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Searched: Comprehensive Neuromuscular Sequencing Panel with CNV Detection
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Test CodeMethodPrice10433Sequencing with CNV PGxome$1290
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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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…for specific neuromuscular disorders (NMDs) including Congenital Myopathy, Limb-Girdle Muscular Dystrophy, and Myofibrillar Myopathy. A 124 gene Comprehensive Neuromuscular Panel as well as a 83 gene Metabolic Myopathies, Rhabdomyolysis…
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Test CodeMethodPrice10427Sequencing with CNV PGxome$990
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Test CodeMethodPrice12001Sequencing with CNV PGxome$1290
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Test CodeMethodPrice2663Sequencing with CNV PGxome$1290
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Test CodeMethodPrice7941Sequencing with CNV PGxome$990
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Test CodeMethodPrice10423Sequencing with CNV PGxome$990
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Test CodeMethodPrice12619Sequencing with CNV PGxome$1490
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Test CodeMethodPrice15185Sequencing with CNV PG-Select$990
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Test CodeMethodPrice11477Sequencing with CNV PGxome$990406Sanger Sequencing$930
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Test CodeMethodPrice4379Sequencing with CNV PGxome$1790
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Test CodeMethodPrice16004Sequencing with CNV PGxome$1790
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Test CodeMethodPrice12005Sequencing with CNV PGxome$1790
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Test CodeMethodPrice16005Sequencing with CNV PGxome$1790
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Test CodeMethodPrice2673Sequencing with CNV PGxome$1290
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Test CodeMethodPrice7003Sequencing with CNV PG-Select$990
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Test CodeMethodPrice4419Sanger Sequencing$7808373Sequencing with CNV PGxome$990
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Test CodeMethodPrice13008Sequencing with CNV PGxome$1790
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Test CodeMethodPrice10419Sequencing with CNV PGxome$990
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