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First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency). [electronic resource] by
- Speiser, P W
- Laforgia, N
- Kato, K
- Pareira, J
- Khan, R
- Yang, S Y
- Whorwood, C
- White, P C
- Elias, S
- Schriock, E
Producer: 19900510
In:
The Journal of clinical endocrinology and metabolism vol. 70
Availability: No items available.
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