APA citiranje

Krawitz, P. M., Schiska, D., Krüger, U., Appelt, S., Heinrich, V., Parkhomchuk, D., . . . Gross, M. (2014). Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndrome. Blackwell Publishing Ltd.

Citação norma Chicago

Krawitz, Peter M., et al. Screening for Single Nucleotide Variants, Small Indels and Exon Deletions With a Next-generation Sequencing Based Gene Panel Approach for Usher Syndrome. Blackwell Publishing Ltd, 2014.

MLA citiranje

Krawitz, Peter M., et al. Screening for Single Nucleotide Variants, Small Indels and Exon Deletions With a Next-generation Sequencing Based Gene Panel Approach for Usher Syndrome. Blackwell Publishing Ltd, 2014.