Abstract
Congenital 21-hydroxylase deficiency as a new mutation: Detection during prenatal diagnosis by HLA typing and DNA analysis : Marilyn S. Pollack, Michael C. Carroll, Susan Black, Stephen H. Leech, Cynthia Callaway, Stanley Harris, Patricia A. Ward, Jeffrey Morris, and J. Fielding Hejtmancik; Baylor College of Medicine/The Methodist Hospital, Houston, TX
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