HLA and 21 hydroxylase deficiency: (congenital and late onset adrenal hyperplasia):in the French population
- 1 February 1982
- journal article
- research article
- Published by Wiley in Tissue Antigens
- Vol. 19 (2), 100-107
- https://doi.org/10.1111/j.1399-0039.1982.tb01424.x
Abstract
No abstract availableThis publication has 26 references indexed in Scilit:
- Prenatal diagnosis of congenital adrenal hyperplasia (21-OH deficiency type) by HLA typingPrenatal Diagnosis, 1981
- Linkage and association between HLA and 21-hydroxylase deficiency.Journal of Medical Genetics, 1980
- Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: A new Allele at the 21-hydroxylase locusHuman Immunology, 1980
- Amniotic 17-α hydroxyprogesterone and HLA typing for the prenatal diagnosis of 21-α hydroxylase deficiency — congenital adrenal hyperplasiaAmerican Journal of Medical Genetics, 1980
- HLA and Congenital Adrenal Hyperplasia due to 11‐Hydroxylase DeficiencyTissue Antigens, 1979
- GENETICS OF ACQUIRED AND CONGENITAL ADRENAL HYPERPLASIAThe Lancet, 1979
- PRENATAL DIAGNOSIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) BY HLA TYPINGThe Lancet, 1979
- 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
- VIRILIZING ADRENAL HYPERPLASIA; A GENETIC AND HORMONAL STUDY 1Journal of Clinical Investigation, 1956