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