👤 Osnat Admoni

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Articles

articles

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

Rita Bertalan, Osnat Admoni, Anu Bashamboo +2 more · 2017 · Clinical endocrinology · Blackwell Publishing · added 2026-04-24

Rita Bertalan, Osnat Admoni, Anu Bashamboo, Yardena Tenenbaum-Rakover, Kenneth McElreavey Show less

no PDF DOI: 10.1111/cen.13396

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