Wedell, A., Ritzén, E. M., Haglund-Stengler, B., & Luthman, H. (1992). Steroid 21-hydroxylase deficiency: Three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations.
Styl ChicagoWedell, A., E M. Ritzén, B. Haglund-Stengler, a H. Luthman. Steroid 21-hydroxylase Deficiency: Three Additional Mutated Alleles and Establishment of Phenotype-genotype Relationships of Common Mutations. 1992.
Citace podle MLAWedell, A., E M. Ritzén, B. Haglund-Stengler, a H. Luthman. Steroid 21-hydroxylase Deficiency: Three Additional Mutated Alleles and Establishment of Phenotype-genotype Relationships of Common Mutations. 1992.
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