De Novo and Inherited Deletions of the 5q13 Region in Spinal Muscular Atrophies von Melki, Judith, Lefebvre, Suzie, Burglen, Lydie, Burlet, Philippe, Clermont, Olivier, Millasseau, Philippe, Reboullet, Sophie, Bénichou, Bernard, Zeviani, Massimo, Le Paslier, Denis, Cohen, Daniel, Weissenbach, Jean, Munnich, Arnold

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Genetic and Physiological Data Implicating the New Human Gene G72 and the Gene for D-Amino Acid Oxidase in Schizophrenia von Chumakov, Ilya, Blumenfeld, Marta, Guerassimenko, Oxana, Cavarec, Laurent, Palicio, Marta, Abderrahim, Hadi, Bougueleret, Lydie, Barry, Caroline, Tanaka, Hiroaki, La Rosa, Philippe, Puech, Anne, Tahri, Nadia, Cohen-Akenine, Annick, Delabrosse, Sylvain, Lissarrague, Sébastien, Picard, Françoise-Pascaline, Maurice, Karelle, Essioux, Laurent, Millasseau, Philippe, Grel, Pascale, Debailleul, Virginie, Simon, Anne-Marie, Caterina, Dominique, Dufaure, Isabelle, Malekzadeh, Kattayoun, Belova, Maria, Luan, Jian-Jian, Bouillot, Michel, Sambucy, Jean-Luc, Primas, Gwenael, Saumier, Martial, Boubkiri, Nadia, Martin-Saumier, Sandrine, Nasroune, Myriam, Peixoto, Hélène, Delaye, Arnaud, Pinchot, Virginie, Bastucci, Mariam, Guillou, Sophie, Chevillon, Magali, Sainz-Fuertes, Ricardo, Meguenni, Said, Aurich-Costa, Joan, Cherif, Dorra, Gimalac, Anne, van Duijn, Cornelia, Gauvreau, Denis, Ouelette, Gail, Fortier, Isabel, Realson, John, Sherbatich, Tatiana, Riazanskaia, Nadejda, Rogaev, Evgeny, Raeymaekers, Peter, Aerssens, Jeroen, Konings, Frank, Luyten, Walter, Macciardi, Fabio, Sham, Pak C., Straub, Richard E., Weinberger, Daniel R., Cohen, Nadine, Cohen, Daniel

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Isolation of 10 Differentially Expressed cDNAs in p53-Induced Apoptosis: Activation of the Vertebrate Homologue of the Drosophila Seven in Absentia Gene von Amson, Robert B., Nemani, Mona, Roperch, Jean-Pierre, Israeli, David, Bougueleret, Lydie, Le Gall, Isabelle, Medhioub, Monia, Linares-Cruz, Gustavo, Lethrosne, Florence, Pasturaud, Patricia, Piouffre, Laurence, Prieur, Sylvie, Susini, Laurent, Alvaro, Véronique, Millasseau, Philippe, Guidicelli, Catherine, Bui, Hung, Massart, Catherine, Cazes, Lucien, Dufour, Fabienne, Bruzzoni-Giovanelli, Heriberto, Owadi, Houman, Hennion, Claude, Charpak, Georges, Dausset, Jean, Calvo, Fabien, Oren, Moshe, Cohen, Daniel, Telerman, Adam

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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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Identification and characterization of a spinal muscular atrophy-determining gene von Lefebvre, Suzie, Bürglen, Lydie, Reboullet, Sophie, Clermont, Olivier, Burlet, Philippe, Viollet, Louis, Benichou, Bernard, Cruaud, Corinne, Millasseau, Philippe, Zeviani, Massimo, Le Paslier, Denis, Frézal, Jean, Cohen, Daniel, Weissenbach, Jean, Munnich, Arnold, Melki, Judith

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The 1993-94 Généthon human genetic linkage map von Bernardi, Giorgio, Vignal, Alain, Morissette, Jean, Marc, Sophie, Millasseau, Philippe, Weissenbach, Jean, Fizames, Cécile, Lathrop, Mark, Gyapay, Gabor, Dib, Colette

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A second-generation linkage map of the human genome von Weissenbach, Jean, Gyapay, Gabor, Dib, Colette, Vignal, Alain, Morissette, Jean, Millasseau, Philippe, Vaysseix, Guy, Lathrop, Mark

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E-box- and MEF-2-independent muscle-specific expression, positive autoregulation, and cross-activation of the chicken MyoD (CMD1) promoter reveal an indirect regulatory pathway von Dechesne, C A, Wei, Q, Eldridge, J, Gannoun-Zaki, L, Millasseau, P, Bougueleret, L, Caterina, D, Paterson, B M

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Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3 von Gecz, J., Pollaord, H., Consalez, G., Villard, L., Stayton, C., Millasseau, P., Khrestchatisky, M., Fontes, M.

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Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and de... von Plassart, E, Reboul, J, Rime, C S, Recan, D, Millasseau, P, Eymard, B, Pelletier, J, Thomas, C, Chapon, F, Desnuelle, C

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The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules von Legouis, Renaud, Hardelin, Jean-Pierre, Levilliers, Jacqueline, Claverie, Jean-Michel, Compain, Sylvia, Wunderle, Véronique, Millasseau, Philippe, Le Paslier, Denis, Cohen, Daniel, Caterina, Dominique, Bougueleret, Lydie, Delemarre-Van de Waal, Henriette, Lutfalla, Georges, Weissenbach, Jean, Petit, Christine

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Predisposing Gene for Early-Onset Prostate Cancer, Localized on Chromosome 1q42.2-43 von Berthon, Philippe, Valeri, Antoine, Cohen-Akenine, Annick, Drelon, Eric, Paiss, Thomas, Wöhr, Gudrun, Latil, Alain, Millasseau, Philippe, Mellah, Imène, Cohen, Nadine, Blanché, Hélène, Bellané-Chantelot, Christine, Demenais, Florence, Teillac, Pierre, Le Duc, Alain, de Petriconi, Robert, Hautmann, Richard, Chumakov, Ilya, Bachner, Lucien, Maitland, Norman J., Lidereau, Rosette, Vogel, Walther, Fournier, Georges, Mangin, Philippe, Cohen, Daniel, Cussenot, Olivier

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Two DRβ Allelic Series Defined by Exon II-Specific Synthetic Oligonucleotide Genomic Hybridization: A Method of HLA Typing? von Le Gall, Isabelle, Millasseau, Philippe, Dausset, Jean, Cohen, Daniel

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Use of Synthetic Oligonucleotides for Genomic DNA Dot Hybridization to Split the DQw3 Haplotype von Martell, Maria, Le Gall, Isabelle, Millasseau, Philippe, Dausset, Jean, Cohen, Daniel

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Survey of CAG/CTG Repeats in Human cDNAs Representing New Genes: Candidates for Inherited Neurological Disorders von Néri, Christian, Albanèse, Véronique, Lebre, Anne-Sophie, Holbert, Sébastien, Saada, Claudine, Bougueleret, Lydie, Meier-Ewert, Sebastian, Le Gall, Isabelle, Millasseau, Philippe, Bui, Hung, Giudicelli, Catherine, Massart, Catherine, Guillou, Sophie, Gervy, Patricia, Poullier, Eric, Rigault, Philippe, Weissenbach, Jean, Lennon, Greg, Chumakov, Ilya, Dausset, Jean, Lehrach, Hans, Cohen, Daniel, Cann, Howard M.

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Down-regulation of mitochondrial mRNAs in the mdx mouse model for Duchenne muscular dystrophy von Gannoun-Zaki, L, Fournier-Bidoz, S, Le Cam, G, Chambon, C, Millasseau, Ph, Léger, J.J, Dechesne, C.A

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IIlegitimate transcription of the phenylalanine hydroxylase gene in lymphocytes for identification of mutations in phenylketonuria von Abadie, V., Jaruzelska, J., Lyonnet, S., Millasseau, P., Berthelon, M., Rey, F., Munnich, A., Rey, J.

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Illegitimate transcription of the phenylalanine hydroxylase gene in lymphocytes for identification of mutations in phenylketonuria von ABADIE, V, JARUZELSKA, J, LYONNET, S, MILLASSEAU, P, BERTHELON, M, REY, F, MUNNICH, A, REY, J

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Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: identification of three new transcripts von Gecz, J., Vlllard, L., Lossl, A.M., Mlllasseau, P., Djaball, M., Fontes, M.

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The 1993-94 Généthon human genetic linkage map von GYAPAY, G, MORISSETTE, J, VIGNAL, A, DIB, C, FIZAMES, C, MILLASSEAU, P, MARC, S, BERNARDI, G, LATHROP, M, WEISSENBACH, J

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