219 related articles for article (PubMed ID: 2882404)
1. Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene region.
Boehm BO; Rosak C; Boehm TL; Kuehnl P; White PC; Schöffling K
Mol Biol Med; 1986 Oct; 3(5):437-48. PubMed ID: 2882404
[TBL] [Abstract][Full Text] [Related]
2. Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein.
Donohoue PA; van Dop C; McLean RH; White PC; Jospe N; Migeon CJ
J Clin Endocrinol Metab; 1986 May; 62(5):995-1002. PubMed ID: 3007562
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.
Schneider PM; Carroll MC; Alper CA; Rittner C; Whitehead AS; Yunis EJ; Colten HR
J Clin Invest; 1986 Sep; 78(3):650-7. PubMed ID: 3018042
[TBL] [Abstract][Full Text] [Related]
5. Adrenal 21-hydroxylase cytochrome P-450 genes within the MHC class III region.
White PC; New MI; Dupont B
Immunol Rev; 1985 Oct; 87():123-50. PubMed ID: 3902620
[TBL] [Abstract][Full Text] [Related]
6. DNA polymorphism unique for a complotype with deletion of HLA-linked C4B and 21-hydroxylase B genes causing congenital adrenal hyperplasia.
Partanen J; Koskimies S; Sipilä I
Hum Genet; 1988 Apr; 78(4):372-3. PubMed ID: 2896160
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency.
Mornet E; Couillin P; Kutten F; Raux MC; White PC; Cohen D; Boué A; Dausset J
Hum Genet; 1986 Dec; 74(4):402-8. PubMed ID: 2878869
[TBL] [Abstract][Full Text] [Related]
9. Identification of a new HLA-B7-associated C21-hydroxylase deficiency gene by restriction enzyme length polymorphism.
Keller E; Andreas-Zietz A; Knorr D; Scholz S; Albert ED
Immunogenetics; 1987; 25(2):123-5. PubMed ID: 2880800
[No Abstract] [Full Text] [Related]
10. Frequent deletion and duplication of the steroid 21-hydroxylase genes.
Werkmeister JW; New MI; Dupont B; White PC
Am J Hum Genet; 1986 Oct; 39(4):461-9. PubMed ID: 3490178
[TBL] [Abstract][Full Text] [Related]
11. HLA haplotypes and hormonal studies in 25 Italian families of patients with classical and non-classical 21-OH deficiency.
Einaudi S; Borelli I; Lala R; Praticŏ L; Curtoni ES; De Sanctis C
J Pediatr Endocrinol; 1994; 7(4):349-55. PubMed ID: 7735374
[TBL] [Abstract][Full Text] [Related]
12. Late-onset form of congenital adrenal hyperplasia in the HLA-B14; DR1 haplotype is caused by a duplication in the 21-OH MHC gene region.
Boehm BO; Rosak C; Kuehnl P; Schöffling K
Horm Metab Res; 1986 Nov; 18(11):791-2. PubMed ID: 3491779
[No Abstract] [Full Text] [Related]
13. Genetics and biochemical variability of variants of 21 hydroxylase deficiency.
Gordon MT; Conway DI; Anderson DC; Harris R
J Med Genet; 1985 Oct; 22(5):354-60. PubMed ID: 3001309
[TBL] [Abstract][Full Text] [Related]
14. Restriction fragment length polymorphism study of families with congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Taiwan.
Lee JS; Tsai HM; Shieh RP; Chen SH; Tsai WY; Chung BC
J Formos Med Assoc; 1990 Jul; 89(7):534-40. PubMed ID: 1979594
[TBL] [Abstract][Full Text] [Related]
15. Prevalence of polymorphic 21-hydroxylase gene (CA21HB) mutations in salt-losing congenital adrenal hyperplasia.
Jospe N; Donohoue PA; Van Dop C; McLean RH; Bias WB; Migeon CJ
Biochem Biophys Res Commun; 1987 Feb; 142(3):798-804. PubMed ID: 3030300
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency.
Levine LS; Dupont B; Lorenzen F; Pang S; Pollack M; Oberfield SE; Kohn B; Lerner A; Cacciari E; Mantero F; Cassio A; Scaroni C; Chiumello G; Rondanini GF; Gargantini L; Giovannelli G; Virdis R; Bartolotta E; Migliori C; Pintor C; Tato L; Barboni F; New MI
J Clin Endocrinol Metab; 1981 Dec; 53(6):1193-8. PubMed ID: 6271801
[TBL] [Abstract][Full Text] [Related]
18. Molecular cloning of steroid 21-hydroxylase.
White PC; Dupont B; New MI
Endocr Res; 1984-1985; 10(3-4):335-45. PubMed ID: 6336060
[TBL] [Abstract][Full Text] [Related]
19. Family studies of the steroid 21-hydroxylase and complement C4 genes define 11 haplotypes in classical congenital adrenal hyperplasia in The Netherlands.
Koppens PF; Hoogenboezem T; Halley DJ; Barendse CA; Oostenbrink AJ; Degenhart HJ
Eur J Pediatr; 1992 Dec; 151(12):885-92. PubMed ID: 1473541
[TBL] [Abstract][Full Text] [Related]
20. [Genetic of the 21 hydroxylase deficiency].
Boué A; Couillin P; Pomarède R; Rappaport R; Boué J
Ann Endocrinol (Paris); 1982; 43(1):3-14. PubMed ID: 6982657
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
