Associated Papers
Ethnic disparity in 21-hydroxylase gene mutations identified in Pakistani congenital adrenal hyperplasia patients.
Khan AH et al.
Bmc Endocrine Disorders, 2011
Molecular characterization of mutations in Indian children with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
Mathur R et al.
Journal of Pediatric Endocrinology & Metabolism : Jpem, 2001
Select a paper to view details