First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency)

P. W. Speiser, N. Laforgia, K. Kato, J. Pareira, R. Khan, S. Y. Yang, C. Whorwood, P. C. White, S. Elias, E. Schriock, E. Schriock, J. L. Simpson, M. Taslimi, J. Najjar, S. May, G. Mills, C. Crawford, M. I. New