1ST TRIMESTER PRENATAL TREATMENT AND MOLECULAR GENETIC DIAGNOSIS OF CONGENITAL ADRENAL-HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) Article

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 and Metabolism (JCEM), 70(4), 838-848. 10.1210/jcem-70-4-838

Open Access

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

sustainable development goals

authors

publication date

  • April 1, 1990

published in

keywords

  • Endocrinology & Metabolism
  • Life Sciences & Biomedicine
  • Science & Technology

Digital Object Identifier (DOI)

start page

  • 838

end page

  • 848

volume

  • 70

issue

  • 4