Diagnosis of homozygosity and heterozygosity in congenital adrenal hyperplasia (CAH) and control of treatment
- 31 July 1983
- journal article
- research article
- Published by Elsevier in Journal of Steroid Biochemistry
- Vol. 19 (1) , 645-653
- https://doi.org/10.1016/0022-4731(83)90231-5
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Hormonal profiles of heterozygotes in humans for 21-hydroxylase deficiency defined by HLA B typingJournal of Steroid Biochemistry, 1981
- Determination of 14 steroid hormones in amniotic fluid (AF): its usefulness in the antenatal diagnosis of 21-hydroxylase deficiencyPediatric Research, 1981
- Concentration of 14 Steroid Hormones in Human Amniotic Fluid of Midpregnancy*Journal of Clinical Endocrinology & Metabolism, 1980
- HLA-A, B, C, DR alleles in congenital adrenal hyperplasiaHuman Genetics, 1980
- Genetic linkage studies between congenital adrenal hyperplasia and the HLA blood group systemImmunogenetics, 1979
- ANTENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIAThe Lancet, 1979
- Detection of the heterozygous state in siblings of patientswith congenital adrenal hyperplasia due to 21-hydroxylase deficiencyThe Journal of Pediatrics, 1979
- CLOSE GENETIC LINKAGE BETWEEN HLA AND CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY)The Lancet, 1977
- The detection of the heterozygous carrier for congenital virilizing adrenal hyperplasiaThe Journal of Pediatrics, 1977
- Elevated amniotic fluid concentration of 17 α-hydroxyprogesterone in congenital adrenal hyperplasiaThe Journal of Pediatrics, 1975