DETECTION OF HETEROZYGOTE OF 21-HYDROXYLASE DEFICIENCY
- 1 January 1980
- journal article
- letter
- Published by Elsevier in The Lancet
- Vol. 315 (8158) , 47
- https://doi.org/10.1016/s0140-6736(80)90585-1
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Detection of Circulating Heart/Reactive Antibodies by Immunofluorescence in Patients with CardiomyopathyClinical Science, 1979
- Detection of the heterozygous state in siblings of patientswith congenital adrenal hyperplasia due to 21-hydroxylase deficiencyThe Journal of Pediatrics, 1979
- PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) BY HLA TYPINGThe Lancet, 1979
- HLA AND CONGENITAL ADRENAL HYPERPLASIAThe Lancet, 1978
- HLA AND CONGENITAL ADRENAL HYPERPLASIA LINKAGE CONFIRMEDThe Lancet, 1978
- CLOSE GENETIC LINKAGE BETWEEN HLA AND CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY)The Lancet, 1977