P

    p16(D9S1749-D9S1752)/CEP9 Single locus probes
    p16(D9S1749-D9S1752)/CEP9 Single locus probes
    PAX3 Breakapart
    PAX3 Breakapart
    PDGFRA /LNX/ SCFD2 Breakapart
    PDGFRA /LNX/ SCFD2 Breakapart
    PDGFRB Breakapart
    PDGFRB Breakapart
    Peptidylprolyl Isomerase B (cyclophilin B) PPIB
    Peptidylprolyl Isomerase B (cyclophilin B) PPIB
    Peroxisomal Biogenesis Disorders – Zellweger Syndrome Spectrum (PEX1, PEX6, PEX10, PEX12, PEX26)
    Peroxisomal Biogenesis Disorders – Zellweger Syndrome Spectrum (PEX1, PEX6, PEX10, PEX12, PEX26)
    Phosphoglycerate Mutase (muscle deficiency)
    Phosphoglycerate Mutase (muscle deficiency)
    PIK3CA (Phosphatidylinositol 3- kinase, catalytic, alpha polypeptide)
    PIK3CA (Phosphatidylinositol 3- kinase, catalytic, alpha polypeptide)
    PIK3CA Single locus probe
    PIK3CA Single locus probe
    PKD1/2 Multiplex Ligation Probe-dependent Amplification (MLPA)
    PKD1/2 Multiplex Ligation Probe-dependent Amplification (MLPA)
    Platelet-type pseudo von Willebrand Disease (GP1BA gene)
    Platelet-type pseudo von Willebrand Disease (GP1BA gene)
    PML/RARA Dual Fusion
    PML/RARA Dual Fusion
    Polycystic Kidney Disease (autosomal dominant) PKD1 & PKD 2 genes
    Polycystic Kidney Disease (autosomal dominant) PKD1 & PKD 2 genes
    PROSTATE PANEL Mix 1 – TMPRSS2/ERG Breakapart Mix 2 - PTEN/CEP10 Single locus probes
    PROSTATE PANEL Mix 1 – TMPRSS2/ERG Breakapart Mix 2 - PTEN/CEP10 Single locus probes
    Protein C Deficiency
    Protein C Deficiency
    Protein S Deficiency
    Protein S Deficiency
    Prothrombin (3’ non 20210G>A prothrombin variants)
    Prothrombin (3’ non 20210G>A prothrombin variants)
    Pseudoxanthoma Elasticum
    Pseudoxanthoma Elasticum
    PTEN/CEP10 Single locus probes
    PTEN/CEP10 Single locus probes
    Sections
    Tests
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