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• W2063835265 abstract "Prenatal DiagnosisVolume 27, Issue 11 p. 1062-1063 Research Letter Prenatal detection of Pierre Robin sequence with deletion Xp and additional trisomy 14q by telomere screening M. Gerard-Blanluet, Corresponding Author M. Gerard-Blanluet [email protected] Clinical genetics, AP-HP, Hôpital Robert Debré, Paris, FranceGénétique Médicale, Hôpital Robert Debré, 48 Boulevard Serrurier, 75019 Paris, France.Search for more papers by this authorE. Pipiras, E. Pipiras Cytogenetics, AP-HP, Hôpital Jean Verdier, Bondy, FranceSearch for more papers by this authorJ. M. Levaillant, J. M. Levaillant Ultrasonography, Hôpital Antoine Béclère, Clamart, FranceSearch for more papers by this authorN. Joye, N. Joye Cytogenetics, AP-HP, Hôpital Saint Antoine, Paris, FranceSearch for more papers by this authorV. Koubi, V. Koubi Cytogenetics, Pasteur-CERBA laboratory, Pontoise, FranceSearch for more papers by this authorS. Kanafani, S. Kanafani Cytogenetics, AP-HP, Hôpital Jean Verdier, Bondy, FranceSearch for more papers by this authorA. Vergnaud, A. Vergnaud Ultrasonography, Centre Hospitalier Intercommunal de Créteil, Créteil, FranceSearch for more papers by this authorA. Verloes, A. Verloes Clinical genetics, AP-HP, Hôpital Robert Debré, Paris, FranceSearch for more papers by this authorM. Gonzales, M. Gonzales Fetopathology, AP-HP, Hôpital Trousseau, Paris, FranceSearch for more papers by this authorR. Jeny, R. Jeny Obstetrics, Hôpital Esquirol, Saint Maurice, FranceSearch for more papers by this authorB. Benzacken, B. Benzacken Cytogenetics, AP-HP, Hôpital Jean Verdier, Bondy, FranceSearch for more papers by this author M. Gerard-Blanluet, Corresponding Author M. Gerard-Blanluet [email protected] Clinical genetics, AP-HP, Hôpital Robert Debré, Paris, FranceGénétique Médicale, Hôpital Robert Debré, 48 Boulevard Serrurier, 75019 Paris, France.Search for more papers by this authorE. Pipiras, E. Pipiras Cytogenetics, AP-HP, Hôpital Jean Verdier, Bondy, FranceSearch for more papers by this authorJ. M. Levaillant, J. M. Levaillant Ultrasonography, Hôpital Antoine Béclère, Clamart, FranceSearch for more papers by this authorN. Joye, N. Joye Cytogenetics, AP-HP, Hôpital Saint Antoine, Paris, FranceSearch for more papers by this authorV. Koubi, V. Koubi Cytogenetics, Pasteur-CERBA laboratory, Pontoise, FranceSearch for more papers by this authorS. Kanafani, S. Kanafani Cytogenetics, AP-HP, Hôpital Jean Verdier, Bondy, FranceSearch for more papers by this authorA. Vergnaud, A. Vergnaud Ultrasonography, Centre Hospitalier Intercommunal de Créteil, Créteil, FranceSearch for more papers by this authorA. Verloes, A. Verloes Clinical genetics, AP-HP, Hôpital Robert Debré, Paris, FranceSearch for more papers by this authorM. Gonzales, M. Gonzales Fetopathology, AP-HP, Hôpital Trousseau, Paris, FranceSearch for more papers by this authorR. Jeny, R. Jeny Obstetrics, Hôpital Esquirol, Saint Maurice, FranceSearch for more papers by this authorB. Benzacken, B. Benzacken Cytogenetics, AP-HP, Hôpital Jean Verdier, Bondy, FranceSearch for more papers by this author First published: 17 August 2007 https://doi.org/10.1002/pd.1818Citations: 2AboutPDF 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 No abstract is available for this article.Citing Literature Volume27, Issue11November 2007Pages 1062-1063 RelatedInformation" @default.
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• W2063835265 title "Prenatal detection of Pierre Robin sequence with deletion Xp and additional trisomy 14q by telomere screening" @default.
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