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This page is a summary of: An Unusual Phenotype of Frasier Syndrome due to IVS9 +4C>T Mutation in the WT1 Gene: Predominantly Male Ambiguous Genitalia and Absence of Gonadal Dysgenesis, The Journal of Clinical Endocrinology & Metabolism, June 2002, Endocrine Society,
DOI: 10.1210/jcem.87.6.8521.
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