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Links from PubMed

Items: 6

1.

The immunological detection of a 21-OH deficiency mutation HLA supratype.

Pollack MS, Keenan B, Christiansen FT, Cobain TJ, Dawkins RL, Clayton G.

Am J Hum Genet. 1986 May;38(5):688-98.

2.

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
3.
4.

Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Morel Y, Miller WL.

Adv Hum Genet. 1991;20:1-68. Review. No abstract available.

PMID:
1801590
5.

[Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis].

Lambotte C.

Rev Med Liege. 1986 Jan 15;41(2):37-44. Review. French. No abstract available.

PMID:
3006204
6.

Basic and clinical aspects of congenital adrenal hyperplasia.

New MI.

J Steroid Biochem. 1987;27(1-3):1-7. Review.

PMID:
3320531

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