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Reference20 articles.
1. 1. Huynh T, McGown I, Cowley D, Nyunt O, Leong GM, et al. The clinical and biochemical spectrum of congenital adrenal hyperplasia secondary to 21- hydroxylase deficiency. Clin Biochem Rev 2009; 30: 75-86. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/19565027
2. 2. Khalid JM, Oerton JM, Dezateux C, Hindmarsh PC, Kelnar CJ, et al. Incidence and clinical features of congenital adrenal hyperplasia in Great Britain. Arch Dis Child. 2012; 97: 101-106. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/22241917
3. 3. Kanaka GC, Chrousos GP, Dacou VC. The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the CYP21A2 gene. Clin Endocrinol (Oxf). 2015; 82: 543-549. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/25041270
4. 4. Avilal NA, Premkumar A, Merke DP. TesticularAdrenal RestTissue in Congenital Adrenal Hyperplasia: Comparison of MR Imaging and Sonographic Findings. AJR. 1999; 172: 1003-1006. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/10587136
5. 5. White PC, Speiser PW. Congenital Adrenal Hyperplasia due to21-Hydroxylase Deficiency. Endocrine Reviews. 2000; 21: 245-291. PubMed: https://www.ncbi.nlm.nih.gov/pubmed/28450075
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