Society for fetal urology panel discussion: Prenatal diagnosis and treatment of genital anomalies

Urology

Volumn 53, Issue 5, 1999, Pages 1029-1031

  Baskin, Laurence S ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GROWTH FACTOR; HORMONE; RECEPTOR; STEROID; STEROID 21 MONOOXYGENASE; TESTIS DETERMINING FACTOR;

CONGENITAL ADRENAL HYPERPLASIA; ECHOGRAPHY; GENE; GENITAL MALFORMATION; HUMAN; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW; SEX DETERMINATION; SEXUAL DEVELOPMENT; X CHROMOSOME; Y CHROMOSOME;

EID: 0033005502     PISSN: 00904295     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0090-4295(99)00082-5     Document Type: Article

References (8)

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7. Spieser P., Laforgia N., Kato K., et al. First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency). J Clin Endocrinol Metab. 70:1990;838-848.
8. Miller W. Prenatal treatment of congenital adrenal hyperplasia - a promising experimental therapy of unproven safety. Trends Endocrinol Metab. 9:1998;290-293.