Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleAn Unusual Phenotype of Frasier Syndrome due to IVS9 +4C>T Mutation in the WT1 Gene: Predominantly Male Ambiguous Genitalia and Absence of Gonadal Dysgenesis.AuthorsMELO, KARLA F. S.; MARTIN, REGINA M.; COSTA, ELAINE M. F.; CARVALHO, FILOMENA M.; JORGE, ALEXANDER A.; ARNHOLD, IVO J. P.; MENDONCA, BERENICE B.PublicationJournal of Clinical Endocrinology & Metabolism, 2002, Vol 87, Issue 6, p2500ISSN0021-972XPublication typeArticleDOI10.1210/jcem.87.6.8521