A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes von Besseau-Ayasse, J., Violle-Poirsier, C., Bazin, A., Gruchy, N., Moncla, A., Girard, F., Till, M., Mugneret, F., Coussement, A., Pelluard, F., Jimenez, M., Vago, P., Portnoï, M. F., Dupont, C., Beneteau, C., Amblard, F., Valduga, M., Bresson, J. L., Carré-Pigeon, F., Le Meur, N., Tapia, S., Yardin, C., Receveur, A., Lespinasse, J., Pipiras, E., Beaujard, M. P., Teboul, P., Brisset, S., Catty, M., Nowak, E., Douet Guilbert, N., Lallaoui, H., Bouquillon, S., Gatinois, V., Joly-Helas, G., Prieur, F., Cartault, F., Martin, D., Kleinfinger, P., Molina Gomes, D., Doco-Fenzy, M., Vialard, F.

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Molecular cytogenetic characterization of two small chromosome 8 derived supernumerary mosaic markers von Herry, A., Morel, F., Le Bris, M.-J., Bellec, V., Lallaoui, H., Parent, P., De Braekeleer, Marc

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Down syndrome maternal serum marker screening after 18 weeks of gestation: a countrywide study von Dreux, Sophie, MD, Nguyen, Claire, MD, Czerkiewicz, Isabelle, MD, Schmitz, Thomas, MD, PhD, Azria, Elie, MD, PhD, Fouré, Marc-Antoine, Muller, Françoise, MD, PhD

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A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes: Prenatal diagnosis of the 22q11.2 deletion of 272 f... von Besseau-Ayasse, J., Violle-Poirsier, C., Bazin, A., Gruchy, N., Moncla, A., Girard, F., Till, M., Mugneret, F., Coussement, A., Pelluard, F., Jimenez, M., Vago, P., Portnoï, M. F., Dupont, C., Beneteau, C., Amblard, F., Valduga, M., Bresson, J. L., Carré-Pigeon, F., Le Meur, N., Tapia, S., Yardin, C., Receveur, A., Lespinasse, J., Pipiras, E., Beaujard, M. P., Teboul, P., Brisset, S., Catty, M., Nowak, E., Douet Guilbert, N., Lallaoui, H., Bouquillon, S., Gatinois, V., Joly-Helas, G., Prieur, F., Cartault, F., Martin, D., Kleinfinger, P., Molina Gomes, D., Doco-Fenzy, M., Vialard, F.

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Second-trimester Down syndrome maternal serum marker screening: a prospective study of 11 040 twin pregnancies von Garchet-Beaudron, Aurélie, Dreux, Sophie, Leporrier, Nathalie, Oury, Jean-François, Muller, Françoise

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Fluorescent in-situ hybridization and sequence-tagged sites for delineation of an X :Y translocation in a patient with secondary amenorrhoea von DELON, B, LALLAOUI, H, ABEL-LABLANCHE, C, GENEIX, A, BELLEC, V, BENKHALIFA, M

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French multi-centric study of 2000 amniotic fluid interphase FISH analyses from high-risk pregnancies and review of the literature von Luquet, I, Mugneret, F, Athis, P.D, Nadal, N, Favre, B, Abel, C, Chelloug, N, Lespinasse, J, Portnoi, M.F, Joyé, N, Dupont, J.M, Lebbar, A, Bresson, J.L, Fellmann, F, Siffroi, J.P, Chantot-Bastaraud, S, Chiesa, J, Amblard, F, Devillard, F, Jeandidier, E, Boceno, M, Rival, J.M, Bellec, V, Lallaoui, H, Delobel, B, Croquette, M.F, Benzacken, B

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Down syndrome maternal serum screening: results' comments recommended by accredited biologists von Muller, F., Dreux, S., Czerkiewicz, Isabelle, Bernard, M., Guibourdenche, J., Lacroix, I., Moineau, M.-P., Read, M.-H., Sault, C., Thibaud, D., Veyrat, B., Bidat, L.

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Oral contraceptive use and ovarian cancer risk for BRCA1/2 mutation carriers: an international cohort study von Schrijver, Lieske H., Antoniou, Antonis C., Olsson, Håkan, Mooij, Thea M., Roos-Blom, Marie-José, Azarang, Leyla, Adlard, Julian, Ahmed, Munaza, Barrowdale, Daniel, Davidson, Rosemarie, Donaldson, Alan, Eeles, Ros, Henderson, Alex, Izatt, Louise, Ong, Kai-Ren, Bonadona, Valérie, van Engelen, Klaartje, Menko, Fred H., Mourits, Marian J.E., Singer, Christian F., Tan, Yen Y., Schmutzler, Rita K., Gerdes, Anne-Marie, Simard, Jacques, Rantala, Johanna, Osorio, Ana, Hopper, John L., Beth Terry, Mary, Noguès, Catherine, Engel, Christoph, Kast, Karin, Goldgar, David E., van Leeuwen, Flora E., Easton, Douglas F., Andrieu, Nadine, Rookus, Matti A., Noguès, Catherine, Laborde, Lilian, Pontois, Pauline, Breysse, Emanuelle, Berline, Margot, Stoppa-Lyonnet, Dominique, Buecher, Bruno, Caron, Olivier, Mouret-Fourme, Emmanuelle, Saule, Claire, Fricker, Jean-Pierre, Lasset, Christine, Berthet, Pascaline, Faivre, Laurence, Luporsi, Elisabeth, Gladieff, Laurence, Chieze-Valéro, Stéphanie, Moretta, Jessica, Popovici, Cornel, Longy, Michel, Soubrier, Florent, Coupier, Isabelle, Corsini, Carole, Morin-Meschin, Marie-Emmanuelle, Lortholary, Alain, Adenis, Claude, Maillez, Audrey, Nguyen, Tan Dat, Tennevet, Isabelle, Maugard, Christine, Bignon, Yves-Jean, Gay Bellile, Mathilde, Penet, Clotilde, Dreyfus, Hélène, Cohen-Haguenauer, Odile, Venat-Bouvet, Laurence, Leroux, Dominique, Layet, Valérie, Lacaze, Elodie, Fert-Ferrer, Sandra, Bera, Odile, Tougeron, David, Lallaoui, Hakima, van Leeuwen, F.E., Schmidt, M.K., Jenner, D.J., Collée, J.M., van den Ouweland, A.M.W., Hooning, M.J., Boere, I.A., van Cronenburg, T.C.T.E.F., Wevers, M.R., Mensenkamp, A.R., Ausems, M.G.E.M., van de Beek, I., Gille, J.J.P., Gómez García, E.B., Blok, M.J., de Boer, M., Berger, L.P.V., de Bock, G.H., Siesling, S., Verloop, J., van den Broek, E.C.

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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Dennis, Joe, Tyrer, Jonathan P., McGuffog, Lesley, Bolla, Manjeet K., Adank, Muriel A., Ahearn, Thomas, Aittomäki, Kristiina, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arun, Banu K., Baynes, Caroline, Becher, Heiko, Bernstein, Leslie, Białkowska, Katarzyna, Blomqvist, Carl, Bojesen, Stig E., Brenner, Hermann, Buys, Saundra S., Caligo, Maria A., Castelao, Jose E., Chang-Claude, Jenny, Chanock, Stephen J., Chung, Wendy K., Collée, J. Margriet, Czene, Kamila, Devilee, Peter, Dwek, Miriam, Evans, D. Gareth, Flyger, Henrik, Fostira, Florentia, García-Closas, Montserrat, García-Sáenz, José A., Gaudet, Mia M., Gehrig, Andrea, Giles, Graham G., Goldgar, David E., Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A., Hall, Per, Hamann, Ute, Harrington, Patricia A., Hart, Steven N., He, Wei, Hogervorst, Frans B. L., Hollestelle, Antoinette, Hulick, Peter J., Hunter, David J., Jager, Agnes, Jones, Michael E., Kaaks, Rudolf, Kapoor, Pooja Middha, Karlan, Beth Y., Keeman, Renske, Kiiski, Johanna I., Kraft, Peter, Lambrechts, Diether, Lesueur, Fabienne, Lindstrom, Tricia, Mannermaa, Arto, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, O’Brien, Katie M., Olsson, Håkan, Ottini, Laura, Park-Simon, Tjoung-Won, Pedersen, Inge Sokilde, Peterlongo, Paolo, Peto, Julian, Pharoah, Paul D. P., Polley, Eric C., Pujana, Miquel Angel, Punie, Kevin, Rashid, Muhammad U., Rennert, Gad, Saloustros, Emmanouil, Santella, Regina, Scheuner, Maren T., Schmidt, Gunnar, Scott, Christopher, Swerdlow, Anthony, Tamimi, Rulla M., Taylor, Jack A., Thull, Darcy L., Tung, Nadine, Vachon, Celine M., Vega, Ana, Wang, Qin, Wendt, Camilla, Yang, Xiaohong R., Ziogas, Argyrios, Park, Sue K., Thomassen, Mads, Simard, Jacques, Chenevix-Trench, Georgia

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