Idkowiak, J., Randell, T., Dhir, V., Patel, P., Shackleton, C. H. L., Taylor, N. F., . . . Arlt, W. (2012). A Missense Mutation in the Human Cytochrome b5 Gene causes 46,XY Disorder of Sex Development due to True Isolated 17,20 Lyase Deficiency. Endocrine Society.

Idkowiak, Jan, Tabitha Randell, Vivek Dhir, Pushpa Patel, Cedric H. L. Shackleton, Norman F. Taylor, Nils Krone, and Wiebke Arlt. A Missense Mutation in the Human Cytochrome B5 Gene Causes 46,XY Disorder of Sex Development Due to True Isolated 17,20 Lyase Deficiency. Endocrine Society, 2012.

Idkowiak, Jan, et al. A Missense Mutation in the Human Cytochrome B5 Gene Causes 46,XY Disorder of Sex Development Due to True Isolated 17,20 Lyase Deficiency. Endocrine Society, 2012.