- Mutation detection in the CYP21B gene determining virilized and non-classical forms of steroid 21-hydroxylase deficiency2000 | Second Faculty of Medicine, Central Library of Charles University
- Frequency of CYP21 gene mutations in Czech patients with steroid 21-hydroxylase deficiency and statistical comparison with other populations2003 | Second Faculty of Medicine
- Rapid and Efficient Method for Detection of A/C 655G Mutation in Patients with Congenital Steroid 21-hydroxylase Deficiency1996 | Second Faculty of Medicine, Central Library of Charles University
- Genetic analysis of the CYP21A2 gene in neonatal dried blood spots from children with transiently elevated 17-hydroxyprogesterone2012 | Second Faculty of Medicine, Third Faculty of Medicine