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• W1985778855 abstract "American Journal of Medical Genetics Part AVolume 155, Issue 5 p. 1178-1183 Research Letter Expanding the skeletal phenotype of Loeys-Dietz syndrome† Sérgio B. Sousa, Sérgio B. Sousa Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, France Serviço de Genética Médica, Hospital Pediátrico de Coimbra, Coimbra, PortugalSearch for more papers by this authorKaren Lambot-Juhan, Karen Lambot-Juhan Service de Radiologie Pédiatrique, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorMarlène Rio, Marlène Rio Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorGeneviève Baujat, Geneviève Baujat Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorVicken Topouchian, Vicken Topouchian Service de Chirurgie Orthopédique Pédiatrique, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorNadine Hanna, Nadine Hanna Université Versailles-SQY, Service de Biochimie et Génétique Moléculaire (AP-HP), Hôpital Ambroise Paré, Boulogne-Billancourt, FranceSearch for more papers by this authorMartine Le Merrer, Martine Le Merrer Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorFrancis Brunelle, Francis Brunelle Service de Radiologie Pédiatrique, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorArnold Munnich, Arnold Munnich Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorCatherine Boileau, Catherine Boileau Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, France Université Versailles-SQY, Service de Biochimie et Génétique Moléculaire (AP-HP), Hôpital Ambroise Paré, Boulogne-Billancourt, FranceSearch for more papers by this authorValérie Cormier-Daire, Corresponding Author Valérie Cormier-Daire cormier-daire@inserm.fr Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, FranceDépartement de Génétique, Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, France.Search for more papers by this author Sérgio B. Sousa, Sérgio B. Sousa Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, France Serviço de Genética Médica, Hospital Pediátrico de Coimbra, Coimbra, PortugalSearch for more papers by this authorKaren Lambot-Juhan, Karen Lambot-Juhan Service de Radiologie Pédiatrique, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorMarlène Rio, Marlène Rio Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorGeneviève Baujat, Geneviève Baujat Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorVicken Topouchian, Vicken Topouchian Service de Chirurgie Orthopédique Pédiatrique, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorNadine Hanna, Nadine Hanna Université Versailles-SQY, Service de Biochimie et Génétique Moléculaire (AP-HP), Hôpital Ambroise Paré, Boulogne-Billancourt, FranceSearch for more papers by this authorMartine Le Merrer, Martine Le Merrer Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorFrancis Brunelle, Francis Brunelle Service de Radiologie Pédiatrique, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorArnold Munnich, Arnold Munnich Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, FranceSearch for more papers by this authorCatherine Boileau, Catherine Boileau Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, France Université Versailles-SQY, Service de Biochimie et Génétique Moléculaire (AP-HP), Hôpital Ambroise Paré, Boulogne-Billancourt, FranceSearch for more papers by this authorValérie Cormier-Daire, Corresponding Author Valérie Cormier-Daire cormier-daire@inserm.fr Department of Medical Genetics (AP-HP), Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, FranceDépartement de Génétique, Université Paris Descartes, INSERM U781, Hôpital Necker-Enfants Malades, Paris, France.Search for more papers by this author First published: 11 April 2011 https://doi.org/10.1002/ajmg.a.33813Citations: 15 † How to Cite this Article: Sousa SB, Lambot-Juhan K, Rio M, Baujat G, Topouchian V, Le Merrer M, Brunelle F, Munnich A, Boileau C, Cormier-Daire V. 2011. Expanding the skeletal phenotype of Loeys-Dietz syndrome. Am J Med Genet Part A 155:1178–1183. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume155, Issue5May 2011Pages 1178-1183 RelatedInformation" @default.
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