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Comments to “A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency”

✍ Scribed by Coeli-Lacchini, Fernanda Borchers; Turatti, Wendy; Elias, Paula Conde Lamparelli; Elias, Lucila Leico Kagohara; Martinelli, Carlos Eduardo; Moreira, Ayrton Custodio; Antonini, Sonir Roberto; de Castro, Margaret

Book ID: 123454318
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 195 KB
Volume: 534
Category: Article
ISSN: 0378-1119
DOI: 10.1016/j.gene.2013.09.109

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