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Reversion SAMD9 Mutations Modifying Phenotypic Expression of MIRAGE Syndrome and Allowing Inheritance in a Usually de novo Disorder by Florence Roucher-Boulez, Florence Roucher-Boulez, Florence Roucher-Boulez, Florence Roucher-Boulez, Delphine Mallet, Delphine Mallet, Nicolas Chatron, Nicolas Chatron, Nicolas Chatron, Frédérique Dijoud, Daniela Brindusa Gorduza, Daniela Brindusa Gorduza, Patricia Bretones, Patricia Bretones, Yves Morel, Yves Morel, Yves Morel
Published 2019-09-01
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Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in France by Estelle Bonnet, Mathias Winter, Delphine Mallet, Ingrid Plotton, Claire Bouvattier, Maryse Cartigny, Laetiti Martinerie, Michel Polak, Anne Bachelot, Frédéric Huet, Sabine Baron, Muriel Houang, Sylvie Soskin, Anne Lienhardt, Jérôme Bertherat, Cyril Amouroux, Aurore Bouty, Lise Duranteau, Rémi Besson, Alaa El Ghoneimi, Dinane Samara-Boustani, François Becmeur, Nicolas Kalfa, Françoise Paris, François Medjkane, Aude Brac de la Perrière, Patricia Bretones, Hervé Lejeune, Marc Nicolino, Pierre Mouriquand, Daniela-Brindusa Gorduza, Claire-Lise Gay
Published 2023-02-01
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