Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia
KK Dumic, Z Grubic, T Yuen, RC Wilson… - The Journal of Steroid …, 2017 - Elsevier
Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency is caused by mutation in
the CYP21A2 gene. The frequency and spectrum of CYP21A2 mutations and genotype …
the CYP21A2 gene. The frequency and spectrum of CYP21A2 mutations and genotype …
Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia.
KK Dumic, Z Grubic, T Yuen, RC Wilson… - The Journal of Steroid …, 2016 - europepmc.org
Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency is caused by mutation in
the CYP21A2 gene. The frequency and spectrum of CYP21A2 mutations and genotype …
the CYP21A2 gene. The frequency and spectrum of CYP21A2 mutations and genotype …
Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia
KK Dumic, Z Grubic, T Yuen, RC Wilson… - The Journal of Steroid …, 2017 - infona.pl
Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency is caused by mutation in
the CYP21A2 gene. The frequency and spectrum of CYP21A2 mutations and genotype …
the CYP21A2 gene. The frequency and spectrum of CYP21A2 mutations and genotype …
Molecular genetic analysis in 93 patients and 193 family members with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Croatia
KK Dumic, Z Grubic, T Yuen… - The Journal of …, 2017 - pubmed.ncbi.nlm.nih.gov
Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency is caused by mutation in
the CYP21A2 gene. The frequency and spectrum of CYP21A2 mutations and genotype …
the CYP21A2 gene. The frequency and spectrum of CYP21A2 mutations and genotype …