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Congenital 21-hydroxylase deficiency as a new mutation: Detection during prenatal diagnosis by HLA typing and DNA analysis

Book ID: 121992847
Publisher: Elsevier Science
Year: 1986
Tongue: English
Weight: 78 KB
Volume: 17
Category: Article
ISSN: 0198-8859
DOI: 10.1016/0198-8859(86)90220-X

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