Assessing the risk of having a child with classic 21-hydroxylase deficiency: a new paradigm
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference42 articles.
1. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline;Speiser;J. Clin. Endocrinol. Metab.,2018
2. Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women;Carmina;Hum. Reprod. Update,2017
3. Congenital adrenal hyperplasia;El-Maouche;Lancet,2017
4. 21-Hydroxylase deficiancy-induced congenital adrenal hyperplasia in 230 Chinese patients: genotype-phenotype correlation and identification of nine novel mutations;Wang;Steroids,2016
5. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline;Speiser;J. Clin. Endocrinol. Metab.,2010
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Genetics of 21‐hydroxylase deficiency: Clinical presentation should guide the investigation;American Journal of Medical Genetics Part A;2023-12-20
2. Nonclassic Adrenal Hyperplasia (NCAH) due to 21-hydroxylase deficiency: A cohort of 78 patients;The Journal of Steroid Biochemistry and Molecular Biology;2023-01
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