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Results: 1 to 20 of 144

1.

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.

PMID:
2783976
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Layrisse Z, White C, Gunczler P, Gafaro Valera L, Arias S, Yunis EJ, Alper CA, Awdeh ZL.

Immunogenetics. 1987;25(2):99-103.

PMID:
3493216
[PubMed - indexed for MEDLINE]
3.

Italian extended HLA haplotypes in congenital adrenal hyperplasia.

Abbal M, Belvedere MC, Livieri C, De Paoli F, Martinetti M, Severi F, Cambon-Thomsen A.

Tissue Antigens. 1988 Jul;32(1):17-23.

PMID:
3263715
[PubMed - indexed for MEDLINE]
4.

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
[PubMed - indexed for MEDLINE]
5.

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.

PMID:
3007562
[PubMed - indexed for MEDLINE]
6.

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
[PubMed - indexed for MEDLINE]
7.

HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.

White PC, New MI, Dupont B.

Proc Natl Acad Sci U S A. 1984 Dec;81(23):7505-9.

PMID:
6334310
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

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
[PubMed - indexed for MEDLINE]
9.

Diagnosis of classical steroid 21-hydroxylase deficiency using an HLA-B locus-specific DNA-probe.

Killeen AA, Seelig S, Ulstrom RA, Orr HT.

Am J Med Genet. 1988 Mar;29(3):703-12.

PMID:
2897792
[PubMed - indexed for MEDLINE]
10.

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.

PMID:
2983330
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

TaqI HLA-B and -DRB RFLP analysis can predict disease in siblings of affected children with 21-hydroxylase deficiency.

Olerup O, Luthman H, Ritzén EM, Haglund-Stengler B.

Hum Genet. 1990 Oct;85(5):467-72.

PMID:
1977680
[PubMed - indexed for MEDLINE]
12.

Hormonal profiles in Italian late-onset adrenal hyperplasia correlate with HLA class III polymorphisms.

Balsamo A, Revelli A, Borelli I, Amoroso A, Cenderelli G, De Sanso G, Mazzola G, Curtoni ES, Zoppetti G, Massobrio M.

Gynecol Endocrinol. 1992 Jun;6(2):91-8.

PMID:
1354409
[PubMed - indexed for MEDLINE]
13.
14.

HLA-A,B,C,DR typing and 17-OHP determination for second trimester prenatal diagnosis of 21-hydroxylase deficient CAH.

Grosse-Wilde H, Valentine-Thon E, Vögeler U, Passarge E, Lorenzen F, Sippell WG, Bidlingmaier F, Knorr D.

Prenat Diagn. 1988 Feb;8(2):131-43.

PMID:
3258985
[PubMed - indexed for MEDLINE]
15.

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.

PMID:
1677925
[PubMed - indexed for MEDLINE]
16.

HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency.

Stuckey MS, Boyne P, Macdonald WB, Christiansen FT, Houliston JB, Dawkins RL.

Aust N Z J Med. 1980 Oct;10(5):552-4.

PMID:
6258552
[PubMed - indexed for MEDLINE]
17.

Altered CYP21 genes in HLA-haplotypes associated with congenital adrenal hyperplasia (CAH): a family study.

Manfras BJ, Swinyard M, Rudert WA, Ball EJ, Lee PA, Kühnl P, Trucco M, Böhm BO.

Hum Genet. 1993 Aug;92(1):33-9.

PMID:
8365724
[PubMed - indexed for MEDLINE]
18.

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.

PMID:
3018042
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

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.

PMID:
8525475
[PubMed - indexed for MEDLINE]
20.

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.

PMID:
1551657
[PubMed - indexed for MEDLINE]

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