Mutation analysis for prenatal diagnosis and heterozygote detection of Gaucher disease type III (Norrbottnian type).

MLA

Dahl, Niklas, et al. “Mutation Analysis for Prenatal Diagnosis and Heterozygote Detection of Gaucher Disease Type III (Norrbottnian Type).” Prenatal Diagnosis, vol. 12, no. 7, July 1992, pp. 603–08. EBSCOhost, https://doi.org/10.1002/pd.1970120706.

APA

Dahl, N., Wadelius, C., Annerén, G., Gustavson, K.-H., Dahl, N., Wadelius, C., Annerén, G., & Gustavson, K. H. (1992). Mutation analysis for prenatal diagnosis and heterozygote detection of Gaucher disease type III (Norrbottnian type). Prenatal Diagnosis, 12(7), 603–608. https://doi.org/10.1002/pd.1970120706

Chicago

Dahl, Niklas, Claes Wadelius, Göran Annerén, Karl-Henrik Gustavson, N Dahl, C Wadelius, G Annerén, and K H Gustavson. 1992. “Mutation Analysis for Prenatal Diagnosis and Heterozygote Detection of Gaucher Disease Type III (Norrbottnian Type).” Prenatal Diagnosis 12 (7): 603–8. doi:10.1002/pd.1970120706.