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