ℹ️
🇬🇧
Search
Search for people relevant for "21-hydroxylase deficiency"
21-hydroxylase deficiency
Person
Class
Person
Publication
Programmes
S. M. Baumgartner-Parzer
Person without affiliation with CUNI
1 publication
Publication
publication
Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia
2005 |
Third Faculty of Medicine
Loading network view...
