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	1.	PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. [electronic resource] by Jacquet, Hélène Raux, Grégory Thibaut, Florence Hecketsweiler, Bernadette Houy, Emmanuelle Demilly, Caroline Haouzir, Sadeq Allio, Gabrielle Fouldrin, Gael Drouin, Valérie Bou, Jacqueline Petit, Michel Campion, Dominique Frébourg, Thierry Producer: 20030414 In: Human molecular genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Sensorineural hearing loss in OPA1-linked disorders. [electronic resource] by Leruez, Stéphanie Milea, Dan Defoort-Dhellemmes, Sabine Colin, Estelle Crochet, Martine Procaccio, Vincent Ferré, Marc Lamblin, Julie Drouin, Valérie Vincent-Delorme, Catherine Lenaers, Guy Hamel, Christian Blanchet, Catherine Juul, Gitte Larsen, Michael Verny, Christophe Reynier, Pascal Amati-Bonneau, Patrizia Bonneau, Dominique Producer: 20130829 In: Brain : a journal of neurology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans. [electronic resource] by de Pontual, Loïc Yao, Evelyn Callier, Patrick Faivre, Laurence Drouin, Valérie Cariou, Sandra Van Haeringen, Arie Geneviève, David Goldenberg, Alice Oufadem, Myriam Manouvrier, Sylvie Munnich, Arnold Vidigal, Joana Alves Vekemans, Michel Lyonnet, Stanislas Henrion-Caude, Alexandra Ventura, Andrea Amiel, Jeanne Producer: 20111121 In: Nature genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)