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Results: 1-6 |
Results: 6

Authors: Rousseau, F. Vincent, A. Rivella, S. Heitz, D. Triboli, C. Maestrini, E. Warren, S. T. Suthers, G. K. Goodfellow, P. Mandel, J. L. Toniolo, D. Oberle, I.
Citation: F. Rousseau, et al., Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA), American journal of human genetics , 48-I(1), 1991, pp. 108-116

Authors: Hanauer, A. Chery, M. Fujita, R. Driesel, A. J. Gilgenkrantz, S. Mandel, J. L.
Citation: A. Hanauer, et al., The friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15, American journal of human genetics , 46-I(1), 1990, pp. 133-137

Authors: Arveiler, B. Oberlé, I. Vincent, A. Hofker, M. H. Pearson, P. L. Mandel, J. L.
Citation: B. Arveiler, et al., Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families, American journal of human genetics , 42(2), 1988, pp. 380-389

Authors: Sirugo, G. Keats, B. Fujita, R. Duclos, F. Purohit, K. Koenig, M. Mandel, J. L.
Citation: G. Sirugo, et al., Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes., American journal of human genetics , 50-I(3), 1992, pp. 559-566

Authors: Feil, R. Palmieri, G. d'Urso, M. Heilig, R. Oberlé, I. Mandel, J. L.
Citation: R. Feil, et al., Physical and genetic mapping of polymorhpic loci in Xq28 (DXSI5, DXS52, and DXS134): analysis of a cosmid clone and a yeast artificial chromosome, American journal of human genetics , 46-II(4), 1990, pp. 720-728

Authors: Arveiler, B. de Saint-Basile, G. Fischer, A. Griscelli, C. Mandel, J. L.
Citation: B. Arveiler, et al., Germ-line mosaicism stimulates genetic heterogeneity in wiskott-aldrich syndrome, American journal of human genetics , 46-II(5), 1990, pp. 906-911
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