Genetics of steroid 21-hydroxylase deficiency
- 31 December 1985
- journal article
- review article
- Published by Elsevier in Trends in Genetics
- Vol. 1, 275-278
- https://doi.org/10.1016/0168-9525(85)90104-0
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Newborn Screening for Congenital Adrenal Hyperplasia with Special Reference to Screening in AlaskaaAnnals of the New York Academy of Sciences, 1985
- Genotyping Steroid 21-Hydroxylase Deficiency: Hormonal Reference Data*Journal of Clinical Endocrinology & Metabolism, 1983
- HLA AND CONGENITAL ADRENAL HYPERPLASIAThe Lancet, 1978
- 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
- Microfilter Paper Method for 17α-Hydroxyprogesterone Radioimmunoassay: Its Application for Rapid Screening for Congenital Adrenal HyperplasiaJournal of Clinical Endocrinology & Metabolism, 1977
- Incidence of salt-losing form of congenital virilizing adrenal hyperplasia.Archives of Disease in Childhood, 1972
- An unusually high incidence of salt-losing congenital adrenal hyperplasia in the Alaskan EskimoThe Journal of Pediatrics, 1969
- Adrenal Disorders: II. Congenital Virilizing Adrenal HyperplasiaArchives of Disease in Childhood, 1962
- VIRILIZING ADRENAL HYPERPLASIA; A GENETIC AND HORMONAL STUDY 1JCI Insight, 1956