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1. The spectrum of CYP21A2 gene mutations in patients with classic salt wasting form of 2l‐hydroxylase deficiency in a Chinese cohort. Issue 11 (21st September 2020)

2. The spectrum of CYP21A2 gene mutations in patients with classic salt wasting form of 2l‐hydroxylase deficiency in a Chinese cohort. Issue 11 (21st September 2020)

3. High prevalence of elevated serum liver enzymes in Chinese children suggests metabolic syndrome as a common risk factor. (7th August 2020)