A novel HSD17B3 gene mutation in a 46,XY female-phenotype newborn identified by whole-exome sequencing. [electronic resource]

By: Contributor(s): Producer: 20190617Description: 407-408 p. digitalISSN:
  • 1365-2265
Subject(s): Online resources: In: Clinical endocrinology vol. 87
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Publication Type: Case Reports; Letter

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