Associated Papers
Combined 17α-hydroxylase/17,20-lyase deficiency with short stature: case study.
Ma L et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology, 2016
A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17{alpha}-hydroxylase deficiency.
Qiao J et al.
European Journal of Endocrinology, 2011
Phenotype-genotype correlation in eight Chinese 17alpha-hydroxylase/17,20 lyase-deficiency patients with five novel mutations of CYP17A1 gene.
Yang J et al.
The Journal of Clinical Endocrinology and Metabolism, 2006
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