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Elsevier, Journal of Clinical and Translational Endocrinology Case Reports, (7), p. 5-7, 2018

DOI: 10.1016/j.jecr.2017.10.002

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

Journal article published in 2018 by Catherine A. Sullivan, Jodi D. Hoffman, Joshua D. Safer
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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