Fingerprint
Dive into the research topics of 'Clinical, endocrine, and molecular genetic findings in patients with 17β-hydroxysteroid dehydrogenase deficiency'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Clinical, endocrine, and molecular genetic findings in patients with 17β-hydroxysteroid dehydrogenase deficiency
Wiebke Twesten, Paul Martin Holterhus, Wolfgang G. Sippell, Michel Morlot, Heinz Schumacher, Bernd Schenk, Olaf Hiort*
*Corresponding author for this work
34
Citations
(Scopus)