Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse) von de Pontual, Loïc, Népote, Virginie, Attié-Bitach, Tania, Al Halabiah, Hassan, Trang, Ha, Elghouzzi, Vincent, Levacher, Béatrice, Benihoud, Karim, Augé, Joëlle, Faure, Christophe, Laudier, Béatrice, Vekemans, Michel, Munnich, Arnold, Perricaudet, Michel, Guillemot, François, Gaultier, Claude, Lyonnet, Stanislas, Simonneau, Michel, Amiel, Jeanne

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PAX8, TITF1, and FOXE1 Gene Expression Patterns during Human Development: New Insights into Human Thyroid Development and Thyroid Dysgenesis-Associated Malformations von Trueba, Sylvia Sura, Augé, Joëlle, Mattei, Géraldine, Etchevers, Heather, Martinovic, Jélééna, Czernichow, Paul, Vekemans, Michel, Polak, Michel, Attié-Bitach, Tania

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Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome von Karmous-Benailly, Houda, Martinovic, Jelena, Gubler, Marie-Claire, Sirot, Yoann, Clech, Laure, Ozilou, Catherine, Augé, Joëlle, Brahimi, Nora, Etchevers, Heather, Detrait, Eric, Esculpavit, Chantal, Audollent, Sophie, Goudefroye, Géraldine, Gonzales, Marie, Tantau, Julia, Loget, Philippe, Joubert, Madeleine, Gaillard, Dominique, Jeanne-Pasquier, Corinne, Delezoide, Anne-Lise, Peter, Marie-Odile, Plessis, Ghislaine, Simon-Bouy, Brigitte, Dollfus, Hélène, Le Merrer, Martine, Munnich, Arnold, Encha-Razavi, Férechté, Vekemans, Michel, Attié-Bitach, Tania

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Long-chain fatty acid oxidation during early human development von STRAUSS, Arnold W, OEY, Nadia A, ATTIE-BITACH, Tania, DEN BOER, Margarethe E. J, WIJBURG, Frits A, VEKEMANS, Michel, AUGE, Joëlle, STEINER, Céline, WANDERS, Ronald J. A, WATERHAM, Hans R, RUITER, Jos P. N

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Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental Retardation von Molinari, Florence, Rio, Marlène, Meskenaite, Virginia, Encha-Razavi, Férechté, Augé, Joelle, Bacq, Delphine, Briault, Sylvain, Vekemans, Michel, Munnich, Arnold, Attié-Bitach, Tania, Sonderegger, Peter, Colleaux, Laurence

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PAX2 mutations in renal-coloboma syndrome: mutational hotspot and germline mosaicism von Amiel, J, Audollent, S, Joly, D, Dureau, P, Salomon, R, Tellier, A L, Augé, J, Bouissou, F, Antignac, C, Gubler, M C, Eccles, M R, Munnich, A, Vekemans, M, Lyonnet, S, Attié-Bitach, T

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Neurological Phenotype in Waardenburg Syndrome Type 4 Correlates with Novel SOX10 Truncating Mutations and Expression in Developing Brain von Touraine, Renaud L., Attié-Bitach, Tania, Manceau, Eric, Korsch, Eckhard, Sarda, Pierre, Pingault, Véronique, Encha-Razavi, Féréchté, Pelet, Anna, Augé, Joelle, Nivelon-Chevallier, Annie, Holschneider, Alexander Mathias, Munnes, Marc, Doerfler, Walter, Goossens, Michel, Munnich, Arnold, Vekemans, Michel, Lyonnet, Stanislas

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Expression of the SMADIP1 gene during early human development von Espinosa-Parrilla, Yolanda, Amiel, Jeanne, Augé, Joëlle, Encha-Razavi, Férechté, Munnich, Arnold, Lyonnet, Stanislas, Vekemans, Michel, Attié-Bitach, Tania

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Expression of the RET proto-oncogene in human Embryos von Attié-Bitach, Tania, Abitbol, Marc, Gérard, Marion, Delezoide, Anne-Lise, Augé, Joelle, Pelet, Anna, Amiel, Jeanne, Pachnis, Vassilis, Munnich, Arnold, Lyonnet, Stanislas, Vekemans, Michel

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Gene expression in pharyngeal arch 1 during human embryonic development von Cai, Juanliang, Ash, David, Kotch, Lori E., Jabs, Ethylin Wang, Attie-Bitach, Tania, Auge, Joelle, Mattei, Geraldine, Etchevers, Heather, Vekemans, Michel, Korshunova, Yulia, Tidwell, Rose, Messina, David N., Winston, Julia B., Lovett, Michael

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Salvage of 5′-deoxy-5′-methylthioadenosine and L-homocysteine into methionine in cells cultured in a methionine-free medium: A study of “methionine-dependence” von Christa, Laurence, Kersual, Joëlle, Auge, Joëlle, Perignon, Jean-Louis

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Expression of the PAX2 gene in human embryos and exclusion in the CHARGE syndrome von Tellier, Anne-Lorraine, Amiel, Jeanne, Delezoide, Anne-Lise, Audollent, Sophie, Augé, Joelle, Esnault, Dominique, Encha-Razavi, Férechté, Munnich, Arnold, Lyonnet, Stanislas, Vekemans, Michel, Attié-Bitach, Tania

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Expression of the Sonic Hedgehog gene in human embryos with neural tube defects von Kirillova, Irena, Novikova, Irena, Augé, Joelle, Audollent, Sophie, Esnault, Dominique, Encha-Razavi, Férechté, Lazjuk, Gennady, Attié-Bitach, Tania, Vekemans, Michel

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Mythe et fiction von Behmenburg, Lena, Boulogne, Jacques, Bréan, Simon, Bréchet, Christophe, Briand, Michel, Calame, Claude, Delattre, Charles, Fabre-Serris, Jacqueline, Férez, Juan Antonio López, García, Francisco Javier González, Gély, Véronique, Gourmelen, Laurent, Lochin, Catherine, Maréchaux, Pierre, Maugier-Sinha, Anne, Muller-Dufeu, Marion, Pellizer, Ezio, Picouet, Maud, Platas, Fátima Díez, Saïd, Suzanne, Soler, Joëlle, Tallet, Gaëlle, Videau, Anne, Webb, Ruth, Wolff, Étienne, Wyler, Stéphanie

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Les complexités de l'alliance, Volume 2: Les systèmes complexes d'alliance matrimoniale (Françoise Héritier-Augé and Elisabeth Copet-Rougier, eds.) (Book Review) von Bahloul, Joëlle

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