HETEROGENEITY OF STEROID 21-HYDROXYLASE GENES IN CLASSICAL CONGENITAL ADRENAL HYPERPLASIA
Author:
Publisher
Wiley
Subject
Genetics,Immunology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1744-313X.1987.tb00367.x/fullpdf
Reference26 articles.
1. GENETIC POLYMORPHISM IN HUMAN GLYCINE-RICH BETA-GLYCOPROTEIN
2. Inherited structural polymorphism of the fourth component of human complement.
3. Molecular Genetics of the Fourth Component of Human Complement and Steroid 21-Hydroxylase
4. Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region.
5. COMPLEMENT ALLOTYPING IN SLE: ASSOCIATION WITH C4A NULL
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1. Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency*;Endocrine Reviews;2000-06-01
2. 5 Studies of MHC haplotypes by pulsed field gel electrophoresis;Baillière's Clinical Endocrinology and Metabolism;1991-06
3. Clinical and Molecular Genetics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency;Advances in Human Genetics;1991
4. CHARACTERIZATION OF MHC ANCESTRAL HAPLOTYPES ASSOCIATED WITH INSULIN-DEPENDENT DIABETES MELLITUS: EVIDENCE FOR INVOLVEMENT OF NON-HLA GENES;European Journal of Immunogenetics;1990-12
5. MOLECULAR PATHOLOGY OF CONGENITAL ADRENAL HYPERPLASIA;Clinical Endocrinology;1990-03
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