Ohcanbohtosat - Randrianaivo, Hanitra

Cost and outcomes of the ultrasound screening program for birth defects over time: a population-based study in France Dahkki Ferrier, Clément, Khoshnood, Babak, Dhombres, Ferdinand, Randrianaivo, Hanitra, Perthus, Isabelle, Jouannic, Jean-Marie, Durand-Zaleski, Isabelle

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Trends in resource use and effectiveness of ultrasound detection of fetal structural anomalies in France: a multiple registry-based study Dahkki Ferrier, Clément, Dhombres, Ferdinand, Khoshnood, Babak, Randrianaivo, Hanitra, Perthus, Isabelle, Guilbaut, Lucie, Durand-Zaleski, Isabelle, Jouannic, Jean-Marie

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Expanding the clinical spectrum of B4GALT7 deficiency: homozygous p.R270C mutation with founder effect causes Larsen of Reunion Island syndrome Dahkki Cartault, François, Munier, Patrick, Jacquemont, Marie-Line, Vellayoudom, Jeannine, Doray, Bérénice, Payet, Christine, Randrianaivo, Hanitra, Laville, Jean-Marc, Munnich, Arnold, Cormier-Daire, Valérie

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Pregnancy outcomes of Q fever: prospective follow-up study on Reunion island Dahkki Mboussou, Yoan, Jaubert, Julien, Larrieu, Sophie, Atiana, Laura, Naze, Florence, Folio, Christine, Randrianaivo, Hanitra, Bertolotti, Antoine, Picot, Sandrine, Robillard, Pierre-Yves, Boukerrou, Malik, Gérardin, Patrick

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Low Clinical Burden of 2009 Pandemic Influenza A (H1N1) Infection during Pregnancy on the Island of La Réunion Dahkki Gérardin, Patrick, El Amrani, Rachid, Cyrille, Béatrice, Gabrièle, Marc, Guillermin, Philippe, Boukerrou, Malik, Boumahni, Brahim, Randrianaivo, Hanitra, Winer, Arnaud, Rouanet, Jean-Fabien, Bohrer, Michel, Jaffar-Bandjee, Marie-Christine, Robillard, Pierre-Yves, Barau, Georges, Michault, Alain

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Multidisciplinary Prospective Study of Mother-to-Child Chikungunya Virus Infections on the Island of La Réunion Dahkki Gérardin, Patrick, Barau, Georges, Michault, Alain, Bintner, Marc, Randrianaivo, Hanitra, Choker, Ghassan, Lenglet, Yann, Touret, Yasmina, Bouveret, Anne, Grivard, Philippe, Roux, Karin Le, Blanc, Séverine, Schuffenecker, Isabelle, Couderc, Thérèse, Arenzana-Seisdedos, Fernando, Lecuit, Marc, Robillard, Pierre-Yves

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Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study Dahkki Bergman, Jorieke E. H., Lutke, L. Renée, Gans, Rijk O. B., Addor, Marie-Claude, Barisic, Ingeborg, Cavero-Carbonell, Clara, Garne, Ester, Gatt, Miriam, Klungsoyr, Kari, Lelong, Nathalie, Lynch, Catherine, Mokoroa, Olatz, Nelen, Vera, Neville, Amanda J., Pierini, Anna, Randrianaivo, Hanitra, Rissmann, Anke, Tucker, David, Wiesel, Awi, Dolk, Helen, Loane, Maria, Bakker, Marian K.

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Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease Dahkki Audrézet, Marie-Pierre, Corbiere, Christine, Lebbah, Said, Morinière, Vincent, Broux, Françoise, Louillet, Ferielle, Fischbach, Michel, Zaloszyc, Ariane, Cloarec, Sylvie, Merieau, Elodie, Baudouin, Véronique, Deschênes, Georges, Roussey, Gwenaelle, Maestri, Sandrine, Visconti, Chiara, Boyer, Olivia, Abel, Carine, Lahoche, Annie, Randrianaivo, Hanitra, Bessenay, Lucie, Mekahli, Djalila, Ouertani, Ines, Decramer, Stéphane, Ryckenwaert, Amélie, Cornec-Le Gall, Emilie, Salomon, Rémi, Ferec, Claude, Heidet, Laurence

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Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndrome Dahkki Alessandri, Jean-Luc, Gordon, Christopher T., Jacquemont, Marie-Line, Gruchy, Nicolas, Ajeawung, Norbert F, Benoist, Guillaume, Oufadem, Myriam, Chebil, Asma, Duffourd, Yannis, Dumont, Coralie, Gérard, Marion, Kuentz, Paul, Jouan, Thibaud, Filippini, Francesca, Nguyen, Thi Tuyet Mai, Alibeu, Olivier, Bole-Feysot, Christine, Nitschké, Patrick, Omarjee, Asma, Ramful, Duksha, Randrianaivo, Hanitra, Doray, Bérénice, Faivre, Laurence, Amiel, Jeanne, Campeau, Philippe M., Thevenon, Julien

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Trends in congenital anomalies in Europe from 1980 to 2012 Dahkki Morris, Joan K., Springett, Anna L., Greenlees, Ruth, Loane, Maria, Addor, Marie-Claude, Arriola, Larraitz, Barisic, Ingeborg, Bergman, Jorieke E. H., Csaky-Szunyogh, Melinda, Dias, Carlos, Draper, Elizabeth S., Garne, Ester, Gatt, Miriam, Khoshnood, Babak, Klungsoyr, Kari, Lynch, Catherine, McDonnell, Robert, Nelen, Vera, Neville, Amanda J., O'Mahony, Mary, Pierini, Anna, Queisser-Luft, Annette, Randrianaivo, Hanitra, Rankin, Judith, Rissmann, Anke, Kurinczuk, Jennifer, Tucker, David, Verellen-Dumoulin, Christine, Wellesley, Diana, Dolk, Helen

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Prevalence of microcephaly in Europe: population based study Dahkki Morris, Joan K, Rankin, Judith, Garne, Ester, Loane, Maria, Greenlees, Ruth, Addor, Marie-Claude, Arriola, Larraitz, Barisic, Ingeborg, Bergman, Jorieke E H, Csaky-Szunyogh, Melinda, Dias, Carlos, Draper, Elizabeth S, Gatt, Miriam, Khoshnood, Babak, Klungsoyr, Kari, Kurinczuk, Jennifer J, Lynch, Catherine, McDonnell, Robert, Nelen, Vera, Neville, Amanda J, O’Mahony, Mary T, Pierini, Anna, Randrianaivo, Hanitra, Rissmann, Anke, Tucker, David, Verellen-Dumoulin, Christine, de Walle, Hermien E K, Wellesley, Diana, Wiesel, Awi, Dolk, Helen

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Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data Dahkki Boyle, Breidge, Addor, Marie-Claude, Arriola, Larraitz, Barisic, Ingeborg, Bianchi, Fabrizio, Csáky-Szunyogh, Melinda, de Walle, Hermien E K, Dias, Carlos Matias, Draper, Elizabeth, Gatt, Miriam, Garne, Ester, Haeusler, Martin, Källén, Karin, Latos-Bielenska, Anna, McDonnell, Bob, Mullaney, Carmel, Nelen, Vera, Neville, Amanda J, O’Mahony, Mary, Queisser-Wahrendorf, Annette, Randrianaivo, Hanitra, Rankin, Judith, Rissmann, Anke, Ritvanen, Annukka, Rounding, Catherine, Tucker, David, Verellen-Dumoulin, Christine, Wellesley, Diana, Wreyford, Ben, Zymak-Zakutnia, Natalia, Dolk, Helen

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Maternal risk factors for the VACTERL association: A EUROCAT case–control study Dahkki van de Putte, Romy, van Rooij, Iris A.L.M., Haanappel, Cynthia P., Marcelis, Carlo L.M., Brunner, Han G., Addor, Marie‐Claude, Cavero‐Carbonell, Clara, Dias, Carlos M., Draper, Elizabeth S., Etxebarriarteun, Larraitz, Gatt, Miriam, Khoshnood, Babak, Kinsner‐Ovaskainen, Agnieszka, Klungsoyr, Kari, Kurinczuk, Jenny J., Latos‐Bielenska, Anna, Luyt, Karen, O'Mahony, Mary T., Miller, Nicola, Mullaney, Carmel, Nelen, Vera, Neville, Amanda J., Perthus, Isabelle, Pierini, Anna, Randrianaivo, Hanitra, Rankin, Judith, Rissmann, Anke, Rouget, Florence, Schaub, Bruno, Tucker, David, Wellesley, Diana, Wiesel, Awi, Zymak‐Zakutnia, Natalya, Loane, Maria, Barisic, Ingeborg, de Walle, Hermien E.K., Bergman, Jorieke E.H., Roeleveld, Nel

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Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders Dahkki Mannucci, Ilaria, Dang, Nghi D. P., Huber, Hannes, Murry, Jaclyn B., Abramson, Jeff, Althoff, Thorsten, Banka, Siddharth, Baynam, Gareth, Bearden, David, Beleza-Meireles, Ana, Benke, Paul J., Berland, Siren, Bierhals, Tatjana, Bilan, Frederic, Bindoff, Laurence A., Braathen, Geir Julius, Busk, Øyvind L., Chenbhanich, Jirat, Denecke, Jonas, Escobar, Luis F., Estes, Caroline, Fleischer, Julie, Groepper, Daniel, Haaxma, Charlotte A., Hempel, Maja, Holler-Managan, Yolanda, Houge, Gunnar, Jackson, Adam, Kellogg, Laura, Keren, Boris, Kiraly-Borri, Catherine, Kraus, Cornelia, Kubisch, Christian, Le Guyader, Gwenael, Ljungblad, Ulf W., Brenman, Leslie Manace, Martinez-Agosto, Julian A., Might, Matthew, Miller, David T., Minks, Kelly Q., Moghaddam, Billur, Nava, Caroline, Nelson, Stanley F., Parant, John M., Prescott, Trine, Rajabi, Farrah, Randrianaivo, Hanitra, Reiter, Simone F., Schuurs-Hoeijmakers, Janneke, Shieh, Perry B., Slavotinek, Anne, Smithson, Sarah, Stegmann, Alexander P. A., Tomczak, Kinga, Tveten, Kristian, Wang, Jun, Whitlock, Jordan H., Zweier, Christiane, McWalter, Kirsty, Juusola, Jane, Quintero-Rivera, Fabiola, Fischer, Utz, Yeo, Nan Cher, Kreienkamp, Hans-Jürgen, Lessel, Davor

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Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita Dahkki Laquerriere, Annie, Jaber, Dana, Abiusi, Emanuela, Maluenda, Jérome, Mejlachowicz, Dan, Vivanti, Alexandre, Dieterich, Klaus, Stoeva, Radka, Quevarec, Loic, Nolent, Flora, Biancalana, Valerie, Latour, Philippe, Sternberg, Damien, Capri, Yline, Verloes, Alain, Bessieres, Bettina, Loeuillet, Laurence, Attie-Bitach, Tania, Martinovic, Jelena, Blesson, Sophie, Petit, Florence, Beneteau, Claire, Whalen, Sandra, Marguet, Florent, Bouligand, Jerome, Héron, Delphine, Viot, Géraldine, Amiel, Jeanne, Amram, Daniel, Bellesme, Céline, Bucourt, Martine, Faivre, Laurence, Jouk, Pierre-Simon, Khung, Suonavy, Sigaudy, Sabine, Delezoide, Anne-Lise, Goldenberg, Alice, Jacquemont, Marie-Line, Lambert, Laetitia, Layet, Valérie, Lyonnet, Stanislas, Munnich, Arnold, Van Maldergem, Lionel, Piard, Juliette, Guimiot, Fabien, Landrieu, Pierre, Letard, Pascaline, Pelluard, Fanny, Perrin, Laurence, Saint-Frison, Marie-Hélène, Topaloglu, Haluk, Trestard, Laetitia, Vincent-Delorme, Catherine, Amthor, Helge, Barnerias, Christine, Benachi, Alexandra, Bieth, Eric, Boucher, Elise, Cormier-Daire, Valerie, Delahaye-Duriez, Andrée, Desguerre, Isabelle, Eymard, Bruno, Francannet, Christine, Grotto, Sarah, Lacombe, Didier, Laffargue, Fanny, Legendre, Marine, Martin-Coignard, Dominique, Mégarbané, André, Mercier, Sandra, Nizon, Mathilde, Rigonnot, Luc, Prieur, Fabienne, Quélin, Chloé, Ranjatoelina-Randrianaivo, Hanitra, Resta, Nicoletta, Toutain, Annick, Verhelst, Helene, Vincent, Marie, Colin, Estelle, Fallet-Bianco, Catherine, Granier, Michèle, Grigorescu, Romulus, Saada, Julien, Gonzales, Marie, Guiochon-Mantel, Anne, Bessereau, Jean-Louis, Tawk, Marcel, Gut, Ivo, Gitiaux, Cyril, Melki, Judith

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