Mutation-haplotype analysis of steroid 21-hydroxylase (CYP21) deficiency in Finland. Implications for the population history of defective alleles (Q47797169)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutation-haplotype analysis of steroid 21-hydroxylase (CYP21) deficiency in Finland. Implications for the population history of defective alleles |
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Mutation-haplotype analysis of steroid 21-hydroxylase (CYP21) deficiency in Finland. Implications for the population history of defective alleles (English)
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A Levo
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1 April 1997
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99
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4
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488-497
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