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#NOVA-6003-16 / #6003-16Simplifies the identification of relevant single nucleotide variants (SNVs), small insertion and deletions (indels), and copy number variants (CNVs) in more than 75 genes.
NEXTflex® Targeted NGS Hybridization Panel 1 - This Targeted NGS Hybridization Panel 1 simplifies the identification of relevant single nucleotide variants (SNVs), small insertion and deletions (indels), and
copy number variants (CNVs) in more than 75 genes related to endocrine and metabolic disorders, hemoglobinopathies, and primary immunodeficiencies.
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.