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Dive into the research topics of 'Detection of the heterozygous state in siblings of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency'. Together they form a unique fingerprint.- Sort by
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James P. Gutai, Peter A. Lee, Roger E. Johnsonbaugh, Frank Gareis, Maria D. Urban, Claude J. Migeon
Research output: Contribution to journal › Article › peer-review