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: Francke, U. Harper, J.F. Darras, B.T. Cowan, J.M. McCabe, E.R.B. Kohlschutter, A. Seltzer, W.K.

Citation: U. Francke, et al., Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions, American journal of human genetics , 40(3), 1987, pp. 212-227

Authors: de Martinville, B. Wyman, A. R. White, R. Francke, U.

Citation: B. De Martinville, et al., Assignment of the First Random Restriction Fragment Lenght Polymorphism (RFLP) Locus (D14S1) to a Region of Human Chromosome 14, American journal of human genetics , 34(2), 1982, pp. 216-226

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: Yang-Feng, T.L. Floyd-Smith, G. Nemer, M. Drouin, J. Francke, U.

Citation: Yang-feng, T.l et al., The pronatriodilatin gene is located on the distal short arm of human chromosome 1 and on mouse chromosome 4, American journal of human genetics , 37(6), 1985, pp. 1117-1128