PubMed for id: 1590

Year	Number of Results
1986	2
1987	1
1988	1
1992	1
2002	2
2003	2
2004	2
2005	2
2007	3
2008	1
2009	4
2010	1
2011	2
2013	2
2019	1
2024	0

1

High-Throughput Screening for CYP21A1P-TNXA/TNXB Chimeric Genes Responsible for Ehlers-Danlos Syndrome in Patients with Congenital Adrenal Hyperplasia.

Lao Q, Brookner B, Merke DP. Lao Q, et al. J Mol Diagn. 2019 Sep;21(5):924-931. doi: 10.1016/j.jmoldx.2019.06.001. Epub 2019 Jun 21. J Mol Diagn. 2019. PMID: 31229653 Free PMC article.

2

Analysis of the CYP21A1P pseudogene: indication of mutational diversity and CYP21A2-like and duplicated CYP21A2 genes.

Tsai LP, Cheng CF, Chuang SH, Lee HH. Tsai LP, et al. Anal Biochem. 2011 Jun 15;413(2):133-41. doi: 10.1016/j.ab.2011.02.016. Epub 2011 Feb 13. Anal Biochem. 2011. PMID: 21324303

3

Estimation of the false-negative rate in newborn screening for congenital adrenal hyperplasia.

Votava F, Török D, Kovács J, Möslinger D, Baumgartner-Parzer SM, Sólyom J, Pribilincová Z, Battelino T, Lebl J, Frisch H, Waldhauser F; Middle European Society for Paediatric Endocrinology -- Congenital Adrenal Hyperplasia (MESPE-CAH) Study Group. Votava F, et al. Eur J Endocrinol. 2005 Jun;152(6):869-74. doi: 10.1530/eje.1.01929. Eur J Endocrinol. 2005. PMID: 15941926

4

Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiency.

Lee HH, Lee YJ, Wang YM, Chao HT, Niu DM, Chao MC, Tsai FJ, Lo FS, Lin SJ. Lee HH, et al. Mol Genet Metab. 2008 Apr;93(4):450-7. doi: 10.1016/j.ymgme.2007.10.008. Epub 2007 Nov 26. Mol Genet Metab. 2008. PMID: 18039588

5

[Screening 21-hydroxylase deficiency carriers in androgen excess women of Chinese Han nationality].

Tao H, Lu Z, Zhang B, Wang Y, Sun M. Tao H, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Apr;22(2):195-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005. PMID: 15793784 Chinese.

6

Phenotype and genotype correlation of the microconversion from the CYP21A1P to the CYP21A2 gene in congenital adrenal hyperplasia.

Torres N, Mello MP, Germano CM, Elias LL, Moreira AC, Castro M. Torres N, et al. Braz J Med Biol Res. 2003 Oct;36(10):1311-8. doi: 10.1590/s0100-879x2003001000006. Epub 2003 Sep 16. Braz J Med Biol Res. 2003. PMID: 14502362 Free article.

7

Structure of human steroid 21-hydroxylase genes.

White PC, New MI, Dupont B. White PC, et al. Proc Natl Acad Sci U S A. 1986 Jul;83(14):5111-5. doi: 10.1073/pnas.83.14.5111. Proc Natl Acad Sci U S A. 1986. PMID: 3487786 Free PMC article.

8

Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene.

Higashi Y, Yoshioka H, Yamane M, Gotoh O, Fujii-Kuriyama Y. Higashi Y, et al. Proc Natl Acad Sci U S A. 1986 May;83(9):2841-5. doi: 10.1073/pnas.83.9.2841. Proc Natl Acad Sci U S A. 1986. PMID: 3486422 Free PMC article.

9

Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia.

Rodrigues NR, Dunham I, Yu CY, Carroll MC, Porter RR, Campbell RD. Rodrigues NR, et al. EMBO J. 1987 Jun;6(6):1653-61. doi: 10.1002/j.1460-2075.1987.tb02414.x. EMBO J. 1987. PMID: 3038528 Free PMC article.

10

Microconversion between CYP21A2 and CYP21A1P promoter regions causes the nonclassical form of 21-hydroxylase deficiency.

Araújo RS, Mendonca BB, Barbosa AS, Lin CJ, Marcondes JA, Billerbeck AE, Bachega TA. Araújo RS, et al. J Clin Endocrinol Metab. 2007 Oct;92(10):4028-34. doi: 10.1210/jc.2006-2163. Epub 2007 Jul 31. J Clin Endocrinol Metab. 2007. PMID: 17666484

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