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1. Clinical and haplotypic variability of Slovenian USH2A patients homozygous for the c. 11864G>A nonsense mutation Andrej Zupan, Ana Fakin, Saba Battelino, Martina Jarc-Vidmar, Marko Hawlina, Crystel Bonnet, Christine Petit, Damjan Glavač, 2019, izvirni znanstveni članek Ključne besede: USH2A, haplotypic variability, homozygous mutation, usher syndrome, founder effect, haplotype analysis, high resolution melting analysis |
2. Genomic characterization of Serbian Holstein-Friesian cattle population Momčilo Šaran, Ljuba Štrbac, Dobrila Janković, Mihajla Djan, Snežana Trivunović, Minja Zorc, 2023, izvirni znanstveni članek Ključne besede: single nucleotide polymorphism, genetic diversity, genomic analysis, linkage disequilibrium, haplotype block |