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Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency
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- Nordenstrom, A (author)
- Karolinska Institutet
- Thilen, A (author)
- Hagenfeldt, L (author)
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- The Endocrine Society, 1999
- 1999
- English.
- In: The Journal of clinical endocrinology and metabolism. - : The Endocrine Society. - 0021-972X. ; 84:5, s. 1505-1509
- Journal article (peer-reviewed)
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- Nordenstrom, A
- Thilen, A
- Hagenfeldt, L
- Larsson, A
- Wedell, A
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