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• W2068268210 abstract "American Journal of Medical Genetics Part AVolume 149A, Issue 12 p. 2865-2866 Research Letter Vertebral defects as an unusual mode of presentation of 22q11.2 deletion† L. Faivre, Corresponding Author L. Faivre laurence.faivre@chu-dijon.fr Centre de Référence Maladies Rares “Anomalies du Développement et Syndromes Malformatifs”, Hôpital d'Enfants, CHU Dijon, FranceCentre de Génétique, Hôpital d'Enfants, 10 bd Maréchal de Lattre de Tassigny, 21034 Dijon Cedex, France.Search for more papers by this authorA. Masurel-Paulet, A. Masurel-Paulet Centre de Référence Maladies Rares “Anomalies du Développement et Syndromes Malformatifs”, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this authorP. Callier, P. Callier Cytogénétique, Plateau Technique de Biologie, CHU Dijon, FranceSearch for more papers by this authorN. Mejean, N. Mejean Radiologie Pédiatrique, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this authorS. Gay, S. Gay Service de Pédiatrie, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this authorM. Grimaldi, M. Grimaldi Service de Pédiatrie, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this authorF. Mugneret, F. Mugneret Cytogénétique, Plateau Technique de Biologie, CHU Dijon, FranceSearch for more papers by this authorF. Huet, F. Huet Service de Pédiatrie, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this authorC. Thauvin-Robinet, C. Thauvin-Robinet Centre de Référence Maladies Rares “Anomalies du Développement et Syndromes Malformatifs”, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this author L. Faivre, Corresponding Author L. Faivre laurence.faivre@chu-dijon.fr Centre de Référence Maladies Rares “Anomalies du Développement et Syndromes Malformatifs”, Hôpital d'Enfants, CHU Dijon, FranceCentre de Génétique, Hôpital d'Enfants, 10 bd Maréchal de Lattre de Tassigny, 21034 Dijon Cedex, France.Search for more papers by this authorA. Masurel-Paulet, A. Masurel-Paulet Centre de Référence Maladies Rares “Anomalies du Développement et Syndromes Malformatifs”, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this authorP. Callier, P. Callier Cytogénétique, Plateau Technique de Biologie, CHU Dijon, FranceSearch for more papers by this authorN. Mejean, N. Mejean Radiologie Pédiatrique, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this authorS. Gay, S. Gay Service de Pédiatrie, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this authorM. Grimaldi, M. Grimaldi Service de Pédiatrie, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this authorF. Mugneret, F. Mugneret Cytogénétique, Plateau Technique de Biologie, CHU Dijon, FranceSearch for more papers by this authorF. Huet, F. Huet Service de Pédiatrie, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this authorC. Thauvin-Robinet, C. Thauvin-Robinet Centre de Référence Maladies Rares “Anomalies du Développement et Syndromes Malformatifs”, Hôpital d'Enfants, CHU Dijon, FranceSearch for more papers by this author First published: 16 November 2009 https://doi.org/10.1002/ajmg.a.32974 † How to Cite this Article: Faivre L, Masurel-Paulet A, Callier P, Mejean N, Gay S, Grimaldi M, Mugneret F, Huet F, Thauvin-Robinet C. 2009. Vertebral defects as an unusual mode of presentation of 22q11.2 deletion. Am J Med Genet Part A 149A:2865–2866. 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 No abstract is available for this article. Volume149A, Issue12December 2009Pages 2865-2866 RelatedInformation" @default.
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