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High carrier frequency of 21-hydroxylase deficiency in Cyprus.
Phedonos AA, Shammas C, Skordis N, Kyriakides TC, Neocleous V, Phylactou LA. Phedonos AA, et al. Among authors: shammas c. Clin Genet. 2013 Dec;84(6):585-8. doi: 10.1111/cge.12153. Epub 2013 Apr 22. Clin Genet. 2013. PMID: 23600966
Genetic defects of the CYP21A2 gene in girls with premature adrenarche.
Skordis N, Shammas C, Phedonos AA, Kyriakou A, Toumba M, Neocleous V, Phylactou LA. Skordis N, et al. Among authors: shammas c. J Endocrinol Invest. 2015 May;38(5):535-9. doi: 10.1007/s40618-014-0223-1. Epub 2014 Dec 7. J Endocrinol Invest. 2015. PMID: 25481255
43 results