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Searched: Stickler Syndrome Type III, Otospondylomegaepiphyseal Dysplasia, Weissenbacher-Zweymuller Syndrome, and Deafness, Autosomal Dominant 13 via the COL11A2 Gene
Search Results
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Test CodeMethodPrice11189Sequencing with CNV PGxome$990829Sanger Sequencing$2040
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Test CodeMethodPrice11191Sequencing with CNV PGxome$990788Sanger Sequencing$2020
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Test CodeMethodPrice7947Sequencing with CNV PGxome$1290
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Test CodeMethodPrice10271Sequencing with CNV PGxome$990
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Test CodeMethodPrice15487Sequencing with CNV PGxome$1290
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Test CodeMethodPrice5063Sequencing with CNV PGxome$1290
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Test CodeMethodPrice10247Sequencing with CNV PGxome$990
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Test CodeMethodPrice11205Sequencing with CNV PGxome$990817Sanger Sequencing$1290
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Test CodeMethodPrice11203Sequencing with CNV PGxome$990805Sanger Sequencing$1830
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Test CodeMethodPrice13065Sequencing with CNV PGxome$1290
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Test CodeMethodPrice10631Sequencing with CNV PGxome$1790
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Test CodeMethodPrice12005Sequencing with CNV PGxome$1790
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Test CodeMethodPrice10657Sequencing with CNV PGxome$1290
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Test CodeMethodPrice4379Sequencing with CNV PGxome$1790
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Test CodeMethodPrice11187Sequencing with CNV PGxome$990831Sanger Sequencing$2490
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Test CodeMethodPrice3091Sequencing with CNV PG-Select$990
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Test CodeMethodPrice11367Sequencing with CNV PGxome$990
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Test CodeMethodPrice10383Sequencing with CNV PGxome$1290
RESULTS KEY
- Tests & Panels
- Categories
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- Pages & Documents
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