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  1. 1.Detection and validation of subchromosomal aberrations detected as additional findings in routine noninvasive prenatal testing for common trisomies

    Detection and validation of subchromosomal aberrations detected as additional findings in routine noninvasive prenatal testing for common trisomies  / Martina Sekelská ... [et al.] .  Newslab : časopis laboratórnej medicíny. - ISSN 1338-9661 . - Roč. 10, č. 2 (2019), s. 69-[71]  : ilustr., fareb., obr.  
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  2. 2.Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions

    Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions  / Kucharik M. ... [et al.] .  Plos One . - Vol. 15 (2020), s. e0238245   [Dokument nie je vo fonde knižnice]
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  3. 3.Potenciál novej generácie sekvenovania pri skríningu Lynchovho syndrómu

    Potenciál novej generácie sekvenovania pri skríningu Lynchovho syndrómu  / Ondrej Pös, Mária Haršanyová, Tomáš Szemes .  Newslab : časopis laboratórnej medicíny. - ISSN 1338-9661 . - Roč. 9, č. 2 (2018), s. 125-[127]  : ilustr., fareb. grafy  
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