Low risk of embryonic and other cancers in PIK3CA‐related overgrowth spectrum: Impact on screening recommendations von Faivre, Laurence, Crépin, Jean‐Charles, Réda, Manon, Nambot, Sophie, Carmignac, Virginie, Abadie, Caroline, Mirault, Tristan, Faure‐Conter, Cécile, Mazereeuw‐Hautier, Juliette, Maza, Aude, Puzenat, Eve, Collonge‐Rame, Marie‐Agnès, Bursztejn, Anne‐Claire, Philippe, Christophe, Thauvin‐Robinet, Christel, Chevarin, Martin, Abasq‐Thomas, Claire, Amiel, Jeanne, Arpin, Stéphanie, Barbarot, Sébastien, Baujat, Geneviève, Bessis, Didier, Bourrat, Emmanuelle, Boute, Odile, Chassaing, Nicolas, Coubes, Christine, Demeer, Bénédicte, Edery, Patrick, El Chehadeh, Salima, Goldenberg, Alice, Hadj‐Rabia, Smail, Haye, Damien, Isidor, Bertrand, Jacquemont, Marie‐Line, Van Kien, Philippe Khau, Lacombe, Didier, Lehalle, Daphné, Lambert, Laetitia, Martin, Ludovic, Maruani, Annabel, Morice‐Picard, Fanny, Petit, Florence, Phan, Alice, Pinson, Lucile, Rossi, Massimiliano, Touraine, Renaud, Vanlerberghe, Clémence, Vincent, Marie, Vincent‐Delorme, Catherine, Whalen, Sandra, Willems, Marjolaine, Marle, Nathalie, Verkarre, Virginie, Devalland, Christine, Devouassoux‐Shisheboran, Mojgan, Abad, Marine, Rioux‐Leclercq, Nathalie, Bonniaud, Bertille, Duffourd, Yannis, Martel, Jehanne, Binquet, Christine, Kuentz, Paul, Vabres, Pierre

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Clinical relevance of 8q23, 15q13 and 18q21 SNP genotyping to evaluate colorectal cancer risk von Baert-Desurmont, Stéphanie, Charbonnier, Françoise, Houivet, Estelle, Ippolito, Lorena, Mauillon, Jacques, Bougeard, Marion, Abadie, Caroline, Malka, David, Duffour, Jacqueline, Desseigne, Françoise, Colas, Chrystelle, Pujol, Pascal, Lejeune, Sophie, Dugast, Catherine, Buecher, Bruno, Faivre, Laurence, Leroux, Dominique, Gesta, Paul, Coupier, Isabelle, Guimbaud, Rosine, Berthet, Pascaline, Manouvrier, Sylvie, Cauchin, Estelle, Prieur, Fabienne, Laurent-Puig, Pierre, Lebrun, Marine, Jonveaux, Philippe, Chiesa, Jean, Caron, Olivier, Morin-Meschin, Marie-Emmanuelle, Polycarpe-Osaer, Florence, Giraud, Sophie, Zaanan, Aziz, Bonnet, Delphine, Mansuy, Ludovic, Bonadona, Valérie, El Chehadeh, Salima, Duhoux, François, Gauthier-Villars, Marion, Saurin, Jean-Christophe, Collonge-Rame, Marie-Agnès, Brugières, Laurence, Wang, Qing, Bressac-de Paillerets, Brigitte, Rey, Jean-Marc, Toulas, Christine, Buisine, Marie-Pierre, Bronner, Myriam, Sokolowska, Joanna, Hardouin, Agnès, Cailleux, Anne-Françoise, Sebaoui, Hakim, Blot, Julien, Tinat, Julie, Benichou, Jacques, Frebourg, Thierry

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TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing von Lesueur, Fabienne, Eon-Marchais, Severine, Bonnet-Boissinot, Sarah, Beauvallet, Juana, Dondon, Marie-Gabrielle, Golmard, Lisa, Rouleau, Etienne, Garrec, Celine, Martinez, Mathilde, Toulas, Christine, Tan Dat Nguyen, Brayotel, Fanny, Crivelli, Louise, Maugard, Christine M., Bubien, Virginie, Sevenet, Nicolas, Gesta, Paul, Chieze-Valero, Stephanie, Nambot, Sophie, Goussot, Vincent, Mari, Veronique, Popovici, Cornel, Prieur, Fabienne, Morin-Meschin, Marie-Emmanuelle, Tinat, Julie, Lortholary, Alain, Dreyfus, Helene, Bidart, Marie, Collonge-Rame, Marie-Agnes, Mozelle-Nivoix, Monique, Gladieff, Laurence, Giraud, Sophie, Boutry-Kryza, Nadia, Chiesa, Jean, Denizeau, Philippe, Bignon, Yves-Jean, Uhrhammer, Nancy, Cohen-Haguenauer, Odile, Vilquin, Paul, Mailliez, Audrey, Coupier, Isabelle, Rey, Jean-Marc, Lacaze, Elodie, Bera, Odile, Colas, Chrystelle, Coulet, Florence, Delnatte, Capucine, Houdayer, Claude, Lasset, Christine, Lemonnier, Jerome, Longy, Michel, Nogues, Catherine, Stoppa-Lyonnet, Dominique, Vaur, Dominique, Andrieu, Nadine, Caron, Olivier

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Genetic characterization of B-cell prolymphocytic leukemia: a prognostic model involving MYC and TP53 von Chapiro, Elise, Pramil, Elodie, Diop, M'boyba, Roos-Weil, Damien, Dillard, Clémentine, Gabillaud, Clémentine, Maloum, Karim, Settegrana, Catherine, Baseggio, Lucile, Lesesve, Jean-François, Yon, Mélanie, Jondreville, Ludovic, Lesty, Claude, Davi, Frédéric, Le Garff-Tavernier, Magali, Droin, Nathalie, Dessen, Philippe, Algrin, Caroline, Leblond, Véronique, Gabarre, Jean, Bouzy, Simon, Eclache, Virginie, Gaillard, Baptiste, Callet-Bauchu, Evelyne, Muller, Marc, Lefebvre, Christine, Nadal, Nathalie, Ittel, Antoine, Struski, Stéphanie, Collonge-Rame, Marie-Agnès, Quilichini, Benoit, Fert-Ferrer, Sandra, Auger, Nathalie, Radford-Weiss, Isabelle, Wagner, Lena, Scheinost, Sebastian, Zenz, Thorsten, Susin, Santos A., Bernard, Olivier A., Nguyen-Khac, Florence

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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study von 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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Association and performance of polygenic risk scores for breast cancer among French women presenting or not a familial predisposition to the disease von Jiao, Yue, Truong, Thérèse, Eon-Marchais, Séverine, Mebirouk, Noura, Caputo, Sandrine M., Dondon, Marie-Gabrielle, Karimi, Mojgan, Le Gal, Dorothée, Beauvallet, Juana, Le Floch, Édith, Dandine-Roulland, Claire, Bacq-Daian, Delphine, Olaso, Robert, Albuisson, Juliette, Audebert-Bellanger, Séverine, Berthet, Pascaline, Bonadona, Valérie, Buecher, Bruno, Caron, Olivier, Cavaillé, Mathias, Chiesa, Jean, Colas, Chrystelle, Collonge-Rame, Marie-Agnès, Coupier, Isabelle, Delnatte, Capucine, De Pauw, Antoine, Dreyfus, Hélène, Fert-Ferrer, Sandra, Gauthier-Villars, Marion, Gesta, Paul, Giraud, Sophie, Gladieff, Laurence, Golmard, Lisa, Lasset, Christine, Lejeune-Dumoulin, Sophie, Léoné, Mélanie, Limacher, Jean-Marc, Lortholary, Alain, Luporsi, Élisabeth, Mari, Véronique, Maugard, Christine M., Mortemousque, Isabelle, Mouret-Fourme, Emmanuelle, Nambot, Sophie, Noguès, Catherine, Popovici, Cornel, Prieur, Fabienne, Pujol, Pascal, Sevenet, Nicolas, Sobol, Hagay, Toulas, Christine, Uhrhammer, Nancy, Vaur, Dominique, Venat, Laurence, Boland-Augé, Anne, Guénel, Pascal, Deleuze, Jean-François, Stoppa-Lyonnet, Dominique, Andrieu, Nadine, Lesueur, Fabienne

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Patterns of genomic aberrations suggest that Burkitt lymphomas with complex karyotype are distinct from other aggressive B-cell lymphomas with MYC rearrangement von Havelange, Violaine, Ameye, Geneviève, Théate, Ivan, Callet-Bauchu, Evelyne, Mugneret, Francine, Michaux, Lucienne, Dastugue, Nicole, Penther, Dominique, Barin, Carole, Collonge-Rame, Marie-Agnès, Baranger, Laurence, Terré, Christine, Nadal, Nathalie, Lippert, Eric, Laï, Jean-Luc, Cabrol, Christine, Tigaud, Isabelle, Herens, Christian, Hagemeijer, Anne, Raphael, Martine, Libouton, Jeanne-Marie, Poirel, Hélène A.

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The t(X;20)(q13;q13) translocation is a good prognostic factor in myeloid neoplasms: A report of 25 cases from the Groupe Francophone de Cytogénétique Hématologique von Nguyen‐Khac, Florence, Muller, Marc, Chapiro, Elise, Abermil, Nassera, Collonge‐Rame, Marie‐Agnes, Daudignon, Agnes, Gaillard, Baptiste, Guzun, Doina, Ittel, Antoine, Lefebvre, Christine, Lesesve, Jean‐Francois, Mozziconacci, Marie‐Joelle, Penther, Dominique, Quessada, Julie, Settegrana, Catherine, Smagghe, Luce, Terre, Christine, Veronese, Lauren, Hirsch, Pierre, Troadec, Marie‐Bérengère

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Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers von Kuchenbaecker, Karoline B, McGuffog, Lesley, Barrowdale, Daniel, Lee, Andrew, Soucy, Penny, Dennis, Joe, Domchek, Susan M, Robson, Mark, Spurdle, Amanda B, Ramus, Susan J, Mavaddat, Nasim, Terry, Mary Beth, Neuhausen, Susan L, Schmutzler, Rita Katharina, Simard, Jacques, Pharoah, Paul D P, Offit, Kenneth, Couch, Fergus J, Chenevix-Trench, Georgia, Easton, Douglas F, Antoniou, Antonis C

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First description of a double heterozygosity for BRCA1 and BRCA2 pathogenic variants in a French metastatic breast cancer patient: A case report von Meynard, Guillaume, Mansi, Laura, Lebahar, Pierre, Villanueva, Cristian, Klajer, Elodie, Calcagno, Fabien, Vivalta, Adrian, Chaix, Marie, Collonge-Rame, Marie-Agnès, Populaire, Céline, Algros, Marie-Paule, Colpart, Prudence, Neidich, Julie, Pivot, Xavier, Curtit, Elsa

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The "extreme phenotype approach" applied to male breast cancer allows the identification of rare variants of ATR as potential breast cancer susceptibility alleles von Chevarin, Martin, Alcantara, Diana, Albuisson, Juliette, Collonge-Rame, Marie-Agnès, Populaire, Céline, Selmani, Zohair, Baurand, Amandine, Sawka, Caroline, Bertolone, Geoffrey, Callier, Patrick, Duffourd, Yannis, Jonveaux, Philippe, Bignon, Yves-Jean, Coupier, Isabelle, Cornelis, François, Cordier, Christophe, Mozelle-Nivoix, Monique, Rivière, Jean-Baptiste, Kuentz, Paul, Thauvin, Christel, Boidot, Romain, Ghiringhelli, François, O'Driscoll, Marc, Faivre, Laurence, Nambot, Sophie

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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes von Fachal, Laura, Kar, Siddhartha, Moradi Marjaneh, Mahdi, Alonso, M. Rosario, Anton-Culver, Hoda, Arason, Adalgeir, Arun, Banu K., Auer, Paul L., Barrowdale, Daniel, Białkowska, Katarzyna, Bolla, Manjeet K., Brooks-Wilson, Angela, Caldés, Trinidad, Campbell, Ian, Carter, Brian D., Christiansen, Hans, Collée, J. Margriet, Couch, Fergus J., Cox, Angela, Cross, Simon S., de la Hoya, Miguel, Ding, Yuan Chun, Dite, Gillian S., Domchek, Susan M., Dwek, Miriam, Eriksson, Mikael, Evans, D. Gareth, Floris, Giuseppe, Gambino, Gaetana, Gapstur, Susan M., García-Sáenz, José A., Gaudet, Mia M., Giles, Graham G., Glendon, Gord, Goldgar, David E., Greene, Mark H., Grip, Mervi, Guénel, Pascal, Håkansson, Niclas, Hall, Per, Harrington, Patricia A., Heyworth, Jane, Hogervorst, Frans B. L., Howell, Anthony, Huang, Guanmengqian, Hulick, Peter J., Jakimovska, Milena, Jakubowska, Anna, Janavicius, Ramunas, Johnson, Nichola, Kaaks, Rudolf, Kapoor, Pooja Middha, Ko, Yon-Dschun, Konstantopoulou, Irene, Laitman, Yael, Lee, Eunjung, Lindblom, Annika, Lo, Wing-Yee, Lophatananon, Artitaya, Manoukian, Siranoush, Margolin, Sara, Martinez, Maria Elena, Mayes, Rebecca, McLean, Catriona, Mebirouk, Noura, Miller, Austin, Moreno, Fernando, Mulligan, Anna Marie, Narod, Steven A., Nassir, Rami, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, Osorio, Ana, Pankratz, V. Shane, Park, Sue K., Parsons, Michael T., Paul, James, Pedersen, Inge Sokilde, Prokofyeva, Darya, Ramus, Susan J., Rantala, Johanna, Risch, Harvey A., Saloustros, Emmanouil, Schoemaker, Minouk J., Scott, Rodney J., Shah, Mitul, Shen, Chen-Yang, Smichkoska, Snezhana, Tamimi, Rulla M., Thomassen, Mads, Toland, Amanda E., Tollenaar, Rob A. E. M., Troester, Melissa A., Vachon, Celine M., van Asperen, Christi J., Vega, Ana, Viel, Alessandra, Wildiers, Hans, Zhang, Yan

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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants von Barnes, Daniel R., Rookus, Matti A., Dennis, Joe, Mavaddat, Nasim, Ahmed, Munaza, Aittomäki, Kristiina, Andrulis, Irene L., Arun, Banu K., Barkardottir, Rosa B., Barrowdale, Daniel, Benitez, Javier, Białkowska, Katarzyna, Blok, Marinus J., Bonanni, Bernardo, Bozsik, Aniko, Buys, Saundra S., Caldés, Trinidad, Campbell, Ian, Christensen, Lise Lotte, Colas, Chrystelle, Berthet, Pascaline, Faivre, Laurence, Giraud, Sophie, Lasset, Christine, Mebirouk, Noura, Adlard, Julian, Antoniou, Antonis, Brennan, Paul, Brewer, Carole, Cook, Jackie, Easton, Douglas, Eeles, Ros, Hanson, Helen, Izatt, Louise, Ong, Kai-ren, O’Shaughnessy-Kirwan, Aoife, Daly, Mary B., Davidson, Rosemarie, Ding, Yuan Chun, Dorfling, Cecilia M., Engel, Christoph, Evans, D. Gareth, Friedlander, Michael, Friedman, Eitan, Ganz, Patricia A., Gerdes, Anne-Marie, Giraud, Sophie, Glendon, Gord, Godwin, Andrew K., Gschwantler-Kaulich, Daphne, Hamann, Ute, Hu, Chunling, Hulick, Peter J., Hogervorst, Frans, Koudijs, Marco, Kruse, Torben A., Lazaro, Conxi, Lester, Jenny, Mai, Phuong L., Mari, Véronique, Meijers-Heijboer, Hanne E.J., Meindl, Alfons, Mensenkamp, Arjen R., Montagna, Marco, Mukherjee, Semanti, Mulligan, Anna Marie, Nevanlinna, Heli, Niederacher, Dieter, Olopade, Olufunmilayo I., Ott, Claus-Eric, Papi, Laura, Park, Sue K., Peissel, Bernard, Pfeiler, Georg, Phillips, Kelly-Anne, Prajzendanc, Karolina, Pujana, Miquel Angel, Ramus, Susan J., Rantala, Johanna, Rennert, Gad, Risch, Harvey A., Schuster, Hélène, Senter, Leigha, Side, Lucy E., Slavin, Thomas P., Soucy, Penny, Sutter, Christian, Thull, Darcy L., Toland, Amanda E., Tung, Nadine, van Engelen, Klaartje, van Rensburg, Elizabeth J., Wang-Gohrke, Shan, Wappenschmidt, Barbara, Yang, Xin, Zimbalatti, Dario, Offit, Kenneth, Couch, Fergus J., Schmutzler, Rita K., Antoniou, Antonis C.

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Systematic donor blood qualification by flow cytometry would have been able to avoid CLL‐type MBL transmission after unrelated hematopoietic stem cell transplantation von Ferrand, Christophe, Garnache‐Ottou, Francine, Collonge‐Rame, Marie Agnès, Larosa, Fabrice, Blanc, Michel, Behar, Catherine, Giannoli, Catherine, Garnier, Frédérico, Tiberghien, Pierre, Deconinck, Eric, Rohrlich, Pierre Simon

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Post-Essential Thrombocythemia Myelofibrosis and Multiple Isodicentric Y Chromosomes: A Unique Case among a Rare Association von Dahlen, Eric, Sarghi, Sinziana I., Renosi, Florian, Ferrand, Christophe, Collonge-Rame, Marie-Agnes, Kuentz, Paul

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Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus von Li, Qiyuan, Andrulis, Irene L., Arndt, Volker, Arver, Brita, Bandera, Elisa V., Barkardottir, Rosa B., Barrowdale, Daniel, Beckmann, Matthias W., Benitez, Javier, Bisogna, Maria, Bogdanova, Natalia, Bonanni, Bernardo, Børresen-Dale, Anne-Lise, Brauch, Hiltrud, Bruinsma, Fiona, Buhari, Shaik Ahmad, Burwinkel, Barbara, Campbell, Ian, Chang-Claude, Jenny, Chiquette, Jocelyne, Choi, Ji-Yeob, Czene, Kamila, Diez, Orland, Doherty, Jennifer A., Domchek, Susan M., Dörk, Thilo, Dumont, Martine, Figueroa, Jonine, Flyger, Henrik, Fostira, Florentia, Foulkes, William D., Friedman, Eitan, Frost, Debra, Gambino, Gaetana, Ganz, Patricia A., Garber, Judy, Gentry-Maharaj, Aleksandra, Ghoussaini, Maya, Giles, Graham G., Glasspool, Rosalind, Goldgar, David E., González-Neira, Anna, Goodman, Marc T., Guénel, Pascal, Haiman, Christopher A., Hallberg, Emily, Hartman, Mikael, Healey, Sue, Heitz, Florian, Høgdall, Estrid, Hogervorst, Frans B. L., Huzarski, Tomasz, Imyanitov, Evgeny N., John, Esther M., Kapuscinski, Miroslav, Karlan, Beth Y., Knight, Julia A., Konstantopoulou, Irene, Kosma, Veli-Matti, Kupryjanczyk, Jolanta, de la Hoya, Miguel, Lambrechts, Diether, De Leeneer, Kim, Li, Jingmei, Lubinski, Jan, Margolin, Sara, McGuffog, Lesley, McNeish, Iain, Meindl, Alfons, Mulligan, Anna Marie, Ness, Roberta B., Neuhausen, Susan L., Odunsi, Kunle, Olah, Edith, Orr, Nick, Osorio, Ana, Park, Sue Kyung, Poole, Elizabeth M., Rantala, Johanna, Risch, Harvey A., Sangrajrang, Suleeporn, Schildkraut, Joellen M., Schmidt, Marjanka K., Shu, Xiao-Ou, Sieh, Weiva, Singer, Christian F., Sinilnikova, Olga M., Slager, Susan, Southey, Melissa C., Stenmark-Askmalm, Marie, Tihomirova, Laima, Tung, Nadine, van Doorn, Helena C., Van't Veer, Laura J., Wentzensen, Nicolas, Wildiers, Hans, Zheng, Wei, Simard, Jacques, Pharoah, Paul D., Chenevix-Trench, Georgia

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Chromosomal abnormalities in transformed Ph-negative myeloproliferative neoplasms are associated to the transformation subtype and independent of JAK2 and the TET2 mutations von Nguyen-Khac, Florence, Lesty, Claude, Eclache, Virginie, Couronné, Lucile, Kosmider, Olivier, Andrieux, Joris, Collonge-Rame, Marie-Agnes, Penther, Dominique, Lafage, Marina, Bilhou-Nabera, Chrystele, Chapiro, Elise, Mozziconacci, Marie-Joelle, Mugneret, Francine, Gachard, Nathalie, Nadal, Nathalie, Lippert, Eric, Struski, Stephanie, Dastugue, Nicole, Cabrol, Christine, Bernard, Olivier A.

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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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Renal cell tumour characteristics in patients with the Birt-Hogg-Dubé cancer susceptibility syndrome: a retrospective, multicentre study von Benusiglio, Patrick R, Giraud, Sophie, Deveaux, Sophie, Méjean, Arnaud, Correas, Jean-Michel, Joly, Dominique, Timsit, Marc-Olivier, Ferlicot, Sophie, Verkarre, Virginie, Abadie, Caroline, Chauveau, Dominique, Leroux, Dominique, Avril, Marie-Françoise, Cordier, Jean-François, Richard, Stéphane

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Cytogenetics in the management of hematologic neoplasms with germline predisposition: guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH) von Gachard, Nathalie, Lafage-Pochitaloff, Marina, Quessada, Julie, Auger, Nathalie, Collonge-Rame, Marie-Agnès

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