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17-β-hydroxysteroid dehydrogenase type 3 deficiency: Identifying a rare cause of 46, XY female phenotype in adulthood

17-β-hydroxysteroid dehydrogenase type 3 deficiency: Identifying a rare cause of 46, XY female phenotype in adulthood

Sullivan, Catherine A.; Hoffman, Jodi D.; Safer, Joshua D.

期刊名称Journal of Clinical and Translational Endocrinology: Case Reports
作者Sullivan, Catherine A.; Hoffman, Jodi D.; Safer, Joshua D.
卷第7卷
印刷ISSN2214-6245
文件大小118.77KB
发表时间2018-03
DOI10.1016/j.jecr.2017.10.002
页码5-7

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