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Searched: Congenital Central Hypoventilation Syndrome (CCHS) via PHOX2B Gene Sequencing with CNV Detection
Search Results
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Test CodeMethodPrice8967Sequencing with CNV PG-Select$990
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Test CodeMethodPrice10239Sequencing with CNV PGxome$990
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Test CodeMethodPrice777Sanger Sequencing$5408963Sequencing with CNV PGxome$990
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Test CodeMethodPrice1834Sanger Sequencing$5408965Sequencing with CNV PGxome$990
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Test CodeMethodPrice2161Sanger Sequencing$6108733Sequencing with CNV PGxome$990
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Test CodeMethodPrice15149Sequencing with CNV PG-Select$990
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Test CodeMethodPrice8993Sequencing with CNV PG-Select$990
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Test CodeMethodPrice1566Sanger Sequencing$5408995Sequencing with CNV PGxome$990
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Test CodeMethodPrice7383Sequencing with CNV PGxome$1790
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Test CodeMethodPrice7985Sequencing with CNV PG-Select$990
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Test CodeMethodPrice10225Sequencing with CNV PGxome$990
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Test CodeMethodPrice4383Sequencing with CNV PG-Select$990
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Test CodeMethodPrice5057Sequencing with CNV PGxome$990
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Test CodeMethodPrice11225Sequencing with CNV PGxome$990382Sanger Sequencing$1650
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Test CodeMethodPrice1471Sanger Sequencing$58011007Sequencing with CNV PGxome$990
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Test CodeMethodPrice11389Sequencing with CNV PGxome$9901510Sanger Sequencing$1130
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