Prenatal diagnosis with molecular probes and successful treatment of classical steroid 21 hydroxylase deficiency (CAH) Meeting Abstract


Authors: Laforgia, N.; Yang, S. Y.; Khan, R.; Kato, K.; White, P. C.; Elias, S.; Schriock, E.; Schriock, E.; Speiser, P. W.; Simpson, J. L.; New, M. I.
Abstract Title: Prenatal diagnosis with molecular probes and successful treatment of classical steroid 21 hydroxylase deficiency (CAH)
Meeting Title: Meeting of the American Pediatric Society and the Society for Pediatric Research
Journal Title: Pediatric Research
Volume: 25
Issue: 4 Pt. 2
Meeting Dates: 1989 May 1-4
Meeting Location: Washington, DC
ISSN: 0031-3998
Publisher: Int Pediatric Research Foundation, Inc  
Date Published: 1989-04-01
Start Page: A87
Language: English
ACCESSION: WOS:A1989T947100506
PROVIDER: wos
PUBMED: 2927977
Notes: Meeting Abstract: 505 -- Source: Wos
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MSK Authors
  1. Soo Y Yang
    108 Yang