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1. A de novo variant in OTX2 in a lamb with otocephaly Julia Maria Paris, Anna Letko, Irene Monika Häflinger, Tanja Švara, Mitja Gombač, Primož Klinc, Andrej Škibin, Estera Pogorevc, Cord Drögemüller, 2020, drugi znanstveni članki Ključne besede: Agnathia, microstomia, precision medicine, rare disease, synotia, whole-genome sequencing, sheep |
2. Diagnostics of genetic disorders with whole genome and mRNA sequencing Gaber Bergant, 2025, doktorska disertacija Ključne besede: genetic diagnostics, genome sequencing, next-generation sequencing, rare disease, RNA sequencing |
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