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Authors: Francke, U. Darras, B. T. Hersh, I. H. Berg, B. O. Miller, R. G.
Citation: U. Francke, et al., Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneity, American journal of human genetics , 45-I(1), 1989, pp. 63-72

Authors: Koenig, M. Beggs, A. H. Moyer, M. Scherpf, S. Heinrich, K. Bettecken, T. Meng, G. Muller, C. R. Lindlof, M. Kaariainen, H. de la Chapelle, A. Kiuru, A. Savontaus, M.-L. Gilgenkrantz, H. Recan, D. Chelly, J. Kaplan, J.-C. Covone, A. E Archidiacono, N. Romeo, G. Liechti-Gallati, S. Schneider, V. Braga, S. Moser, H. Darras, B. T. Murphy, P. Francke, U. Chen, J. D. Morgan, G. Denton, M. Greenberg, C. R. Wrogemann, K. Blonden, L. A. J. van Paassen, H. M. B. van Ommen, G. J. B. Kunkel, L. M.
Citation: M. Koenig, et al., The molecular basis for duchenne versus becker muscular dystrophy: correlation of severity with type of deletion, American journal of human genetics , 45-I(4), 1989, pp. 498-506
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