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.
Chicago Style citaatKrawitz, 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 citatieKrawitz, 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.
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