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26. Non-classic congenital adrenal hyperplasia due to 21-hydoxylase deficiency as a cause of infertility and miscarriages. Falhammar H N Z Med J; 2010 Apr; 123(1312):77-80. PubMed ID: 20389322 [TBL] [Abstract][Full Text] [Related]
28. Erroneous prenatal diagnosis of congenital adrenal hyperplasia owing to a duplication of the CYP21A2 gene. Lekarev O; Tafuri K; Lane AH; Zhu G; Nakamoto JM; Buller-Burckle AM; Wilson TA; New MI J Perinatol; 2013 Jan; 33(1):76-8. PubMed ID: 23269230 [TBL] [Abstract][Full Text] [Related]
29. Genetics of congenital adrenal hyperplasia. New MI Prog Clin Biol Res; 1985; 200():233-41. PubMed ID: 3878527 [No Abstract] [Full Text] [Related]
30. Acne and non-classic congenital adrenal hyperplasia. Falhammar H N Z Med J; 2008 Jun; 121(1275):94-5. PubMed ID: 18551162 [No Abstract] [Full Text] [Related]
31. Steroid 21 hydroxylase deficiency congenital adrenal hyperplasia. Nimkarn S; Lin-Su K; New MI Endocrinol Metab Clin North Am; 2009 Dec; 38(4):699-718. PubMed ID: 19944288 [TBL] [Abstract][Full Text] [Related]
36. [Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype]. Dumić M; Brkljacić L; Krzisnik C; Radica A; Tajić M; Kastelan A Lijec Vjesn; 1983; 105(7-8):290-2. PubMed ID: 6605467 [No Abstract] [Full Text] [Related]
37. Over 50 years of progress in the treatment of the hypertensive form of congenital adrenal hyperplasia due to steroid 11-beta-hydroxylase deficiency. Commentary on Simm PJ and Zacharin MR: Successful pregnancy in a patient with severe 11-beta-hydroxylase deficiency and novel mutations in CYP11B1 gene (Horm Res 2007;68:294-297). Migeon CJ Horm Res; 2007; 68(6):298-9. PubMed ID: 17726334 [No Abstract] [Full Text] [Related]
38. [Congenital adrenal hyperplasia due to 21-hydroxylase deficiency]. Fujieda K; Mukai T Nihon Rinsho; 2004 Feb; 62(2):361-7. PubMed ID: 14968546 [TBL] [Abstract][Full Text] [Related]
39. Detection and management of late-onset 21-hydroxylase deficiency in women with hyperandrogenism. Young J; Tardy V; de la Perrière AB; Bachelot A; Morel Y; Ann Endocrinol (Paris); 2010 Feb; 71(1):14-8. PubMed ID: 20070950 [TBL] [Abstract][Full Text] [Related]
40. First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy. Concolino P; Corsello S; Carrozza C; Minucci A; Santonocito C; Lovicu RM; Santini SA; Ameglio F; Zuppi C; Capoluongo E Clin Biochem; 2007 Dec; 40(18):1435-6. PubMed ID: 18028896 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]