Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development von Sanlaville, D, Etchevers, H C, Gonzales, M, Martinovic, J, Clément-Ziza, M, Delezoide, A-L, Aubry, M-C, Pelet, A, Chemouny, S, Cruaud, C, Audollent, S, Esculpavit, C, Goudefroye, G, Ozilou, C, Fredouille, C, Joye, N, Morichon-Delvallez, N, Dumez, Y, Weissenbach, J, Munnich, A, Amiel, J, Encha-Razavi, F, Lyonnet, S, Vekemans, M, Attié-Bitach, T

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Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis von Bouton, Jean Marie, Neuhaus, Thomas, Aziza, Jacqueline, Makni, Saloua, Delezoide, Anne-Lise, Dijoud, Frédérique, Antignac, Corinne, Bouvier, Raymonde, Joubert, Madeleine, Roume, Joelle, Laube, Guido, Laurent, Nicole, Amar, Hatem Ben, Bieth, Eric, Gribouval, Olivier, Gubler, Marie Claire, Feuillet, François, Ollagnon-Roman, Elisabeth, Gonzales, Marie

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Fetal phenotypes in otopalatodigital spectrum disorders von Naudion, S., Moutton, S., Coupry, I., Sole, G., Deforges, J., Guerineau, E., Hubert, C., Deves, S., Pilliod, J., Rooryck, C., Abel, C., Le Breton, F., Collardeau-Frachon, S., Cordier, M.P., Delezoide, A.L., Goldenberg, A., Loget, P., Melki, J., Odent, S., Patrier, S., Verloes, A., Viot, G., Blesson, S., Bessières, B., Lacombe, D., Arveiler, B., Goizet, C., Fergelot, P.

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Safety study of Ciprofloxacin in newborn mice von Bourgeois, Thomas, Delezoide, Anne-Lise, Zhao, Wei, Guimiot, Fabien, Adle-Biassette, Homa, Durand, Estelle, Ringot, Maud, Gallego, Jorge, Storme, Thomas, Le Guellec, Chantal, Kassaï, Behrouz, Turner, Mark A., Jacqz-Aigrain, Evelyne, Matrot, Boris

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Dynamics of Thymus-Colonizing Cells during Human Development von Haddad, Rima, Guimiot, Fabien, Six, Emmanuelle, Jourquin, Frederic, Setterblad, Niclas, Kahn, Edmond, Yagello, Micael, Schiffer, Cecile, Andre-Schmutz, Isabelle, Cavazzana-Calvo, Marina, Gluckman, Jean Claude, Delezoide, Anne-Lise, Pflumio, Françoise, Canque, Bruno

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Paradoxic activation of the renin-angiotensin system in twin-twin transfusion syndrome : An explanation for cardiovascular disturbances in the recipient von MAHIEU-CAPUTO, Dominique, MEULEMANS, Alain, MARTINOVIC, Jelena, GUBLER, Marie-Claire, DELEZOIDE, Anne-Lise, MULLER, Francoise, MADELENAT, Patrick, FISK, Nicholas M, DOMMERGUES, Marc

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Molecular characterization of early human T/NK and B-lymphoid progenitor cells in umbilical cord blood von Haddad, Rima, Guardiola, Philippe, Izac, Brigitte, Thibault, Christelle, Radich, Jerry, Delezoide, Anne-Lise, Baillou, Claude, Lemoine, François M., Gluckman, Jean Claude, Pflumio, Françoise, Canque, Bruno

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Twin-to-Twin Transfusion Syndrome : Role of the Fetal Renin-Angiotensin System von Mahieu-Caputo, Dominique, Dommergues, Marc, Delezoide, Anne-Lise, Lacoste, Mireille, Cai, Yi, Narcy, Francoise, Jolly, Dominique, Gonzales, Marie, Dumez, Yves, Gubler, Marie-Claire

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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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Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome von Karmous-Benailly, Houda, Martinovic, Jelena, Gubler, Marie-Claire, Sirot, Yoann, Clech, Laure, Ozilou, Catherine, Augé, Joëlle, Brahimi, Nora, Etchevers, Heather, Detrait, Eric, Esculpavit, Chantal, Audollent, Sophie, Goudefroye, Géraldine, Gonzales, Marie, Tantau, Julia, Loget, Philippe, Joubert, Madeleine, Gaillard, Dominique, Jeanne-Pasquier, Corinne, Delezoide, Anne-Lise, Peter, Marie-Odile, Plessis, Ghislaine, Simon-Bouy, Brigitte, Dollfus, Hélène, Le Merrer, Martine, Munnich, Arnold, Encha-Razavi, Férechté, Vekemans, Michel, Attié-Bitach, Tania

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Developmental toxicity of the angiotensin II type 1 receptor antagonists during human pregnancy: a report of 10 cases von Serreau, Raphael, Luton, Dominique, Macher, Marie‐Alice, Delezoide, Anne‐Lise, Garel, Catherine, Jacqz‐Aigrain, Evelyne

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Absence of functional type 1 parathyroid hormone (PTH)/PTH-related protein receptors in humans is associated with abnormal breast development and tooth impaction von WYSOLMERSKI, John J, CORMIER, Sarah, PHILBRICK, William M, DANN, Pamela, ZHANG, Jian-Ping, ROUME, Joelle, DELEZOIDE, Anne-Lise, SILVE, Caroline

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Fibroblast Growth Factor Receptor 3 Mutations Promote Apoptosis but Do Not Alter Chondrocyte Proliferation in Thanatophoric Dysplasia von Legeai-Mallet, Laurence, Benoist-Lasselin, Catherine, Delezoide, Anne-Lise, Munnich, Arnold, Bonaventure, Jacky

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Organ weights in human fetuses after formalin fixation: standards by gestational age and body weight von Guihard-Costa, Anne-Marie, Ménez, Françoise, Delezoide, Anne-Lise

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The Distribution of SMN Protein Complex in Human Fetal Tissues and Its Alteration in Spinal Muscular Atrophy von Burlet, P., Huber, C., Bertrandy, S., Ludosky, M. A., Zwaenepoel, I., Clermont, O., Roume, J., Delezoide, A. L., Cartaud, J., Munnich, A., Lefebvre, S.

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Contribution of Fetal MR Imaging in the Evaluation of Cerebral Ischemic Lesions von Garel, Catherine, Delezoide, Anne-Lise, Elmaleh-Berges, Monique, Menez, Francoise, Fallet-Bianco, Catherine, Vuillard, Edith, Luton, Dominique, Oury, Jean-Francois, Sebag, Guy

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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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MR imaging of fetal cerebral anomalies von SONIGO, P. C, RYPENS, F. F, CARTERET, M, DELEZOIDE, A.-L, BRUNELLE, F. O

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Missense FGFR3 Mutations Create Cysteine Residues in Thanatophoric Dwarfism Type I (TD1) von Rousseau, F., El Ghouzzi, V., Delezoide, A. L., Legeai-Mallet, L., Le Merrer, M., Munnich, A., Bonaventure, J.

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Stop codon FGFR3 mutations in thanatophoric dwarfism type 1 von Munnich, Arnold, Sanak, Marek, Rousseau, Francis, Bonaventure, Jacky, Merrer, Martine Le, Maroteaux, Pierre, Delezoide, Anne-Lise, Narcy, Françoise, Saugier, Pascale

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