Concolino, Paola, Enrica Mello, Cecilia Zuppi, et al. "Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations" Clinical Chemistry and Laboratory Medicine, 48.8 (2010): 1057-1062. Retrieved 19 Jun. 2013, from doi:10.1515/cclm.2010.239

Concolino, P., Mello, E., Zuppi, C., et al. (2010). Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations. Clinical Chemistry and Laboratory Medicine, 48(8), pp. 1053-A77. Retrieved 19 Jun. 2013, from doi:10.1515/cclm.2010.239

Concolino, Paola, Enrica Mello, Cecilia Zuppi, et al. 2010. Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations. Clinical Chemistry and Laboratory Medicine. 48(8): 1053-A77. Retrieved 19 Jun. 2013, from doi:10.1515/cclm.2010.239