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    ← Guides & Articles

    Blogs

    Guides, explainers, and the latest thinking on pediatric genetic health from the Fore Genomics team.

    • Comparing DNA Tests for Rare Disease Diagnosis: A Simplified Explanation
    • A Solution for Adverse Drug Reactions
    • How is Fore Genomics’ Pediatric Genetic Health Screening Unique?
    • Empowered by Knowledge: Genetic Disorders with Manageable Treatment Options
    • Newborn Genome Sequencing: New Study On Rare Diseases
    • Navigating Family Healthcare: Precision Medicine Solutions
    Comparing DNA Tests for Rare Disease Diagnosis
    A Solution for Adverse Drug Reactions
    How is Fore Genomics’ Screening Unique?
    Empowered by Knowledge: Manageable Genetic Disorders
    Newborn Genome Sequencing: New Study On Rare Diseases
    Navigating Family Healthcare: Precision Medicine Solutions

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    Fore screens for 1,000+ clinically actionable childhood conditions with an at-home cheek swab.

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    These tests were developed and performance characteristics were determined by Fore Genomics, Inc. in collaboration with Fore’s service providers. The US Food and Drug Administration (FDA) has not approved or cleared these tests; however, FDA clearance approval is not currently required for clinical use. These tests are used for clinical purposes, and therefore validation was done as required under the requirements of the Clinical Laboratory Improvement Act (CLIA) of 1988. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions. The chance of a false negative or a false-positive result due to laboratory error cannot be completely excluded. These results should not be regarded as investigational or for research.

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