Cited by 27Sexual Differentiation and DisordersAdrenal Hormones and DisordersOvarian function and disorders

Prenatal treatment of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency: European experience in 223 pregnancies at risk

Forest, M G, Dörr, H G·1993·Pediatric Research

Integrity signals

Registry

Crossref · 10.1203/00006450-199305001-00011

Cites

Statistics

Recomputing p-values needs the paper’s full text.

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Authors
Forest, M. G., & Dörr, H. G.
Affiliations
Inserm (FR)
Venue
Pediatric Research
Published
1993-05
Volume
33
Pages
S3-S3
ISSN
  • 0031-3998 (ISSN-L)
  • 1530-0447
OpenAlex
W2050208514
Cited by
23
References
0
Citations by year
2021: 1 · 2019: 1 · 2014: 1 · 2012: 1
FWCI
0.64
Type
journal article
Language
en
Open access
closed
Locations
Pediatric Research (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
  • Health Sciences › Medicine › Reproductive Medicine › Ovarian function and disorders
Keywords
congenital adrenal hyperplasia, 21-hydroxylase deficiency, fetal therapy, prenatal diagnosis, chorionic villus sampling, HLA typing, fetal virilization, external genitalia, pregnancy outcomes, maternal side effects

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