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Results: 1-4 |
Results: 4

Authors: Romero, NB De Lonlay, P Llense, S Leturcq, F Touati, G Urtizberea, JA Saudubray, JM Munnich, A Kaplan, JC Recan, D
Citation: Nb. Romero et al., Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomaticcarrier with 'de novo' duplication of dystrophin gene, NEUROMUSC D, 11(5), 2001, pp. 494-498

Authors: Canki-Klain, N Recan, D Milicic, D Llense, S Leturcq, F Deburgrave, N Kaplan, JC Debevec, M Zurak, N
Citation: N. Canki-klain et al., Clinical variability and molecular diagnosis in a four-generation family with X-linked Emery-Dreifuss muscular dystrophy, CROAT MED J, 41(4), 2000, pp. 389-395

Authors: Merlini, L Kaplan, JC Navarro, C Barois, A Bonneau, D Brasa, J Echenne, B Gallano, P Jarre, L Jeanpierre, M Kalaydjieva, L Leturcq, F Levi-Gomes, A Toutain, A Tournev, I Urtizberea, A Vallat, JM Voit, T Warter, JM
Citation: L. Merlini et al., Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation, NEUROLOGY, 54(5), 2000, pp. 1075-1079

Authors: Dincer, P Piccolo, F Leturcq, F Kaplan, JC Jeanpierre, M Topaloglu, H
Citation: P. Dincer et al., Prenatal diagnosis of limb-girdle muscular dystrophy Type 2C, PRENAT DIAG, 18(12), 1998, pp. 1300-1303
Risultati: 1-4 |