Duplicated distal phalanx of thumb or hallux in trisomy 13: A recurrent feature in a series of 42 fetuses von Létard, Pascaline, Guimiot, Fabien, Dupont, Céline, Rosenblatt, Jonathan, Delezoide, Anne‐Lise, Khung‐Savatovsky, Suonavy

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Biometry of face and brain in fetuses with trisomy 21 von GUIHARD-COSTA, Anne-Marie, KHUNG, Suonavy, DELBECQUE, Kathy, MENEZ, Francoise, DELEZOIDE, Anne-Lise

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Management strategy in pregnancies with elevated second-trimester maternal serum alpha-fetoprotein based on a second assay von Spaggiari, Emmanuel, MD, Ruas, Marie, MD, Dreux, Sophie, MD, Valat, Anne-Sylvie, MD, Czerkiewicz, Isabelle, MD, Guimiot, Fabien, PhD, Schmitz, Thomas, MD, PhD, Delezoide, Anne-Lise, MD, PhD, Muller, Françoise, MD, PhD

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Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy von Mariot, Virginie, Roche, Stephane, Hourdé, Christophe, Portilho, Debora, Sacconi, Sabrina, Puppo, Francesca, Duguez, Stephanie, Rameau, Philippe, Caruso, Nathalie, Delezoide, Anne-Lise, Desnuelle, Claude, Bessières, Bettina, Collardeau, Sophie, Feasson, Leonard, Maisonobe, Thierry, Magdinier, Frederique, Helmbacher, Françoise, Butler-Browne, Gillian, Mouly, Vincent, Dumonceaux, Julie

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DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III von Dagoneau, Nathalie, Goulet, Marie, Geneviève, David, Sznajer, Yves, Martinovic, Jelena, Smithson, Sarah, Huber, Céline, Baujat, Geneviève, Flori, Elisabeth, Tecco, Laura, Cavalcanti, Denise, Delezoide, Anne-Lise, Serre, Valérie, Le Merrer, Martine, Munnich, Arnold, Cormier-Daire, Valérie

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Dynamic Expression Patterns of Progenitor and Pyramidal Neuron Layer Markers in the Developing Human Hippocampus von Cipriani, Sara, Nardelli, Jeannette, Verney, Catherine, Delezoide, Anne-Lise, Guimiot, Fabien, Gressens, Pierre, Adle-Biassette, Homa

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Unilateral agenesis of the abdominal wall musculature: An early muscle deficiency von Gerard‐Blanluet, Marion, Port‐Lis, Marylin, Baumann, Clarisse, Perrin‐Sabourin, Laurence, Ebrad, Patrick, Audry, Georges, Delezoide, Anne‐Lise, Verloes, Alain

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Entry and Distribution of Microglial Cells in Human Embryonic and Fetal Cerebral Cortex von Monier, Anne, Adle-Biassette, Homa, Delezoide, Anne-Lise, Evrard, Philippe, Gressens, Pierre, Verney, Catherine

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Spatial and temporal localization during embryonic and fetal human development of the transcription factor SIM2 in brain regions altered in Down syndrome von Rachidi, Mohammed, Lopes, Carmela, Charron, Giselle, Delezoide, Anne‐Lise, Paly, Evelyne, Bloch, Bernard, Delabar, Jean‐Maurice

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Outcome and etiologies of fetal megacystis according to the gestational age at diagnosis von Bornes, Marie, Spaggiari, Emmanuel, Schmitz, Thomas, Dreux, Sophie, Czerkiewicz, Isabelle, Delezoide, Anne-Lise, El-Ghoneimi, Alaa, Oury, Jean-François, Muller, Françoise

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Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions von Teixeira, Luis, Guimiot, Fabien, Dodé, Catherine, Fallet-Bianco, Catherine, Millar, Robert P, Delezoide, Anne-Lise, Hardelin, Jean-Pierre

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Two Novel Homozygous Mutations in Phosphoglucomutase 3 Leading to Severe Combined Immunodeficiency, Skeletal Dysplasia, and Malformations von Fusaro, Mathieu, Vincent, Aline, Castelle, Martin, Rosain, Jérémie, Fournier, Benjamin, Veiga-da-Cunha, Maria, Kentache, Takfarinas, Serre, Jill, Fallet-Bianco, Catherine, Delezoide, Anne-Lise, Renesme, Laurent, Picard, Fanny Morice, Lasseaux, Eulalie, Aladjidi, Nathalie, Seta, Nathalie, Cormier-Daire, Valérie, Schaftingen, Emile van, Neven, Bénédicte, Moshous, Despina, Blesson, Sophie, Picard, Capucine

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Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry von Beaussant Cohen, Sarah, Fenneteau, Odile, Plouvier, Emmanuel, Rohrlich, Pierre-Simon, Daltroff, Gerard, Plantier, Isabelle, Dupuy, Alain, Kerob, Delphine, Beaupain, Blandine, Bordigoni, Pierre, Fouyssac, Fanny, Delezoide, Anne-Lise, Devouassoux, Gilles, Nicolas, Jean François, Bensaid, Philippe, Bertrand, Yves, Balabanian, Karl, Chantelot, Christine Bellanne, Bachelerie, Françoise, Donadieu, Jean

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Asphyxiating thoracic dysplasia: clinical and molecular review of 39 families von Baujat, Geneviève, Huber, Céline, El Hokayem, Joyce, Caumes, Roseline, Do Ngoc Thanh, Claire, David, Albert, Delezoide, Anne-Lise, Dieux-Coeslier, Anne, Estournet, Brigitte, Francannet, Christine, Kayirangwa, Honorine, Lacaille, Florence, Le Bourgeois, Muriel, Martinovic, Jelena, Salomon, Rémi, Sigaudy, Sabine, Malan, Valérie, Munnich, Arnold, Le Merrer, Martine, Le Quan Sang, Kim Hanh, Cormier-Daire, Valérie

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Fetal phenotype associated with the 22q11 deletion von Noël, Anne-Claire, Pelluard, Fanny, Delezoide, Anne-Lise, Devisme, Louise, Loeuillet, Laurence, Leroy, Brigitte, Martin, Alain, Bouvier, Raymonde, Laquerriere, Annie, Jeanne-Pasquier, Corinne, Bessieres-Grattagliano, Betty, Mechler, Charlotte, Alanio, Elisabeth, Leroy, Camille, Gaillard, Dominique

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Prenatal diagnosis of focal dermal hypoplasia: Report of three fetuses and review of the literature von Mary, Laura, Scheidecker, Sophie, Kohler, Monique, Lombardi, Maria‐Paola, Delezoide, Anne‐Lise, Auberger, Elisabeth, Triau, Stéphane, Colin, Estelle, Gerard, Marion, Grzeschik, Karl‐Heinz, Dollfus, Hélène, Antal, Maria Cristina

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Phenotypic spectrum of STRA6 mutations: from matthew-wood syndrome to non-lethal anophthalmia von Chassaing, Nicolas, Golzio, Christelle, Odent, Sylvie, Lequeux, Léopoldine, Vigouroux, Adeline, Martinovic-Bouriel, Jelena, Tiziano, Francesco Danilo, Masini, Lucia, Piro, Francesca, Maragliano, Giovanna, Delezoide, Anne-Lise, Attié-Bitach, Tania, Manouvrier-Hanu, Sylvie, Etchevers, Heather C, Calvas, Patrick

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Fetal anomalies associated with HNF1B mutations: report of 20 autopsy cases von Duval, Hélène, Michel-Calemard, Laurence, Gonzales, Marie, Loget, Philippe, Beneteau, Claire, Buenerd, Annie, Joubert, Madeleine, Denis-Musquer, Marielee, Clemenson, Alix, Chesnais, Anne-Laure, Blesson, Sophie, De Pinieux, Isabelle, Delezoide, Anne-Lise, Bonyhay, Gheorghe, Bellanné-Chantelot, Christine, Heidet, Laurence, Dupré, Florence, Collardeau-Frachon, Sophie

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CD117hi expression identifies a human fetal hematopoietic stem cell population with high proliferation and self-renewal potential von Maillard, Loïc, Sanfilippo, Sandra, Domenech, Carine, Kasmi, Nassima, Petit, Laurence, Jacques, Sébastien, Delezoide, Anne-Lise, Guimiot, Fabien, Eladak, Soria, Moison, Delphine, Nicolas, Nour, Rouiller-Fabre, Virginie, Pozzi-Godin, Stéphanie, Mennesson, Benoit, Brival, Marie-Laure, Letourneur, Franck, Jaffredo, Thierry, Chomienne, Christine, Souyri, Michèle

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A dramatic fetal outcome following transplacental transfer of dasatinib von Berveiller, Paul, Andreoli, Annalisa, Mir, Olivier, Anselem, Olivia, Delezoide, Anne-Lise, Sauvageon, Hélène, Chapuis, Nicolas, Tsatsaris, Vassilis

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