Group adaptation, formal darwinism and contextual analysis von OKASHA, S., PATERNOTTE, C.

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Campagnes anti-genre en Europe: Des mobilisations contre l’égalité

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Campagnes anti-genre en Europe von Bracke, Sarah, Cornejo, Monica, Dupont, Wannes, Garbagnoli, Sara, Giorgi, Alberta, Graff, Agnieszka, Hodžić, Amir, Kováts, Eszter, Kuhar, Roman, Mayer, Stefanie, McAuliffe, Mary, Moss, Kevin, Paternotte, David, Rochefort, Florence, Stambolis-Ruhstorfer, Michael, Tricou, Josselin, Villa, Paula-Irene

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A new locus for autosomal recessive spastic paraplegia (SPG32) on chromosome 14q12-q21 von STEVANIN, G, PATERNOTTE, C, WEISSENBACH, J, BRICE, A, HAZAN, J, COUTINHO, P, KLEBE, S, ELLEUCH, N, LOUREIRO, J. L, DENIS, E, CRUZ, V. T, DÜRR, A, PRUD'HOMME, J.-F

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Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patients von Doudney, K., Moore, G.E., Stanier, P., Ybot-Gonzalez, P., Paternotte, C., Greene, N.D.E., Copp, A.J., Stevenson, R.E.

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Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2 von Dürr, A., Davoine, C.-S., Paternotte, C., von Fellenberg, J., Cogilnicean, S., Coutinho, P., Lamy, C., Bourgeois, S., Prud'homme, J.-F., Penet, C., Mas, J.-L., Burgunder, J.-M., Hazan, J., Weissenbach, J., Brice, A., Fontaine, B.

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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia von Heilig, Roland, Dürr, Alexandra, Brottier, Philippe, Fontaine, Bertrand, Weissenbach, Jean, Burgunder, Jean-Marc, Paternotte, Caroline, Fonknechten, Nùria, Samson, Delphine, Cruaud, Corinne, Wincker, Patrick, Davoine, Claire-Sophie, Brice, Alexis, Hazan, Jamilé, Cattolico, Laurence, Mavel, Delphine, Artiguenave, François, Barbe, Valérie, Prud'homme, Jean-François

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Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse von Murdoch, Jennifer N., Henderson, Deborah J., Doudney, Kit, Gaston-Massuet, Carles, Phillips, Helen M., Paternotte, Caroline, Arkell, Ruth, Stanier, Philip, Copp, Andrew J.

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Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification von MURDOCH, Jennifer N, DOUDNEY, Kit, PATERNOTTE, Caroline, COPP, Andrew J, STANIER, Philip

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Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay in Two Unrelated Turkish Families von Gücüyener, K., Özgül, Köksal, Paternotte, Caroline, Erdem, H., Prud'homme, J. F., Özgüç, M., Topaloğlu, H.

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Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralog Vangl1 in neural tube defect patients (Am J Med Genet 136A: 90-92, 2005) von Doudney, K., Moore, G.E., Stanier, P., Ybot-Gonzalez, P., Paternotte, C., Greene, N.D.E., Copp, A.J., Stevenson, R.E.

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A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34 von Fontaine, Bertrand, Davoine, Claire-Sophie, Dürr, Alexandra, Paternotte, Caroline, Feki, Imed, Weissenbach, Jean, Hazan, Jamilé, Brice, Alexis

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Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p von Heinzlef, O, Paternotte, C, Mahieux, F, Prud'homme, J F, Dien, J, Madigand, M, Pouget, J, Weissenbach, J, Roullet, E, Hazan, J

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Cloning and Characterization of Igsf9 in Mouse and Human: A New Member of the Immunoglobulin Superfamily Expressed in the Developing Nervous System von Doudney, Kit, Murdoch, Jennifer N, Braybrook, Claire, Paternotte, Caroline, Bentley, Louise, Copp, Andrew J, Stanier, Philip

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Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia von Murdoch, Jennifer N, Doudney, Kit, Gerrelli, Dianne, Wortham, Noel, Paternotte, Caroline, Stanier, Philip, Copp, Andrew J

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Comparative Physical and Transcript Maps of similar to 1 Mb around loop-tail, a Gene for Severe Neural Tube Defects on Distal Mouse Chromosome 1 and Human Chromosome 1q22-q23 von Doudney, K, Murdoch, J N, Paternotte, C, Bentley, L, Gregory, S, Copp, A J, Stanier, P

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Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family von BÜRGER, J, METZKE, H, PATERNOTTE, C, SCHILLING, F, HAZAN, J, REIS, A

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Comparative physical and transcript maps of approximately 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23 von Doudney, K, Murdoch, J N, Paternotte, C, Bentley, L, Gregory, S, Copp, A J, Stanier, P

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Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q von Paternotte, C, Rudnicki, D, Fizames, C, Davoine, C S, Mavel, D, Dürr, A, Samson, D, Marquette, C, Muselet, D, Vega-Czarny, N, Drouot, N, Voit, T, Fontaine, B, Gyapay, G, Auburger, G, Weissenbach, J, Hazan, J

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Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation von Wlodarska, Iwona, Selleri, Licia, La Starza, Roberta, Paternotte, Caroline, Evans, Glen A., Boogaerts, Marc, Van den Berghe, Herman, Mecucci, Cristina

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