Detection of the heterozygous state in siblings of patientswith congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- 31 May 1979
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 94 (5), 770-772
- https://doi.org/10.1016/s0022-3476(79)80152-3
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- UNUSUAL HETEROZYGOTES OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCYActa Endocrinologica, 1978
- 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
- EVIDENCE FOR PARTIAL 21-HYDROXYLASE DEFICIENCY AMONG HETEROZYGOTE CARRIERS OF CONGENITAL ADRENAL HYPERPLASIAJournal of Clinical Endocrinology & Metabolism, 1975
- VIRILIZING ADRENAL HYPERPLASIA; A GENETIC AND HORMONAL STUDY 1Journal of Clinical Investigation, 1956