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Items: 1 to 20 of 109

1.

Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies.

Aston CE, Sherman SL, Morton NE, Speiser PW, New MI.

Am J Hum Genet. 1988 Sep;43(3):304-10.

2.

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.

PMID:
2822757
4.

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. Review.

PMID:
3902620
5.

Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region.

Carroll MC, Palsdottir A, Belt KT, Porter RR.

EMBO J. 1985 Oct;4(10):2547-52.

6.

Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.

White PC, Grossberger D, Onufer BJ, Chaplin DD, New MI, Dupont B, Strominger JL.

Proc Natl Acad Sci U S A. 1985 Feb;82(4):1089-93.

7.
10.

The absence of 21-OH A and C4 B genes is a constant characteristic of the "Sardinian" HLA extended haplotype A30 Cw5 B18 BfF1 DR3 DRw52 DQw2.

Carcassi C, Porcella R, Manca ML, Orrù S, La Nasa G, Contu L.

Tissue Antigens. 1989 Aug;34(2):85-9.

PMID:
2609326
11.

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.

12.

[Localization of the pathologic gene for 21-hydroxylase enzyme deficiency within the HLA system].

Brkljacić-Surkalović L, Dumić M, Mardesić D, Plavsić V, Kastelan A.

Lijec Vjesn. 1988 Sep-Oct;110(9-10):306-11. Croatian. No abstract available.

PMID:
3264873
13.

Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus.

O'Neill GJ, Dupont B, Pollack MS, Levine LS, New MI.

Clin Immunol Immunopathol. 1982 May;23(2):312-22. No abstract available.

PMID:
6980755
14.

Molecular genetics of the fourth component of human complement and steroid 21-hydroxylase.

Carroll MC, Belt KT, Palsdottir A, Yu Y.

Immunol Rev. 1985 Oct;87:39-60. Review. No abstract available.

PMID:
2997023
15.

C4B gene polymorphism detected in a human cosmid clone.

Prentice HL, Schneider PM, Strominger JL.

Immunogenetics. 1986;23(4):274-6. No abstract available.

PMID:
3009318
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.

17.

Steroid 21-hydroxylase deficiency and the major histocompatibility complex.

White PC, Werkmeister J, New MI, Dupont B.

Hum Immunol. 1986 Apr;15(4):404-15.

PMID:
3009365
18.

C4 complement allotypes in juvenile dermatomyositis.

Robb SA, Fielder AH, Saunders CE, Davey NJ, Burley MW, Lord DH, Batchelor JR, Dubowitz V.

Hum Immunol. 1988 May;22(1):31-8.

PMID:
3260584
19.

21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.

Sinnott PJ, Dyer PA, Price DA, Harris R, Strachan T.

J Med Genet. 1989 Jan;26(1):10-7.

20.

Map of the human MHC.

Trowsdale J, Ragoussis J, Campbell RD.

Immunol Today. 1991 Dec;12(12):443-6. No abstract available.

PMID:
1786080

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