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This page is a summary of: 46,XY Disorder of Sex Development Caused by 17α-Hydroxylase/17,20-Lyase Deficiency due to Homozygous Mutation ofCYP17A1Gene: Consequences of Late Diagnosis, Case Reports in Endocrinology, January 2018, Hindawi Publishing Corporation,
DOI: 10.1155/2018/2086861.
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