APA način citiranja

Walsh, T., Shahin, H., Elkan-Miller, T., Lee, M. K., Thornton, A. M., Roeb, W., . . . Kanaan, M. (2010). Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82. Elsevier.

Čikaški stil citiranja

Walsh, Tom, et al. Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 As the Cause of Nonsyndromic Hearing Loss DFNB82. Elsevier, 2010.

MLA način citiranja

Walsh, Tom, et al. Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 As the Cause of Nonsyndromic Hearing Loss DFNB82. Elsevier, 2010.