Genetic Mapping of the 21-Hydroxylase-Deficiency Gene within the HLA Linkage Group
- 26 October 1978
- journal article
- research article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 299 (17), 911-915
- https://doi.org/10.1056/nejm197810262991702
Abstract
To document further the proposed genetic linkage between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and HLA, 34 unrelated families from New York and Zurich, with a total of 48 patients, 48 siblings and their parents, were studied. All patients were HLA genotypically different from the healthy sibs; when two or more children were affected in the same sibship they were always HLA-B identical.This publication has 13 references indexed in Scilit:
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