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Page 1
Mapping of two chromosome 15 microsatellites.
Fougerousse F, Richard I, Broux O, Cohen D, Beckmann JS. Fougerousse F, et al. Among authors: beckmann js. Genomics. 1992 Jul;13(3):903-4. doi: 10.1016/0888-7543(92)90184-t. Genomics. 1992. PMID: 1639425 No abstract available.
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.
Richard I, Brenguier L, Dinçer P, Roudaut C, Bady B, Burgunder JM, Chemaly R, Garcia CA, Halaby G, Jackson CE, Kurnit DM, Lefranc G, Legum C, Loiselet J, Merlini L, Nivelon-Chevallier A, Ollagnon-Roman E, Restagno G, Topaloglu H, Beckmann JS. Richard I, et al. Among authors: beckmann js. Am J Hum Genet. 1997 May;60(5):1128-38. Am J Hum Genet. 1997. PMID: 9150160 Free PMC article.
A diagnostic fluorescent marker kit for six limb girdle muscular dystrophies.
Richard I, Bourg N, Marchand S, Alibert O, Eymard B, van der Kooi AJ, Jackson CE, Garcia C, Burgunder JM, Legum C, de Visser M, Fardeau M, Beckmann JS. Richard I, et al. Among authors: beckmann js. Neuromuscul Disord. 1999 Dec;9(8):555-63. doi: 10.1016/s0960-8966(99)00037-1. Neuromuscul Disord. 1999. PMID: 10619713
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies.
Beckmann JS, Richard I, Broux O, Fougerousse F, Allamand V, Chiannilkulchai N, Lim LE, Duclos F, Bourg N, Brenguier L, Pasturaud P, Quétier F, Roudaut C, Sunada Y, Meyer J, Dinçer P, Lefranc G, Merlini L, Topaloglu H, Tomé FM, Cohen D, Jackson CE, Campbell KP, Fardeau M. Beckmann JS, et al. Neuromuscul Disord. 1996 Dec;6(6):455-62. doi: 10.1016/s0960-8966(96)00386-0. Neuromuscul Disord. 1996. PMID: 9027855
409 results