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.
استشهاد بنمط شيكاغوWedell, A., E M. Ritzén, B. Haglund-Stengler, و H. Luthman. Steroid 21-hydroxylase Deficiency: Three Additional Mutated Alleles and Establishment of Phenotype-genotype Relationships of Common Mutations. 1992.
MLA استشهادWedell, A., E M. Ritzén, B. Haglund-Stengler, و H. Luthman. Steroid 21-hydroxylase Deficiency: Three Additional Mutated Alleles and Establishment of Phenotype-genotype Relationships of Common Mutations. 1992.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.