𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations

✍ Scribed by Concolino, Paola; Mello, Enrica; Zuppi, Cecilia; Capoluongo, Ettore


Book ID
118750787
Publisher
Walter de Gruyter GmbH & Co. KG
Year
2010
Tongue
English
Weight
136 KB
Volume
48
Category
Article
ISSN
1434-6621

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES