HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency.
暂无分享,去创建一个
[1] P. A. Lee,et al. Detection of the heterozygous state in siblings of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. , 1979, The Journal of pediatrics.
[2] A. Prader,et al. Genetic mapping of the 21-hydroxylase-deficiency gene within the HLA linkage group. , 1978, The New England journal of medicine.
[3] D. Price,et al. HLA AND CONGENITAL ADRENAL HYPERPLASIA LINKAGE CONFIRMED , 1978, The Lancet.
[4] B. Dupont,et al. CLOSE GENETIC LINKAGE BETWEEN HLA AND CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) , 1977, The Lancet.
[5] A. Krensky,et al. Identification of heterozygote carriers of congenital adrenal hyperplasia by radioimmunoassay of serum 17-OH progesterone. , 1977, The Journal of pediatrics.
[6] J. Gutai,et al. The detection of the heterozygous carrier for congenital virilizing adrenal hyperplasia. , 1977, The Journal of pediatrics.
[7] I. Hughes,et al. The application of a serum 17OH-progesterone radioimmunoassay to the diagnosis and management of congenital adrenal hyperplasia. , 1976, The Journal of pediatrics.
[8] Wardle En. Letter: Endotoxaemia in liver disease. , 1974, Lancet.
[9] C. Alper,et al. GENETIC POLYMORPHISM IN HUMAN GLYCINE-RICH BETA-GLYCOPROTEIN , 1972, The Journal of experimental medicine.
[10] Baig Ar,et al. Sex-chromatin values in rat epithelium. , 1967 .