Risultati della ricerca - Gaston, Véronique

In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene di Gicquel, Christine, Gaston, Véronique, Mandelbaum, Jacqueline, Siffroi, Jean-Pierre, Flahault, Antoine, Le Bouc, Yves

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Identification of Mutations in SDR9C7 in Three Patients with Autosomal Recessive Congenital Ichthyosis di MAZEREEUW-HAUTIER, Juliette, SEVERINO-FREIRE, Maella, GASTON, Véronique, TEXIER, Hélène, VINCENT, Marie, AUBERT, Hélène, MORICE-PICARD, Fanny, JONCA, Nathalie

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Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome di Bieth, Eric, Eddiry, Sanaa, Gaston, Véronique, Lorenzini, Françoise, Buffet, Alexandre, Conte Auriol, Françoise, Molinas, Catherine, Cailley, Dorothée, Rooryck, Caroline, Arveiler, Benoit, Cavaillé, Jérome, Salles, Jean Pierre, Tauber, Maïthé

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Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens di Patat, Olivier, Pagin, Adrien, Siegfried, Aurore, Mitchell, Valérie, Chassaing, Nicolas, Faguer, Stanislas, Monteil, Laetitia, Gaston, Véronique, Bujan, Louis, Courtade-Saïdi, Monique, Marcelli, François, Lalau, Guy, Rigot, Jean-Marc, Mieusset, Roger, Bieth, Eric

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Confirmation of FZD5 implication in a cohort of 50 patients with ocular coloboma di Aubert-Mucca, Marion, Pernin-Grandjean, Julie, Marchasson, Sébastien, Gaston, Veronique, Habib, Christophe, Meunier, Isabelle, Sigaudy, Sabine, Kaplan, Josseline, Roche, Olivier, Denis, Danièle, Bitoun, Pierre, Haye, Damien, Verloes, Alain, Calvas, Patrick, Chassaing, Nicolas, Plaisancié, Julie

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