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	1.	[Is there a single form of Charcot-Marie-Tooth disease, or are there several variations? A classification difficulty]. [electronic resource] by Ben Hamida, M Ben Othmane, K Belal, S Hentati, F Producer: 19951129 In: Revue neurologique vol. 151 Availability: No items available. Save to lists Add to cart (remove)
	2.	The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24). [electronic resource] by Le Merrer, M Ben Othmane, K Stanescu, V Lyonnet, S Van Maldergem, L Royer, G Munnich, A Maroteaux, P Producer: 19921127 In: Journal of medical genetics vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Fine localization of the CMT4A locus using a PAC contig and haplotype analysis. [electronic resource] by Ben Othmane, K Rochelle, J M Ben Hamida, M Slotterbeck, B Rao, N Hentati, F Pericak-Vance, M A Vance, J M Producer: 20000407 In: Neurogenetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C) [electronic resource] by Ben Othmane, K Speer, M C Stauffer, J Blel, S Middleton, L Ben Hamida, C Etribi, A Loeb, D Hentati, F Roses, A D Producer: 19951012 In: American journal of human genetics vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	5.	Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. [electronic resource] by 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 Producer: 19940203 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Report and abstracts of the First International Workshop on Human Chromosome 8 Mapping. Vancouver, British Columbia, May 2-4, 1993. [electronic resource] by Wood, S Ben Othmane, K Bergerheim, U S Blanton, S H Bookstein, R Clarke, R A Daiger, S P Donis-Keller, H Drayna, D Kumar, S Producer: 19931103 In: Cytogenetics and cell genetics vol. 64 Availability: No items available. Save to lists Add to cart (remove)
	7.	Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. [electronic resource] by Ben Othmane, K Ben Hamida, M Pericak-Vance, M A Ben Hamida, C Blel, S Carter, S C Bowcock, A M Petruhkin, K Gilliam, T C Roses, A D Producer: 19930623 In: Nature genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity. [electronic resource] by Ben Othmane, K Middleton, L T Loprest, L J Wilkinson, K M Lennon, F Rozear, M P Stajich, J M Gaskell, P C Roses, A D Pericak-Vance, M A Producer: 19931028 In: Genomics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy. [electronic resource] by Noguchi, S McNally, E M Ben Othmane, K Hagiwara, Y Mizuno, Y Yoshida, M Yamamoto, H Bönnemann, C G Gussoni, E Denton, P H Kyriakides, T Middleton, L Hentati, F Ben Hamida, M Nonaka, I Vance, J M Kunkel, L M Ozawa, E Producer: 19951206 In: Science (New York, N.Y.) vol. 270 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)