@article{article6b134692,
title   = {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},
author = {Melo, Karla F. S. and Martin, Regina M. and Costa, Elaine M. F. and Carvalho, Filomena and Jorge, Alexander A. and Arnhold, Ivo J. P. and Mendonça, Berenice B.},
year = {2002},
journal   = {The Journal of Clinical Endocrinology & Metabolism}
}