1. Linkage analysis of French families with facioscapulohumeral muscular dystrophy. Issue 8 (August 1989) Authors: Lucotte, G; Berriche, S; Fardeau, M Journal: Journal of medical genetics Issue: Volume 26:Issue 8(1989) Page Start: 485 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D). Issue 6 (June 1997) Authors: Carrié, A; Piccolo, F; Leturcq, F; de Toma, C; Azibi, K; Beldjord, C; Vallat, J M; Merlini, L; Voit, T; Sewry, C; Urtizberea, J A; Romero, N; Tomé, F M; Fardeau, M; Sunada, Y; Campbell, K P; Kaplan, J C; Jeanpierre, M Journal: Journal of medical genetics Issue: Volume 34:Issue 6(1997) Page Start: 470 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy. Issue 3 (March 1998) Authors: Guicheney, P; Vignier, N; Zhang, X; He, Y; Cruaud, C; Frey, V; Helbling-Leclerc, A; Richard, P; Estournet, B; Merlini, L; Topaloglu, H; Mora, M; Harpey, J P; Haenggeli, C A; Barois, A; Hainque, B; Schwartz, K; Tomé, F M; Fardeau, M; Tryggvason, K Journal: Journal of medical genetics Issue: Volume 35:Issue 3(1998) Page Start: 211 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Polyneuropathy after perhexiline maleate therapy. Issue 6020 (22nd May 1976) Authors: Lhermitte, F; Fardeau, M; Chedru, F; Mallecourt, J Journal: BMJ Issue: Volume 1:Issue 6020(1976) Page Start: 1256 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Possible founder effect of rapsyn N88K mutation and identification of novel rapsyn mutations in congenital myasthenic syndromes. Issue 6 (1st June 2003) Authors: Richard, P; Gaudon, K; Andreux, F; Yasaki, E; Prioleau, C; Bauché, S; Barois, A; Ioos, C; Mayer, M; Routon, M C; Mokhtari, M; Leroy, J P; Fournier, E; Hainque, B; Koenig, J; Fardeau, M; Eymard, B; Hantaï, D Journal: Journal of medical genetics Issue: Volume 40:Issue 6(2003) Page Start: e81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies. Issue 9 (September 1995) Authors: Wallgren-Pettersson, C; Clarke, A; Samson, F; Fardeau, M; Dubowitz, V; Moser, H; Grimm, T; Barohn, R J; Barth, P G Journal: Journal of medical genetics Issue: Volume 32:Issue 9(1995) Page Start: 673 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗