A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype.

MLA

Hergersberg, M., et al. “A New Mutation, 3905insT, Accounts for 4.8% of 1173 CF Chromosomes in Switzerland and Causes a Severe Phenotype.” Human Genetics, vol. 100, no. 2, Aug. 1997, pp. 220–23. EBSCOhost, https://doi.org/10.1007/s004390050494.

APA

Hergersberg, M., Balakrishnan, J., Bettecken, T., Chevalier-Porst, F., Brägger, C., Burger, R., Einschenk, I., Liechti-Gallati, S., Morris, M., Schorderet, D., Thonney, F., Moser, H., & Malik, N. (1997). A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype. Human Genetics, 100(2), 220–223. https://doi.org/10.1007/s004390050494

Chicago

Hergersberg, M, J Balakrishnan, T Bettecken, F Chevalier-Porst, C Brägger, R Burger, I Einschenk, et al. 1997. “A New Mutation, 3905insT, Accounts for 4.8% of 1173 CF Chromosomes in Switzerland and Causes a Severe Phenotype.” Human Genetics 100 (2): 220–23. doi:10.1007/s004390050494.