Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleIdentification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome.AuthorsHarbuz, Radu; Lespinasse, James; Boulet, Stéphanie; Francannet, Christine; Creveaux, Isabelle; Benkhelifa, Mariem; Jouk, Pierre-Simon; Lunardi, Joël; Ray, Pierre F.PublicationPrenatal Diagnosis, 2010, Vol 30, Issue 11, p1072ISSN0197-3851Publication typeArticleDOI10.1002/pd.2613