Rančelis, T. (2013). Next-generation whole-exome sequencing contribution to identification of rare autosomal recessive diseases. Vilniaus Universitetas.
Chicago Style (17th ed.) CitationRančelis, Tautvydas. Next-generation Whole-exome Sequencing Contribution to Identification of Rare Autosomal Recessive Diseases. Vilniaus Universitetas, 2013.
MLA (9th ed.) CitationRančelis, Tautvydas. Next-generation Whole-exome Sequencing Contribution to Identification of Rare Autosomal Recessive Diseases. Vilniaus Universitetas, 2013.
Warning: These citations may not always be 100% accurate.