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Searched: Brugada Syndrome via SLMAP Gene Sequencing with CNV Detection
Search Results
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Test CodeMethodPrice11693Sequencing with CNV PGxome$990
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Test CodeMethodPrice10329Sequencing with CNV PGxome$990
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Test CodeMethodPrice1017Sanger Sequencing$5808845Sequencing with CNV PGxome$990
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Test CodeMethodPrice1011Sanger Sequencing$7109955Sequencing with CNV PGxome$990
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Test CodeMethodPrice10423Sequencing with CNV PGxome$990
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Test CodeMethodPrice1016Sanger Sequencing$3509247Sequencing with CNV PGxome$990
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Test CodeMethodPrice11417Sequencing with CNV PGxome$990
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Test CodeMethodPrice11131Sequencing with CNV PGxome$9901013Sanger Sequencing$1020
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Test CodeMethodPrice2488Sanger Sequencing$5403977Sequencing with CNV PGxome$990
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Test CodeMethodPrice11127Sequencing with CNV PGxome$990
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…the SCN3B Gene Test Code Method Price 1017 Sanger Sequencing $580 8845 Sequencing with CNV PGxome $990 Brugada Syndrome via the SLMAP Gene Test Code Method Price 11693 Sequencing with CNV PGxome $990 Brunner Syndrome via the MAOA Gene Test…
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…Price 1017 Sanger Sequencing $580 8845 Sequencing with CNV PGxome $990 Brugada Syndrome via the SLMAP Gene Test Code Method Price 11693 Sequencing with CNV PGxome $990 Brunner Syndrome via the MAOA Gene Test Code Method Price 10697…
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Test CodeMethodPrice11123Sequencing with CNV PGxome$9901012Sanger Sequencing$2110
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Test CodeMethodPrice2663Sequencing with CNV PGxome$1290
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Test CodeMethodPrice3113Sequencing with CNV PG-Select$990
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Test CodeMethodPrice11369Sequencing with CNV PGxome$990947Sanger Sequencing$960
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Test CodeMethodPrice13008Sequencing with CNV PGxome$1790
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…contributors to non-syndromic obesity control energy balance via the leptin-melanocortin signaling pathway (LEP, LEPR, POMC, PCSK1, and MC4R). Several cell-signaling genes interact with this pathway peripherally or influence the development…
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Test CodeMethodPrice2609Sequencing with CNV PGxome$990
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…Syndrome Panel Brugada Syndrome Panel Kabuki Syndrome Panel Holt-Oram Syndrome (HOS) Testing via TBX5 Sequencing Noonan Spectrum Disorders/Rasopathies Panel For those who prefer genomes or exomes rather than defined panels, PreventionGenetics…
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