Schwab,, Karl Otfried, Moisan,, Anne-Marie, Homoki,, Janos, Peter,, Michael and Simard,, Jacques. "17α-Hydroxylase/17,20-Lyase Deficiency Due to Novel Compound Heterozygote Mutations: Treatment for Tall Stature in a Female with Male Pseudohermaphroditism and Spontaneous Puberty in her Affected Sister"
Journal of Pediatric Endocrinology and Metabolism, vol. 18, no. 4, 2005, pp. 403-412.
https://doi.org/10.1515/JPEM.2005.18.4.403Schwab,, K., Moisan,, A., Homoki,, J., Peter,, M. & Simard,, J. (2005). 17α-Hydroxylase/17,20-Lyase Deficiency Due to Novel Compound Heterozygote Mutations: Treatment for Tall Stature in a Female with Male Pseudohermaphroditism and Spontaneous Puberty in her Affected Sister.
Journal of Pediatric Endocrinology and Metabolism,
18(4), 403-412.
https://doi.org/10.1515/JPEM.2005.18.4.403Schwab,, K., Moisan,, A., Homoki,, J., Peter,, M. and Simard,, J. (2005) 17α-Hydroxylase/17,20-Lyase Deficiency Due to Novel Compound Heterozygote Mutations: Treatment for Tall Stature in a Female with Male Pseudohermaphroditism and Spontaneous Puberty in her Affected Sister. Journal of Pediatric Endocrinology and Metabolism, Vol. 18 (Issue 4), pp. 403-412.
https://doi.org/10.1515/JPEM.2005.18.4.403Schwab,, Karl Otfried, Moisan,, Anne-Marie, Homoki,, Janos, Peter,, Michael and Simard,, Jacques. "17α-Hydroxylase/17,20-Lyase Deficiency Due to Novel Compound Heterozygote Mutations: Treatment for Tall Stature in a Female with Male Pseudohermaphroditism and Spontaneous Puberty in her Affected Sister"
Journal of Pediatric Endocrinology and Metabolism 18, no. 4 (2005): 403-412.
https://doi.org/10.1515/JPEM.2005.18.4.403Schwab, K, Moisan, A, Homoki, J, Peter, M, Simard, J. 17α-Hydroxylase/17,20-Lyase Deficiency Due to Novel Compound Heterozygote Mutations: Treatment for Tall Stature in a Female with Male Pseudohermaphroditism and Spontaneous Puberty in her Affected Sister.
Journal of Pediatric Endocrinology and Metabolism. 2005;18(4): 403-412.
https://doi.org/10.1515/JPEM.2005.18.4.403Copied to clipboard
