First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) Article
Speiser, PW, Laforgia, N, Kato, K et al. (1990). First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)
. 70(4), 838-848. 10.1210/jcem-70-4-838