Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene.
- DOI
- 10.6065/apem.2346014.007
- Published
- 2024 Feb
- Container
- Annals of pediatric endocrinology & metabolism
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.6065/apem.2346014.007,
title = {Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene.},
author = {Yoon JH and Hwang S and Kim JH and Kim GH and Yoo HW and Choi JH},
year = {2024},
journal = {Annals of pediatric endocrinology \& metabolism},
doi = {10.6065/apem.2346014.007},
url = {https://doi.org/10.6065/apem.2346014.007}
}RIS
TY - JOUR TI - Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene. AU - Yoon JH AU - Hwang S AU - Kim JH AU - Kim GH AU - Yoo HW AU - Choi JH PY - 2024 JO - Annals of pediatric endocrinology & metabolism DO - 10.6065/apem.2346014.007 UR - https://doi.org/10.6065/apem.2346014.007 ER -
APA
JH, Y., S, H., JH, K., GH, K., HW, Y., & JH, C. (2024). Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency through molecular genetic analysis of the CYP21A2 gene.. Annals of pediatric endocrinology & metabolism. https://doi.org/10.6065/apem.2346014.007
Source records
- pubmed · retrieved 2026-09-24T21:01:09.806Z
- europe-pmc · retrieved 2026-09-24T21:01:09.830Z