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

Authors: Laing, N. G. Majda, B. T. Akkari, P. A. Layton, M. G. Mulley, J. C. Phillips, H. Haan, E. A. White, S. J. Beggs, A. H. Kunkel, L. M. Groth, D. M. Boundy, K. L. Kneebone, C. S. Blumberg, P. C. Wilton, S. D. Speer, M. C. Kakulas, B. A.

Citation: G. Laing, N. et al., Assignment of a gene (NEM1) for autosomal dominant nemaline myopathy to chromosome 1, American journal of human genetics , 50-I(3), 1992, pp. 576-583

Authors: Feener, C. A. Boyce, F. M. Kunkel, L. M.

Citation: A. Feener, C. et al., Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene., American journal of human genetics , 48-I(3), 1991, pp. 621-627

Authors: Richards, C. S. Watkins, S. C. Hoffman, E. P. Schneider, N. R. Milsark, I. W. Katz, K. S. Cook, I. D. Kunkel, L. M. Cortada, J. M.

Citation: S. Richards, C. et al., Skewed X inactivation in a female MZ twin results in duchenne muscular dystrophy, American journal of human genetics , 46-II(4), 1990, pp. 672-681

Authors: Bertelson, C.J. Pogo, A. O. Chaudhuri, A. Marsh, W. L. Redman, C. M. Banerjee, D. Symmans, W. A. Simon, T. Frey, D. Kunkel, L. M.

Citation: Bertelson, C.j et al., Localization of the McLeod Locus (XK) within XP21 by deletion analysis, American journal of human genetics , 42(5), 1988, pp. 703-711