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Mutation-haplotype analysis of steroid 21-hydroxylase (CYP21) deficiency in Finland. Implications for the population history of defective alleles

✍ Scribed by Antti Levo; Jukka Partanen


Publisher
Springer
Year
1997
Tongue
English
Weight
88 KB
Volume
99
Category
Article
ISSN
0340-6717

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