182 related articles for article (PubMed ID: 1971153)
1. Gene conversion in steroid 21-hydroxylase genes.
Urabe K; Kimura A; Harada F; Iwanaga T; Sasazuki T
Am J Hum Genet; 1990 Jun; 46(6):1178-86. PubMed ID: 1971153
[TBL] [Abstract][Full Text] [Related]
2. [Mutations in 21-hydroxylase gene caused by gene conversion-like events].
Urabe K
Fukuoka Igaku Zasshi; 1990 Feb; 81(2):77-87. PubMed ID: 2328938
[TBL] [Abstract][Full Text] [Related]
3. Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21B.
Donohoue PA; Jospe N; Migeon CJ; Van Dop C
Genomics; 1989 Oct; 5(3):397-406. PubMed ID: 2613228
[TBL] [Abstract][Full Text] [Related]
4. Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.
Amor M; Parker KL; Globerman H; New MI; White PC
Proc Natl Acad Sci U S A; 1988 Mar; 85(5):1600-4. PubMed ID: 3257825
[TBL] [Abstract][Full Text] [Related]
5. Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.
White PC; Vitek A; Dupont B; New MI
Proc Natl Acad Sci U S A; 1988 Jun; 85(12):4436-40. PubMed ID: 3260033
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Exon 7 Ncol restriction site within CYP21B (steroid 21-hydroxylase) is a normal polymorphism.
Donohoue PA; Sandrini Neto R; Collins MM; Migeon CJ
Mol Endocrinol; 1990 Sep; 4(9):1354-62. PubMed ID: 1978247
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes.
Collier S; Sinnott PJ; Dyer PA; Price DA; Harris R; Strachan T
EMBO J; 1989 May; 8(5):1393-402. PubMed ID: 2788573
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Major-histocompatibility-complex gene markers and restriction-fragment analysis of steroid 21-hydroxylase (CYP21) and complement C4 genes in classical congenital adrenal hyperplasia patients in a single population.
Partanen J; Koskimies S; Sipilä I; Lipsanen V
Am J Hum Genet; 1989 May; 44(5):660-70. PubMed ID: 2565078
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Direct analysis of CYP21B genes in 21-hydroxylase deficiency using polymerase chain reaction amplification.
Owerbach D; Crawford YM; Draznin MB
Mol Endocrinol; 1990 Jan; 4(1):125-31. PubMed ID: 2325662
[TBL] [Abstract][Full Text] [Related]
14. Molecular and endocrine characterization of a mutation involving a recombination between the steroid 21-hydroxylase functional gene and pseudogene.
Killeen AA; Sane KS; Orr HT
J Steroid Biochem Mol Biol; 1991 Jun; 38(6):677-86. PubMed ID: 1905948
[TBL] [Abstract][Full Text] [Related]
15. Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia.
Ghanem N; Lobaccaro JM; Buresi C; Abbal M; Halaby G; Sultan C; Lefranc G
Hum Genet; 1990 Dec; 86(2):117-25. PubMed ID: 1979956
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families.
Sinnott PJ; Livieri C; Sampietro M; Marconi M; Harris R; Severi F; Strachan T
Hum Genet; 1992 Mar; 88(5):545-51. PubMed ID: 1551657
[TBL] [Abstract][Full Text] [Related]
18. Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency.
Rumsby G; Fielder AH; Hague WM; Honour JW
J Med Genet; 1988 Sep; 25(9):596-9. PubMed ID: 3263505
[TBL] [Abstract][Full Text] [Related]
19. Identification of the recombination site within the steroid 21-hydroxylase gene (CYP21) of the HLA-B47,DR7 haplotype.
Chu X; Braun-Heimer L; Rittner C; Schneider PM
Exp Clin Immunogenet; 1992; 9(2):80-5. PubMed ID: 1489553
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
