FP54-FR-05 Genotype and phenotype study in Sudanese and Yemeni families with axonal recessive Charcot-Marie-Tooth disease von Salih, M.A.M, Mikesova, E, Elmalik, S.A, Mukhtar, M.M, LeGuern, E, Azzedine, H

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PO19-WE-05 Linkage analysis and mutation screening in PANK2 and PLA2G6 genes in 7 consanguineous Saudi Arabian families with Karak syndrome von Azzedine, H, Salih, M.A.M, Khan, A, Mundwiller, E, Aldriss, A, Elmalik, S.A, Kabiraj, M.M, Stevanin, G

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P1.16 Novel mutations and loci are associated with limb girdle muscular dystrophy type 2 von Boyden, S.E, Salih, M.A.M, Estrella, E.A, White, A.J, Duncan, A.R, Burgess, S.L, Seidahmed, M.Z, Bennett, R.R, Kunkel, L.M, Kang, P.B

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EM.P.2.04 Unraveling the genetic complexity of alpha-dystroglycanopathies: Ethnically diverse pathogenic mutations von Manzini, M.C, Gleason, D, Chang, B.S, Hill, R.S, Partlow, J.N, Barry, B.J, Poduri, A, Basel-Vanagaite, L, Seidhamed, M.Z, Salih, M.A.M, Dobyns, W.B, Walsh, C.A

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REFINEMENT OF THE CLINICAL PHENOTYPE IN MUSK-RELATED CONGENITAL MYASTHENIC SYNDROMES von MIHAYLOVA, V, SALIH, M. A. M, LOCHMÜLLER, H, GUERGUELTCHEVA, V, MUKHTAR, M. M, ABUZEID, H. A, EL-SADIG, S. M, VON DER HAGEN, M, HUEBNER, A, NÜRNBERG, G, ABICHT, A, MÜLLER, J. S

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Genetic polymorphisms of fecundity genes in Watish Sudanese desert sheep von Mohamed, Sara E Ibrahim, Ahmed, Romaz M, Jawasreh, Khaleel I Z, Salih, M A M, Abdelhalim, Dalia Mursi, Abdelgadir, A W, Obeidat, Md T, Musa, L M A, Ahmed, Mohammed-Khair A

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Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25 von JEN, J, COULIN, C. J, BOSLEY, T. M, SALIH, M. A. M, SABATTI, C, NELSON, S. F, BALOH, R. W

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Government policy and options in pastoral development in the Sudan von Salih, M.A.M. (Nordiska Afrikainst., Uppsala (Sweden))

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Pastoralism and the state in African arid lands. An overview von Salih, M.A.M. (Nordiska Afrikainst., Uppsala (Sweden))

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Ecospace, humanspace and climate change von Dietz, A.J.

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Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity von Salih, M A, Maisonobe, T, Kabiraj, M, al Rayess, M, al-Turaiki, M H, Akbar, M, Tahan, A, Urtizberea, J A, Grid, D, Hamadouche, T, Guilbot, A, Brice, A, Leguern, E

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Moyamoya syndrome with unusual angiographic findings and protein C deficiency: Review of the literature von Andeejani, A.M.I, Salih, M.A.M, Kolawole, T, Gader, AMA, Malabarey, T.O, Al Damegh, S, Al Boukai, A

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Genetic Refinement And Physical Mapping Of The CMT4B Gene On Chromosome 11Q22 von Bolino, A., Levy, E.R., Muglia, M., Conforti, F.L., LeGuern, E., Salih, M.A.M., Georgiou, D.M., Hausmanowa‐Petrusewicz, I., Mandich, P., Gambardella, A., Quattrone, A., Devoto, M., Monaco, A.P.

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AIDS and HIV infection in Sudanese children: a clinical and epidemiological study von Hashim, M S, Salih, M A, el Hag, A A, Karrar, Z A, Osman, E M, el-Shiekh, F S, el Tilib, I A, Attala, N E

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Etudes sur les caractéristiques de l'agent causal Mycobacterium farcinogenes du farcin du bouf au Soudan von El Sanousi, S.M., Salih, M.A.M., Mousa, M.T., Tag el Din, M.H., Soad, A.M.A.

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Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndrome von Seidahmed, M. Zein, Rooney, D.E., Salih, M.A.M., Basit, O. Bashir Abdel, Shaheed, M.M., Abdullah, M.A., Abomelha, A.

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Miliary bovine farcy experimentally induced in a Zebu calf [Mycobacterium farcinogenes] von Sanousi, S. M. El, Salih, M. A. M.

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Multiple congenital malformations in two sibs reminiscent of hydrolethalus and pseudotrisomy 13 syndromes von Dincsoy, Mehmet Y., Salih, Mustafa A. M., Al-Jurayyan, Nasir, Al Saadi, Muslim, Patel, Pravinchandra J.

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Further studies on the properties of the aetiology of bovine farcy isolated from Sudanese cattle von El Sanousi, S.M, Salih, M.A.M, Mousa, M.T, Tag El Din, M.H, Ali, S.A.M

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New hybrid priority scheduling algorithm based on a round Robin with dynamic time quantum von Najm, Nahlah M. A. M.

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