SPEISER, PW, LAFORGIA, N, KATO, K
et al. (1990). 1ST TRIMESTER PRENATAL TREATMENT AND MOLECULAR GENETIC DIAGNOSIS OF CONGENITAL ADRENAL-HYPERPLASIA (21-HYDROXYLASE DEFICIENCY)
.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 70(4), 838-848. 10.1210/jcem-70-4-838
SPEISER, PW, LAFORGIA, N, KATO, K et al. (1990). 1ST TRIMESTER PRENATAL TREATMENT AND MOLECULAR GENETIC DIAGNOSIS OF CONGENITAL ADRENAL-HYPERPLASIA (21-HYDROXYLASE DEFICIENCY)
. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 70(4), 838-848. 10.1210/jcem-70-4-838