Non-association of Crohn's disease with NOD2 gene variants in Moroccan patients von Hama, I., Ratbi, I., Reggoug, S., Elkerch, F., Kharrasse, G., Errabih, I., Ouazzani, H., Sefiani, A.

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Cytogenetic and epidemiological profiles of Down syndrome in a Moroccan population: a report of 852 cases von Jaouad, I C, Cherkaoui Deqaqi, S, Sbiti, A, Natiq, A, Elkerch, F, Sefiani, A

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Frequencies of CYP3A51/3 variants in a Moroccan population and effect on tacrolimus daily dose requirements in renal transplant patients von Elmachad, Mustapha, Elkabbaj, Driss, Elkerch, Fatiha, Laarabi, Fatima Zahra, Barkat, Amina, Oualim, Zouhir, Sefiani, Abdelaziz

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Cytogenetic analysis of 5572 patients referred for suspected chromosomal abnormalities in Morocco von Aboussair, Nisrine, Jaouad, Imane Cherkaoui, Dequaqui, Souad Cherkaoui, Sbiti, Aziza, Elkerch, Fatiha, Yahya, Benbouchta, Natiq, Abdelhafid, Sefiani, Abdelaziz

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Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity von Piccolo, F, Chaouch, M, Jeanpierre, M, Romero, N.B, Campbell, K.P, Voit, T, Kaplan, J-C, El Kerch, F, Collin, H, Roberds, S.L, Eymard, B, Fardeau, M, Leturcq, F, Beckmann, J.S, Sefiani, A, Tomé, F.M.S, Azibi, K, Récan, D, Reghis, A, Merlini, L, Beldjord, C, Carrié, A

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Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa von el Kerch, F, Sefiani, A, Azibi, K, Boutaleb, N, Yahyaoui, M, Bentahila, A, Vinet, M C, Leturcq, F, Bachner, L, Beckmann, J

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Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency von ROMERO, N. B, TOME, F. M. S, KAPLAN, J.-C, LETURCQ, F, FATIHA EL KERCH, KEMAL AZIBI, BACHNER, L, ANDERSON, R. D, ROBERDS, S. L, CAMPBELL, K. P, FARDEAU, M

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