Zain, F. M., Isa, M. N., & Awang, R. A. (2000). Molecular detection of genetic defects in ambiguous genitalia (AG) and congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency.
Chicago Style (17th ed.) CitationZain, Fuziah Md, Mohd Nizam Isa, and Rus Anida Awang. Molecular Detection of Genetic Defects in Ambiguous Genitalia (AG) and Congenital Adrenal Hyperplasia (CAH) Due to 21-hydroxylase Deficiency. 2000.
MLA (9th ed.) CitationZain, Fuziah Md, et al. Molecular Detection of Genetic Defects in Ambiguous Genitalia (AG) and Congenital Adrenal Hyperplasia (CAH) Due to 21-hydroxylase Deficiency. 2000.
Warning: These citations may not always be 100% accurate.