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2. Genotyping of CYP21, linked chromosome 6p markers, and a sex-specific gene in neonatal screening for congenital adrenal hyperplasia. Fitness J; Dixit N; Webster D; Torresani T; Pergolizzi R; Speiser PW; Day DJ J Clin Endocrinol Metab; 1999 Mar; 84(3):960-6. PubMed ID: 10084579 [TBL] [Abstract][Full Text] [Related]
3. Molecular analysis of the CYP21 gene and prenatal diagnosis in families with 21-hydroxylase deficiency in northeastern Iran. Vakili R; Baradaran-Heravi A; Barid-Fatehi B; Gholamin M; Ghaemi N; Abbaszadegan MR Horm Res; 2005; 63(3):119-24. PubMed ID: 15775714 [TBL] [Abstract][Full Text] [Related]
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7. 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]
8. Congenital adrenal hyperplasia due to 21 hydroxylase deficiency: from birth to adulthood. White PC; Bachega TA Semin Reprod Med; 2012 Oct; 30(5):400-9. PubMed ID: 23044877 [TBL] [Abstract][Full Text] [Related]
9. Neonatal screening for congenital adrenal hyperplasia: 17-hydroxyprogesterone levels and CYP21 genotypes in preterm infants. Nordenström A; Wedell A; Hagenfeldt L; Marcus C; Larsson A Pediatrics; 2001 Oct; 108(4):E68. PubMed ID: 11581476 [TBL] [Abstract][Full Text] [Related]
10. High frequency of non-classical congenital adrenal hyperplasia form among children with persistently elevated levels of 17-hydroxyprogesterone after newborn screening. Castro PS; Rassi TO; Araujo RF; Pezzuti IL; Rodrigues AS; Bachega TASS; Silva IN J Pediatr Endocrinol Metab; 2019 May; 32(5):499-504. PubMed ID: 31028712 [TBL] [Abstract][Full Text] [Related]
11. Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Forest MG Hum Reprod Update; 2004; 10(6):469-85. PubMed ID: 15514016 [TBL] [Abstract][Full Text] [Related]
12. Molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia: implications for genetic counseling. Speiser PW Am J Pharmacogenomics; 2001; 1(2):101-10. PubMed ID: 12174671 [TBL] [Abstract][Full Text] [Related]
13. Predicting phenotype in steroid 21-hydroxylase deficiency? Comprehensive genotyping in 155 unrelated, well defined patients from southern Germany. Krone N; Braun A; Roscher AA; Knorr D; Schwarz HP J Clin Endocrinol Metab; 2000 Mar; 85(3):1059-65. PubMed ID: 10720040 [TBL] [Abstract][Full Text] [Related]
14. How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency. L'Allemand D; Tardy V; Grüters A; Schnabel D; Krude H; Morel Y J Clin Endocrinol Metab; 2000 Dec; 85(12):4562-7. PubMed ID: 11134109 [TBL] [Abstract][Full Text] [Related]
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