An unusual phenotype of fraiser syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis - Melo, Karla F. S.; Martin, Regina M.; Costa, Elaine M. F.; Carvalho, Filomena; Jorge, Alexander A.; Arnhold, Ivo J. P.; Mendonça, Berenice B. (The Journal of Clinical Endocrinology & Metabolism, 2002)