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Dive into the research topics of 'First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)'. Together they form a unique fingerprint.- Sort by
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Phyllis W. Speiser, Nicola Laforgia, Koji Kato, Judith Pareira, Rafiya Khan, Soo Young Yang, Christopher Whorwood, Perrin C. White, Sherman Elias, Elizabeth Schriock, Eldon Schriock, Joe Leigh Simpson, Mark Taslimi, Jennifer Najjar, Steven May, Gary Mills, Christopher Crawford, Maria I. New
Research output: Contribution to journal › Article › peer-review