PRENATAL-DIAGNOSIS WITH MOLECULAR PROBES AND SUCCESSFUL TREATMENT OF CLASSICAL STEROID 21-HYDROXYLASE DEFICIENCY (CAH) Conference

LAFORGIA, N, YANG, SY, KHAN, R et al. (1989). PRENATAL-DIAGNOSIS WITH MOLECULAR PROBES AND SUCCESSFUL TREATMENT OF CLASSICAL STEROID 21-HYDROXYLASE DEFICIENCY (CAH) . PEDIATRIC RESEARCH, 25(4), A87-A87.

cited authors

  • LAFORGIA, N; YANG, SY; KHAN, R; KATO, K; WHITE, PC; ELIAS, S; SCHRIOCK, E; SCHRIOCK, E; SPEISER, PW; SIMPSON, JL; NEW, MI

sustainable development goals

authors

publication date

  • April 1, 1989

published in

keywords

  • Life Sciences & Biomedicine
  • Pediatrics
  • Science & Technology

publisher

  • WILLIAMS & WILKINS

start page

  • A87

end page

  • A87

volume

  • 25

issue

  • 4