· June 2010

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Duchenne and Becker muscular dystrophy: contribution of a molecular and immunohistochemical analysis in diagnosis in Morocco.
Hanane Bellayou, Khalil Hamzi, Mohamed Abdou Rafai, Mehdi Karkouri, Ilham Slassi

J Biomed Biotechnol· July 2009

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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.
Klaus Dieterich, Raoudha Zouari, Radu Harbuz, François Vialard, Delphine Martinez, Hanane Bellayou

Hum Mol Genet· April 2009

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