Adverse perinatal outcomes of chronic intervillositis of unknown etiology: an observational retrospective study of 122 cases von Mattuizzi, Aurélien, Sauvestre, Fanny, André, Gwenaëlle, Poingt, Marion, Camberlein, Camille, Carles, Dominique, Pelluard, Fanny, Blanco, Patrick, Sentilhes, Loïc, Lazaro, Estibaliz

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Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome von Alby, Caroline, Piquand, Kevin, Huber, Céline, Megarbané, André, Ichkou, Amale, Legendre, Marine, Pelluard, Fanny, Encha-Ravazi, Ferechté, Abi-Tayeh, Georges, Bessières, Bettina, El Chehadeh-Djebbar, Salima, Laurent, Nicole, Faivre, Laurence, Sztriha, László, Zombor, Melinda, Szabó, Hajnalka, Failler, Marion, Garfa-Traore, Meriem, Bole, Christine, Nitschké, Patrick, Nizon, Mathilde, Elkhartoufi, Nadia, Clerget-Darpoux, Françoise, Munnich, Arnold, Lyonnet, Stanislas, Vekemans, Michel, Saunier, Sophie, Cormier-Daire, Valérie, Attié-Bitach, Tania, Thomas, Sophie

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Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions von Tan, Tiong Yang, Gonzaga-Jauregui, Claudia, Bhoj, Elizabeth J., Strauss, Kevin A., Brigatti, Karlla, Puffenberger, Erik, Li, Dong, Xie, LiQin, Das, Nanditha, Skubas, Ioanna, Deckelbaum, Ron A., Hughes, Virginia, Brydges, Susannah, Hatsell, Sarah, Siao, Chia-Jen, Dominguez, Melissa G., Economides, Aris, Overton, John D., Mayne, Valerie, Simm, Peter J., Jones, Bryn O., Eggers, Stefanie, Le Guyader, Gwenaël, Pelluard, Fanny, Haack, Tobias B., Sturm, Marc, Riess, Angelika, Waldmueller, Stephan, Hofbeck, Michael, Steindl, Katharina, Joset, Pascal, Rauch, Anita, Hakonarson, Hakon, Baker, Naomi L., Farlie, Peter G.

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Reduced placental telomere length during pregnancies complicated by intrauterine growth restriction von Toutain, Jérôme, Prochazkova-Carlotti, Martina, Cappellen, David, Jarne, Ana, Chevret, Edith, Ferrer, Jacky, Idrissi, Yamina, Pelluard, Fanny, Carles, Dominique, Maugey-Laulon, Brigitte, Lacombe, Didier, Horovitz, Jacques, Merlio, Jean-Philippe, Saura, Robert

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Fraser syndrome: features suggestive of prenatal diagnosis in a review of 38 cases von Tessier, Aude, Sarreau, Mélie, Pelluard, Fanny, André, Gwenaelle, Blesson, Sophie, Bucourt, Martine, Dechelotte, Pierre, Faivre, Laurence, Frébourg, Thierry, Goldenberg, Alice, Goua, Valérie, Jeanne-Pasquier, Corinne, Guimiot, Fabien, Laquerriere, Annie, Laurent, Nicole, Lefebvre, Mathilde, Loget, Philippe, Maréchaud, Martine, Mechler, Charlotte, Perez, Marie-Josée, Sabourin, Jean Christophe, Verloes, Alain, Patrier, Sophie, Guerrot, Anne-Marie

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Foetal onset of EIF2B related disorder in two siblings: cerebellar hypoplasia with absent Bergmann glia and severe hypomyelination von Trimouille, Aurélien, Marguet, Florent, Sauvestre, Fanny, Lasseaux, Eulalie, Pelluard, Fanny, Martin-Négrier, Marie-Laure, Plaisant, Claudio, Rooryck, Caroline, Lacombe, Didier, Arveiler, Benoît, Boespflug-Tanguy, Odile, Naudion, Sophie, Laquerrière, Annie

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Rhombencephalosynapsis and related anomalies: a neuropathological study of 40 fetal cases von Pasquier, Laurent, Marcorelles, Pascale, Loget, Philippe, Pelluard, Fanny, Carles, Dominique, Perez, Marie-Josée, Bendavid, Claude, de La Rochebrochard, Céline, Ferry, Mathilde, David, Véronique, Odent, Sylvie, Laquerrière, Annie

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Omphalocele: a review of common genetic etiologies von Poaty, Henriette, Pelluard, Fanny, Diallo, Mama Sy, Ondima, Irène Patricia Lucienne, André, Gwenaelle, Silou-Massamba, Jacques François

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Genetic rescue of Cdk4 null mice restores pancreatic β-cell proliferation but not homeostatic cell number von Martín, Javier, Hunt, Sarah L, Dubus, Pierre, Sotillo, Rocío, Néhmé-Pélluard, Fanny, Magnuson, Mark A, Parlow, Albert F, Malumbres, Marcos, Ortega, Sagrario, Barbacid, Mariano

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Elastase 2A: a new player in skin barrier function von Nehmé-Pelluard, Fanny, Deraison, Céline, Dubus, Pierre

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Human interleukin-2 receptor β mutations associated with defects in immunity and peripheral tolerance von Zhang, Zinan, Gothe, Florian, Pennamen, Perrine, James, John R, McDonald, David, Mata, Carlos P, Modis, Yorgo, Alazami, Anas M, Acres, Meghan, Haller, Wolfram, Bowen, Claire, Döffinger, Rainer, Sinclair, Jan, Brothers, Shannon, Zhang, Yu, Matthews, Helen F, Naudion, Sophie, Pelluard, Fanny, Alajlan, Huda, Yamazaki, Yasuhiro, Notarangelo, Luigi D, Thaventhiran, James E, Engelhardt, Karin R, Al-Mousa, Hamoud, Hambleton, Sophie, Rooryck, Caroline, Smith, Kenneth G C, Lenardo, Michael J

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An Atypical Case of Congenital Erythropoietic Porphyria von Sudrié-Arnaud, Bénédicte, Legendre, Marine, Snanoudj, Sarah, Pelluard, Fanny, Bekri, Soumeya, Tebani, Abdellah

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Morphological and genetic causes of fetal cardiomyopathies von Kohaut, Eva, Ader, Flavie, Rooryck, Caroline, Pelluard, Fanny, Bonnière, Maryse, André, Gwenaelle, Sauvestre, Fanny, Roth, Philippe, Khraiche, Diala, Bessières, Bettina, Attié‐Bitach, Tania, Richard, Pascale

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Occupational Exposure to Ultrafine Particles and Placental Histopathological Lesions: A Retrospective Study about 130 Cases von Pasquiou, Anaïs, Pelluard, Fanny, Manangama, Guyguy, Brochard, Patrick, Audignon, Sabyne, Sentilhes, Loïc, Delva, Fleur

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Extending the prenatal Noonan's phenotype by review of ultrasound and autopsy data von Lamouroux, Audrey, Dauge, Coralie, Wells, Constance, Mousty, Eve, Pinson, Lucile, Cavé, Hélène, Capri, Yline, Faure, Jean‐Michel, Grosjean, Frédéric, Sauvestre, Fanny, Attié‐Bitach, Tania, Pelluard, Fanny, Geneviève, David

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p57-discordant villi in hydropic products of conception: a clinicopathological study of 70 cases von Gaillot-Durand, Lucie, Patrier, Sophie, Aziza, Jacqueline, Devisme, Louise, Riera, Anne-Claude, Marcorelles, Pascale, Pelluard, Fanny, Gasser, Bernard, Mauduit, Claire, Hajri, Touria, Massardier, Jérôme, Bolze, Pierre-Adrien, Golfier, François, Devouassoux-Shisheboran, Mojgan, Allias, Fabienne

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COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage von Coste, Thibault, Vincent‐Delorme, Catherine, Stichelbout, Morgane, Devisme, Louise, Gelot, Antoinette, Deryabin, Igor, Pelluard, Fanny, Aloui, Chaker, Leutenegger, Anne‐Louise, Jouannic, Jean‐Marie, Héron, Delphine, Gould, Douglas B, Tournier‐Lasserve, Elisabeth

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TAR syndrome: Clinical and molecular characterization of a cohort of 26 patients and description of novel noncoding variants of RBM8A von Boussion, Simon, Escande, Fabienne, Jourdain, Anne‐Sophie, Smol, Thomas, Brunelle, Perrine, Duhamel, Céline, Alembik, Yves, Attié‐Bitach, Tania, Baujat, Geneviève, Bazin, Anne, Bonnière, Maryse, Carassou, Philippe, Carles, Dominique, Devisme, Louise, Goizet, Cyril, Goldenberg, Alice, Grotto, Sarah, Guichet, Agnès, Jouk, Pierre‐Simon, Loeuillet, Laurence, Mechler, Charlotte, Michot, Caroline, Pelluard, Fanny, Putoux, Audrey, Whalen, Sandra, Ghoumid, Jamal, Manouvrier‐Hanu, Sylvie, Petit, Florence

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Bardet‐Biedl syndrome: Antenatal presentation of forty‐five fetuses with biallelic pathogenic variants in known Bardet‐Biedl syndrome genes von Mary, Laura, Chennen, Kirsley, Stoetzel, Corinne, Antin, Manuela, Leuvrey, Anne, Nourisson, Elsa, Alanio‐Detton, Elisabeth, Antal, Maria C., Attié‐Bitach, Tania, Bouvagnet, Patrice, Bouvier, Raymonde, Buenerd, Annie, Clémenson, Alix, Devisme, Louise, Gasser, Bernard, Gilbert‐Dussardier, Brigitte, Guimiot, Fabien, Khau Van Kien, Philippe, Leroy, Brigitte, Loget, Philippe, Martinovic, Jelena, Pelluard, Fanny, Perez, Marie‐Josée, Petit, Florence, Pinson, Lucile, Rooryck‐Thambo, Caroline, Poch, Olivier, Dollfus, Hélène, Schaefer, Elise, Muller, Jean

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Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies von Devisme, Louise, Bouchet, Céline, Gonzalès, Marie, Alanio, Elisabeth, Bazin, Anne, Bessières, Bettina, Bigi, Nicole, Blanchet, Patricia, Bonneau, Dominique, Bonnières, Maryse, Bucourt, Martine, Carles, Dominique, Clarisse, Bénedicte, Delahaye, Sophie, Fallet-Bianco, Catherine, Figarella-Branger, Dominique, Gaillard, Dominique, Gasser, Bernard, Delezoide, Anne-Lise, Guimiot, Fabien, Joubert, Madeleine, Laurent, Nicole, Laquerrière, Annie, Liprandi, Agnès, Loget, Philippe, Marcorelles, Pascale, Martinovic, Jelena, Menez, Francoise, Patrier, Sophie, Pelluard, Fanny, Perez, Marie-José, Rouleau, Caroline, Triau, Stéphane, Attié-Bitach, Tania, Vuillaumier-Barrot, Sandrine, Seta, Nathalie, Encha-Razavi, Férechté

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