Correct operation determining means for motor vehicle sensor e.g. exhaust von AFONSO VASCO, QUELIN JEAN MARIE

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PROCEDE DE CONTROLE D'UN CAPTEUR EQUIPANT UN MOTEUR A COMBUSTION INTERNE von AFONSO VASCO, QUELIN JEAN MARIE

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Multiple congenital anomalies in two fetuses with glutathione‐synthetase deficit (GSS) von Jury, Jeanne, Benoist, Jean‐François, Joubert, Madeleine, Quelin, Chloé, Besnard, Thomas, Conrad, Solène, Le Vaillant, Claudine, Bézieau, Stéphane, Isidor, Bertrand, Attié‐Bitach, Tania, Cogné, Benjamin, Vincent, Marie

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The wide spectrum of tubulinopathies: what are the key features for the diagnosis? von BAHI-BUISSON, Nadia, POIRIER, Karine, LASCELLES, Karine, SOUVILLE, Isabelle, BELDJORD, Cherif, CHELLY, Jamel, FOURNIOL, Franck, SAILLOUR, Yoann, VALENCE, Stéphanie, LEBRUN, Nicolas, HULLY, Marie, BIANCO, Catherine Fallet, BODDAERT, Nathalie, ELIE, Caroline

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Clinical and molecular data in cases of prenatal localized overgrowth disorder: major implication of genetic variants in PI3K‐AKT‐mTOR signaling pathway von Bourgon, N., Carmignac, V., Sorlin, A., Duffourd, Y., Philippe, C., Thauvin‐Robinet, C., Guibaud, L., Faivre, L., Vabres, P., Kuentz, P., Tisserand, Emilie, Chevarin, Martin, Delanne, Julian, Jouan, Thibaud, Pöe, Charlotte, Abel, Carine, Allory, Patrick, Amram, Daniel, Attie‐Bitach, Tania, Aziza, Jacqueline, Benevent, Jean‐Baptiste, Bidat, Laurent, Bessières, Bettina, Boussion, Françoise, Cabaret‐Dufour, Anne‐Sophie, Chanoz‐Poulard, Geneviève, Chassaing, Nicolas, Ciorna‐Monferrato, Viorica, Cordier, Anne‐Gaëlle, Cordier, Marie‐Pierre, Cuillier, Fabrice, Doray, Berenice, Encha‐Razavi, Ferechte, Eszto, Marie‐Laure, Bianco, Catherine Fallet, Fernandez, Carla, Ferry, Mathilde, Fichez, Axel, Vequeau, Valérie Goua, Grevent, David, Guichet, Agnès, Laurent, Nicole, Le Gac, Marie‐Pascale, Lefebvre, Mathilde, Letard, Pascaline, Loget, Philippe, Loisel, Didier, Martinovich, Jelena, Masutti, Jean‐Paul, Millischer, Anne‐Elodie, Musizzano, Yuri, Nord, Jean‐François, Perez, Marie‐Josée, Prieur, Fabienne, Proisy, Maia, Quelin, Chloé, Roth, Philippe, Rousseau, Thierry, Salomon, Laurent, Sonigo, Pascale, Spaggiari, Emmanuel, Stempfle, Noëlle, Stirnemann, Julien, Tanteau, Julia, Triau, Stéphane, Vasiljevic, Alexandre, Ville, Yves, Zidane‐Marinnes, Merzouka, Kaltenbach, Sophie, Rivière, Jean‐Baptiste

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Congenital mirror movements: Mutational analysis of RAD51 and DCC in 26 cases von Méneret, Aurélie, Depienne, Christel, Riant, Florence, Trouillard, Oriane, Bouteiller, Delphine, Cincotta, Massimo, Bitoun, Pierre, Wickert, Julia, Lagroua, Isabelle, Westenberger, Ana, Borgheresi, Alessandra, Doummar, Diane, Romano, Marcello, Rossi, Simone, Defebvre, Luc, De Meirleir, Linda, Espay, Alberto J, Fiori, Simona, Klebe, Stephan, Quélin, Chloé, Rudnik-Schöneborn, Sabine, Plessis, Ghislaine, Dale, Russell C, Sklower Brooks, Susan, Dziezyc, Karolina, Pollak, Pierre, Golmard, Jean-Louis, Vidailhet, Marie, Brice, Alexis, Roze, Emmanuel

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Scarcity of available information resources for patients and clinicians after a diagnosis of ultra-rare diseases: retrospective on a cohort of 626 individuals with congenital abnor... von Rollier, Paul, de Montgolfier, Sandrine, Dubourg, Christèle, Carre, Wilfrid, David, Véronique, Galibert, Marie-Dominique, Quelin, Chloe, Fradin, Mélanie, Lavillaureix, Alinoe, Morel, Godelieve, Pasquier, Laurent, Odent, Sylvie, Jean-Marcais, Nolwenn

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Correction to: Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities von Carmignac, Virginie, Mignot, Cyril, Blanchard, Emmanuelle, Kuentz, Paul, Aubriot-Lorton, Marie-Hélène, Parker, Victoria E.R., Sorlin, Arthur, Fraitag, Sylvie, Courcet, Jean-Benoît, Duffourd, Yannis, Rodriguez, Diana, Knox, Rachel G., Polubothu, Satyamaanasa, Boland, Anne, Olaso, Robert, Delepine, Marc, Darmency, Véronique, Riachi, Melissa, Quelin, Chloé, Rollier, Paul, Goujon, Louise, Grotto, Sarah, Capri, Yline, Jacquemont, Marie-Line, Odent, Sylvie, Amram, Daniel, Chevarin, Martin, Vincent-Delorme, Catherine, Catteau, Benoît, Guibaud, Laurent, Arzimanoglou, Alexis, Keddar, Malika, Sarret, Catherine, Callier, Patrick, Bessis, Didier, Geneviève, David, Deleuze, Jean-François, Thauvin, Christel, Semple, Robert K., Philippe, Christophe, Rivière, Jean-Baptiste, Kinsler, Veronica A., Faivre, Laurence, Vabres, Pierre

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Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmentalabnormalities von Carmignac Virginie, Mignot Cyril, Blanchard, Emmanuelle, Kuentz, Paul, Marie-Hélène, Aubriot-Lorton, Parker, Victoria E, Sorlin Arthur, Fraitag Sylvie, Jean-Benoît, Courcet, Duffourd Yannis, Rodriguez, Diana, Knox, Rachel G, Satyamaanasa, Polubothu, Boland, Anne, Olaso, Robert, Delepine, Marc, Darmency Véronique, Riachi, Melissa, Quelin Chloé, Rollier, Paul, Goujon Louise, Grotto, Sarah, Capri Yline, Marie-Line, Jacquemont, Odent Sylvie, Amram, Daniel, Chevarin Martin, Vincent-Delorme, Catherine, Catteau Benoît, Guibaud Laurent, Arzimanoglou Alexis, Keddar Malika, Sarret, Catherine, Callier, Patrick, Bessis Didier, David, Geneviève, Deleuze Jean-François, Thauvin Christel, Semple, Robert K, Christophe, Philippe, Rivière Jean-Baptiste, Kinsler, Veronica A, Faivre, Laurence, Vabres Pierre

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The expanding spectrum of COL2A1 gene variants IN 136 patients with a skeletal dysplasia phenotype von Barat-Houari, Mouna, Dumont, Bruno, Fabre, Aurélie, Them, Frédéric Tm, Alembik, Yves, Alessandri, Jean-Luc, Amiel, Jeanne, Audebert, Séverine, Baumann-Morel, Clarisse, Blanchet, Patricia, Bieth, Eric, Brechard, Marie, Busa, Tiffany, Calvas, Patrick, Capri, Yline, Cartault, François, Chassaing, Nicolas, Ciorca, Vidrica, Coubes, Christine, David, Albert, Delezoide, Anne-Lise, Dupin-Deguine, Delphine, El Chehadeh, Salima, Faivre, Laurence, Giuliano, Fabienne, Goldenberg, Alice, Isidor, Bertrand, Jacquemont, Marie-Line, Julia, Sophie, Kaplan, Josseline, Lacombe, Didier, Lebrun, Marine, Marlin, Sandrine, Martin-Coignard, Dominique, Martinovic, Jelena, Masurel, Alice, Melki, Judith, Mozelle-Nivoix, Monique, Nguyen, Karine, Odent, Sylvie, Philip, Nicole, Pinson, Lucile, Plessis, Ghislaine, Quélin, Chloé, Shaeffer, Elise, Sigaudy, Sabine, Thauvin, Christel, Till, Marianne, Touraine, Renaud, Vigneron, Jacqueline, Baujat, Geneviève, Cormier-Daire, Valérie, Le Merrer, Martine, Geneviève, David, Touitou, Isabelle

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Developmental and symptom profiles in early-onset psychosis von Giannitelli, Marianna, Levinson, Douglas F., Cohen, David, Xavier, Jean, Laurent-Levinson, Claudine

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Twelve new patients with 13q deletion syndrome: Genotype–phenotype analyses in progress von Quélin, Chloé, Bendavid, Claude, Dubourg, Christèle, de la Rochebrochard, Céline, Lucas, Josette, Henry, Catherine, Jaillard, Sylvie, Loget, Philippe, Loeuillet, Laurence, Lacombe, Didier, Rival, Jean-Marie, David, Véronique, Odent, Sylvie, Pasquier, Laurent

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10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in France von Messiaen, Claude, Racine, Caroline, Khatim, Ahlem, Soussand, Louis, Odent, Sylvie, Lacombe, Didier, Manouvrier, Sylvie, Sigaudy, Sabine, Geneviève, David, Thauvin-Robinet, Christel, Pasquier, Laurent, Petit, Florence, Rossi, Massimiliano, Willems, Marjolaine, Attié-Bitach, Tania, Demougeot, Laurent, Slama, Lilia Ben, Landais, Paul, Doco-Fenzy, Martine, Poirsier, Céline, Spodenkiewicz, Marta, Lissy, Lola, Lannoy, Audrey, Shaefer, Elise, Chehadeh, Salima El, Amiel, Jeanne, Mignot, Cyril, Melki, Judith, Whalen, Sandra, Lackmy, Marilyn Irène, Funalot, Benoit, Morin, Gilles, Gérard, Marion, Gruchy, Nicolas, Molin, Arnaud, Toutain, Annick, Arpin, Stéphanie, Blesson, Sophie, Jeanne, Médéric, Isidor, Bertrand, Vincent, Marie, Nizon, Mathilde, Mercier, Sandra, Bonneau, Dominique, Colin, Estelle, Ziegler, Alban, Audebert-Bellanger, Séverine, Stoeva, Radka, Demurger, Florence, Thevenon, Julien, Francannet, Christine, Troude, Baptiste, Haye, Damien, Collignon, Patrick, Gilbert-Dussardier, Brigitte, Egloff, Mattieu, Le Guyader, Gwenaël, Letard, Pascaline, Sarrazin, Elisabeth, Giguet-Valard, Anna-Gaëlle, Damaj, Léna, Fradin, Mélanie, Lavillaureix, Alinoe, Jean-Marçais, Nolwenn, Morel, Godelieve, Quelin, Chloé, Naudion, Sophie, Legendre, Marine, Van-Gils, Julien, Rooryck-Thambo, Caroline, Boute, Odile, Dieux, Anne, Vincent-Delorme, Catherine, Ghoumid, Jamal, Vanlerberghe, Clémence, Caumes, Roseline, Colson, Cindy, Marsili, Luisa, Wyrebski, Antoine, Bellengier, Laurence, Houdayer, Françoise, Putoux, Audrey, Busa, Tiffany, Riccardi, Florence, Missirian, Chantal, Blanchet, Patricia, Haquet, Emmanuelle, Pinson, Lucile, Puechberty, Jacques, Wells, Constance, Capri, Yline, Perrin, Laurence, Passemard, Sandrine, Ruand, Lyse, Nambot, Sophie, Delanne, Julian, Moutton, Sébastien, Sorlin, Arthur, Lehalle, Daphné, Garde, Aurore

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The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (AαCys36Gly, AαCys36Arg and AαCys45Tyr) confirms the role of N-terminal Aα disulfide bond... von HANSS, Michel, POUYMAYOU, Catherine, BLOUCH, Marie-Thérèse, LELLOUCHE, Franck, FFRENCH, Patrick, ROUSSON, Robert, ABGRALL, Jean-François, MORANGE, Pierre-Emmanuel, QUELIN, Florence, DE MAZANCOURT, Philippe

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Phenotypic spectrum of fetal Smith–Lemli–Opitz syndrome von Quélin, Chloé, Loget, Philippe, Verloes, Alain, Bazin, Anne, Bessières, Bettina, Laquerrière, Annie, Patrier, Sophie, Grigorescu, Romulus, Encha-Razavi, Ferechté, Delahaye, Sophie, Jouannic, Jean-Marie, Carbonne, Bruno, D’Hervé, Dominique, Aubry, Marie-Cécile, Macé, Guillaume, Harvey, Thierry, Ville, Yves, Viot, Geraldine, Joyé, Nicole, Odent, Sylvie, Attié-Bitach, Tania, Wolf, Claude, Chevy, Françoise, Benlian, Pascale, Gonzales, Marie

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The natural occurrence of human fibrinogen variants disrupting inter-chain disulfide bonds (A{alpha}Cys36Gly, A{alpha}Cys36Arg and A{alpha}Cys45Tyr) confirms the role of N-terminal... von Hanss, Michel, Pouymayou, Catherine, Blouch, Marie-Thérèse, Lellouche, Franck, Ffrench, Patrick, Rousson, Robert, Abgrall, Jean-François, Morange, Pierre-Emmanuel, Quélin, Florence, de Mazancourt, Philippe

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Erratum: Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome von Tabet, Anne-Claude, Rolland, Thomas, Ducloy, Marie, Lévy, Jonathan, Buratti, Julien, Mathieu, Alexandre, Haye, Damien, Perrin, Laurence, Dupont, Céline, Passemard, Sandrine, Capri, Yline, Verloes, Alain, Drunat, Séverine, Keren, Boris, Mignot, Cyril, Marey, Isabelle, Jacquette, Aurélia, Whalen, Sandra, Pipiras, Eva, Benzacken, Brigitte, Chantot-Bastaraud, Sandra, Afenjar, Alexandra, Héron, Delphine, Le Caignec, Cédric, Beneteau, Claire, Pichon, Olivier, Isidor, Bertrand, David, Albert, El Khattabi, Laila, Kemeny, Stephan, Gouas, Laetitia, Vago, Philippe, Mosca-Boidron, Anne-Laure, Faivre, Laurence, Missirian, Chantal, Philip, Nicole, Sanlaville, Damien, Edery, Patrick, Satre, Véronique, Coutton, Charles, Devillard, Françoise, Dieterich, Klaus, Vuillaume, Marie-Laure, Rooryck, Caroline, Lacombe, Didier, Pinson, Lucile, Gatinois, Vincent, Puechberty, Jacques, Chiesa, Jean, Lespinasse, James, Dubourg, Christèle, Quelin, Chloé, Fradin, Mélanie, Journel, Hubert, Toutain, Annick, Martin, Dominique, Benmansour, Abdelamdjid, Leblond, Claire S, Toro, Roberto, Amsellem, Frédérique, Delorme, Richard, Bourgeron, Thomas

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Author Correction: A framework to identify contributing genes in patients with Phelan-McDermid syndrome von Tabet, Anne-Claude, Rolland, Thomas, Ducloy, Marie, Lévy, Jonathan, Buratti, Julien, Mathieu, Alexandre, Haye, Damien, Perrin, Laurence, Dupont, Céline, Passemard, Sandrine, Capri, Yline, Verloes, Alain, Drunat, Séverine, Keren, Boris, Mignot, Cyril, Marey, Isabelle, Jacquette, Aurélia, Whalen, Sandra, Pipiras, Eva, Benzacken, Brigitte, Chantot-Bastaraud, Sandra, Afenjar, Alexandra, Héron, Delphine, Le Caignec, Cédric, Beneteau, Claire, Pichon, Olivier, Isidor, Bertrand, David, Albert, El Khattabi, Laila, Kemeny, Stephan, Gouas, Laetitia, Vago, Philippe, Mosca-Boidron, Anne-Laure, Faivre, Laurence, Missirian, Chantal, Philip, Nicole, Sanlaville, Damien, Edery, Patrick, Satre, Véronique, Coutton, Charles, Devillard, Françoise, Dieterich, Klaus, Vuillaume, Marie-Laure, Rooryck, Caroline, Lacombe, Didier, Pinson, Lucile, Gatinois, Vincent, Puechberty, Jacques, Chiesa, Jean, Lespinasse, James, Dubourg, Christèle, Quelin, Chloé, Fradin, Mélanie, Journel, Hubert, Toutain, Annick, Martin, Dominique, Benmansour, Abdelamdjid, Leblond, Claire S., Toro, Roberto, Amsellem, Frédérique, Delorme, Richard, Bourgeron, Thomas

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A framework to identify contributing genes in patients with Phelan-McDermid syndrome von Tabet, Anne-Claude, Rolland, Thomas, Ducloy, Marie, Lévy, Jonathan, Buratti, Julien, Mathieu, Alexandre, Haye, Damien, Perrin, Laurence, Dupont, Céline, Passemard, Sandrine, Capri, Yline, Verloes, Alain, Drunat, Séverine, Keren, Boris, Mignot, Cyril, Marey, Isabelle, Jacquette, Aurélia, Whalen, Sandra, Pipiras, Eva, Benzacken, Brigitte, Chantot-Bastaraud, Sandra, Afenjar, Alexandra, Héron, Delphine, Le Caignec, Cédric, Beneteau, Claire, Pichon, Olivier, Isidor, Bertrand, David, Albert, El Khattabi, Laila, Kemeny, Stephan, Gouas, Laetitia, Vago, Philippe, Mosca-Boidron, Anne-Laure, Faivre, Laurence, Missirian, Chantal, Philip, Nicole, Sanlaville, Damien, Edery, Patrick, Satre, Véronique, Coutton, Charles, Devillard, Françoise, Dieterich, Klaus, Vuillaume, Marie-Laure, Rooryck, Caroline, Lacombe, Didier, Pinson, Lucile, Gatinois, Vincent, Puechberty, Jacques, Chiesa, Jean, Lespinasse, James, Dubourg, Christèle, Quelin, Chloé, Fradin, Mélanie, Journel, Hubert, Toutain, Annick, Martin, Dominique, Benmansour, Abdelamdjid, Leblond, Claire S., Toro, Roberto, Amsellem, Frédérique, Delorme, Richard, Bourgeron, Thomas

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Mental Stress-Induced Increase in Blood Pressure Is Not Related to Baroreflex Sensitivity in Middle-Aged Healthy Men von Fauvel, Jean Pierre, Cerutti, Catherine, Quelin, Pierre, Laville, Maurice, Gustin, Marie Paule, Paultre, Christian Zacharie, Ducher, Michel

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