Detection of heterozygotes for congenital adrenal hyperplasia: 21-Hydroxylase deficiency—a comparison of HLA typing and 17-OH progesterone response to ACTH infusion
- 1 November 1980
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 97 (5) , 749-753
- https://doi.org/10.1016/s0022-3476(80)80257-5
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) BY HLA TYPINGThe Lancet, 1979
- Genetic Mapping of the 21-Hydroxylase-Deficiency Gene within the HLA Linkage GroupNew England Journal of Medicine, 1978
- CLOSE GENETIC LINKAGE BETWEEN HLA AND CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY)The Lancet, 1977
- Identification of heterozygote carriers of congenital adrenal hyperplasia by radioimmunoassay of serum 17-OH progesteroneThe Journal of Pediatrics, 1977
- The detection of the heterozygous carrier for congenital virilizing adrenal hyperplasiaThe Journal of Pediatrics, 1977
- Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.The Journal of Experimental Medicine, 1976
- EVIDENCE FOR PARTIAL 21-HYDROXYLASE DEFICIENCY AMONG HETEROZYGOTE CARRIERS OF CONGENITAL ADRENAL HYPERPLASIAJournal of Clinical Endocrinology & Metabolism, 1975
- GENETIC POLYMORPHISM IN HUMAN GLYCINE-RICH BETA-GLYCOPROTEINThe Journal of Experimental Medicine, 1972
- An unusually high incidence of salt-losing congenital adrenal hyperplasia in the Alaskan EskimoThe Journal of Pediatrics, 1969
- VIRILIZING ADRENAL HYPERPLASIA; A GENETIC AND HORMONAL STUDY 1Journal of Clinical Investigation, 1956