Fertility preservation and cancer: How many persons are concerned? by Le Bihan-Benjamin, Christine, Hoog-Labouret, Natalie, Lefeuvre, Delphine, Carré-Pigeon, Frédérique, Bousquet, Philippe Jean

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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study by Gruchy, Nicolas, Blondeel, Eleonore, Le Meur, Nathalie, Joly-Hélas, Géraldine, Chambon, Pascal, Till, Marianne, Herbaux, Martine, Vigouroux-Castera, Adeline, Coussement, Aurélie, Lespinasse, James, Amblard, Florence, Jimenez Pocquet, Mélanie, Lebel-Roy, Camille, Carré-Pigeon, Frédérique, Flori, Elisabeth, Mugneret, Francine, Jaillard, Sylvie, Yardin, Catherine, Harbuz, Radu, Collonge-Rame, Marie-Agnès, Vago, Philippe, Valduga, Mylène, Leporrier, Nathalie, Vialard, François

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Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots by ELLNATI, Elias, KUENTZ, Paul, LOUANJLI, Noureddine, IQBAL, Naeem, BISHARAH, Mazen, CARRE PIGEON, Frédérique, GOURABI, H, DE BRIEL, Dominique, BRUGNON, Florence, GITLIN, Susan A, GRILLO, Jean-Marc, GHAEDI, Kamran, REDIN, Claire, DEEMEH, Mohammad R, TANHAEI, Somayeh, MODARRES, Parastoo, HEINDRYCKX, Björn, BENKHALIFA, Moncef, NIKIFORAKI, Dimitra, OEHNINGER, Sergio C, DE SUTTER, Petra, MULLER, Jean, VIVILLE, Stephane, JABER, Sara, MEERSCHAUT, Frauke Vanden, MAKARIAN, Joelle, KOSCINSKI, Isabelle, NASR-ESFAHANI, Mohammad H, DEMIROL, Aygul, GURGAN, Timur

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Testicular germ cell tumour risk by occupation and industry: a French case–control study – TESTIS by Guth, Margot, Coste, Astrid, Ahmadi, Shukrullah, Boyle, Helen, Schüz, Joachim, Bujan, Louis, Giscard d’Estaing, Sandrine, Teletin, Marius, Ducrocq, Berengere, Frapsauce, Cynthia, Pirtea, Paul, Lecarpentier, Edouard, Goffinet, François, Ziegler, Dominique De, Barraud-Lange, Virginie, Wolf, Jean-Philippe, Auger, Jacques, Kremer, Laurianne, Ferreux, Lucile, Peretout, Pauline, Rivet, Diane, Rulle, Sandrine, Levy, Rachel, Sermondade, Nathalie, Belaid, Yassine, Durand, Marine, Harbemont, Charlène, Larouziere, Vanina De, Eustache, Florence, Berthaut, Isabelle, Saias-Magnan, Jacqueline, Perrin, Jeanne, Daoud-Deveze, Carole, Nasca, Laurent, Moinard, Nathalie, Isus, François, Bettiol, Célia, Janny, Laurent, Bruhat, Valérie, Brugnon, Florence, Bouche, Cyril, Koscinski, Isabelle, Ladureau-Fritsch, Laëtitia, Schmitt, Françoise, Pax, Charles, Papaxanthos, Aline, Jimenez, Clément, Chansel, Lucie, Delorme, Olivier, Dehee, Pascale, Bouillon, Céline, Guerif, Fabrice, Couet, Marie-Laure, Gervereau, Olivia, Poisson, Elodie, Lanoue, Michel, Guerin, Catherine, Clarotti, Marie-Ange, Szerman, Ethel, Ancelle, Amélie, Muris, Catherine, Chatel, Corinne Fourmy, Denoual-Ziad, Christine, Vienne, Claire De, Delesalle, Cécile, Bouiller, Jean-Paul, Clergeau, Antoine, Blagosklonov, Oxana, Bey, Séverine, Jouve, Guilhem, Veau, Ségolène, Vandenbroucke, Laurent, Letremy, Agnès, Fauque, Patricia, Barberet, Julie, Thibault, Emmanuelle, Besnier, Pierre, Martin, Clémence, Diligent, Catherine, Touati, Françoise, Monnin, Nicolas, Hersant, Christel, Loup-Cabaniols, Vanessa, Gala, Anna, Scalici, Elodie, Sablayrolles, Lucile, Mullet, Tiffany, Chabert, Audrey, Saintpeyre, Christelle, Caro, Mélanie, Sicard, Marie, Hennebicq, Sylvianne, Hoffmann, Pascale, Quenard, Nicole, Villaret, Laure, Blocquaux, Marie-Claude, Carre-Pigeon, Frédérique, Graesslin, Olivier, Béranger, Rémi, Fléchon, Aude

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DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins by Sailani, M Reza, Santoni, Federico A, Letourneau, Audrey, Borel, Christelle, Makrythanasis, Periklis, Hibaoui, Youssef, Popadin, Konstantin, Bonilla, Ximena, Guipponi, Michel, Gehrig, Corinne, Vannier, Anne, Carre-Pigeon, Frederique, Feki, Anis, Nizetic, Dean, Antonarakis, Stylianos E

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Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene by Béroud, Christophe, Carrié, Alain, Beldjord, Chérif, Deburgrave, Nathalie, Llense, Stéphane, Carelle, Nadège, Peccate, Cécile, Cuisset, Jean-Marie, Pandit, Florence, Carré-Pigeon, Frédérique, Mayer, Michèle, Bellance, Rémi, Récan, Dominique, Chelly, Jamel, Kaplan, Jean-Claude, Leturcq, France

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Automated nephelometric assay for seminal fluid transferrin by LEFEVRE, F, MOUTEL, G, CARRE-PIGEON, F, CARON, J, GILLERY, P

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Development of Ovarian Tissue Autograft to Restore Ovarian Function: Protocol for a French Multicenter Cohort Study by Pretalli, Jean-Baptiste, Frontczak Franck, Sophie, Pazart, Lionel, Roux, Christophe, Amiot, Clotilde

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Identification of four novel mutations in the cystic fibrosis transmembrane conductance regulator gene: E664X, 2113delA, 306delTAGA, and [Delta]M1140 by Clavel, Christine, Pennaforte, François, Pigeon, Frédérique, Verlingue, Claudine, Birembaut, Philippe, Férec, Claude

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Primary application of three-dimensional ultrasonography to early diagnosis of ectopic pregnancy by Harika, Ghassan, Gabriel, René, Carre-Pigeon, Frédérique, Alemany, Laurence, Quereux, Christian, Wahl, Paul

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Identification of four novel mutations in the cystic fibrosis transmembrane conductance regulator gene: E664X, 2113delA, 306delTAGA, and ΔM1140 by Clavel, Christine, Pennaforte, François, Pigeon, Frédérique, Verlingue, Claudine, Birembaut, Philippe, Férec, Claude

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Multinodular goitre is a gateway for molecular testing of DICER1 syndrome by Oliver‐Petit, Isabelle, Bertozzi, Anne‐Isabelle, Grunenwald, Solange, Gambart, Marion, Pigeon‐Kerchiche, Patricia, Sadoul, Jean‐Louis, Caron, Philippe J., Savagner, Frédérique

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