The biochemical basis for genotyping 21-hydroxylase deficiency
- 1 August 1981
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 58 (1) , 123-127
- https://doi.org/10.1007/bf00284159
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
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- The Attenuated Form of Congenital Adrenal Hyperplasia as an Allelic Form of 21-Hydroxylase Deficiency*Journal of Clinical Endocrinology & Metabolism, 1980
- Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: A new Allele at the 21-hydroxylase locusHuman Immunology, 1980
- Adult-onset familial adrenal 21-hydroxylase deficiencyThe American Journal of Medicine, 1980
- UNUSUAL HETEROZYGOTES OF CONGENITAL ADRENAL HYPERPLASIA DUE TO 21-HYDROXYLASE DEFICIENCY CONFIRMED BY HLA TISSUE TYPINGActa Endocrinologica, 1979
- GENETICS OF ACQUIRED AND CONGENITAL ADRENAL HYPERPLASIAThe Lancet, 1979
- Genetic Mapping of the 21-Hydroxylase-Deficiency Gene within the HLA Linkage GroupNew England Journal of Medicine, 1978
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- Partial 11- and 21-hydroylase deficiencies in hirsute women.1977