Genetic and Physical Analyses of the Centromeric and Pericentromeric Regions of Human Chromosome 5: Recombination across 5cen by Puechberty, Jacques, Laurent, Anne-Marie, Gimenez, Sylvie, Billault, Alain, Brun-Laurent, Marie-Elisabeth, Calenda, Alphonse, Marçais, Bertrand, Prades, Catherine, Ioannou, Panos, Yurov, Yuri, Roizès, Gérard

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Organization of the variant domains of α satellite DNA on human chromosome 21 by MARCAIS, B, LAURENT, A.-M, CHARLIEU, J.-P, ROIZES, G

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High resolution multicolor fluorescence in situ hybridization using cyanine and fluorescein dyes : rapid chromosome identification by directly fluorescently labeled alphoid DNA pro... by YUROV, YU. B, SOLOVIEV, I. V, VORSANOVA, S. G, MARCAIS, B, ROIZES, G, LEWIS, R

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Analysis of pericentromeric chromosome 21 specific YAC clones by FISH : identification of new markers for molecular-cytogenetic application by YUROV, Y. B, LAURENT, A.-M, MARCAIS, B, VORSANOVA, S. G, ROIZES, G

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OMIXCARE: OMICS technologies solved about 33% of the patients with heterogeneous rare neuro-developmental disorders and negative exome sequencing results and identified 13% additio... by Colin, Estelle, Duffourd, Yannis, Tisserant, Emilie, Relator, Raissa, Bruel, Ange-Line, Tran Mau-Them, Frédéric, Denommé-Pichon, Anne-Sophie, Safraou, Hana, Delanne, Julian, Jean-Marçais, Nolwenn, Keren, Boris, Isidor, Bertrand, Vincent, Marie, Mignot, Cyril, Heron, Delphine, Afenjar, Alexandra, Heide, Solveig, Faudet, Anne, Charles, Perrine, Odent, Sylvie, Herenger, Yvan, Sorlin, Arthur, Moutton, Sébastien, Kerkhof, Jennifer, McConkey, Haley, Chevarin, Martin, Poë, Charlotte, Couturier, Victor, Bourgeois, Valentin, Callier, Patrick, Boland, Anne, Olaso, Robert, Philippe, Christophe, Sadikovic, Bekim, Thauvin-Robinet, Christel, Faivre, Laurence, Deleuze, Jean-François, Vitobello, Antonio

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ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder by Carapito, Raphael, Ivanova, Ekaterina L., Morlon, Aurore, Meng, Linyan, Molitor, Anne, Erdmann, Eva, Kieffer, Bruno, Pichot, Angélique, Naegely, Lydie, Kolmer, Aline, Paul, Nicodème, Hanauer, Antoine, Tran Mau-Them, Frédéric, Jean-Marçais, Nolwenn, Hiatt, Susan M., Cooper, Gregory M., Tvrdik, Tatiana, Muir, Alison M., Dimartino, Clémantine, Chopra, Maya, Amiel, Jeanne, Gordon, Christopher T., Dutreux, Fabien, Garde, Aurore, Thauvin-Robinet, Christel, Wang, Xia, Leduc, Magalie S., Phillips, Meredith, Crawford, Heather P., Kukolich, Mary K., Hunt, David, Harrison, Victoria, Kharbanda, Mira, Smigiel, Robert, Gold, Nina, Hung, Christina Y., Viskochil, David H., Dugan, Sarah L., Bayrak-Toydemir, Pinar, Joly-Helas, Géraldine, Guerrot, Anne-Marie, Schluth-Bolard, Caroline, Rio, Marlène, Wentzensen, Ingrid M., McWalter, Kirsty, Schnur, Rhonda E., Lewis, Andrea M., Lalani, Seema R., Mensah-Bonsu, Noël, Céraline, Jocelyn, Sun, Zijie, Ploski, Rafal, Bacino, Carlos A., Mefford, Heather C., Faivre, Laurence, Bodamer, Olaf, Chelly, Jamel, Isidor, Bertrand, Bahram, Seiamak

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ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder by Carapito, Raphael, Ivanova, Ekaterina L., Morlon, Aurore, Meng, Linyan, Molitor, Anne, Erdmann, Eva, Kieffer, Bruno, Pichot, Angélique, Naegely, Lydie, Kolmer, Aline, Paul, Nicodème, Hanauer, Antoine, Tran Mau-Them, Frédéric, Jean-Marçais, Nolwenn, Hiatt, Susan M., Cooper, Gregory M., Tvrdik, Tatiana, Muir, Alison M., Dimartino, Clémantine, Chopra, Maya, Amiel, Jeanne, Gordon, Christopher T., Dutreux, Fabien, Garde, Aurore, Thauvin-Robinet, Christel, Wang, Xia, Leduc, Magalie S., Phillips, Meredith, Crawford, Heather P., Kukolich, Mary K., Hunt, David, Harrison, Victoria, Kharbanda, Mira, Smigiel, Robert, Gold, Nina, Hung, Christina Y., Viskochil, David H., Dugan, Sarah L., Bayrak-Toydemir, Pinar, Joly-Helas, Géraldine, Guerrot, Anne-Marie, Schluth-Bolard, Caroline, Rio, Marlène, Wentzensen, Ingrid M., McWalter, Kirsty, Schnur, Rhonda E., Lewis, Andrea M., Lalani, Seema R., Mensah-Bonsu, Noël, Céraline, Jocelyn, Sun, Zijie, Ploski, Rafal, Bacino, Carlos A., Mefford, Heather C., Faivre, Laurence, Bodamer, Olaf, Chelly, Jamel, Isidor, Bertrand, Bahram, Seiamak

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Correction to ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder by Carapito, Raphaël, Ivanova, Ekaterina, Morlon, Aurore, Meng, Linyan, Molitor, Anne, Erdmann, Eva, Kieffer, Bruno, Pichot, Angélique, Naegely, Lydie, Kolmer, Aline, Paul, Nicodème, Hanauer, Antoine, Tran Mau-Them, Frédéric, Jean-Marçais, Nolwenn, Hiatt, Susan, Cooper, Gregory, Tvrdik, Tatiana, Muir, Alison, Dimartino, Clémantine, Chopra, Maya, Amiel, Jeanne, Gordon, Christopher, Dutreux, Fabien, Garde, Aurore, Thauvin-Robinet, Christel, Wang, Xia, Leduc, Magalie, Phillips, Meredith, Crawford, Heather, Kukolich, Mary, Hunt, David, Harrison, Victoria, Kharbanda, Mira, Smigiel, Robert, Gold, Nina, Hung, Christina, Viskochil, David, Dugan, Sarah, Bayrak-Toydemir, Pinar, Joly-Helas, Géraldine, Guerrot, Anne-Marie, Schluth-Bolard, Caroline, Rio, Marlène, Wentzensen, Ingrid M., Mcwalter, Kirsty, Schnur, Rhonda, Lewis, Andrea, Lalani, Seema, Mensah-Bonsu, Noël, Céraline, Jocelyn, Sun, Zijie, Ploski, Rafal, Bacino, Carlos, Mefford, Heather, Faivre, Laurence, Bodamer, Olaf, Chelly, Jamel, Isidor, Bertrand, Bahram, Seiamak

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Lessons from two series by physicians and caregivers' self‐reported data in DDX3X‐related disorders by Ruault, Valentin, Burger, Pauline, Gradels‐Hauguel, Johanna, Ruiz, Nathalie, Jamra, Rami Abou, Afenjar, Alexandra, Alembik, Yves, Alessandri, Jean‐Luc, Arpin, Stéphanie, Barcia, Giulia, Bendová, Šárka, Bruel, Ange‐Line, Charles, Perrine, Chatron, Nicolas, Chopra, Maya, Conrad, Solène, Daire, Valérie Cormier, Cospain, Auriane, Coubes, Christine, Coursimault, Juliette, Delahaye‐Duriez, Andrée, Doco, Martine, Dufour, William, Durand, Benjamin, Engel, Camille, Faivre, Laurence, Ferroul, Fanny, Fradin, Mélanie, Frenkiel, Hélène, Fusco, Carlo, Garavelli, Livia, Garde, Aurore, Gerard, Bénédicte, Germanaud, David, Goujon, Louise, Gouronc, Aurélie, Ginglinger, Emmanuelle, Goldenberg, Alice, Hancarova, Miroslava, Havlovicová, Markéta, Heron, Delphine, Isidor, Bertrand, Marçais, Nolwenn Jean, Keren, Boris, Koch‐Hogrebe, Margarete, Kuentz, Paul, Lamure, Victoria, Lebre, Anne‐Sophie, Lecoquierre, François, Lehman, Natacha, Lesca, Gaetan, Lyonnet, Stanislas, Martin, Delphine, Mignot, Cyril, Neuhann, Teresa M., Nicolas, Gaël, Nizon, Mathilde, Petit, Florence, Philippe, Christophe, Piton, Amélie, Pollazzon, Marzia, Prchalová, Darina, Putoux, Audrey, Rio, Marlène, Rondeau, Sophie, Rossi, Massimiliano, Sabbagh, Quentin, Saugier‐Veber, Pascale, Schmetz, Ariane, Steffann, Julie, Thauvin‐Robinet, Christel, Toutain, Annick, Them, Frederic Tran Mau, Trimarchi, Gabriele, Vincent, Marie, Vlčková, Markéta, Wieczorek, Dagmar, Willems, Marjolaine, Yauy, Kevin, Zelinová, Michaela, Ziegler, Alban, Chaumette, Boris, Sadikovic, Bekim, Mandel, Jean‐Louis, Geneviève, David

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Pregnancy in primary immunodeficiency diseases: The PREPI study by Mallart, Elise, Françoise, Ugo, Driessen, Marine, Blanche, Stéphane, Lortholary, Olivier, Lefort, Agnès, Caseris, Marion, Fischer, Alain, Mahlaoui, Nizar, Charlier, Caroline, Amazzough, Karima, Bertrand, Yves, Boutboul, David, Catherinot, Émilie, Chandesris, Olivia, Cheminant, Morgane, Couderc, Anne, D’Aveni, Maud, Delarue, Richard, Fieschi, Claire, Frenzel, Laurent, Galicier, Lionel, Gardembas, Martine, Goujard, Cécile, Gounot, Romain, Hermine, Olivier, Jaccard, Arnaud, Lambotte, Olivier, Lanternier, Fanny, Levy, Romain, Malphettes, Marion, Marcais, Ambroise, Mouthon, Luc, Oksenhendler, Eric, Perlat, Antoinette, Picard, Capucine, Queyrel, Viviane, Robin, Maris, Suarez, Felipe, Viallard, Jean François

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Characterization of a CD44/CD122int Memory CD8 T Cell Subset Generated under Sterile Inflammatory Conditions by Mbitikon-Kobo, Florentin-Martial, Vocanson, Marc, Michallet, Marie-Cecile, Tomkowiak, Martine, Cottalorda, Anne, Angelov, Georgi S, Coupet, Charles-Antoine, Djebali, Sophia, Marcais, Antoine, Dubois, Bertrand, Bonnefoy-Berard, Nathalie, Nicolas, Jean-Francois, Arpin, Christophe, Marvel, Jacqueline

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HTLV-1-associated arthropathy treated with anti-TNF-alpha agent by Frenzel, Laurent, Moura, Bertrand, Marcais, Ambroise, Chapdelaine, Hugo, Hermine, Olivier

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Integrated genome and transcriptome analyses solves about one third of the patients with rare developmental disorders and negative first-line molecular investigations by Vitobello, A., Mau-Them, F. T., Bruel, A. L., Duffourd, Y., Tisserant, E., Callier, P., Moutton, S., Nambot, S., Lehalle, D., Jean-Marcais, N., Delanne, J., Racine, C., Thevenon, J., Poe, C., Jouan, T., Chevarin, M., Willems, M., Coubes, C., Genevieve, D., Houcinat, N., Masurel-Paulet, A., Mosca-Boidron, A., Sorlin, A., Isidor, Bertrand, Heide, S., Afenjar, A., Rodriguez, D., Mignot, C., Heron, D., Vincent, M., Charles, P., Odent, S., Dubourg, C., Faudet, A., Keren, B., Cogné, Benjamin, Boland, Anne, Olaso, Robert, Philippe, C., Deleuze, Jean-François, Faivre, L., Thauvin-Robinet, C.

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Late relapse after hematopoietic stem cell transplantation for acute leukemia: a retrospective study by SFGM-TC by Kaphan, Eléonore, Bettega, François, Forcade, Edouard, Labussière-Wallet, Hélène, Fegueux, Nathalie, Robin, Marie, Peffault De Latour, Régis, Huynh, Anne, Lapierre, Léopoldine, Berceanu, Ana, Marcais, Ambroise, Debureaux, Pierre-Edouard, Vanlangendonck, Nicolas, Bulabois, Claude-Eric, Magro, Leonardo, Daniel, Adrien, Galtier, Jean, Lioure, Bruno, Chevallier, Patrice, Antier, Chloé, Loschi, Michael, Guillerm, Gaelle, Mear, Jean-Baptiste, Chantepie, Sylvain, Cornillon, Jérome, Rey, Gaelle, Poire, Xavier, Bazarbachi, Ali, Rubio, Marie-Thérèse, Contentin, Nathalie, Orvain, Corentin, Dulery, Rémy, Bay, Jacques Olivier, Croizier, Carolyne, Beguin, Yves, Charbonnier, Aude, Skrzypczak, Caroline, Desmier, Déborah, Villate, Alban, Carré, Martin, Thiebaut-Bertrand, Anne

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Arthropathie associée à l’HTLV-1 traitée par anti-TNF alpha by Frenzel, Laurent, Moura, Bertrand, Marcais, Ambroise, Chapdelaine, Hugo, Hermine, Olivier

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Reducing the risk of anaphylaxis during anaesthesia. Short text. Société française d'anesthésie et réanimation. Société française d'allergologie by Société française d'anesthésie et réanimation (Sfar), Société française d'allergologie (SFA)

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