APA

Speiser P. W., Laforgia N., Kato K., Pareira J., Khan R., Yang S. Y., Whorwood C., White P. C., Elias S. & Schriock E. (19900510). First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency). : The Journal of clinical endocrinology and metabolism.

Chicago

Speiser P W, Laforgia N, Kato K, Pareira J, Khan R, Yang S Y, Whorwood C, White P C, Elias S and Schriock E. 19900510. First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency). : The Journal of clinical endocrinology and metabolism.

Harvard

Speiser P. W., Laforgia N., Kato K., Pareira J., Khan R., Yang S. Y., Whorwood C., White P. C., Elias S. and Schriock E. (19900510). First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency). : The Journal of clinical endocrinology and metabolism.

MLA

Speiser P W, Laforgia N, Kato K, Pareira J, Khan R, Yang S Y, Whorwood C, White P C, Elias S and Schriock E. First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency). : The Journal of clinical endocrinology and metabolism. 19900510.