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Clinical Genomics Test Requisition Form
Clinical Genomics Requisition
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Newborn screening follow-up requisition
This form is useful to order follow-up testing once newborn screening is completed
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Brochure for cytokine assays portfolio
This leaflet presents the analytical performances of each assay, the associated standard curve* and the list of available references.
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Whole Exome Sequencing - Secondary Findings - Carrier Status
Flyer contains carrier status genes as secondary findings; Carrier status tests can detect genetic changes that can cause hereditary disorders in future generations.
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PhenoVue Hoechst 33342 Nuclear Stain Product Information Sheet
Product Information Sheet for PhenoVue Hoechst 33342 Nuclear Stain
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PhenoVue HypoxiTRAK, Hypoxia Indicator Product Sheet
PhenoVue HypoxiTRAK, Hypoxia Indicator Product Sheet
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PhenoVue DRAQ7, Dead Cell Nuclear Stain Product Sheet
Product Information Sheet for PhenoVue DRAQ7, Dead Cell Nuclear Stain
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PhenoPlate 384-well Product Information Sheet
Product information sheet for PhenoPlate 384-well microplates.
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PhenoPlate 96-well Product Information Sheet
Product information sheet for PhenoPlate 96-well microplates.
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Comprehensive genetic testing gives a high diagnostic yield in the Indian sub-continent compared to the western population
The diagnostic yield achieved through Focused exome sequencing in Indian patients is high. Revvity Omics' Focused exome Sequencing's proprietary bioinformatics pipelines helps in enhanced detection of sequencing variants (SNVs), copy number variants (CNVs) and mitochondrial DNA (mtDNA) in a single assay making it the most comprehensive testing options available in Indian markets.
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Genetic testing for APOB, LDLR, PCSK9, and LDLRAP1 suggest that FH testing may be underutilized
This eposter highlights the prevalence of Familial hypercholesterolemia, to inform of disease risk and response to treatment, leading to positive health outcomes for patients and their families.
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Shining a light on diagnosis of rare genetic disorders: the lantern project
The study helps to identify a larhger patient pool with potential to attract more interest in these rare disorders, increaing the developmental landscape of alternative therapies.
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