153 related articles for article (PubMed ID: 2613228)
21. Molecular pathology of 21-hydroxylase deficiency.
Strachan T
J Inherit Metab Dis; 1994; 17(4):430-41. PubMed ID: 7967493
[TBL] [Abstract][Full Text] [Related]
22. Analysis of mutations causing steroid 21-hydroxylase deficiency.
White PC
Endocr Res; 1989; 15(1-2):239-56. PubMed ID: 2788080
[TBL] [Abstract][Full Text] [Related]
23. Mutations in steroid 21-hydroxylase (CYP21).
White PC; Tusie-Luna MT; New MI; Speiser PW
Hum Mutat; 1994; 3(4):373-8. PubMed ID: 8081391
[TBL] [Abstract][Full Text] [Related]
24. Structural analysis of the chimeric CYP21P/CYP21 gene in steroid 21-hydroxylase deficiency.
Lee HH; Niu DM; Lin RW; Chan P; Lin CY
J Hum Genet; 2002; 47(10):517-22. PubMed ID: 12376740
[TBL] [Abstract][Full Text] [Related]
25. Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1.
Speiser PW; New MI; White PC
N Engl J Med; 1988 Jul; 319(1):19-23. PubMed ID: 3260007
[TBL] [Abstract][Full Text] [Related]
26. Concordance of 21-hydroxylase gene ratio, human leukocyte antigen haplotyping and adrenal testing results in a family with late-onset adrenal hyperplasia.
Wells G; Acton RT; Azziz R
J Reprod Med; 1993 Aug; 38(8):615-20. PubMed ID: 8410868
[TBL] [Abstract][Full Text] [Related]
27. Determination of deletion sizes in the MHC-linked complement C4 and steroid 21-hydroxylase genes by pulsed-field gel electrophoresis.
Partanen J; Kere J; Wessberg S; Koskimies S
Genomics; 1989 Aug; 5(2):345-9. PubMed ID: 2551816
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. R339H and P453S: CYP21 mutations associated with nonclassic steroid 21-hydroxylase deficiency that are not apparent gene conversions.
Helmberg A; Tusie-Luna MT; Tabarelli M; Kofler R; White PC
Mol Endocrinol; 1992 Aug; 6(8):1318-22. PubMed ID: 1406709
[TBL] [Abstract][Full Text] [Related]
30. Nonsense mutation causing steroid 21-hydroxylase deficiency.
Globerman H; Amor M; Parker KL; New MI; White PC
J Clin Invest; 1988 Jul; 82(1):139-44. PubMed ID: 3267225
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Preliminary investigation of mutations in 21-hydroxylase gene in patients with congenital adrenal hyperplasia in Russia.
Evgrafov OV; Polyakov AV; Dzenis IG; Baharev VA
Hum Mutat; 1995; 5(2):131-6. PubMed ID: 7749411
[TBL] [Abstract][Full Text] [Related]
33. [Gene heterogeneity in adrenal 21-hydroxylase].
Morel Y
Presse Med; 1991 May; 20(20):945-9. PubMed ID: 1829200
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Extended MHC haplotypes and CYP21/C4 gene organisation in Irish 21-hydroxylase deficiency families.
Sinnott PJ; Costigan C; Dyer PA; Harris R; Strachan T
Hum Genet; 1991 Jul; 87(3):361-6. PubMed ID: 1677925
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Molecular genetics of congenital adrenal hyperplasia.
White PC; New MI
Baillieres Clin Endocrinol Metab; 1988 Nov; 2(4):941-65. PubMed ID: 3077248
[TBL] [Abstract][Full Text] [Related]
38. Coupling of HLA-A3,Cw6,Bw47,DR7 and a normal CA21HB steroid 21-hydroxylase gene in the Old Order Amish.
Donohoue PA; Van Dop C; Migeon CJ; McLean RH; Bias WB
J Clin Endocrinol Metab; 1987 Nov; 65(5):980-6. PubMed ID: 2822757
[TBL] [Abstract][Full Text] [Related]
39. Clinical and genetic characterization of nonclassic 21-hydroxylase deficiency.
Speiser PW; New MI; White PC
Endocr Res; 1989; 15(1-2):257-76. PubMed ID: 2788081
[TBL] [Abstract][Full Text] [Related]
40. Gene conversions and unequal crossovers between CYP21 (steroid 21-hydroxylase gene) and CYP21P involve different mechanisms.
TusiƩ-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]
[Previous] [Next] [New Search]