Mild and severe muscular dystrophy caused by a single γ-sarcoglycan mutation
MCNALLY, E. M, PASSOS-BUENO, M. R, KUNKEL, L. M, BÖNNEMANN, C. G, VAINZOF, M, DE SA MOREIRA, E, LIDOV, H. G. W, OTHMANE, K. B, DENTON, P. H, VANCE, J. M, ZATZ, M
Published in American journal of human genetics (01.11.1996)
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Published in American journal of human genetics (01.11.1996)
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Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21
Vance, Jeffery M, Baxter, Rachel V, Ben Othmane, Kamel, Rochelle, Julie M, Stajich, Jason E, Hulette, Christine, Dew-Knight, Susan, Hentati, Faycal, Ben Hamida, Mongi, Bel, S, Stenger, Judy E, Gilbert, John R, Pericak-Vance, Margaret A
Published in Nature genetics (01.01.2002)
Published in Nature genetics (01.01.2002)
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Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
Ben Othmane, K, Hentati, F, Lennon, F, Ben Hamida, C, Blel, S, Roses, A D, Pericak-Vance, M A, Ben Hamida, M, Vance, J M
Published in Human molecular genetics (01.10.1993)
Published in Human molecular genetics (01.10.1993)
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Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2B
Vance, J M, Speer, M C, Stajich, J M, West, S, Wolpert, C, Gaskell, P, Lennon, F, Tim, R M, Rozear, M, Othmane, K B
Published in American journal of human genetics (01.07.1996)
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Published in American journal of human genetics (01.07.1996)
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Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)
Ben Othmane, K, Speer, M C, Stauffer, J, Blel, S, Middleton, L, Ben Hamida, C, Etribi, A, Loeb, D, Hentati, F, Roses, A D
Published in American journal of human genetics (01.09.1995)
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Published in American journal of human genetics (01.09.1995)
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The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24)
Le Merrer, M, Ben Othmane, K, Stanescu, V, Lyonnet, S, Van Maldergem, L, Royer, G, Munnich, A, Maroteaux, P
Published in Journal of medical genetics (01.10.1992)
Published in Journal of medical genetics (01.10.1992)
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Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15
Othmane, Kamel Ben, Johnson, Ellen, Menold, Marisa, Graham, Felicia L., Hamida, Mongi Ben, Hasegawa, Osamu, Rogala, Allison D., Ohnishi, Akio, Pericak-Vance, Margaret, Hentati, Faycal, Vance, Jeffery M.
Published in Genomics (San Diego, Calif.) (15.12.1999)
Published in Genomics (San Diego, Calif.) (15.12.1999)
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Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q
Ben Othmane, Kamel, Ben Hamida, Mongi, Pericak-Vance, Margaret A, Ben Hamida, Christiane, Blel, Samir, Carter, Susan C, Bowcock, Anne M, Petruhkin, Konstantin, Conrad Gilliam, T, Roses, Allen D, Hentati, Faycal, Vance, Jeffery M
Published in Nature genetics (01.12.1992)
Published in Nature genetics (01.12.1992)
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Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A
Othmane, K.Ben, Loeb, D., Hayworth-Hodgte, R., Hentati, F., Rao, N., Roses, A.D., Hamida, M.Ben, Pericak-Vance, M.A., Vance, J.M.
Published in Genomics (San Diego, Calif.) (20.07.1995)
Published in Genomics (San Diego, Calif.) (20.07.1995)
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