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) . OBSTETRICAL & GYNECOLOGICAL SURVEY, 45(10), 707-709. 10.1097/00006254-199010000-00020

cited authors

  • Speiser, PW; Laforgia, N; Kato, K; Pareira, J; Khan, R; Yang, SY; Whorwood, C; White, PC; Elias, S; Schriock, E; Schriock, E; Simpson, JL; Taslimi, M; Najjar, J; May, S; Mills, G; Crawford, C; New, MI

authors

publication date

  • January 1, 1990

published in

Digital Object Identifier (DOI)

start page

  • 707

end page

  • 709

volume

  • 45

issue

  • 10