- Substituce v promotoru CYP21 genu ovlivňují fenotyp nemoci u pacientů s deficitem 21-hydroxylázy2009 | 3. lékařská fakulta
- Frequency of CYP21 gene mutations in Czech patients with steroid 21-hydroxylase deficiency and statistical comparison with other populations2003 | 2. lékařská fakulta
- Common CYP21 gene mutations in Czech patients and statistical analysis of worldwide mutation distribution2003 | 2. lékařská fakulta, Ústřední knihovna
- Molecular genetic analysis of steroid 21-hydroxylase gene2004 | 2. lékařská fakulta
- Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia2005 | 3. lékařská fakulta
- Lessons learned from 5 years of newborn screening for congenital adrenal hyperplasia in the Czech Republic: 17-hydroxyprogesterone, genotypes, and screening performance2012 | 2. lékařská fakulta, 3. lékařská fakulta, Lékařská fakulta v Hradci Králové
- Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia2005 | 2. lékařská fakulta, 3. lékařská fakulta