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Case Reports
. 2017 Oct;87(4):407-408.
doi: 10.1111/cen.13396. Epub 2017 Jul 24.

A novel HSD17B3 gene mutation in a 46,XY female-phenotype newborn identified by whole-exome sequencing

Rita Bertalan  1 , Osnat Admoni  2 , Anu Bashamboo  1 , Yardena Tenenbaum-Rakover  2   3 , Kenneth McElreavey  1
Affiliations
Case Reports

A novel HSD17B3 gene mutation in a 46,XY female-phenotype newborn identified by whole-exome sequencing

Rita Bertalan et al. Clin Endocrinol (Oxf). 2017 Oct.
No abstract available

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