Response

Publisher Website

1 July 1993

journal article
other
Published by Elsevier in Human Immunology

Vol. 37 (3) , 196-197
https://doi.org/10.1016/0198-8859(93)90187-6

Abstract

No abstract available

This publication has 1 reference indexed in Scilit:

Congenital 21-hydroxylase deficiency as a new deletion mutation: Detection in a proband during subsequent prenatal diagnosis by HLA typing and DNA analysis
Human Immunology, 1992