Contemporary Predictors of Conversion from Laparoscopic to Open Appendectomy von Wagner, Patrick L., Eachempati, Soumitra R., Aronova, Anna, Hydo, Lynn J., Pieracci, Frederic M., Bartholdi, Marie, Umunna, Ben-Paul N., Shou, Jian, Barie, Philip S.

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The clinical significance of small copy number variants in neurodevelopmental disorders von Asadollahi, Reza, Oneda, Beatrice, Joset, Pascal, Azzarello-Burri, Silvia, Bartholdi, Deborah, Steindl, Katharina, Vincent, Marie, Cobilanschi, Joana, Sticht, Heinrich, Baldinger, Rosa, Reissmann, Regina, Sudholt, Irene, Thiel, Christian T, Ekici, Arif B, Reis, André, Bijlsma, Emilia K, Andrieux, Joris, Dieux, Anne, FitzPatrick, David, Ritter, Susanne, Baumer, Alessandra, Latal, Beatrice, Plecko, Barbara, Jenni, Oskar G, Rauch, Anita

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New insights into genotype―phenotype correlations for the doublecortin-related lissencephaly spectrum von BAHI-BUISSON, Nadia, SOUVILLE, Isabelle, LOUIS LEGER, Pierre, ELIE, Caroline, BODDAERT, Nathalie, BELDJORD, Cherif, CHELLY, Jamel, FRANCIS, Fiona, EUROPEAN CONSORTIUM, Sbh-Lis, FOURNIOL, Franck J, TOUSSAINT, Aurelie, MOORES, Carolyn A, HOUDUSSE, Anne, YVES LEMAITRE, Jean, POIRIER, Karine, KHALAF-NAZZAL, Reham, HULLY, Marie

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Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis von Gribouval, Olivier, Morinière, Vincent, Pawtowski, Audrey, Arrondel, Christelle, Sallinen, Satu-Leena, Saloranta, Carola, Clericuzio, Carol, Viot, Géraldine, Tantau, Julia, Blesson, Sophie, Cloarec, Sylvie, Machet, Marie Christine, Chitayat, David, Thauvin, Christelle, Laurent, Nicole, Sampson, Julian R., Bernstein, Jonathan A, Clemenson, Alix, Prieur, Fabienne, Daniel, Laurent, Levy-Mozziconacci, Annie, Lachlan, Katherine, Alessandri, Jean Luc, Cartault, François, Rivière, Jean Pierre, Picard, Nicole, Baumann, Clarisse, Delezoide, Anne Lise, Belar Ortega, Maria, Chassaing, Nicolas, Labrune, Philippe, Yu, Sui, Firth, Helen, Wellesley, Diana, Bitzan, Martin, Alfares, Ahmed, Braverman, Nancy, Krogh, Lotte, Tolmie, John, Gaspar, Harald, Doray, Bérénice, Majore, Silvia, Bonneau, Dominique, Triau, Stéphane, Loirat, Chantal, David, Albert, Bartholdi, Deborah, Peleg, Amir, Brackman, Damien, Stone, Rosario, DeBerardinis, Ralph, Corvol, Pierre, Michaud, Annie, Antignac, Corinne, Gubler, Marie Claire

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Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations von Jaureguiberry, Graciana, De la Dure-Molla, Muriel, Parry, David, Quentric, Mickael, Himmerkus, Nina, Koike, Toshiyasu, Poulter, James, Klootwijk, Enriko, Robinette, Steven L., Howie, Alexander J., Patel, Vaksha, Figueres, Marie-Lucile, Stanescu, Horia C., Issler, Naomi, Nicholson, Jeremy K., Bockenhauer, Detlef, Laing, Christopher, Walsh, Stephen B., McCredie, David A., Povey, Sue, Asselin, Audrey, Picard, Arnaud, Coulomb, Aurore, Medlar, Alan J., Bailleul-Forestier, Isabelle, Verloes, Alain, Le Caignec, Cedric, Roussey, Gwenaelle, Guiol, Julien, Isidor, Bertrand, Logan, Clare, Shore, Roger, Johnson, Colin, Inglehearn, Christopher, Al-Bahlani, Suhaila, Schmittbuhl, Matthieu, Clauss, François, Huckert, Mathilde, Laugel, Virginie, Ginglinger, Emmanuelle, Pajarola, Sandra, Spartà, Giuseppina, Bartholdi, Deborah, Rauch, Anita, Addor, Marie-Claude, Yamaguti, Paulo M., Safatle, Heloisa P., Acevedo, Ana Carolina, Martelli-Júnior, Hercílio, dos Santos Netos, Pedro E., Coletta, Ricardo D., Gruessel, Sandra, Sandmann, Carolin, Ruehmann, Denise, Langman, Craig B., Scheinman, Steven J., Ozdemir-Ozenen, Didem, Hart, Thomas C., Hart, P. Suzanne, Neugebauer, Ute, Schlatter, Eberhard, Houillier, Pascal, Gahl, William A., Vikkula, Miikka, Bloch-Zupan, Agnès, Bleich, Markus, Kitagawa, Hiroshi, Unwin, Robert J., Mighell, Alan, Berdal, Ariane, Kleta, Robert

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Identification of the genetic defect in the original Wagner syndrome family von Kloeckener-Gruissem, Barbara, Bartholdi, Deborah, Abdou, Marie-Therese, Zimmermann, Dieter R, Berger, Wolfgang

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The clinical significance of small copy number variants in neurodevelopmental disorders von Asadollahi, Reza, Oneda, Beatrice, Joset, Pascal, Azzarello-Burri, Silvia, Bartholdi, Deborah, Steindl, Katharina, Vincent, Marie, Cobilanschi, Joana, Sticht, Heinrich, Baldinger, Rosa, Reissmann, Regina, Sudholt, Irene, Thiel, Christian T, Ekici, Arif B, Reis, André, Bijlsma, Emilia K, Andrieux, Joris, Dieux, Anne, FitzPatrick, David, Ritter, Susanne, Baumer, Alessandra, Latal, Beatrice, Plecko, Barbara, Jenni, Oskar G, Rauch, Anita

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Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis von Gribouval, Olivier, Morinière, Vincent, Pawtowski, Audrey, Arrondel, Christelle, Sallinen, Satu-Leena, Saloranta, Carola, Clericuzio, Carol, Viot, Géraldine, Tantau, Julia, Blesson, Sophie, Cloarec, Sylvie, Machet, Marie Christine, Chitayat, David, Thauvin, Christelle, Laurent, Nicole, Sampson, Julian R, Bernstein, Jonathan A, Clemenson, Alix, Prieur, Fabienne, Daniel, Laurent, Levy-Mozziconacci, Annie, Lachlan, Katherine, Alessandri, Jean Luc, Cartault, François, Rivière, Jean Pierre, Picard, Nicole, Baumann, Clarisse, Delezoide, Anne Lise, Belar Ortega, Maria, Chassaing, Nicolas, Labrune, Philippe, Yu, Sui, Firth, Helen, Wellesley, Diana, Bitzan, Martin, Alfares, Ahmed, Braverman, Nancy, Krogh, Lotte, Tolmie, John, Gaspar, Harald, Doray, Bérénice, Majore, Silvia, Bonneau, Dominique, Triau, Stéphane, Loirat, Chantal, David, Albert, Bartholdi, Deborah, Peleg, Amir, Brackman, Damien, Stone, Rosario, Deberardinis, Ralph, Corvol, Pierre, Michaud, Annie, Antignac, Corinne, Gubler, Marie Claire

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Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations von JAUREGUIBERRY, Graciana, DE LA DURE-MOLLA, Muriel, PATEL, Vaksha, FIGUERES, Marie-Lucile, STANESCU, Horia C, ISSLER, Naomi, NICHOLSON, Jeremy K, BOCKENHAUER, Detlef, LAING, Christopher, WALSH, Stephen B, MCCREDIE, David A, POVEY, Sue, PARRY, David, ASSELIN, Audrey, PICARD, Arnaud, COULOMB, Aurore, MEDLAR, Alan J, BAILLEUL-FORESTIER, Isabelle, VERLOES, Alain, LE CAIGNEC, Cedric, ROUSSEY, Gwenaelle, GUIOL, Julien, ISIDOR, Bertrand, QUENTRIC, Mickael, LOGAN, Clare, SHORE, Roger, JOHNSON, Colin, INGLEHEARN, Christopher, AL-BAHLANI, Suhaila, SCHMITTBUHL, Matthieu, CLAUSS, François, HUCKERT, Mathilde, LAUGEL, Virginie, GINGLINGER, Emmanuelle, HIMMERKUS, Nina, PAJAROLA, Sandra, SPARTA, Giuseppina, BARTHOLDI, Deborah, RAUCH, Anita, ADDOR, Marie-Claude, YAMAGUTI, Paulo M, SAFATLE, Heloisa P, ACEVEDO, Ana Carolina, MARTELLI-JUNIOR, Hercílio, DOS SANTOS NETOS, Pedro E, KOIKE, Toshiyasu, COLETTA, Ricardo D, GRUESSEL, Sandra, SANDMANN, Carolin, RUEHMANN, Denise, LANGMAN, Craig B, SCHEINMAN, Steven J, OZDEMIR-OZENEN, Didem, HART, Thomas C, SUZANNE HART, P, NEUGEBAUER, Ute, POULTER, James, KLOOTWIJK, Enriko, ROBINETTE, Steven L, HOWIE, Alexander J

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Theœ clinical significance of small copy number variants in neurodevelopmental disorders von Asadollahi, Reza

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Autographes, Carton 36 : Sculpteurs Ada-Bri von Adam, Lambert-Sigisbert (1700-1759), Adam, Gaspard-Louis-Charles (1760-18??), Allegrain, Christophe Gabriel (1710-1795), Allouard, Henri (1844-1929), Anguier, Michel (1612?-1686), Arnoult, Philippe-François (17??-17??), Aubanel, Joseph (1816-1879), Auvray, Louis (1810-1890), Baffier, Jean (1851-1920), Barrau, Théophile Eugène Victor (1848-1913), Barré, Jean Baptiste (1807-1877), Barrias, Louis-Ernest (1841-1905), Barrois, François (1656-1726), Bartholdi, Auguste (1834-1904), Bartolini, Lorenzo (1777-1850), Barye, Antoine Louis (1795?-1875), Bauchery, Francis Roland (1798-1863?), Becquet, Just (1829-1907), Bernard, Joseph Antoine (1866-1931), Berruer, Pierre-François (1733-1797), Bertaux, Hélène (1825-1909), Bloch, Armand Lucien (1866-1933), Bloch, Elisa (1848-1904), Blondat, Max (1879-1925), Bonheur, Isidore Jules (1827-1901), Bonnassieux, Jean-Marie (1810-1892), Bordoni, Francesco (1580-1654), Bosio, François Joseph (1768-1845), Bouchardon, Edme (1698-1762), Boudard, Jean-Baptiste (1710-1768), Bougron, Louis Victor (1798-1886), Bourdelle, Antoine (1861-1929), Bourgeois, Louis Maximilien (1838-1901), Boutry, Edgar Henri (1857-1938?), Bra, Théophile François Marcel (1797-1863), Brion, Isidore Hippolyte (1799-1863)

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