Association of spermatogenic failure with the b2/b3 partial AZFc deletion von Eloualid, Abdelmajid, Rhaissi, Houria, Reguig, Ahmed, Bounaceur, Safaa, El Houate, Brahim, Abidi, Omar, Charif, Majida, Louanjli, Noureddine, Chadli, Elbakkay, Barakat, Abdelhamid, Bashamboo, Anu, McElreavey, Ken, Rouba, Hassan

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The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population von Charif, Majida, Bounaceur, Safaa, Abidi, Omar, Nahili, Halima, Rouba, Hassan, Kandil, Mostafa, Boulouiz, Redouane, Barakat, Abdelhamid

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Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss von Nahili, Halima, Charif, Majida, Boulouiz, Redouane, bounaceur, Safaa, Benrahma, Houda, Abidi, Omar, Chafik, Abdelaziz, Rouba, Hassan, Kandil, Mostafa, Barakat, Abdelhamid

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Maternal Effect and Familial Aggregation in a Type 2 Diabetic Moroccan Population von Benrahma, Houda, Arfa, Imen, Charif, Majida, Bounaceur, Safaa, Eloualid, Abdelmajid, Boulouiz, Redouane, Nahili, Halima, Abidi, Omar, Rouba, Hassan, Chadli, Asmaa, Oudghiri, Mounia, Farouqui, Ahmed, Abdelhak, Sonia, Barakat, Abdelhamid

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