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.
80 related articles for article (PubMed ID: 12746407)
1. Mapping of a de novo unequal crossover causing a deletion of the steroid 21-hydroxylase (CYP21A2) gene and a non-functional hybrid tenascin-X (TNXB) gene. Koppens PF; Smeets HJ; de Wijs IJ; Degenhart HJ J Med Genet; 2003 May; 40(5):e53. PubMed ID: 12746407 [No Abstract] [Full Text] [Related]
2. Carriership of a defective tenascin-X gene in steroid 21-hydroxylase deficiency patients: TNXB -TNXA hybrids in apparent large-scale gene conversions. Koppens PF; Hoogenboezem T; Degenhart HJ Hum Mol Genet; 2002 Oct; 11(21):2581-90. PubMed ID: 12354783 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. An unequal crossover between the RCCX modules of the human MHC leading to the presence of a CYP21B gene and a tenascin TNXB/TNXA-RP2 recombinant between C4A and C4B genes in a patient with juvenile rheumatoid arthritis. Rupert KL; Rennebohm RM; Yu CY Exp Clin Immunogenet; 1999; 16(2):81-97. PubMed ID: 10343159 [TBL] [Abstract][Full Text] [Related]
5. Chimeric CYP21P/CYP21 and TNXA/TNXB genes in the RCCX module. Lee HH Mol Genet Metab; 2005 Jan; 84(1):4-8. PubMed ID: 15639189 [TBL] [Abstract][Full Text] [Related]
6. The phenotypic spectrum of contiguous deletion of CYP21A2 and tenascin XB: quadricuspid aortic valve and other midline defects. Chen W; Kim MS; Shanbhag S; Arai A; VanRyzin C; McDonnell NB; Merke DP Am J Med Genet A; 2009 Dec; 149A(12):2803-8. PubMed ID: 19921645 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency. Sinnott P; Collier S; Costigan C; Dyer PA; Harris R; Strachan T Proc Natl Acad Sci U S A; 1990 Mar; 87(6):2107-11. PubMed ID: 2315306 [TBL] [Abstract][Full Text] [Related]
9. PCR-based detection of the CYP21 deletion and TNXA/TNXB hybrid in the RCCX module. Lee HH; Lee YJ; Lin CY Genomics; 2004 May; 83(5):944-50. PubMed ID: 15081125 [TBL] [Abstract][Full Text] [Related]
11. Analysis of the CYP21A1P pseudogene: indication of mutational diversity and CYP21A2-like and duplicated CYP21A2 genes. Tsai LP; Cheng CF; Chuang SH; Lee HH Anal Biochem; 2011 Jun; 413(2):133-41. PubMed ID: 21324303 [TBL] [Abstract][Full Text] [Related]
12. Unequal meiotic crossover: a frequent cause of NF1 microdeletions. López Correa C; Brems H; Lázaro C; Marynen P; Legius E Am J Hum Genet; 2000 Jun; 66(6):1969-74. PubMed ID: 10775528 [TBL] [Abstract][Full Text] [Related]
13. Genes, pseudogenes and like genes: the case of 21-hydroxylase in Italian population. Concolino P; Mello E; Minucci A; Giardina B; Capoluongo E Clin Chim Acta; 2013 Sep; 424():85-9. PubMed ID: 23721949 [TBL] [Abstract][Full Text] [Related]
14. Duplication of the CYP21A2 gene complicates mutation analysis of steroid 21-hydroxylase deficiency: characteristics of three unusual haplotypes. Koppens PF; Hoogenboezem T; Degenhart HJ Hum Genet; 2002 Oct; 111(4-5):405-10. PubMed ID: 12384784 [TBL] [Abstract][Full Text] [Related]
15. Mutational analysis of CYP21A2 gene and CYP21A1P pseudogene: long-range PCR on genomic DNA. Lee HH Methods Mol Biol; 2014; 1167():275-87. PubMed ID: 24823785 [TBL] [Abstract][Full Text] [Related]
16. Predisposition for de novo gene aberrations in the offspring of mothers with a duplicated CYP21A2 gene. Baumgartner-Parzer SM; Fischer G; Vierhapper H J Clin Endocrinol Metab; 2007 Mar; 92(3):1164-7. PubMed ID: 17164306 [TBL] [Abstract][Full Text] [Related]
17. Intraspecific evolution of human RCCX copy number variation traced by haplotypes of the CYP21A2 gene. Bánlaki Z; Szabó JA; Szilágyi Á; Patócs A; Prohászka Z; Füst G; Doleschall M Genome Biol Evol; 2013; 5(1):98-112. PubMed ID: 23241443 [TBL] [Abstract][Full Text] [Related]
18. Chimeric CYP21A1P/CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia. Vrzalová Z; Hrubá Z; Hrabincová ES; Vrábelová S; Votava F; Koloušková S; Fajkusová L Eur J Med Genet; 2011; 54(2):112-7. PubMed ID: 20970527 [TBL] [Abstract][Full Text] [Related]
19. CYP21 and CYP21P variability in steroid 21-hydroxylase deficiency patients and in the general population in the Netherlands. Koppens PF; Hoogenboezem T; Degenhart HJ Eur J Hum Genet; 2000 Nov; 8(11):827-36. PubMed ID: 11093272 [TBL] [Abstract][Full Text] [Related]
20. Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms. Tusié-Luna MT; White PC Proc Natl Acad Sci U S A; 1995 Nov; 92(23):10796-800. PubMed ID: 7479886 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]