Bhangoo,, A., Aisenberg,, J., Chartoff,, Α., Ten,, S., Wallerstein,, R.J., Wolf,, R. and Auchus,, R.J.. "Novel Mutation in Cytochrome P450c17 Causes Complete Combined 17α-Hydroxylase/17,20-Lyase Deficiency"
Journal of Pediatric Endocrinology and Metabolism, vol. 21, no. 2, 2008, pp. 185-190.
https://doi.org/10.1515/JPEM.2008.21.2.185Bhangoo,, A., Aisenberg,, J., Chartoff,, Α., Ten,, S., Wallerstein,, R., Wolf,, R. & Auchus,, R. (2008). Novel Mutation in Cytochrome P450c17 Causes Complete Combined 17α-Hydroxylase/17,20-Lyase Deficiency.
Journal of Pediatric Endocrinology and Metabolism,
21(2), 185-190.
https://doi.org/10.1515/JPEM.2008.21.2.185Bhangoo,, A., Aisenberg,, J., Chartoff,, Α., Ten,, S., Wallerstein,, R., Wolf,, R. and Auchus,, R. (2008) Novel Mutation in Cytochrome P450c17 Causes Complete Combined 17α-Hydroxylase/17,20-Lyase Deficiency. Journal of Pediatric Endocrinology and Metabolism, Vol. 21 (Issue 2), pp. 185-190.
https://doi.org/10.1515/JPEM.2008.21.2.185Bhangoo,, A., Aisenberg,, J., Chartoff,, Α., Ten,, S., Wallerstein,, R.J., Wolf,, R. and Auchus,, R.J.. "Novel Mutation in Cytochrome P450c17 Causes Complete Combined 17α-Hydroxylase/17,20-Lyase Deficiency"
Journal of Pediatric Endocrinology and Metabolism 21, no. 2 (2008): 185-190.
https://doi.org/10.1515/JPEM.2008.21.2.185Bhangoo, A, Aisenberg, J, Chartoff, Α, Ten, S, Wallerstein, R, Wolf, R, Auchus, R. Novel Mutation in Cytochrome P450c17 Causes Complete Combined 17α-Hydroxylase/17,20-Lyase Deficiency.
Journal of Pediatric Endocrinology and Metabolism. 2008;21(2): 185-190.
https://doi.org/10.1515/JPEM.2008.21.2.185Copied to clipboard
