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Searched: Complex Hereditary Spastic Paraplegia Sequencing Panel with CNV Detection
Search Results
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Test CodeMethodPrice2677Sequencing with CNV PGxome$990
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Test CodeMethodPrice2673Sequencing with CNV PGxome$1290
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Test CodeMethodPrice2679Sequencing with CNV PGxome$990
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Test CodeMethodPrice13055Sequencing with CNV PGxome$9902836Sanger Sequencing$780
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Test CodeMethodPrice4355Sequencing with CNV PGxome$990
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…variants (CNVs). This panel will detect all these variant types. Notably, the vast majority of CNVs, including 16p11.2 deletion syndrome and Smith-Magenis syndrome (17p11.2) will be detected. This panel is not designed to diagnose Prader…
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Test CodeMethodPrice11157Sequencing with CNV PGxome$990
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Test CodeMethodPrice11707Sequencing with CNV PGxome$9902169Sanger Sequencing$990
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Test CodeMethodPrice10331Sequencing with CNV PGxome$990
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Test CodeMethodPrice4895Sequencing with CNV PGxome$990
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Test CodeMethodPrice4903Sequencing with CNV PGxome$990
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Test CodeMethodPrice2494Sanger Sequencing$6108799Sequencing with CNV PGxome$990
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Test CodeMethodPrice5403Sequencing with CNV PGxome$990
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Test CodeMethodPrice5401Sequencing with CNV PGxome$990
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Test CodeMethodPrice5405Sequencing with CNV PGxome$990
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Test CodeMethodPrice2859Sanger Sequencing$8704373Sequencing with CNV PGxome$990
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Test CodeMethodPrice15299Sequencing with CNV PG-Select$990
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Test CodeMethodPrice5477Sequencing with CNV PG-Select$990
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Test CodeMethodPrice2846Sanger Sequencing$8408315Sequencing with CNV PGxome$990
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Test CodeMethodPrice2847Sanger Sequencing$6108801Sequencing with CNV PGxome$990
RESULTS KEY
- Tests & Panels
- Categories
- Newsroom
- Custom panels
- Pages & Documents
- Webinars