Speiser, PW, Laforgia, N, Kato, K
et al. (1990). First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)
.
OBSTETRICAL & GYNECOLOGICAL SURVEY, 45(10), 707-709. 10.1097/00006254-199010000-00020
Speiser, PW, Laforgia, N, Kato, K et al. (1990). First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)
. OBSTETRICAL & GYNECOLOGICAL SURVEY, 45(10), 707-709. 10.1097/00006254-199010000-00020