These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
143 related articles for article (PubMed ID: 15684714)
21. Analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency. Lee HH; Chang JG; Tsai CH; Tsai FJ; Chao HT; Chung B Clin Chem; 2000 May; 46(5):606-11. PubMed ID: 10794740 [TBL] [Abstract][Full Text] [Related]
22. The HLA-A3, Cw6,B47,DR7 extended haplotypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with at least two crossover sites in the class III region. Donohoue PA; Guethlein L; Collins MM; Van Dop C; Migeon CJ; Bias WB; Schmeckpeper BJ Tissue Antigens; 1995 Sep; 46(3 ( Pt 1)):163-72. PubMed ID: 8525475 [TBL] [Abstract][Full Text] [Related]
23. The Prevalence of the Chimeric TNXA/TNXB Gene and Clinical Symptoms of Ehlers-Danlos Syndrome with 21-Hydroxylase Deficiency. Gao Y; Lu L; Yu B; Mao J; Wang X; Nie M; Wu X J Clin Endocrinol Metab; 2020 Jul; 105(7):. PubMed ID: 32291442 [TBL] [Abstract][Full Text] [Related]
24. Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia. Lee HH; Chao HT; Ng HT; Choo KB J Med Genet; 1996 May; 33(5):371-5. PubMed ID: 8733045 [TBL] [Abstract][Full Text] [Related]
25. Deficiencies of human complement component C4A and C4B and heterozygosity in length variants of RP-C4-CYP21-TNX (RCCX) modules in caucasians. The load of RCCX genetic diversity on major histocompatibility complex-associated disease. Blanchong CA; Zhou B; Rupert KL; Chung EK; Jones KN; Sotos JF; Zipf WB; Rennebohm RM; Yung Yu C J Exp Med; 2000 Jun; 191(12):2183-96. PubMed ID: 10859342 [TBL] [Abstract][Full Text] [Related]
26. Comparing the Southern blot method and polymerase chain reaction product analysis for chimeric RCCX detection in CYP21A2 deficiency. Lee HH; Lee YJ; Chao MC Anal Biochem; 2010 Apr; 399(2):293-8. PubMed ID: 19961824 [TBL] [Abstract][Full Text] [Related]
27. A novel frameshift mutation (141delT) in exon 1 of the 21-hydroxylase gene (CYP21) in a patient with the salt wasting form of congenital adrenal hyperplasia. Mutation in brief no. 255. Online. Krone N; Braun A; Roscher AA; Schwarz HP Hum Mutat; 1999; 14(1):90-1. PubMed ID: 10447270 [TBL] [Abstract][Full Text] [Related]
28. The suppression effect of DNA sequences within the C4A region on the transcription activity of human CYP21. Chang SF; Cheng CL Endocr Res; 1998; 24(3-4):625-30. PubMed ID: 9888550 [TBL] [Abstract][Full Text] [Related]
29. Molecular approaches for the diagnosis of 21-hydroxylase deficiency and congenital adrenal hyperplasia. Wedell A Clin Lab Med; 1996 Mar; 16(1):125-37. PubMed ID: 8867587 [TBL] [Abstract][Full Text] [Related]
30. An unequal crossover event in RCCX modules of the human MHC resulting in the formation of a TNXB/TNXA hybrid and deletion of the CYP21A. Jaatinen T; Chung EK; Ruuskanen O; Lokki ML Hum Immunol; 2002 Aug; 63(8):683-9. PubMed ID: 12121677 [TBL] [Abstract][Full Text] [Related]
31. Modular variations of the human major histocompatibility complex class III genes for serine/threonine kinase RP, complement component C4, steroid 21-hydroxylase CYP21, and tenascin TNX (the RCCX module). A mechanism for gene deletions and disease associations. Yang Z; Mendoza AR; Welch TR; Zipf WB; Yu CY J Biol Chem; 1999 Apr; 274(17):12147-56. PubMed ID: 10207042 [TBL] [Abstract][Full Text] [Related]
32. Measurement of serum tenascin-X in patients with congenital adrenal hyperplasia at risk for Ehlers-Danlos contiguous gene deletion syndrome CAH-X. Kolli V; Kim H; Rao H; Lao Q; Gaynor A; Milner JD; Merke DP BMC Res Notes; 2019 Oct; 12(1):711. PubMed ID: 31666125 [TBL] [Abstract][Full Text] [Related]
33. 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 Mol Genet Metab; 2008 Apr; 93(4):450-7. PubMed ID: 18039588 [TBL] [Abstract][Full Text] [Related]
34. Salt-wasting congenital adrenal hyperplasia: detection and characterization of mutations in the steroid 21-hydroxylase gene, CYP21, using the polymerase chain reaction. Owerbach D; Ballard AL; Draznin MB J Clin Endocrinol Metab; 1992 Mar; 74(3):553-8. PubMed ID: 1740489 [TBL] [Abstract][Full Text] [Related]
35. A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiency. Tukel T; Uyguner O; Wei JQ; Yuksel-Apak M; Saka N; Song DX; Kayserili H; Bas F; Gunoz H; Wilson RC; New MI; Wollnik B J Clin Endocrinol Metab; 2003 Dec; 88(12):5893-7. PubMed ID: 14671187 [TBL] [Abstract][Full Text] [Related]
37. 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]
39. Revisiting the association of HLA alleles and haplotypes with CYP21A2 mutations in a large cohort of patients with congenital adrenal hyperplasia. Jayakrishnan R; Lao Q; Adams SD; Ward WW; Merke DP Gene; 2019 Mar; 687():30-34. PubMed ID: 30419250 [TBL] [Abstract][Full Text] [Related]
40. Characterization of frequent polymorphisms in intron 2 of CYP21: application to analysis of segregation of CYP21 alleles. Killeen AA; Jiddou RR; Sane KS Clin Chem; 1998 Dec; 44(12):2410-5. PubMed ID: 9836705 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]