APA

Fransen E., Verstreken M., Verhagen W. I., Wuyts F. L., Huygen P. L., D'Haese P., Robertson N. G., Morton C. C., McGuirt W. T., Smith R. J., Declau F., Van de Heyning P. H. & Van Camp G. (19990914). High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. : Human molecular genetics.

Chicago

Fransen E, Verstreken M, Verhagen W I, Wuyts F L, Huygen P L, D'Haese P, Robertson N G, Morton C C, McGuirt W T, Smith R J, Declau F, Van de Heyning P H and Van Camp G. 19990914. High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. : Human molecular genetics.

Harvard

Fransen E., Verstreken M., Verhagen W. I., Wuyts F. L., Huygen P. L., D'Haese P., Robertson N. G., Morton C. C., McGuirt W. T., Smith R. J., Declau F., Van de Heyning P. H. and Van Camp G. (19990914). High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. : Human molecular genetics.

MLA

Fransen E, Verstreken M, Verhagen W I, Wuyts F L, Huygen P L, D'Haese P, Robertson N G, Morton C C, McGuirt W T, Smith R J, Declau F, Van de Heyning P H and Van Camp G. High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. : Human molecular genetics. 19990914.