MANAGEMENT OF ENDOCRINE DISEASE: Gonadal dysfunction in congenital adrenal hyperplasia From Decades of Pioneering Research to Pi
![PDF] CYP21 gene mutation analysis in 198 patients with 21-hydroxylase deficiency in The Netherlands: six novel mutations and a specific cluster of four mutations. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/384f7e497007b610cf23ee55e89190c3c54bbacd/5-Table2-1.png "PDF] CYP21 gene mutation analysis in 198 patients with 21-hydroxylase deficiency in The Netherlands: six novel mutations and a specific cluster of four mutations. | Semantic Scholar")
PDF] CYP21 gene mutation analysis in 198 patients with 21-hydroxylase deficiency in The Netherlands: six novel mutations and a specific cluster of four mutations. | Semantic Scholar
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![PDF] CYP21 gene mutation analysis in 198 patients with 21-hydroxylase deficiency in The Netherlands: six novel mutations and a specific cluster of four mutations. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/384f7e497007b610cf23ee55e89190c3c54bbacd/4-Figure1-1.png "PDF] CYP21 gene mutation analysis in 198 patients with 21-hydroxylase deficiency in The Netherlands: six novel mutations and a specific cluster of four mutations. | Semantic Scholar")
PDF] CYP21 gene mutation analysis in 198 patients with 21-hydroxylase deficiency in The Netherlands: six novel mutations and a specific cluster of four mutations. | Semantic Scholar
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MANAGEMENT OF ENDOCRINE DISEASE: Gonadal dysfunction in congenital adrenal hyperplasia in: European Journal of Endocrinology Volume 184 Issue 3 (2021)
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