APA

Harteveld C. L., van Helden W. C. H., Boxma G. L., van Delft P., Bakker-Verweij M., Wajcman H., Zanella-Cleon I., Becchi M. & Giordano P. C. (20071005). Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype. : Hemoglobin.

Chicago

Harteveld Cornelis L, van Helden Willem C H, Boxma George L, van Delft Peter, Bakker-Verweij Margaretha, Wajcman Henri, Zanella-Cleon Isabelle, Becchi Michel and Giordano Piero C. 20071005. Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype. : Hemoglobin.

Harvard

Harteveld C. L., van Helden W. C. H., Boxma G. L., van Delft P., Bakker-Verweij M., Wajcman H., Zanella-Cleon I., Becchi M. and Giordano P. C. (20071005). Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype. : Hemoglobin.

MLA

Harteveld Cornelis L, van Helden Willem C H, Boxma George L, van Delft Peter, Bakker-Verweij Margaretha, Wajcman Henri, Zanella-Cleon Isabelle, Becchi Michel and Giordano Piero C. Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype. : Hemoglobin. 20071005.