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Searched: Charcot-Marie-Tooth disease, axonal, type 20, Spinal muscular atrophy with lower extremity predominance and Mental retardation, autosomal dominant type 13 via the DYNC1H1 Gene
Search Results
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Test CodeMethodPrice11273Sequencing with CNV PGxome$9901038Sanger Sequencing$3660
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Test CodeMethodPrice10353Sequencing with CNV PGxome$990
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Test CodeMethodPrice10427Sequencing with CNV PGxome$990
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Test CodeMethodPrice16004Sequencing with CNV PGxome$1790
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Test CodeMethodPrice16006Sequencing with CNV PGxome$1790
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Test CodeMethodPrice2677Sequencing with CNV PGxome$990
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Test CodeMethodPrice11347Sequencing with CNV PGxome$990383Sanger Sequencing$940
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Test CodeMethodPrice12619Sequencing with CNV PGxome$1490
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Test CodeMethodPrice1794Sanger Sequencing$5808871Sequencing with CNV PGxome$990
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Test CodeMethodPrice10409Sequencing with CNV PGxome$990
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Test CodeMethodPrice7347Sequencing with CNV PGxome$1490
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Test CodeMethodPrice12675Sequencing with CNV PGxome$990
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Test CodeMethodPrice387Sanger Sequencing$4409177Sequencing with CNV PGxome$990
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Test CodeMethodPrice2136Sanger Sequencing$4909075Sequencing with CNV PGxome$990
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Test CodeMethodPrice11251Sequencing with CNV PGxome$990914Sanger Sequencing$1160
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Test CodeMethodPrice10419Sequencing with CNV PGxome$990
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Test CodeMethodPrice10375Sequencing with CNV PGxome$990
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