A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex von Haines, J.L., Ter-Minassian, M., Bazyk, A., Gusella, J.F., Kim, D.J., Terwedow, H., PericakVance, M.A., Rimmler, J.B., Haynes, C.S., Roses, A.D., Lee, A., Shaner, B., Menold, M., Seboun, E., Fitoussi, R-P., Gartioux, C., Reyes, C., Ribierre, F., Gyapay, G., Weissenbach, J., Hauser, S.L., Goodkin, D.E., Lincoln, R., Usuku, K., Garcia-Merino, A., Gatto, N., Young, S., Oksenberg, J.R.

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A Causative Relationship between Mutant IFNgR1 Alleles and Impaired Cellular Response to IFNγ in a Compound Heterozygous Child von Altare, Frédéric, Jouanguy, Emmanuelle, Lamhamedi-Cherradi, Salma, Fondanèche, Marie-Claude, Fizame, Cécile, Ribiérre, Florence, Merlin, Gilles, Dembic, Zlatko, Schreiber, Robert, Lisowska-Grospierre, Barbara, Fischer, Alain, Seboun, Eric, Casanova, Jean-Laurent

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Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene von SEBOUN, E, BARBAUX, S, KASAHARA, M, BOURGERON, T, NISHI, S, ALGONIK, A, EGASHIRA, M, NIKKAWA, N, BISHOP, C, FELLOUS, M, MCELREAVEY, K

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G.O.5 A new autosomal dominant distal vacuolar myopathy associated with mutation of the nuclear matrix protein, matrin 3 von Senderek, J, Garvey, S.M, Krieger, M, Tournev, I, Elbracht, M, Roos, A, Stendel, C, Urtizberea, A, Guergueltcheva, V, Mihailova, V, Feit, H, Tramonte, J, Hedera, P, Bergmann, C, Rudnik-Schöneborn, S, Zerres, K, Lochmüller, H, Seboun, E, Beckmann, J.S, Hauser, M.A, Jackson, C.E, Weis, J

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A comprehensive genetic map of the human genome based on 5,264 microsatellites von Dib, Colette, Fauré, Sabine, Fizames, Cécile, Samson, Delphine, Drouot, Nathalie, Vignal, Alain, Millasseau, Philippe, Marc, Sophie, Kazan, Jamile, Seboun, Eric, Lathrop, Mark, Gyapay, Gabor, Morissette, Jean, Weissenbach, Jean

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Interferon-γ –Receptor Deficiency in an Infant with Fatal Bacille Calmette–Guérin Infection von Jouanguy, Emmanuelle, Altare, Frédéric, Lamhamedi, Salma, Revy, Patrick, Emile, Jean-François, Newport, Melanie, Levin, Michael, Blanche, Stéphane, Seboun, Eric, Fischer, Alain, Casanova, Jean-Laurent

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A susceptibility locus for multiple sclerosis is linked to the T cell receptor β chain complex von Seboun, E., Robinson, M.A., Doolittle, T.H., Ciulla, T.A., Kindt, T.J., Hauser, S.L.

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Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy von Nakabayashi, Kazuhiko, Amann, Daniela, Ren, Yan, Saarialho-Kere, Ulpu, Avidan, Nili, Gentles, Simone, MacDonald, Jeffrey R., Puffenberger, Erik G., Christiano, Angela M., Martinez-Mir, Amalia, Salas-Alanis, Julio C., Rizzo, Renata, Vamos, Esther, Raams, Anja, Les, Clifford, Seboun, Eric, Jaspers, Nicolaas G.J., Beckmann, Jacques S., Jackson, Charles E., Scherer, Stephen W.

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Vocal Cord and Pharyngeal Weakness with Autosomal Dominant Distal Myopathy: Clinical Description and Gene Localization to 5q31 von Feit, Howard, Silbergleit, Alice, Schneider, Lori B., Gutierrez, Jorge A., Fitoussi, Reine-Paule, Réyès, Cécile, Rouleau, Guy A., Brais, Bernard, Jackson, Charles E., Beckmann, Jacques S., Seboun, Eric

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Unusual Organization of the Human T-Cell Receptor β-Chain Gene Complex is Linked to Recombination Hotspots von Seboun, E., Houghton, L., C. J. Hatem, Jr, Lincoln, R., Hauser, S. L.

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Amish brittle hair syndrome gene maps to 7p14.1 von Seboun, Eric, Lemainque, Arnaud, Jackson, Charles E.

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Insertion/deletion-related polymorphisms in the human T cell receptor β gene complex von SEBOUN, E, ROBINSON, M. A, KONDT, T. J, HAUSER, S. L

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Genetics of Demyelinating Diseases von Oksenberg, Jorge R., Seboun, Eric, Hauser, Stephen L.

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Testis-specific transcripts detected by a human Y-DNA-derived probe von Leroy, P, Seboun, E, Mattei, M G, Fellous, M, Bishop, C E

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Molecular Genotypes of the T-Cell Receptor Beta Chain in Families with Multiple Sclerosis von CIULLA, T. A., ROBINSON, M. A., SEBOUN, E., DOOLITTLE, T. H., HAYASHI, T., KINDT, T. J., HAUSER, S. L.

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Prenatal identification of a Y-chromosome deletion by Y-specific single copy DNA probes von Gilgenkrantz, S., Droulle, P., Seboun, E., Casanova, M., Schweitzer, M., Goosens, M., Fellous, M.

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Vacuoliting megalencephalic leukoencephalopathy with subcortical cysts, mapped to chromosome 22qtel von TOPCU, M, GARTIOUX, C, RIBIERRE, F, YALCINKAYA, C, TOKUS, E, ÖZTEKIN, N, BECKMANN, J. S, OZGUC, M, SEBOUN, E

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Linkage analysis of candidate myelin genes in familial multiple sclerosis von Seboun, E, Oksenberg, J R, Rombos, A, Usuku, K, Goodkin, D E, Lincoln, R R, Wong, M, Pham-Dinh, D, Boesplug-Tanguy, O, Carsique, R, Fitoussi, R, Gartioux, C, Reyes, C, Ribierre, F, Faure, S, Fizames, C, Gyapay, G, Weissenbach, J, Dautigny, A, Rimmler, J B, Garcia, M E, Pericak-Vance, M A, Haines, J L, Hauser, S L

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Etude des facteurs génétiques d'une maladie à hérédité complexe : la sclérose en plaques: Les maladies génétiques multifactorielles von SEBOUN, E

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A causative relationship between mutant IFNgR1 alleles and impaired cellular response to IFNgamma in a compound heterozygous child von Altare, F, Jouanguy, E, Lamhamedi-Cherradi, S, Fondanéche, M C, Fizame, C, Ribiérre, F, Merlin, G, Dembic, Z, Schreiber, R, Lisowska-Grospierre, B, Fischer, A, Seboun, E, Casanova, J L

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