Intra-HLA recombinations localizing the 21-hydroxylase deficiency gene within the HLA complex
- 31 March 1981
- journal article
- Published by Elsevier in Human Immunology
- Vol. 2 (2), 139-145
- https://doi.org/10.1016/0198-8859(81)90060-4
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Genetic linkage studies between congenital adrenal hyperplasia and the HLA blood group systemImmunogenetics, 1979
- Location of the gene for 21-hydroxylase deficiencyPediatric Research, 1979
- Genetic Mapping of the 21-Hydroxylase-Deficiency Gene within the HLA Linkage GroupNew England Journal of Medicine, 1978
- 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
- The detection of the heterozygous carrier for congenital virilizing adrenal hyperplasiaThe Journal of Pediatrics, 1977
- Twenty-four Hour Integrated Concentrations of Progesterone, 17-Hydroxyprogesterone and Cortisol in Normal Male SubjectsJournal of Clinical Endocrinology & Metabolism, 1977
- Simultaneous detection of two cell populations by two-colour fluorescence and application to the recognition of B-cell determinantsNature, 1976