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Genetic Testing

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  • Amniotic Fluid Karyotype Test

    Amniotic Fluid Karyotype Test – Prenatal Chromosomal Analysis for Genetic Disorders

    2.150,00 د.إ

    The Amniotic Fluid Karyotype Test detects chromosomal abnormalities like Down syndrome. Accurate results in 30 days. Book your prenatal test with Lab Tests Dubai.

    Sample Type : Amiotic Fluid

    Methodology : Conventional Cytogenetics: Culture + Chromosome analysis

    TAT : 30 Days

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  • Centoscreen (Duo)

    Centoscreen (Duo)

    9.120,00 د.إ

    Sample Type : EDTA blood
    Methodology : NGS
    TAT : 15 Days

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  • Chromosomal Studies - Blood Karyotype

    Chromosomal Studies – Blood Karyotype

    2.150,00 د.إ

    Sample Type : Whole Blood
    Methodology : Conventional Cytogenetics: Culture + Chromosome analysis
    TAT : 30 Days

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  • HLA Typing - B5 (PCR)

    HLA Typing – B5 (PCR)

    1.250,00 د.إ

    Sample Type : Whole Blood
    Methodology : Real-time PCR
    TAT : 10 Days

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  • MTHFR C677T Gene Mutation Test – DNA Analysis for Genetic Health Insights

    MTHFR C677T Gene Mutation Test – DNA Analysis for Genetic Health Insights

    1.600,00 د.إ

    The MTHFR Mutation (C677T) Analysis is a genetic test that identifies the presence of the C677T variant in the MTHFR gene, which can impact folate metabolism and homocysteine levels. Key features include accurate DNA analysis using a simple saliva or cheek swab sample, fast turnaround time, and clear, actionable results. Benefits include personalized insights into potential health risks such as cardiovascular issues, fertility challenges, and neurological conditions, enabling targeted lifestyle and nutritional interventions. Its unique selling point lies in empowering individuals with genetic knowledge to make informed health decisions and optimize wellness through precision nutrition.

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  • Oncomine Comprehensive myeloid/ Leukemia Panel (DNA + RNA fusions)

    Oncomine Comprehensive myeloid/ Leukemia Panel (DNA + RNA fusions)

    5.500,00 د.إ

    The Oncomine Comprehensive Myeloid/Leukemia Panel (DNA + RNA fusions) is a next-generation sequencing (NGS) assay designed for comprehensive genomic profiling of myeloid malignancies and leukemias. It simultaneously analyzes DNA and RNA to detect key mutations, copy number variations, and gene fusions across a broad range of clinically relevant genes.

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